PMID-sentid	Pub_year	Sent_text	comp_official_name	comp_offset	protein_name	organism	prot_offset
16665340-11	1987	The high affinity of ascorbate peroxidase for H(2)O(2) indicates that this enzyme, rather than catalase, is responsible for most H(2)O(2) removal outside of peroxisomes in root nodules.	Hydrogen Peroxide	46-54	peroxidase	Glycine max	31-41
16665340-2	1987	H(2)O(2) may be removed from root nodules in a series of enzymic reactions involving ascorbate peroxidase, dehydroascorbate reductase, and glutathione reductase.	Hydrogen Peroxide	0-8	peroxidase	Glycine max	95-105
16665340-11	1987	The high affinity of ascorbate peroxidase for H(2)O(2) indicates that this enzyme, rather than catalase, is responsible for most H(2)O(2) removal outside of peroxisomes in root nodules.	Hydrogen Peroxide	129-137	peroxidase	Glycine max	31-41
6811509-1	1982	Peroxidase-labelled lectins specific for various carbohydrate residues were used as histochemical reagents in the investigation of Hurler"s syndrome.	Carbohydrates	49-61	peroxidase	Glycine max	0-10
3800997-5	1986	The data support the hypothesis that hydrogen peroxide generated by peroxidase from NADH may play a role during cell wall breakdown in plants.	Hydrogen Peroxide	37-54	peroxidase	Glycine max	68-78
3800997-5	1986	The data support the hypothesis that hydrogen peroxide generated by peroxidase from NADH may play a role during cell wall breakdown in plants.	NAD	84-88	peroxidase	Glycine max	68-78
16593704-8	1986	The evidence indicates an important role of glutathione, ascorbate, ascorbate peroxidase, dehydroascorbate reductase, and glutathione reductase as components of a peroxide-scavenging mechanism in soybean root nodules.	Peroxides	163-171	peroxidase	Glycine max	78-88
33584766-2	2021	We previously confirmed that the bHLH transcription factor GmPIB1 (P. sojae-inducible bHLH transcription factor) reduces accumulation of reactive oxygen species (ROS) in cells by inhibiting expression of the peroxidase-related gene GmSPOD thus improving the resistance of hairy roots to P. sojae.	Reactive Oxygen Species	137-160	peroxidase	Glycine max	208-218
155124-2	1978	It is used the Con A-Peroxidase-DAB technique described by Bernhard and Avrameas (1971).	diazobenzenesulfonic acid	32-35	peroxidase	Glycine max	21-31
33554371-8	2021	In addition, there was an increase in the activity of superoxide dismutase, catalase, peroxidase, and ascorbate peroxidase antioxidant enzymes in leaves due to HI, regardless of FC.	Ascorbic Acid	102-111	peroxidase	Glycine max	112-122
33554371-8	2021	In addition, there was an increase in the activity of superoxide dismutase, catalase, peroxidase, and ascorbate peroxidase antioxidant enzymes in leaves due to HI, regardless of FC.	Histidine	160-162	peroxidase	Glycine max	86-96
33554371-8	2021	In addition, there was an increase in the activity of superoxide dismutase, catalase, peroxidase, and ascorbate peroxidase antioxidant enzymes in leaves due to HI, regardless of FC.	Histidine	160-162	peroxidase	Glycine max	112-122
33715130-0	2021	Elimination of selected heterocyclic aromatic emerging contaminants from water using soybean peroxidase.	Water	73-78	peroxidase	Glycine max	93-103
33715130-3	2021	In this study, feasibility of soybean peroxidase-catalyzed removal of three selected heterocyclic aromatics from water was investigated, including sensitivity to the most important operational conditions, pH (range 3.6-9.0), H2O2 concentration (range 0.10-1.50 mM), and enzyme activity (range 0.001-5.0 U/mL).	Water	113-118	peroxidase	Glycine max	38-48
33715130-3	2021	In this study, feasibility of soybean peroxidase-catalyzed removal of three selected heterocyclic aromatics from water was investigated, including sensitivity to the most important operational conditions, pH (range 3.6-9.0), H2O2 concentration (range 0.10-1.50 mM), and enzyme activity (range 0.001-5.0 U/mL).	Hydrogen Peroxide	225-229	peroxidase	Glycine max	38-48
33584766-2	2021	We previously confirmed that the bHLH transcription factor GmPIB1 (P. sojae-inducible bHLH transcription factor) reduces accumulation of reactive oxygen species (ROS) in cells by inhibiting expression of the peroxidase-related gene GmSPOD thus improving the resistance of hairy roots to P. sojae.	Reactive Oxygen Species	162-165	peroxidase	Glycine max	208-218
33584766-10	2021	Antioxidant enzymes include peroxidase (POD), glutathione peroxidase (GPX), superoxide dismutase (SOD), catalase (CAT) are responsible for ROS scavenging in soybean.	Reactive Oxygen Species	139-142	peroxidase	Glycine max	28-38
33584766-10	2021	Antioxidant enzymes include peroxidase (POD), glutathione peroxidase (GPX), superoxide dismutase (SOD), catalase (CAT) are responsible for ROS scavenging in soybean.	Reactive Oxygen Species	139-142	peroxidase	Glycine max	40-43
33584766-13	2021	These data suggest that GmPSMD might reduce the production of ROS by improving the activity of antioxidant enzymes such as POD, SOD, GPX, CAT, and GmPSMD plays a significant role in the response of soybean to P. sojae.	Reactive Oxygen Species	62-65	peroxidase	Glycine max	123-126
33477226-5	2021	Elevated CO2 concentration significantly increased peroxidase activity and abscisic acid content of leaves under drought stress, decreased the content of proline, and did not affect the content of soluble saccharides.	Carbon Dioxide	9-12	peroxidase	Glycine max	51-61
32629356-6	2021	The activity of peroxidase (POD), 4-coumarate:CoA ligase (4CL), cinnamyl alcohol dehydrogenase (CAD) and phenylalanine ammonia-lyase (PAL) increased during pre-and post-growth periods, whereas Si also increased lignin accumulation and inhibited lodging.	Silicon	193-195	peroxidase	Glycine max	16-26
32629356-6	2021	The activity of peroxidase (POD), 4-coumarate:CoA ligase (4CL), cinnamyl alcohol dehydrogenase (CAD) and phenylalanine ammonia-lyase (PAL) increased during pre-and post-growth periods, whereas Si also increased lignin accumulation and inhibited lodging.	Lignin	211-217	peroxidase	Glycine max	16-26
33320882-6	2020	However, after seeds soaking with melatonin, the lipid peroxidation of the cell membrane was reduced, and the activities of antioxidant enzymes such as superoxide dismutase (SOD), peroxidase (POD), catalase (CAT), and ascorbate peroxidase (APX) further increased to minimize the excessive generation of ROS.	Melatonin	34-43	peroxidase	Glycine max	192-195
32473423-5	2020	Catalase and peroxidase, possibly performing a signaling function, are involved in the adaptation to the toxicity of Pb salts.	pb salts	117-125	peroxidase	Glycine max	13-23
33320882-6	2020	However, after seeds soaking with melatonin, the lipid peroxidation of the cell membrane was reduced, and the activities of antioxidant enzymes such as superoxide dismutase (SOD), peroxidase (POD), catalase (CAT), and ascorbate peroxidase (APX) further increased to minimize the excessive generation of ROS.	Melatonin	34-43	peroxidase	Glycine max	180-190
32450145-18	2020	Immunoblot analysis depicted that accumulation of ascorbate peroxidase, glutathione reductase, and peroxiredoxin remained unchanged under both GS and CS silver NPs.	Ascorbic Acid	50-59	peroxidase	Glycine max	60-70
31897538-7	2020	It was concluded that strain RP11 alleviated TBBPA-induced harmful effects in soybean seedlings by the secretion of IAA and ALA, the accumulation of carotenoid, soluble sugar and soluble protein, and the induction of SOD, CAT and POD as well as nutrient adjustment of phosphorus and potassium levels.	tetrabromobisphenol A	45-50	peroxidase	Glycine max	230-233
32630094-9	2020	Moreover, the enzymes involved in the ascorbate-glutathione cycle including superoxide dismutase (SOD), catalase (CAT), ascorbate peroxidase (APX) and glutathione reductase (GR) showed a significant increase in their activity with the application of ZnO-NPs to the As-stressed plants.	Ascorbic Acid	38-47	peroxidase	Glycine max	130-140
32630094-9	2020	Moreover, the enzymes involved in the ascorbate-glutathione cycle including superoxide dismutase (SOD), catalase (CAT), ascorbate peroxidase (APX) and glutathione reductase (GR) showed a significant increase in their activity with the application of ZnO-NPs to the As-stressed plants.	zno-nps	250-257	peroxidase	Glycine max	130-140
32412658-7	2020	Acetic acid-sprayed plants suffered less oxidative stress due to the enhancement of antioxidant defense mechanisms, as evidenced by the increased activities of superoxide dismutase, ascorbate peroxidase, catalase, glutathione peroxidase and glutathione S-transferase.	Acetic Acid	0-11	peroxidase	Glycine max	192-202
31947957-5	2020	Additionally, Cd induced the stress levels of Cd, proline, glycine betaine, hydrogen peroxide, malondialdehyde, antioxidant enzymes (i.e., catalase, CAT; ascorbate peroxidase, APX; superoxide dismutase, SOD; peroxidise, POD), and the expression of stress-related genes (i.e., APX, CAT, Fe-SOD, POD, CHI, CHS, PHD2, VSO, NR, and P5CS) in soybean leaves.	Cadmium	14-16	peroxidase	Glycine max	164-174
32117330-6	2019	In addition, Si application normalized the photosynthetic responses, such as transpiration rate (E) and net photosynthesis rate (PN ) in salt-treated plants, and reduced the activity of ascorbate peroxidase and glutathione under salt stress.	Silicon	13-15	peroxidase	Glycine max	196-206
32245276-12	2020	In response to drought and salt stress, lower malondialdehyde (MDA) accumulation and higher peroxidase (POD) and superoxide dismutase (SOD) activities were observed in soybean composite seedlings with an overexpression of hairy roots.	Salts	27-31	peroxidase	Glycine max	92-102
32175178-0	2020	Soybean Peroxidase Catalyzed Decoloration of Acid Azo Dyes.	Azo Compounds	50-58	peroxidase	Glycine max	8-18
31779627-5	2019	RESULTS: In the present study, we present a rapid and robust approach to easily test the degradability of 21 different emerging pollutants by five different peroxidases (soybean peroxidase, chloroperoxidase, lactoperoxidase, manganese peroxidase, and horseradish peroxidase) using an LC-MSMS approach.	Manganese	225-234	peroxidase	Glycine max	157-167
31779627-8	2019	The degradation of furosemide and trimethoprim by soybean peroxidase and chloroperoxidase, respectively, was investigated in detail by examining the transformation products generated during their degradation.	Furosemide	19-29	peroxidase	Glycine max	58-68
31604973-8	2019	Eight DEGs/DEPs enriched in phenylpropanoid biosynthesis were assigned to peroxidase, which catalyzes the conversion of coumaryl alcohol to hydroxy-phenyl lignin in the final step of lignin biosynthesis.	3,4-dihydroxyphenacyl caffeate phenylpropanoid ester	28-43	peroxidase	Glycine max	74-84
31779627-8	2019	The degradation of furosemide and trimethoprim by soybean peroxidase and chloroperoxidase, respectively, was investigated in detail by examining the transformation products generated during their degradation.	Trimethoprim	34-46	peroxidase	Glycine max	58-68
31604973-8	2019	Eight DEGs/DEPs enriched in phenylpropanoid biosynthesis were assigned to peroxidase, which catalyzes the conversion of coumaryl alcohol to hydroxy-phenyl lignin in the final step of lignin biosynthesis.	p-coumaric acid	120-136	peroxidase	Glycine max	74-84
31604973-8	2019	Eight DEGs/DEPs enriched in phenylpropanoid biosynthesis were assigned to peroxidase, which catalyzes the conversion of coumaryl alcohol to hydroxy-phenyl lignin in the final step of lignin biosynthesis.	Lignin	140-161	peroxidase	Glycine max	74-84
31058828-5	2019	The chlorophyll content was significantly reduced but antioxidant activities, viz., superoxide dismutase (SOD), peroxidase (POD) and catalase (CAT), as well as the malondialdehyde (MDA) contents, were detected higher in spl-1 than in the wild-type.	Chlorophyll	4-15	peroxidase	Glycine max	112-122
31370221-0	2019	Overexpression of Peroxidase Gene GsPRX9 Confers Salt Tolerance in Soybean.	Salts	49-53	peroxidase	Glycine max	18-28
31540266-5	2019	Superoxide dismutase and peroxidase isoenzymatic regulation may play a determinant role: 10 superoxide dismutase isoenzymes were observed in both cultivars, but iron superoxide dismutase activity was only detected in efficient plants; 15 peroxidase isoenzymes were observed in the roots and trifoliate leaves of efficient and inefficient cultivars and peroxidase activity levels were only increased in roots of efficient plants.	Iron	161-165	peroxidase	Glycine max	25-35
31058828-5	2019	The chlorophyll content was significantly reduced but antioxidant activities, viz., superoxide dismutase (SOD), peroxidase (POD) and catalase (CAT), as well as the malondialdehyde (MDA) contents, were detected higher in spl-1 than in the wild-type.	Chlorophyll	4-15	peroxidase	Glycine max	124-127
30724183-1	2019	The oxidation of eugenol, isoeugenol and vanillin natural antioxidants catalyzed by the soybean peroxidase enzyme was studied using uv-vis spectroscopy.	Eugenol	17-24	peroxidase	Glycine max	96-106
31051438-9	2019	The result showed that by significantly increasing the concentration of NiO nanoparticles, the activity of catalase and ascorbate peroxidase enzymes was enhanced.	nio	72-75	peroxidase	Glycine max	130-140
30724183-1	2019	The oxidation of eugenol, isoeugenol and vanillin natural antioxidants catalyzed by the soybean peroxidase enzyme was studied using uv-vis spectroscopy.	isoeugenol	26-36	peroxidase	Glycine max	96-106
30653617-7	2019	The methanolic extract of R. marina cutaneous secretions also increased the specific activity of POX and PPO in "Monsoy 8372 IPRO" and "TMG 132 RR", respectively, and decreased the activity of beta-1,3-glucanases in "Monsoy 8372 IPRO".	methanolic	4-14	peroxidase	Glycine max	97-100
30724183-1	2019	The oxidation of eugenol, isoeugenol and vanillin natural antioxidants catalyzed by the soybean peroxidase enzyme was studied using uv-vis spectroscopy.	vanillin	41-49	peroxidase	Glycine max	96-106
30113770-7	2019	The activities and expression levels of enzymatic superoxide dismutase (SOD) and peroxidase (POD) antioxidants were significantly higher in GmBTB/POZ-overexpressing (GmBTB/POZ-OE) transgenic soybean plants than in wild-type (WT) plants treated with sterile water or infected with P. sojae.	gmbtb	140-145	peroxidase	Glycine max	81-91
30113770-7	2019	The activities and expression levels of enzymatic superoxide dismutase (SOD) and peroxidase (POD) antioxidants were significantly higher in GmBTB/POZ-overexpressing (GmBTB/POZ-OE) transgenic soybean plants than in wild-type (WT) plants treated with sterile water or infected with P. sojae.	gmbtb	140-145	peroxidase	Glycine max	93-96
29889651-1	2018	The peroxidase (POD) enzyme, obtained from different sources, has been described in the literature regarding its good results of reduction in concentration or degradation levels of mycotoxins, such as aflatoxin B1, deoxynivalenol and zearalenone (ZEA).	Zearalenone	234-245	peroxidase	Glycine max	16-19
28956655-16	2018	Soybean oil also showed strong antioxidant effects, causing significant (p < .005) increase in kidney homogenate catalases, glutathione peroxidase, and superoxide dismutase and significant (p < .005) decrease in lipid peroxidase in gentamicin- and rifampicin-treated animals.	Oils	8-11	peroxidase	Glycine max	139-149
30077102-5	2018	Exposure of the plants to gamma-Fe2O3 NPs increased cell wall-bound peroxidase (POD) activity but decreased phenylalanine ammonia lyase (PAL) activity due, probably, to the negative feedback of accumulated phenolic compounds.	gamma-fe2o3	26-37	peroxidase	Glycine max	68-78
30077102-5	2018	Exposure of the plants to gamma-Fe2O3 NPs increased cell wall-bound peroxidase (POD) activity but decreased phenylalanine ammonia lyase (PAL) activity due, probably, to the negative feedback of accumulated phenolic compounds.	gamma-fe2o3	26-37	peroxidase	Glycine max	80-83
30077102-6	2018	In contrast, FeCl3 decreased cell wall-bound POD activity.	ferric chloride	13-18	peroxidase	Glycine max	45-48
29889651-0	2018	Zearalenone reduction by commercial peroxidase enzyme and peroxidases from soybean bran and rice bran.	Zearalenone	0-11	peroxidase	Glycine max	36-46
29889651-1	2018	The peroxidase (POD) enzyme, obtained from different sources, has been described in the literature regarding its good results of reduction in concentration or degradation levels of mycotoxins, such as aflatoxin B1, deoxynivalenol and zearalenone (ZEA).	Zearalenone	247-250	peroxidase	Glycine max	4-14
29889651-1	2018	The peroxidase (POD) enzyme, obtained from different sources, has been described in the literature regarding its good results of reduction in concentration or degradation levels of mycotoxins, such as aflatoxin B1, deoxynivalenol and zearalenone (ZEA).	Aflatoxin B1	201-213	peroxidase	Glycine max	4-14
29889651-1	2018	The peroxidase (POD) enzyme, obtained from different sources, has been described in the literature regarding its good results of reduction in concentration or degradation levels of mycotoxins, such as aflatoxin B1, deoxynivalenol and zearalenone (ZEA).	Aflatoxin B1	201-213	peroxidase	Glycine max	16-19
29889651-1	2018	The peroxidase (POD) enzyme, obtained from different sources, has been described in the literature regarding its good results of reduction in concentration or degradation levels of mycotoxins, such as aflatoxin B1, deoxynivalenol and zearalenone (ZEA).	deoxynivalenol	215-229	peroxidase	Glycine max	4-14
29889651-1	2018	The peroxidase (POD) enzyme, obtained from different sources, has been described in the literature regarding its good results of reduction in concentration or degradation levels of mycotoxins, such as aflatoxin B1, deoxynivalenol and zearalenone (ZEA).	deoxynivalenol	215-229	peroxidase	Glycine max	16-19
29889651-1	2018	The peroxidase (POD) enzyme, obtained from different sources, has been described in the literature regarding its good results of reduction in concentration or degradation levels of mycotoxins, such as aflatoxin B1, deoxynivalenol and zearalenone (ZEA).	Zearalenone	234-245	peroxidase	Glycine max	4-14
29889651-1	2018	The peroxidase (POD) enzyme, obtained from different sources, has been described in the literature regarding its good results of reduction in concentration or degradation levels of mycotoxins, such as aflatoxin B1, deoxynivalenol and zearalenone (ZEA).	Zearalenone	247-250	peroxidase	Glycine max	16-19
29889651-3	2018	POD was extracted from SB and RB in phosphate buffer by orbital agitation.	Antimony	23-25	peroxidase	Glycine max	0-3
29889651-3	2018	POD was extracted from SB and RB in phosphate buffer by orbital agitation.	Phosphates	36-45	peroxidase	Glycine max	0-3
29889651-4	2018	Evaluation of the action of commercial POD and POD from SB and RB in ZEA reduction was carried out in phosphate buffer and aqueous solution, respectively.	Phosphates	102-111	peroxidase	Glycine max	39-42
29889651-4	2018	Evaluation of the action of commercial POD and POD from SB and RB in ZEA reduction was carried out in phosphate buffer and aqueous solution, respectively.	Phosphates	102-111	peroxidase	Glycine max	47-50
29578014-2	2018	The activated carbon (AC) was synthesized from the solid waste obtained in the extraction process of the peroxidase enzyme and the magnetic composite was used as support for the immobilization of soybean peroxidase (SP).	Carbon	14-20	peroxidase	Glycine max	105-115
30059870-10	2018	The superoxide dismutase and peroxidase activities increased with the increasing Al availability in the nutrient solution, and they were higher in the roots, showing their role in Al detoxification.	Aluminum	81-83	peroxidase	Glycine max	29-39
30059870-10	2018	The superoxide dismutase and peroxidase activities increased with the increasing Al availability in the nutrient solution, and they were higher in the roots, showing their role in Al detoxification.	Aluminum	180-182	peroxidase	Glycine max	29-39
29776461-0	2018	Soybean Peroxidase-Catalyzed Treatment of Azo Dyes with or without Fe  Pretreatment.	Azo Compounds	42-50	peroxidase	Glycine max	8-18
29776461-0	2018	Soybean Peroxidase-Catalyzed Treatment of Azo Dyes with or without Fe  Pretreatment.	Iron	67-69	peroxidase	Glycine max	8-18
29578014-2	2018	The activated carbon (AC) was synthesized from the solid waste obtained in the extraction process of the peroxidase enzyme and the magnetic composite was used as support for the immobilization of soybean peroxidase (SP).	Carbon	14-20	peroxidase	Glycine max	204-214
29578014-2	2018	The activated carbon (AC) was synthesized from the solid waste obtained in the extraction process of the peroxidase enzyme and the magnetic composite was used as support for the immobilization of soybean peroxidase (SP).	Carbon	22-24	peroxidase	Glycine max	105-115
29578014-2	2018	The activated carbon (AC) was synthesized from the solid waste obtained in the extraction process of the peroxidase enzyme and the magnetic composite was used as support for the immobilization of soybean peroxidase (SP).	Carbon	22-24	peroxidase	Glycine max	204-214
28986654-0	2018	Soybean peroxidase immobilized on delta-FeOOH as new magnetically recyclable biocatalyst for removal of ferulic acid.	delta-feooh	34-45	peroxidase	Glycine max	8-18
30174333-9	2018	The main enzyme involved in the rapid removal of free radicals was superoxide peroxidase, activated by the herbicide treatment, while catalase was not significantly stimulated.	Free Radicals	49-62	peroxidase	Glycine max	78-88
28986654-0	2018	Soybean peroxidase immobilized on delta-FeOOH as new magnetically recyclable biocatalyst for removal of ferulic acid.	ferulic acid	104-116	peroxidase	Glycine max	8-18
28634178-6	2017	A previously unknown ascorbate peroxidase activity of MauG was characterized with a kcat of 0.24 s-1 and a Km of 2.2 microM for ascorbate.	Ascorbic Acid	21-30	peroxidase	Glycine max	31-41
29164108-8	2017	Compared with the plants exposed to Al alone, Al+SA plants possessed higher activities of superoxide dismutase, peroxidase, and ascorbate peroxidase, and lower catalase activity, indicating that SA alleviated Al-induced oxidative damage.	Aluminum	46-48	peroxidase	Glycine max	112-122
29164108-8	2017	Compared with the plants exposed to Al alone, Al+SA plants possessed higher activities of superoxide dismutase, peroxidase, and ascorbate peroxidase, and lower catalase activity, indicating that SA alleviated Al-induced oxidative damage.	Aluminum	46-48	peroxidase	Glycine max	138-148
29164108-8	2017	Compared with the plants exposed to Al alone, Al+SA plants possessed higher activities of superoxide dismutase, peroxidase, and ascorbate peroxidase, and lower catalase activity, indicating that SA alleviated Al-induced oxidative damage.	Salicylic Acid	49-51	peroxidase	Glycine max	112-122
29164108-8	2017	Compared with the plants exposed to Al alone, Al+SA plants possessed higher activities of superoxide dismutase, peroxidase, and ascorbate peroxidase, and lower catalase activity, indicating that SA alleviated Al-induced oxidative damage.	Salicylic Acid	49-51	peroxidase	Glycine max	138-148
29164108-8	2017	Compared with the plants exposed to Al alone, Al+SA plants possessed higher activities of superoxide dismutase, peroxidase, and ascorbate peroxidase, and lower catalase activity, indicating that SA alleviated Al-induced oxidative damage.	Salicylic Acid	195-197	peroxidase	Glycine max	112-122
29164108-8	2017	Compared with the plants exposed to Al alone, Al+SA plants possessed higher activities of superoxide dismutase, peroxidase, and ascorbate peroxidase, and lower catalase activity, indicating that SA alleviated Al-induced oxidative damage.	Salicylic Acid	195-197	peroxidase	Glycine max	138-148
29164108-8	2017	Compared with the plants exposed to Al alone, Al+SA plants possessed higher activities of superoxide dismutase, peroxidase, and ascorbate peroxidase, and lower catalase activity, indicating that SA alleviated Al-induced oxidative damage.	Aluminum	46-48	peroxidase	Glycine max	112-122
29164108-8	2017	Compared with the plants exposed to Al alone, Al+SA plants possessed higher activities of superoxide dismutase, peroxidase, and ascorbate peroxidase, and lower catalase activity, indicating that SA alleviated Al-induced oxidative damage.	Aluminum	46-48	peroxidase	Glycine max	138-148
29026164-8	2017	The PTH-HRP construction was the most sensitive and supported all tested peroxidase co-substrates (TrueBlueTM, tetramethylbenzidine (TMB), luminol, biotin-phenol with streptavidin-Qdots); the 3 latter schemes identified endogenous PTHR1 in the osteoblastic HOS cell line.	3,3',5,5'-tetramethylbenzidine	133-136	peroxidase	Glycine max	73-83
29026164-8	2017	The PTH-HRP construction was the most sensitive and supported all tested peroxidase co-substrates (TrueBlueTM, tetramethylbenzidine (TMB), luminol, biotin-phenol with streptavidin-Qdots); the 3 latter schemes identified endogenous PTHR1 in the osteoblastic HOS cell line.	Biotinyl tyramide	148-161	peroxidase	Glycine max	73-83
29016915-6	2017	Compared with the wild type (WT), GmMYB84-overexpressing soybean mutants (OE lines) exhibited enhanced drought resistance with a higher survival rate, longer primary root length, greater proline and reactive oxygen species (ROS) contents, higher antioxidant enzyme activities [peroxidase (POD), catalase (CAT) and superoxide dismutase (SOD)], a lower dehydration rate and reduced malondialdehyde (MDA) content.	gmmyb84	34-41	peroxidase	Glycine max	277-287
28848576-8	2017	Furthermore, catalase, superoxide dismutase, and peroxidase activities also changed after NaCl treatment.	Sodium Chloride	90-94	peroxidase	Glycine max	49-59
29169120-0	2018	Soybean peroxidase immobilized onto silica-coated superparamagnetic iron oxide nanoparticles: Effect of silica layer on the enzymatic activity.	Silicon Dioxide	36-42	peroxidase	Glycine max	8-18
29169120-0	2018	Soybean peroxidase immobilized onto silica-coated superparamagnetic iron oxide nanoparticles: Effect of silica layer on the enzymatic activity.	ferric oxide	68-78	peroxidase	Glycine max	8-18
29169120-0	2018	Soybean peroxidase immobilized onto silica-coated superparamagnetic iron oxide nanoparticles: Effect of silica layer on the enzymatic activity.	Silicon Dioxide	104-110	peroxidase	Glycine max	8-18
29016915-6	2017	Compared with the wild type (WT), GmMYB84-overexpressing soybean mutants (OE lines) exhibited enhanced drought resistance with a higher survival rate, longer primary root length, greater proline and reactive oxygen species (ROS) contents, higher antioxidant enzyme activities [peroxidase (POD), catalase (CAT) and superoxide dismutase (SOD)], a lower dehydration rate and reduced malondialdehyde (MDA) content.	gmmyb84	34-41	peroxidase	Glycine max	289-292
29016915-7	2017	We also found that ROS could induce SOD/POD/CAT activity in OE lines.	Reactive Oxygen Species	19-22	peroxidase	Glycine max	40-43
28634178-7	2017	A putative binding site for ascorbate was inferred from inspection of the crystal structure of MauG and comparison with the structure of soybean ascorbate peroxidase with bound ascorbate.	Ascorbic Acid	28-37	peroxidase	Glycine max	155-165
28634178-7	2017	A putative binding site for ascorbate was inferred from inspection of the crystal structure of MauG and comparison with the structure of soybean ascorbate peroxidase with bound ascorbate.	Ascorbic Acid	145-154	peroxidase	Glycine max	155-165
28088531-0	2017	The effect of dissolved organic matter on soybean peroxidase-mediated removal of triclosan in water.	organic matter	24-38	peroxidase	Glycine max	50-60
28088531-0	2017	The effect of dissolved organic matter on soybean peroxidase-mediated removal of triclosan in water.	Triclosan	81-90	peroxidase	Glycine max	50-60
28088531-0	2017	The effect of dissolved organic matter on soybean peroxidase-mediated removal of triclosan in water.	Water	94-99	peroxidase	Glycine max	50-60
27942755-0	2017	Tyramine-modified pectins via periodate oxidation for soybean hull peroxidase induced hydrogel formation and immobilization.	Tyramine	0-8	peroxidase	Glycine max	67-77
27942755-0	2017	Tyramine-modified pectins via periodate oxidation for soybean hull peroxidase induced hydrogel formation and immobilization.	metaperiodate	30-39	peroxidase	Glycine max	67-77
27942755-3	2017	All tyramine-pectins showed exceptional gelling properties and could form hydrogel both by cross-linking of carboxyl groups with calcium or by cross-linking phenol groups with peroxidase in the presence of hydrogen peroxide.	Tyramine	4-12	peroxidase	Glycine max	176-186
28135657-6	2017	Reactive oxygen species (ROS) scavenging enzymes activity analysis showed that the activities of peroxidase (POD), polyphenol oxidase (PPO) and superoxide dismutase (SOD) increased significantly in T-soybean pretreated plants.	Reactive Oxygen Species	0-23	peroxidase	Glycine max	97-107
28135657-6	2017	Reactive oxygen species (ROS) scavenging enzymes activity analysis showed that the activities of peroxidase (POD), polyphenol oxidase (PPO) and superoxide dismutase (SOD) increased significantly in T-soybean pretreated plants.	Reactive Oxygen Species	0-23	peroxidase	Glycine max	109-112
28135657-6	2017	Reactive oxygen species (ROS) scavenging enzymes activity analysis showed that the activities of peroxidase (POD), polyphenol oxidase (PPO) and superoxide dismutase (SOD) increased significantly in T-soybean pretreated plants.	Reactive Oxygen Species	25-28	peroxidase	Glycine max	97-107
28135657-6	2017	Reactive oxygen species (ROS) scavenging enzymes activity analysis showed that the activities of peroxidase (POD), polyphenol oxidase (PPO) and superoxide dismutase (SOD) increased significantly in T-soybean pretreated plants.	Reactive Oxygen Species	25-28	peroxidase	Glycine max	109-112
27623850-0	2016	Degradation of orange dyes and carbamazepine by soybean peroxidase immobilized on silica monoliths and titanium dioxide.	Carbamazepine	31-44	peroxidase	Glycine max	56-66
28261569-8	2017	To study this hypothesis, we have adapted a proximity-labeling strategy using APEX2, a mutant soybean ascorbate peroxidase that biotinylates interacting and proximal proteins within minutes in the presence of H2O2 and its exogenous substrate, biotin-phenol.	Hydrogen Peroxide	209-213	peroxidase	Glycine max	112-122
28261569-8	2017	To study this hypothesis, we have adapted a proximity-labeling strategy using APEX2, a mutant soybean ascorbate peroxidase that biotinylates interacting and proximal proteins within minutes in the presence of H2O2 and its exogenous substrate, biotin-phenol.	Biotinyl tyramide	243-256	peroxidase	Glycine max	112-122
27878319-4	2017	TBBPA treatment at low concentrations enhanced soluble sugar and soluble protein content, and it activated superoxide dismutase (SOD; EC:1.15.1.1), catalase (CAT; EC:1.11.1.6), and peroxidase (POD; EC:1.11.1.7); however, high concentrations of TBBPA inhibited activities of antioxidant enzymes and generation of soluble sugar and soluble protein.	tetrabromobisphenol A	0-5	peroxidase	Glycine max	181-191
27878319-4	2017	TBBPA treatment at low concentrations enhanced soluble sugar and soluble protein content, and it activated superoxide dismutase (SOD; EC:1.15.1.1), catalase (CAT; EC:1.11.1.6), and peroxidase (POD; EC:1.11.1.7); however, high concentrations of TBBPA inhibited activities of antioxidant enzymes and generation of soluble sugar and soluble protein.	tetrabromobisphenol A	0-5	peroxidase	Glycine max	193-196
27623850-0	2016	Degradation of orange dyes and carbamazepine by soybean peroxidase immobilized on silica monoliths and titanium dioxide.	Silicon Dioxide	82-88	peroxidase	Glycine max	56-66
27623850-0	2016	Degradation of orange dyes and carbamazepine by soybean peroxidase immobilized on silica monoliths and titanium dioxide.	titanium dioxide	103-119	peroxidase	Glycine max	56-66
27623850-2	2016	Soybean peroxidase (SBP) was used as biocatalyst, both free in solution and immobilized on silica monoliths, and titanium dioxide as photocatalyst.	Silicon Dioxide	91-97	peroxidase	Glycine max	8-18
27040261-2	2016	The catalytic mechanism is an enzymatic cascade reaction in which hydrogen peroxide is the oxidizer and soybean peroxidase, in the presence of acetosyringone, syringaldehyde or vanillin, acts as a natural catalysts.	Hydrogen Peroxide	66-83	peroxidase	Glycine max	112-122
27292084-12	2016	These results suggest that peroxidase and aldehyde dehydrogenase play key roles in post-drought recovery in soybean by scavenging toxic reactive oxygen species and reducing the load of harmful aldehydes.	Reactive Oxygen Species	136-159	peroxidase	Glycine max	27-37
27292084-12	2016	These results suggest that peroxidase and aldehyde dehydrogenase play key roles in post-drought recovery in soybean by scavenging toxic reactive oxygen species and reducing the load of harmful aldehydes.	Aldehydes	193-202	peroxidase	Glycine max	27-37
27292084-19	2016	Peroxidase and aldehyde dehydrogenase reduce the toxic reactive oxygen species and aldehydes from the plant, respectively, and help to recover from drought stress.	Reactive Oxygen Species	55-78	peroxidase	Glycine max	0-10
27292084-19	2016	Peroxidase and aldehyde dehydrogenase reduce the toxic reactive oxygen species and aldehydes from the plant, respectively, and help to recover from drought stress.	Aldehydes	83-92	peroxidase	Glycine max	0-10
27040261-2	2016	The catalytic mechanism is an enzymatic cascade reaction in which hydrogen peroxide is the oxidizer and soybean peroxidase, in the presence of acetosyringone, syringaldehyde or vanillin, acts as a natural catalysts.	acetosyringone	143-157	peroxidase	Glycine max	112-122
27040261-2	2016	The catalytic mechanism is an enzymatic cascade reaction in which hydrogen peroxide is the oxidizer and soybean peroxidase, in the presence of acetosyringone, syringaldehyde or vanillin, acts as a natural catalysts.	vanillin	177-185	peroxidase	Glycine max	112-122
27242811-9	2016	The activities of superoxide dismutase (SOD), peroxidase (POD), catalase (CAT), and ascorbate peroxidase (APX) increases by 40.04, 28.22, 48.53, and 56.79%, respectively, over the control in Ni treated seedlings and further enhancement in the antioxidant activity was observed by the application of JA.	jasmonic acid	299-301	peroxidase	Glycine max	94-104
26691059-9	2016	Enzymatic analysis showed that Ca(2+) and SA stimulated the activities of superoxidase (SOD), peroxidase (POD), and ascorbate peroxidase (APX) in Al-treated roots.	Salicylic Acid	42-44	peroxidase	Glycine max	76-86
26989345-0	2016	Additive Effect on Soybean Peroxidase-Catalyzed Removal of Anilines from Water.	Aniline Compounds	59-67	peroxidase	Glycine max	27-37
26989345-0	2016	Additive Effect on Soybean Peroxidase-Catalyzed Removal of Anilines from Water.	Water	73-78	peroxidase	Glycine max	27-37
26989345-5	2016	These results are enabling advancement of soybean peroxidase-catalyzed treatment of anilines found in wastewaters as a new sustainable method.	Aniline Compounds	84-92	peroxidase	Glycine max	50-60
26502790-3	2016	In this investigation, the influence of the additives polyethylene glycol and Triton X-100 was evaluated in the phenol oxidation, caffeic acid, chlorogenic acid and total phenolic compounds present in coffee processing wastewater (CPW) at different pH values, performed by turnip peroxidase and peroxidase extracted from soybean seed hulls.	Octoxynol	78-90	peroxidase	Glycine max	280-290
26502790-3	2016	In this investigation, the influence of the additives polyethylene glycol and Triton X-100 was evaluated in the phenol oxidation, caffeic acid, chlorogenic acid and total phenolic compounds present in coffee processing wastewater (CPW) at different pH values, performed by turnip peroxidase and peroxidase extracted from soybean seed hulls.	Octoxynol	78-90	peroxidase	Glycine max	295-305
25959717-5	2016	Peroxidase activity in Mandarin (Ottawa) was 31% higher with O3 but was not significantly different in Fiskeby III.	Ozone	61-63	peroxidase	Glycine max	0-10
26691059-9	2016	Enzymatic analysis showed that Ca(2+) and SA stimulated the activities of superoxidase (SOD), peroxidase (POD), and ascorbate peroxidase (APX) in Al-treated roots.	Salicylic Acid	42-44	peroxidase	Glycine max	106-109
26691059-9	2016	Enzymatic analysis showed that Ca(2+) and SA stimulated the activities of superoxidase (SOD), peroxidase (POD), and ascorbate peroxidase (APX) in Al-treated roots.	Salicylic Acid	42-44	peroxidase	Glycine max	94-104
26691059-9	2016	Enzymatic analysis showed that Ca(2+) and SA stimulated the activities of superoxidase (SOD), peroxidase (POD), and ascorbate peroxidase (APX) in Al-treated roots.	Aluminum	146-148	peroxidase	Glycine max	76-86
26691059-9	2016	Enzymatic analysis showed that Ca(2+) and SA stimulated the activities of superoxidase (SOD), peroxidase (POD), and ascorbate peroxidase (APX) in Al-treated roots.	Aluminum	146-148	peroxidase	Glycine max	106-109
26691059-9	2016	Enzymatic analysis showed that Ca(2+) and SA stimulated the activities of superoxidase (SOD), peroxidase (POD), and ascorbate peroxidase (APX) in Al-treated roots.	Aluminum	146-148	peroxidase	Glycine max	94-104
26109045-0	2015	Antimicrobial mechanism of resveratrol-trans-dihydrodimer produced from peroxidase-catalyzed oxidation of resveratrol.	Resveratrol	27-38	peroxidase	Glycine max	72-82
26109045-2	2015	We performed the in vitro oligomerization of resveratrol catalyzed by soybean peroxidase, and the two isomers (resveratrol-trans-dihydrodimer and pallidol) produced were tested for antimicrobial activity.	Resveratrol	45-56	peroxidase	Glycine max	78-88
26230263-4	2015	In the combined treatment of La3+ (0.08 mM) and AR, the cell membrane permeability and the peroxidation of cell membrane lipid of soybean roots increased, and the superoxide dismutase, catalase, peroxidase and reduced ascorbic acid served as scavengers of reactive oxygen species.	lanthanum(3+)	29-33	peroxidase	Glycine max	195-205
25651304-7	2015	Exposure to 48.0 mg L(-1) or 96.0 mg L(-1) BPA caused decreases in the CAT activity and AsA/GSH content, as well as increases in the SOD and POD activities and the proline content, leading to excess ROS accumulation (i.e., H2 O2 and O2 (-) ) and cell membrane damage.	bisphenol A	43-46	peroxidase	Glycine max	141-144
26572024-6	2015	NAA distinctly enhanced the activities of APX, POD, CAT, MDHAR, GPX, and ratios of AsA/DHA and GSH/GSSG, while decreased the levels of ROS and MDA.	1-naphthaleneacetic acid	0-3	peroxidase	Glycine max	47-50
25156196-6	2014	Results Drought treatment (8% PEG) caused a significant increase in TBARS levels as well as a marked decrease in the non-enzymatic (GSH and AS) and enzymatic (CAT, SOD, and POD) antioxidant defense systems.	Polyethylene Glycols	30-33	peroxidase	Glycine max	173-176
26417938-0	2015	Hydrogen peroxide-independent generation of superoxide catalyzed by soybean peroxidase in response to ferrous ion.	Hydrogen Peroxide	0-17	peroxidase	Glycine max	76-86
26417938-0	2015	Hydrogen peroxide-independent generation of superoxide catalyzed by soybean peroxidase in response to ferrous ion.	Superoxides	44-54	peroxidase	Glycine max	76-86
26417938-3	2015	By employing the purified proteins of horseradish peroxidase as a model, we have recently proposed a likely role for free Fe(2+) in reduction of ferric enzyme of plant peroxidases into ferrous intermediate and oxygen-bound form of enzyme known as Compound III which may eventually releases superoxide anion radical (O2( -)), especially under alkaline condition, possibly contributing to the plant defense mechanism.	ammonium ferrous sulfate	122-128	peroxidase	Glycine max	50-60
26417938-3	2015	By employing the purified proteins of horseradish peroxidase as a model, we have recently proposed a likely role for free Fe(2+) in reduction of ferric enzyme of plant peroxidases into ferrous intermediate and oxygen-bound form of enzyme known as Compound III which may eventually releases superoxide anion radical (O2( -)), especially under alkaline condition, possibly contributing to the plant defense mechanism.	Oxygen	210-216	peroxidase	Glycine max	50-60
26417938-3	2015	By employing the purified proteins of horseradish peroxidase as a model, we have recently proposed a likely role for free Fe(2+) in reduction of ferric enzyme of plant peroxidases into ferrous intermediate and oxygen-bound form of enzyme known as Compound III which may eventually releases superoxide anion radical (O2( -)), especially under alkaline condition, possibly contributing to the plant defense mechanism.	Superoxides	290-314	peroxidase	Glycine max	50-60
26417938-3	2015	By employing the purified proteins of horseradish peroxidase as a model, we have recently proposed a likely role for free Fe(2+) in reduction of ferric enzyme of plant peroxidases into ferrous intermediate and oxygen-bound form of enzyme known as Compound III which may eventually releases superoxide anion radical (O2( -)), especially under alkaline condition, possibly contributing to the plant defense mechanism.	Oxygen	316-318	peroxidase	Glycine max	50-60
26417938-4	2015	In the present study, we employed the purified protein of soybean peroxidase (SBP) as an additional model, and examined the changes in the redox status of enzyme accompanying the generation of O2( -) in response to Fe(2+) under alkaline condition.	ammonium ferrous sulfate	215-221	peroxidase	Glycine max	66-76
24454805-5	2014	BABA treatment resulted in a significant increase in the activities of several defense enzymes, such as phenylalanine ammonia-lyase (PAL), peroxidase (POX), polyphenol oxidase (PPO), chitinase (CHI), and beta-1, 3-glucanase (GLU) in soybean seedlings attacked by aphid.	3-aminobutyric acid	0-4	peroxidase	Glycine max	139-149
24504695-5	2014	Native-polyacrylamide gel electrophoresis analysis of the POD and PPO was employed followed by activity staining to find out the isoforms of respective enzymes.	polyacrylamide	7-21	peroxidase	Glycine max	58-61
24956780-1	2014	A continuous tank reactor was used to remove 4-chlorophenol from aqueous solutions, using immobilized soybean peroxidase and hydrogen peroxide.	4-chlorophenol	45-59	peroxidase	Glycine max	110-120
24454805-5	2014	BABA treatment resulted in a significant increase in the activities of several defense enzymes, such as phenylalanine ammonia-lyase (PAL), peroxidase (POX), polyphenol oxidase (PPO), chitinase (CHI), and beta-1, 3-glucanase (GLU) in soybean seedlings attacked by aphid.	3-aminobutyric acid	0-4	peroxidase	Glycine max	151-154
24308857-0	2013	Soybean peroxidase-mediated degradation of an azo dye- a detailed mechanistic study.	Azo Compounds	46-53	peroxidase	Glycine max	8-18
24308857-3	2013	RESULTS: In the present study, the enzymatic degradation of an azo dye (Crystal Ponceau 6R, CP6R) was studied using commercially available soybean peroxidase (SBP) enzyme.	Azo Compounds	63-70	peroxidase	Glycine max	147-157
24308857-3	2013	RESULTS: In the present study, the enzymatic degradation of an azo dye (Crystal Ponceau 6R, CP6R) was studied using commercially available soybean peroxidase (SBP) enzyme.	Crystal Ponceau 6R	72-90	peroxidase	Glycine max	147-157
24308857-3	2013	RESULTS: In the present study, the enzymatic degradation of an azo dye (Crystal Ponceau 6R, CP6R) was studied using commercially available soybean peroxidase (SBP) enzyme.	cp6r	92-96	peroxidase	Glycine max	147-157
23711110-0	2013	Mechanistic study of a diazo dye degradation by Soybean Peroxidase.	diazo dye	23-32	peroxidase	Glycine max	56-66
23653318-4	2013	Compared to treatment with acid rain (pH 4.5 and pH 3.0) or La3+ alone, joint stress of La3+ and acid rain affected more severely the activity of catalase and peroxidase, and induced more H2O2 accumulation and lipid peroxidation.	lanthanum(3+)	88-92	peroxidase	Glycine max	159-169
23796491-1	2013	UNLABELLED: This work evaluates the activity of a few key enzymes involved in combating reactive oxygen species (ROS), such as ascorbate peroxidase (EC 1.11.1.11), catalase (EC 1.11.1.6), glutathione reductase (EC 1.6.4.2), and superoxide dismutase (EC 1.15.1.1), as well as the concentration of malondialdehyde and hydrogen peroxide in transgenic and non-transgenic soybean leaves.	Reactive Oxygen Species	88-111	peroxidase	Glycine max	137-147
23796491-1	2013	UNLABELLED: This work evaluates the activity of a few key enzymes involved in combating reactive oxygen species (ROS), such as ascorbate peroxidase (EC 1.11.1.11), catalase (EC 1.11.1.6), glutathione reductase (EC 1.6.4.2), and superoxide dismutase (EC 1.15.1.1), as well as the concentration of malondialdehyde and hydrogen peroxide in transgenic and non-transgenic soybean leaves.	Reactive Oxygen Species	113-116	peroxidase	Glycine max	137-147
23796491-1	2013	UNLABELLED: This work evaluates the activity of a few key enzymes involved in combating reactive oxygen species (ROS), such as ascorbate peroxidase (EC 1.11.1.11), catalase (EC 1.11.1.6), glutathione reductase (EC 1.6.4.2), and superoxide dismutase (EC 1.15.1.1), as well as the concentration of malondialdehyde and hydrogen peroxide in transgenic and non-transgenic soybean leaves.	Malondialdehyde	296-311	peroxidase	Glycine max	137-147
23796491-1	2013	UNLABELLED: This work evaluates the activity of a few key enzymes involved in combating reactive oxygen species (ROS), such as ascorbate peroxidase (EC 1.11.1.11), catalase (EC 1.11.1.6), glutathione reductase (EC 1.6.4.2), and superoxide dismutase (EC 1.15.1.1), as well as the concentration of malondialdehyde and hydrogen peroxide in transgenic and non-transgenic soybean leaves.	Hydrogen Peroxide	316-333	peroxidase	Glycine max	137-147
23711110-3	2013	RESULTS: The present report describes a detailed study on the use of Soybean Peroxidase to efficiently degrade Trypan Blue, a diazo dye.	Trypan Blue	111-122	peroxidase	Glycine max	77-87
23711110-3	2013	RESULTS: The present report describes a detailed study on the use of Soybean Peroxidase to efficiently degrade Trypan Blue, a diazo dye.	diazo dye	126-135	peroxidase	Glycine max	77-87
23711110-6	2013	CONCLUSION: We report that Soybean peroxidase causes Trypan Blue degradation via symmetrical azo bond cleavage and subsequent radical-initiated ring opening of the metabolites.	Trypan Blue	53-64	peroxidase	Glycine max	35-45
23711110-6	2013	CONCLUSION: We report that Soybean peroxidase causes Trypan Blue degradation via symmetrical azo bond cleavage and subsequent radical-initiated ring opening of the metabolites.	anthrone	93-96	peroxidase	Glycine max	35-45
23711110-7	2013	Interestingly, our results also show that no high molecular weight polymers were produced during the peroxidase-H2O2 mediated degradation of the phenolic Trypan Blue.	Hydrogen Peroxide	112-116	peroxidase	Glycine max	101-111
23711110-7	2013	Interestingly, our results also show that no high molecular weight polymers were produced during the peroxidase-H2O2 mediated degradation of the phenolic Trypan Blue.	Trypan Blue	154-165	peroxidase	Glycine max	101-111
22949256-1	2012	Peroxidase from soybean seed coats catalyzes the oxidation and polymerization of aromatic compounds in the presence of H(2)O(2).	Water	119-124	peroxidase	Glycine max	0-10
23964520-0	2013	[Phenothiazine derivatives as enhancers of peroxidase-dependent chemiluminescence].	phenothiazine	1-14	peroxidase	Glycine max	43-53
23964520-1	2013	Some N-alkyl phenothiazines with different ionic groups were studied as enhancers of chemiluminescence catalyzed by soybean peroxidase.	n-alkyl phenothiazines	5-27	peroxidase	Glycine max	124-134
22588482-11	2012	In addition, increased abundance of antioxidant enzymes, namely superoxide dismutase, ascorbate peroxidase, catalase, ensures cellular protection from reactive oxygen species mediated damages under cadmium stress.	Reactive Oxygen Species	151-174	peroxidase	Glycine max	96-106
22588482-11	2012	In addition, increased abundance of antioxidant enzymes, namely superoxide dismutase, ascorbate peroxidase, catalase, ensures cellular protection from reactive oxygen species mediated damages under cadmium stress.	Cadmium	198-205	peroxidase	Glycine max	96-106
22932812-1	2012	Peroxidase-catalysed reactions are used in a wide variety of analytical applications, most of them based on the final quantification of hydrogen peroxide.	Hydrogen Peroxide	136-153	peroxidase	Glycine max	0-10
22253132-4	2012	Magnetic field treatment resulted in enhanced production of ROS mediated by cell wall peroxidase while ascorbic acid content, superoxide dismutase and ascorbate peroxidase activity decreased in the hypocotyl of germinating seeds.	Reactive Oxygen Species	60-63	peroxidase	Glycine max	86-96
22253132-5	2012	An increase in the cytosolic peroxidase activity indicated that this antioxidant enzyme had a vital role in scavenging the increased H(2)O(2) produced in seedlings from the magnetically treated seeds.	Hydrogen Peroxide	133-141	peroxidase	Glycine max	29-39
23033637-5	2012	Activities of antioxidant enzymes (superoxide dismutase, ascorbate peroxidase and glutathione reductase) and proline content increased significantly in all the cultivars with each NaCl treatment.	Sodium Chloride	180-184	peroxidase	Glycine max	67-77
21479540-5	2011	The single treatment with the high concentration of Cd(2+) (>6 mg L(-1)) or acid rain at pH 2.5 decreased the activities of peroxidase and catalase, damaged the cell membrane and then decreased the seed germination of soybean.	Cadmium ion	52-58	peroxidase	Glycine max	127-137
21501957-3	2011	We investigated the effects of bacteriocins [thuricin 17 (T17) and bacthuricin F4 (BF4)] on the activities of phenylalanine ammonia lyase (PAL), guaiacol peroxidase (POD), ascorbate peroxidase (APX), superoxide dismutase (SOD), and polyphenol oxidase (PPO).	bacthuricin f4	67-81	peroxidase	Glycine max	154-164
21724228-8	2011	The soil residual PCB-5 was correlated with the activity of the following enzymes: catalase (CAT), polyphenol oxidase (PPO) and peroxidase (POD).	2,3-dichlorobiphenyl	18-23	peroxidase	Glycine max	128-138
21489652-2	2011	We found that exogenously applied caffeic acid inhibited root growth, decreased the PAL activity and H(2)O(2) content and increased the soluble and cell wall-bound POD activities.	caffeic acid	34-46	peroxidase	Glycine max	164-167
21724228-8	2011	The soil residual PCB-5 was correlated with the activity of the following enzymes: catalase (CAT), polyphenol oxidase (PPO) and peroxidase (POD).	2,3-dichlorobiphenyl	18-23	peroxidase	Glycine max	140-143
21359959-5	2011	It is concluded that apoplastic hydroxyl radical generation depends fully, or for the most part, on peroxidase localized in the cell wall.	Hydroxyl Radical	32-48	peroxidase	Glycine max	100-110
21710366-8	2011	It was concluded that the reduction in the O -2 and H(2)O(2) contents and lipid peroxidation in soybean roots was due to the enhanced SOD and POD activities and thus a possible antioxidant role of L-DOPA.	Levodopa	197-203	peroxidase	Glycine max	142-145
21494099-0	2011	Nitric oxide increases the enzymatic activity of three ascorbate peroxidase isoforms in soybean root nodules.	Nitric Oxide	0-12	peroxidase	Glycine max	65-75
21359959-4	2011	By contrast, in membranes from other parts of the seedlings a low rate of spontaneous hydroxyl radical formation was observed due to the presence of small amounts of tightly bound peroxidase.	Hydroxyl Radical	86-102	peroxidase	Glycine max	180-190
21494099-1	2011	Ascorbate peroxidase is one of the major enzymes regulating the levels of H2O2 in plants and plays a crucial role in maintaining root nodule redox status.	Hydrogen Peroxide	74-78	peroxidase	Glycine max	10-20
21494099-2	2011	We used fully developed and mature nitrogen fixing root nodules from soybean plants to analyze the effect of exogenously applied nitric oxide, generated from the nitric oxide donor 2,2"-(hydroxynitrosohydrazono)bis-ethanimine, on the enzymatic activity of soybean root nodule ascorbate peroxidase.	Nitric Oxide	129-141	peroxidase	Glycine max	286-296
21494099-3	2011	Nitric oxide caused an increase in the total enzymatic activity of ascorbate peroxidase.	Nitric Oxide	0-12	peroxidase	Glycine max	77-87
21494099-4	2011	The nitric oxide-induced changes in ascorbate peroxidase enzymatic activity were coupled to altered nodule H2O2 content.	Nitric Oxide	4-16	peroxidase	Glycine max	46-56
21494099-4	2011	The nitric oxide-induced changes in ascorbate peroxidase enzymatic activity were coupled to altered nodule H2O2 content.	Hydrogen Peroxide	107-111	peroxidase	Glycine max	46-56
21494099-5	2011	Further analysis of ascorbate peroxidase enzymatic activity identified three ascorbate peroxidase isoforms for which augmented enzymatic activity occurred in response to nitric oxide.	Nitric Oxide	170-182	peroxidase	Glycine max	30-40
21494099-5	2011	Further analysis of ascorbate peroxidase enzymatic activity identified three ascorbate peroxidase isoforms for which augmented enzymatic activity occurred in response to nitric oxide.	Nitric Oxide	170-182	peroxidase	Glycine max	87-97
21494099-6	2011	Our results demonstrate that nitric oxide regulates soybean root nodule ascorbate peroxidase activity.	Nitric Oxide	29-41	peroxidase	Glycine max	82-92
20535473-0	2010	Soybean peroxidase propeptides are functional signal peptides and increase the yield of a foreign protein.	propeptides	19-30	peroxidase	Glycine max	8-18
21204536-1	2011	A direct competitive chemiluminescent enzyme-linked immunosorbent assay (CL-ELISA) for the determination of ochratoxin A (OTA) was developed using soybean peroxidase (SbP) in combination with 3-(10"-phenothiazinyl)propane-1-sulfonate (SPTZ) and 4-morpholinopyridine (MORPH) as a detection system.	ochratoxin A	108-120	peroxidase	Glycine max	155-165
21194634-0	2011	Oxidative degradation of Remazol Turquoise Blue G 133 by soybean peroxidase.	resorcinol	25-32	peroxidase	Glycine max	65-75
21194634-3	2011	In this paper, we report the complete and fast decolourization of a Cu(II)-phthalocyanine based reactive dye (Remazol Turquoise Blue G 133) by means of the soybean peroxidase/H(2)O(2) system.	cu(ii)-phthalocyanine	68-89	peroxidase	Glycine max	164-174
21194634-3	2011	In this paper, we report the complete and fast decolourization of a Cu(II)-phthalocyanine based reactive dye (Remazol Turquoise Blue G 133) by means of the soybean peroxidase/H(2)O(2) system.	resorcinol	110-117	peroxidase	Glycine max	164-174
21141391-0	2010	Soybean peroxidase-catalyzed removal of an aromatic thiol, 2-mercaptobenzothiazole, from water.	aromatic thiol	43-57	peroxidase	Glycine max	8-18
21141391-0	2010	Soybean peroxidase-catalyzed removal of an aromatic thiol, 2-mercaptobenzothiazole, from water.	captax	59-82	peroxidase	Glycine max	8-18
21141391-0	2010	Soybean peroxidase-catalyzed removal of an aromatic thiol, 2-mercaptobenzothiazole, from water.	Water	89-94	peroxidase	Glycine max	8-18
21141391-1	2010	This paper demonstrates, for the first time, the capability of soybean peroxidase (SBP), an enzyme, for catalyzing the removal of an aromatic thiol, 2-mercaptobenzothiazole (MBT), from aqueous solution.	aromatic thiol	133-147	peroxidase	Glycine max	71-81
21141391-1	2010	This paper demonstrates, for the first time, the capability of soybean peroxidase (SBP), an enzyme, for catalyzing the removal of an aromatic thiol, 2-mercaptobenzothiazole (MBT), from aqueous solution.	captax	149-172	peroxidase	Glycine max	71-81
21141391-1	2010	This paper demonstrates, for the first time, the capability of soybean peroxidase (SBP), an enzyme, for catalyzing the removal of an aromatic thiol, 2-mercaptobenzothiazole (MBT), from aqueous solution.	captax	174-177	peroxidase	Glycine max	71-81
20817298-4	2010	PAL activity, soluble and cell wall-bound POD activities, and H(2)O(2) and lignin contents increased significantly after Cd exposure.	Cadmium	121-123	peroxidase	Glycine max	42-45
18592408-4	2009	Natural anacardic acid was enzymatically polymerized using soybean peroxidase.	anacardic acid	8-22	peroxidase	Glycine max	67-77
20338952-10	2010	Addition of Na(2)SiO(3) reduced the K deficiency-induced increases in activities of superoxide dismutase, catalase and peroxidase.	na(2)sio(3)	12-23	peroxidase	Glycine max	119-129
19361921-2	2009	In this study enzyme (free and immobilized soybean peroxidase) and UV (produced by a KrCl excilamp) were used to treat 4-CP solutions at concentrations ranging from 50 to 500 mg L(-1).	4-chlorophenol	119-123	peroxidase	Glycine max	51-61
18038682-0	2007	[Use of soybean peroxidase for the enzyme immunoassay of sulfamethoxipyridazine in milk].	Sulfamethoxypyridazine	57-79	peroxidase	Glycine max	16-26
18703329-0	2009	Hydrogen peroxide biosensor based on direct electrochemistry of soybean peroxidase immobilized on single-walled carbon nanohorn modified electrode.	Hydrogen Peroxide	0-17	peroxidase	Glycine max	72-82
18703329-0	2009	Hydrogen peroxide biosensor based on direct electrochemistry of soybean peroxidase immobilized on single-walled carbon nanohorn modified electrode.	Carbon	112-118	peroxidase	Glycine max	72-82
18703329-2	2009	The direct immobilization of acid-stable and thermostable soybean peroxidase (SBP) on SWCNH modified electrode surface can realize the direct electrochemistry of enzyme.	swcnh	86-91	peroxidase	Glycine max	66-76
18673160-5	2008	The naturally occurring methoxyphenol apocynin has been found to inhibit NADPH oxidase upon activation by peroxidases (e.g. soybean peroxidase, myeloperoxidase) or ROS under mild reaction conditions.	methoxyphenol apocynin	24-46	peroxidase	Glycine max	106-116
18071845-0	2008	Effectiveness of phenoxyl radicals generated by peroxidase/H2O2-catalyzed oxidation of caffeate, ferulate, and p-coumarate in cooxidation of ascorbate and NADH.	phenoxy radical	17-34	peroxidase	Glycine max	48-58
18071845-0	2008	Effectiveness of phenoxyl radicals generated by peroxidase/H2O2-catalyzed oxidation of caffeate, ferulate, and p-coumarate in cooxidation of ascorbate and NADH.	caffeic acid	87-95	peroxidase	Glycine max	48-58
18071845-0	2008	Effectiveness of phenoxyl radicals generated by peroxidase/H2O2-catalyzed oxidation of caffeate, ferulate, and p-coumarate in cooxidation of ascorbate and NADH.	ferulic acid	97-105	peroxidase	Glycine max	48-58
18071845-0	2008	Effectiveness of phenoxyl radicals generated by peroxidase/H2O2-catalyzed oxidation of caffeate, ferulate, and p-coumarate in cooxidation of ascorbate and NADH.	trans-4-coumarate	111-122	peroxidase	Glycine max	48-58
18071845-0	2008	Effectiveness of phenoxyl radicals generated by peroxidase/H2O2-catalyzed oxidation of caffeate, ferulate, and p-coumarate in cooxidation of ascorbate and NADH.	Ascorbic Acid	141-150	peroxidase	Glycine max	48-58
18071845-0	2008	Effectiveness of phenoxyl radicals generated by peroxidase/H2O2-catalyzed oxidation of caffeate, ferulate, and p-coumarate in cooxidation of ascorbate and NADH.	NAD	155-159	peroxidase	Glycine max	48-58
18071845-1	2008	The rate of ascorbate and nicotinamide adenine dinucleotide plus hydrogen (NADH) cooxidation (i.e., their nonenzymic oxidation by peroxidase/H2O2-generated phenoxyl radicals of three hydroxycinnamates: caffeate, ferulate and p-coumarate) was studied in vitro.	Ascorbic Acid	12-21	peroxidase	Glycine max	130-140
18071845-1	2008	The rate of ascorbate and nicotinamide adenine dinucleotide plus hydrogen (NADH) cooxidation (i.e., their nonenzymic oxidation by peroxidase/H2O2-generated phenoxyl radicals of three hydroxycinnamates: caffeate, ferulate and p-coumarate) was studied in vitro.	NAD	26-59	peroxidase	Glycine max	130-140
18071845-1	2008	The rate of ascorbate and nicotinamide adenine dinucleotide plus hydrogen (NADH) cooxidation (i.e., their nonenzymic oxidation by peroxidase/H2O2-generated phenoxyl radicals of three hydroxycinnamates: caffeate, ferulate and p-coumarate) was studied in vitro.	Hydrogen	65-73	peroxidase	Glycine max	130-140
18071845-1	2008	The rate of ascorbate and nicotinamide adenine dinucleotide plus hydrogen (NADH) cooxidation (i.e., their nonenzymic oxidation by peroxidase/H2O2-generated phenoxyl radicals of three hydroxycinnamates: caffeate, ferulate and p-coumarate) was studied in vitro.	NAD	75-79	peroxidase	Glycine max	130-140
18071845-1	2008	The rate of ascorbate and nicotinamide adenine dinucleotide plus hydrogen (NADH) cooxidation (i.e., their nonenzymic oxidation by peroxidase/H2O2-generated phenoxyl radicals of three hydroxycinnamates: caffeate, ferulate and p-coumarate) was studied in vitro.	phenoxy radical	156-173	peroxidase	Glycine max	130-140
18071845-1	2008	The rate of ascorbate and nicotinamide adenine dinucleotide plus hydrogen (NADH) cooxidation (i.e., their nonenzymic oxidation by peroxidase/H2O2-generated phenoxyl radicals of three hydroxycinnamates: caffeate, ferulate and p-coumarate) was studied in vitro.	hydroxycinnamates	183-200	peroxidase	Glycine max	130-140
18071845-1	2008	The rate of ascorbate and nicotinamide adenine dinucleotide plus hydrogen (NADH) cooxidation (i.e., their nonenzymic oxidation by peroxidase/H2O2-generated phenoxyl radicals of three hydroxycinnamates: caffeate, ferulate and p-coumarate) was studied in vitro.	caffeic acid	202-210	peroxidase	Glycine max	130-140
18071845-1	2008	The rate of ascorbate and nicotinamide adenine dinucleotide plus hydrogen (NADH) cooxidation (i.e., their nonenzymic oxidation by peroxidase/H2O2-generated phenoxyl radicals of three hydroxycinnamates: caffeate, ferulate and p-coumarate) was studied in vitro.	ferulic acid	212-220	peroxidase	Glycine max	130-140
18071845-1	2008	The rate of ascorbate and nicotinamide adenine dinucleotide plus hydrogen (NADH) cooxidation (i.e., their nonenzymic oxidation by peroxidase/H2O2-generated phenoxyl radicals of three hydroxycinnamates: caffeate, ferulate and p-coumarate) was studied in vitro.	trans-4-coumarate	225-236	peroxidase	Glycine max	130-140
18071845-4	2008	The peroxidase sources differed both in the rate of H2O2-dependent hydroxycinnamate oxidation and in the order of affinity for the phenolic substrates.	Hydrogen Peroxide	52-56	peroxidase	Glycine max	4-14
18071845-4	2008	The peroxidase sources differed both in the rate of H2O2-dependent hydroxycinnamate oxidation and in the order of affinity for the phenolic substrates.	Coumaric Acids	67-83	peroxidase	Glycine max	4-14
18071845-7	2008	Metal ions (Zn2+ and Al3+) inhibited the reaction of peroxidase with p-coumarate and affected the cooxidation rate of ascorbate and the peroxidase reaction in the same manner with all substrates used.	Metals	0-5	peroxidase	Glycine max	53-63
18071845-7	2008	Metal ions (Zn2+ and Al3+) inhibited the reaction of peroxidase with p-coumarate and affected the cooxidation rate of ascorbate and the peroxidase reaction in the same manner with all substrates used.	Metals	0-5	peroxidase	Glycine max	136-146
18071845-7	2008	Metal ions (Zn2+ and Al3+) inhibited the reaction of peroxidase with p-coumarate and affected the cooxidation rate of ascorbate and the peroxidase reaction in the same manner with all substrates used.	Zinc	12-16	peroxidase	Glycine max	53-63
18071845-7	2008	Metal ions (Zn2+ and Al3+) inhibited the reaction of peroxidase with p-coumarate and affected the cooxidation rate of ascorbate and the peroxidase reaction in the same manner with all substrates used.	Zinc	12-16	peroxidase	Glycine max	136-146
18071845-7	2008	Metal ions (Zn2+ and Al3+) inhibited the reaction of peroxidase with p-coumarate and affected the cooxidation rate of ascorbate and the peroxidase reaction in the same manner with all substrates used.	ALUMINUM ION	21-25	peroxidase	Glycine max	53-63
18071845-7	2008	Metal ions (Zn2+ and Al3+) inhibited the reaction of peroxidase with p-coumarate and affected the cooxidation rate of ascorbate and the peroxidase reaction in the same manner with all substrates used.	ALUMINUM ION	21-25	peroxidase	Glycine max	136-146
18071845-7	2008	Metal ions (Zn2+ and Al3+) inhibited the reaction of peroxidase with p-coumarate and affected the cooxidation rate of ascorbate and the peroxidase reaction in the same manner with all substrates used.	trans-4-coumarate	69-80	peroxidase	Glycine max	53-63
18038682-1	2007	An enzyme immunoassay with colorimetric detection of sulfamethoxipyridazine (SMP), the most widely used sulfamide, was developed with the soybean anionic peroxidase as an enzyme marker.	Sulfamethoxypyridazine	77-80	peroxidase	Glycine max	154-164
17330483-2	2006	Sulfur fertilization also increased the amount of soil bacteria, fungi and actinomycetes and the activities of peroxidase, urease, neutral phosphatase and polyphenoloxidase significantly.	Sulfur	0-6	peroxidase	Glycine max	111-121
17267016-0	2007	Removal of dinitrotoluenes from water via reduction with iron and peroxidase-catalyzed oxidative polymerization: a comparison between Arthromyces ramosus peroxidase and soybean peroxidase.	Dinitrobenzenes	11-26	peroxidase	Glycine max	66-76
19704805-5	2007	In vitro exposure of chloroplasts to a NO-donor (GSNO) decreased both ascorbyl radical content and the activity of ascorbate peroxidase, without modification of the total ascorbate content.	S-Nitrosoglutathione	49-53	peroxidase	Glycine max	125-135
19704805-5	2007	In vitro exposure of chloroplasts to a NO-donor (GSNO) decreased both ascorbyl radical content and the activity of ascorbate peroxidase, without modification of the total ascorbate content.	Ascorbic Acid	115-124	peroxidase	Glycine max	125-135
19704805-8	2007	Taken as a whole, NO seems to be an endogenous metabolite in soybean chloroplasts and reactive nitrogen species could exert either antioxidant or prooxidant effects on chloroplasts, since both a decreased lipid radical content in membranes and a decrease in the activity of ascorbate peroxidase were observed after exposure to a NO donor.	Reactive Nitrogen Species	86-111	peroxidase	Glycine max	284-294
17195115-7	2007	In general, the length, fresh weight, and dry weight of the roots decreased, whereas PAL and POD activities and phenolic compound and lignin content increased after L-DOPA treatments.	Levodopa	165-171	peroxidase	Glycine max	93-96
16769153-9	2007	Under water-stressed conditions, uniconazole increased the content of proline and soluble sugars, and the activities of superoxide dismutase and peroxidase in soybean leaves but not the malondialdehyde content or electrical conductivity.	Water	6-11	peroxidase	Glycine max	145-155
16769153-9	2007	Under water-stressed conditions, uniconazole increased the content of proline and soluble sugars, and the activities of superoxide dismutase and peroxidase in soybean leaves but not the malondialdehyde content or electrical conductivity.	uniconazole	33-44	peroxidase	Glycine max	145-155
17055627-4	2007	Among the enzymatic antioxidants, activity of superoxide dismutase, ascorbate peroxidase and glutathione reductase increased significantly whereas that of catalase declined markedly in relation to increasing concentration of Deltamethrin applied.	decamethrin	225-237	peroxidase	Glycine max	78-88
17267016-0	2007	Removal of dinitrotoluenes from water via reduction with iron and peroxidase-catalyzed oxidative polymerization: a comparison between Arthromyces ramosus peroxidase and soybean peroxidase.	Dinitrobenzenes	11-26	peroxidase	Glycine max	154-164
17267016-0	2007	Removal of dinitrotoluenes from water via reduction with iron and peroxidase-catalyzed oxidative polymerization: a comparison between Arthromyces ramosus peroxidase and soybean peroxidase.	Dinitrobenzenes	11-26	peroxidase	Glycine max	154-164
17267016-0	2007	Removal of dinitrotoluenes from water via reduction with iron and peroxidase-catalyzed oxidative polymerization: a comparison between Arthromyces ramosus peroxidase and soybean peroxidase.	Water	32-37	peroxidase	Glycine max	66-76
17267016-1	2007	A two-step process for the removal of dinitrotoluene from water is presented: zero-valent iron reduction is coupled with peroxidase-catalyzed polymerization of the resulting diaminotoluenes (DAT).	Dinitrobenzenes	38-52	peroxidase	Glycine max	121-131
17267016-1	2007	A two-step process for the removal of dinitrotoluene from water is presented: zero-valent iron reduction is coupled with peroxidase-catalyzed polymerization of the resulting diaminotoluenes (DAT).	Water	58-63	peroxidase	Glycine max	121-131
17267016-1	2007	A two-step process for the removal of dinitrotoluene from water is presented: zero-valent iron reduction is coupled with peroxidase-catalyzed polymerization of the resulting diaminotoluenes (DAT).	Iron	90-94	peroxidase	Glycine max	121-131
17267016-1	2007	A two-step process for the removal of dinitrotoluene from water is presented: zero-valent iron reduction is coupled with peroxidase-catalyzed polymerization of the resulting diaminotoluenes (DAT).	2,4-diaminotoluene	174-189	peroxidase	Glycine max	121-131
17267016-1	2007	A two-step process for the removal of dinitrotoluene from water is presented: zero-valent iron reduction is coupled with peroxidase-catalyzed polymerization of the resulting diaminotoluenes (DAT).	2,4-diaminotoluene	191-194	peroxidase	Glycine max	121-131
17450942-2	2007	The half-life of a model enzyme, soybean peroxidase, adsorbed onto fullerenes at 95 degrees C was 117 min, ca.	Fullerenes	67-77	peroxidase	Glycine max	41-51
17076497-3	2006	The influence of the reaction media on soybean peroxidase-catalyzed oxidation of para-substituted phenols was studied using Hammett analysis for several organic solvent systems.	para-substituted phenols	81-105	peroxidase	Glycine max	47-57
16967316-0	2006	ESR spectroscopy investigation of the denaturation process of soybean peroxidase induced by guanidine hydrochloride, DMSO or heat.	Guanidine	92-115	peroxidase	Glycine max	70-80
16967316-0	2006	ESR spectroscopy investigation of the denaturation process of soybean peroxidase induced by guanidine hydrochloride, DMSO or heat.	Dimethyl Sulfoxide	117-121	peroxidase	Glycine max	70-80
16002139-9	2006	Oxidation of [C(3)H(3)]TNT by peroxidase and phenoloxidase was also studied.	c(3)h(3)	14-22	peroxidase	Glycine max	30-40
16188293-1	2006	This paper describes a comparison between horseradish peroxidase (HRP) and soybean peroxidase (SBP), the two most widely used commercial peroxidases for the removal of phenol from wastewater.	Phenol	168-174	peroxidase	Glycine max	54-64
16188293-1	2006	This paper describes a comparison between horseradish peroxidase (HRP) and soybean peroxidase (SBP), the two most widely used commercial peroxidases for the removal of phenol from wastewater.	Phenol	168-174	peroxidase	Glycine max	83-93
16506804-1	2006	A procedure for the production of conjugates of soybean peroxidase (SbP) oxidized by sodium periodate and anti-mouse IgG antibody (Ab) was optimized.	metaperiodate	85-101	peroxidase	Glycine max	56-66
16337930-1	2006	Reanalysis of the tryptic digests of soybean seed coat peroxidase (SBP) and its carboxyamidated peptide derivatives in the light of more complete sequence data has thrown light on the diglycosylated tryptic peptides, TP13 (Leu[183-205]Arg) and TP15 (Cys[208-231]Arg).	Peptides	207-215	peroxidase	Glycine max	55-65
16337930-1	2006	Reanalysis of the tryptic digests of soybean seed coat peroxidase (SBP) and its carboxyamidated peptide derivatives in the light of more complete sequence data has thrown light on the diglycosylated tryptic peptides, TP13 (Leu[183-205]Arg) and TP15 (Cys[208-231]Arg).	Cysteine	250-253	peroxidase	Glycine max	55-65
16337930-1	2006	Reanalysis of the tryptic digests of soybean seed coat peroxidase (SBP) and its carboxyamidated peptide derivatives in the light of more complete sequence data has thrown light on the diglycosylated tryptic peptides, TP13 (Leu[183-205]Arg) and TP15 (Cys[208-231]Arg).	Arginine	235-238	peroxidase	Glycine max	55-65
15998149-0	2005	Soybean peroxidase-catalyzed oxidation of luminol by hydrogen peroxide.	Luminol	42-49	peroxidase	Glycine max	8-18
15998149-0	2005	Soybean peroxidase-catalyzed oxidation of luminol by hydrogen peroxide.	Hydrogen Peroxide	53-70	peroxidase	Glycine max	8-18
15998149-1	2005	Anionic soybean peroxidase Glycine max (SbP) is shown to efficiently catalyze luminol oxidation by hydrogen peroxide.	Luminol	78-85	peroxidase	Glycine max	16-26
15998149-1	2005	Anionic soybean peroxidase Glycine max (SbP) is shown to efficiently catalyze luminol oxidation by hydrogen peroxide.	Hydrogen Peroxide	99-116	peroxidase	Glycine max	16-26
16086255-3	2005	When compared to laccase in combination with a mediator (ABTS), soybean peroxidase was more effective at oxidative dye removal, especially for the methine dye.	2,2'-azino-di-(3-ethylbenzothiazoline)-6-sulfonic acid	57-61	peroxidase	Glycine max	72-82
15381099-3	2004	Treatment with 200 microM Cd during 48 h caused a 70% increase in thiobarbituric acid reactive substances, whereas GSH decreased 67%, guaiacol peroxidase and total superoxide dismutase also inhibited 49% and 46%, respectively.	Cadmium	26-28	peroxidase	Glycine max	143-153
15877353-0	2005	Synthesis of conducting polyelectrolyte complexes of polyaniline and poly(2-acrylamido-3-methyl-1-propanesulfonic acid) catalyzed by pH-stable palm tree peroxidase.	polyaniline	53-64	peroxidase	Glycine max	153-163
15877353-0	2005	Synthesis of conducting polyelectrolyte complexes of polyaniline and poly(2-acrylamido-3-methyl-1-propanesulfonic acid) catalyzed by pH-stable palm tree peroxidase.	poly(2-acrylamido-3-methyl-1-propanesulfonic acid	69-118	peroxidase	Glycine max	153-163
15877353-3	2005	Using this peroxidase as a catalyst, the enzymatic synthesis of polyelectrolyte complexes of PANI and poly(2-acrylamido-3-methyl-1-propanesulfonic acid) (PAMPS) was developed.	poly(2-acrylamido-3-methyl-1-propanesulfonic acid)	102-152	peroxidase	Glycine max	11-21
15877353-3	2005	Using this peroxidase as a catalyst, the enzymatic synthesis of polyelectrolyte complexes of PANI and poly(2-acrylamido-3-methyl-1-propanesulfonic acid) (PAMPS) was developed.	pamps	154-159	peroxidase	Glycine max	11-21
14571976-0	2003	Polymerization of cardanol using soybean peroxidase and its potential application as anti-biofilm coating material.	cardanol	18-26	peroxidase	Glycine max	41-51
15236572-0	2004	Crystal structure of the ascorbate peroxidase-salicylhydroxamic acid complex.	salicylhydroxamic acid	46-68	peroxidase	Glycine max	35-45
15236572-1	2004	Ascorbate peroxidase is a bifunctional peroxidase that catalyzes the H(2)O(2)-dependent oxidation of both ascorbate and various aromatic substrates.	Hydrogen Peroxide	69-77	peroxidase	Glycine max	10-20
15236572-1	2004	Ascorbate peroxidase is a bifunctional peroxidase that catalyzes the H(2)O(2)-dependent oxidation of both ascorbate and various aromatic substrates.	Hydrogen Peroxide	69-77	peroxidase	Glycine max	39-49
15236572-1	2004	Ascorbate peroxidase is a bifunctional peroxidase that catalyzes the H(2)O(2)-dependent oxidation of both ascorbate and various aromatic substrates.	Ascorbic Acid	106-115	peroxidase	Glycine max	10-20
15236572-1	2004	Ascorbate peroxidase is a bifunctional peroxidase that catalyzes the H(2)O(2)-dependent oxidation of both ascorbate and various aromatic substrates.	Ascorbic Acid	106-115	peroxidase	Glycine max	39-49
15236572-6	2004	In this work, the X-ray crystal structure of recombinant soybean cytosolic ascorbate peroxidase (rsAPX) in complex with salicylhydroxamic acid (SHA) has been determined to 1.46 A.	salicylhydroxamic acid	120-142	peroxidase	Glycine max	85-95
15303323-4	2004	Length, fresh weight, and dry weight of roots decreased, while soluble and cell wall bound POD activity, PAL activity, and lignin content increased after ferulic acid treatment.	ferulic acid	154-166	peroxidase	Glycine max	91-94
14755564-4	2004	Salt-activation, a technique previously demonstrated to substantially increase the transesterification activity of hydrolytic enzymes in organic solvents, was applied to horse liver alcohol dehydrogenase, soybean peroxidase, galactose oxidase, and xanthine oxidase, which are oxidoreductase and oxygenase enzymes.	Salts	0-4	peroxidase	Glycine max	213-223
14571976-1	2003	Soybean peroxidase (20 mg) catalyzed the oxidative polymerization of cardanol in 2-propanol/phospate buffer solution (25 ml, 1:1 v/v) and yielded 62% polycardanol over 6 h. Cobalt naphthenate (0.5% w/w) catalyzed the crosslinking of polycardanol and the final hardness of crosslinked polycardanol film exceeded 9 H scale as pencil scratch hardness, which shows a high potential as a commercial coating material.	cardanol	69-77	peroxidase	Glycine max	8-18
14571976-1	2003	Soybean peroxidase (20 mg) catalyzed the oxidative polymerization of cardanol in 2-propanol/phospate buffer solution (25 ml, 1:1 v/v) and yielded 62% polycardanol over 6 h. Cobalt naphthenate (0.5% w/w) catalyzed the crosslinking of polycardanol and the final hardness of crosslinked polycardanol film exceeded 9 H scale as pencil scratch hardness, which shows a high potential as a commercial coating material.	2-Propanol	81-91	peroxidase	Glycine max	8-18
14571976-1	2003	Soybean peroxidase (20 mg) catalyzed the oxidative polymerization of cardanol in 2-propanol/phospate buffer solution (25 ml, 1:1 v/v) and yielded 62% polycardanol over 6 h. Cobalt naphthenate (0.5% w/w) catalyzed the crosslinking of polycardanol and the final hardness of crosslinked polycardanol film exceeded 9 H scale as pencil scratch hardness, which shows a high potential as a commercial coating material.	phospate	92-100	peroxidase	Glycine max	8-18
14571976-1	2003	Soybean peroxidase (20 mg) catalyzed the oxidative polymerization of cardanol in 2-propanol/phospate buffer solution (25 ml, 1:1 v/v) and yielded 62% polycardanol over 6 h. Cobalt naphthenate (0.5% w/w) catalyzed the crosslinking of polycardanol and the final hardness of crosslinked polycardanol film exceeded 9 H scale as pencil scratch hardness, which shows a high potential as a commercial coating material.	polycardanol	150-162	peroxidase	Glycine max	8-18
14571976-1	2003	Soybean peroxidase (20 mg) catalyzed the oxidative polymerization of cardanol in 2-propanol/phospate buffer solution (25 ml, 1:1 v/v) and yielded 62% polycardanol over 6 h. Cobalt naphthenate (0.5% w/w) catalyzed the crosslinking of polycardanol and the final hardness of crosslinked polycardanol film exceeded 9 H scale as pencil scratch hardness, which shows a high potential as a commercial coating material.	naphthenic acid	173-191	peroxidase	Glycine max	8-18
14571976-1	2003	Soybean peroxidase (20 mg) catalyzed the oxidative polymerization of cardanol in 2-propanol/phospate buffer solution (25 ml, 1:1 v/v) and yielded 62% polycardanol over 6 h. Cobalt naphthenate (0.5% w/w) catalyzed the crosslinking of polycardanol and the final hardness of crosslinked polycardanol film exceeded 9 H scale as pencil scratch hardness, which shows a high potential as a commercial coating material.	polycardanol	233-245	peroxidase	Glycine max	8-18
14571976-1	2003	Soybean peroxidase (20 mg) catalyzed the oxidative polymerization of cardanol in 2-propanol/phospate buffer solution (25 ml, 1:1 v/v) and yielded 62% polycardanol over 6 h. Cobalt naphthenate (0.5% w/w) catalyzed the crosslinking of polycardanol and the final hardness of crosslinked polycardanol film exceeded 9 H scale as pencil scratch hardness, which shows a high potential as a commercial coating material.	polycardanol	233-245	peroxidase	Glycine max	8-18
12514805-0	2003	Microfluidic peroxidase biochip for polyphenol synthesis.	Polyphenols	36-46	peroxidase	Glycine max	13-23
12732522-0	2003	Enhanced killing of Acanthamoeba cysts with a plant peroxidase-hydrogen peroxide-halide antimicrobial system.	Hydrogen Peroxide	63-80	peroxidase	Glycine max	52-62
12732522-0	2003	Enhanced killing of Acanthamoeba cysts with a plant peroxidase-hydrogen peroxide-halide antimicrobial system.	halide	81-87	peroxidase	Glycine max	52-62
12732522-1	2003	The activity of H(2)O(2) against the resistant cyst stage of the pathogenic free-living amoeba Acanthamoeba was enhanced by the addition of KI and either horseradish peroxidase or soybean peroxidase or, to a lesser degree, lactoperoxidase.	Hydrogen Peroxide	16-24	peroxidase	Glycine max	166-176
12732522-1	2003	The activity of H(2)O(2) against the resistant cyst stage of the pathogenic free-living amoeba Acanthamoeba was enhanced by the addition of KI and either horseradish peroxidase or soybean peroxidase or, to a lesser degree, lactoperoxidase.	Hydrogen Peroxide	16-24	peroxidase	Glycine max	188-198
12514805-6	2003	Soybean peroxidase was used as the phenol oxidizing catalyst, and in the presence of p-cresol and H(2)O(2), essentially complete conversion of the H(2)O(2) (the limiting substrate) occurred in the microchannel at a flow rate of ca.	Phenol	35-41	peroxidase	Glycine max	8-18
12514805-6	2003	Soybean peroxidase was used as the phenol oxidizing catalyst, and in the presence of p-cresol and H(2)O(2), essentially complete conversion of the H(2)O(2) (the limiting substrate) occurred in the microchannel at a flow rate of ca.	4-cresol	85-93	peroxidase	Glycine max	8-18
12514805-6	2003	Soybean peroxidase was used as the phenol oxidizing catalyst, and in the presence of p-cresol and H(2)O(2), essentially complete conversion of the H(2)O(2) (the limiting substrate) occurred in the microchannel at a flow rate of ca.	Hydrogen Peroxide	98-106	peroxidase	Glycine max	8-18
12514805-6	2003	Soybean peroxidase was used as the phenol oxidizing catalyst, and in the presence of p-cresol and H(2)O(2), essentially complete conversion of the H(2)O(2) (the limiting substrate) occurred in the microchannel at a flow rate of ca.	Hydrogen Peroxide	147-155	peroxidase	Glycine max	8-18
12514805-9	2003	These results were extended to a series of phenols, thereby demonstrating that the microfluidic peroxidase reactor may have application in high-throughput screening of phenolic polymerization reactions for use in phenolic resin synthesis.	Phenols	43-50	peroxidase	Glycine max	96-106
12514805-11	2003	This finding suggests that solution-phase peroxidase catalysis can be used in the controlled deposition of polymers on the walls of microreactors.	Polymers	107-115	peroxidase	Glycine max	42-52
12396133-1	2002	The peroxidase enzyme from the plants Ipomea palmata (1.003 IU/g of leaf) and Saccharum spontaneum (3.6 IU/g of leaf) can be used as an alternative to the commercial source of horseradish and soybean peroxidase enzyme for the decolorization of textile dyes, mainly azo dyes.	Azo Compounds	265-273	peroxidase	Glycine max	4-14
12682976-3	2002	During 1-6 days of TCB stress, peroxidase (POD) activity gradually increased, and superoxide dismutase (SOD) activity increased firstly, and decreased afterward.	1,2,4-trichlorobenzene	19-22	peroxidase	Glycine max	31-41
12682976-3	2002	During 1-6 days of TCB stress, peroxidase (POD) activity gradually increased, and superoxide dismutase (SOD) activity increased firstly, and decreased afterward.	1,2,4-trichlorobenzene	19-22	peroxidase	Glycine max	43-46
12427040-0	2002	Substrate binding and catalytic mechanism in ascorbate peroxidase: evidence for two ascorbate binding sites.	Ascorbic Acid	45-54	peroxidase	Glycine max	55-65
12427040-1	2002	The catalytic mechanism of recombinant soybean cytosolic ascorbate peroxidase (rsAPX) and a derivative of rsAPX in which a cysteine residue (Cys32) located close to the substrate (L-ascorbic acid) binding site has been modified to preclude binding of ascorbate [Mandelman, D., Jamal, J., and Poulos, T. L. (1998) Biochemistry 37, 17610-17617] has been examined using pre-steady-state and steady-state kinetic techniques.	rsapx	79-84	peroxidase	Glycine max	67-77
12427040-1	2002	The catalytic mechanism of recombinant soybean cytosolic ascorbate peroxidase (rsAPX) and a derivative of rsAPX in which a cysteine residue (Cys32) located close to the substrate (L-ascorbic acid) binding site has been modified to preclude binding of ascorbate [Mandelman, D., Jamal, J., and Poulos, T. L. (1998) Biochemistry 37, 17610-17617] has been examined using pre-steady-state and steady-state kinetic techniques.	Ascorbic Acid	57-66	peroxidase	Glycine max	67-77
12165299-0	2002	Polysaccharide degradation by Fenton reaction--or peroxidase-generated hydroxyl radicals in isolated plant cell walls.	Hydroxyl Radical	71-88	peroxidase	Glycine max	50-60
12165299-4	2002	The peroxidase-catalyzed degradation of cell-wall polysaccharides can be inhibited by KCN and superoxide radical (O(2)*) or OH* scavengers.	Polysaccharides	50-65	peroxidase	Glycine max	4-14
12165299-4	2002	The peroxidase-catalyzed degradation of cell-wall polysaccharides can be inhibited by KCN and superoxide radical (O(2)*) or OH* scavengers.	Potassium Cyanide	86-89	peroxidase	Glycine max	4-14
12165299-4	2002	The peroxidase-catalyzed degradation of cell-wall polysaccharides can be inhibited by KCN and superoxide radical (O(2)*) or OH* scavengers.	Superoxides	94-112	peroxidase	Glycine max	4-14
12165299-4	2002	The peroxidase-catalyzed degradation of cell-wall polysaccharides can be inhibited by KCN and superoxide radical (O(2)*) or OH* scavengers.	Superoxides	114-120	peroxidase	Glycine max	4-14
12125206-1	2002	The influence of the allelochemicals ferulic (FA) and vanillic (VA) acids on peroxidase (POD, EC 1.11.1.7) and phenylalanine ammonia-lyase (PAL, EC 4.3.1.5) activities and their relationships with phenolic acid (PhAs) contents and root growth of soybean (Glycine max (L.) Merr.)	vanillic	54-62	peroxidase	Glycine max	77-87
12150251-0	2002	Removal of nitroaromatics from synthetic wastewater using two-step zero-valent iron reduction and peroxidase-catalyzed oxidative polymerization.	nitroaromatics	11-25	peroxidase	Glycine max	98-108
12150251-2	2002	Zero-valent iron reduction of nitroaromatics coupled with peroxidase-catalyzed capture of the resulting anilines as a two-step strategy for removing nitroaromatics from wastewater and process water is investigated here.	Iron	12-16	peroxidase	Glycine max	58-68
12150251-2	2002	Zero-valent iron reduction of nitroaromatics coupled with peroxidase-catalyzed capture of the resulting anilines as a two-step strategy for removing nitroaromatics from wastewater and process water is investigated here.	nitroaromatics	30-44	peroxidase	Glycine max	58-68
12150251-2	2002	Zero-valent iron reduction of nitroaromatics coupled with peroxidase-catalyzed capture of the resulting anilines as a two-step strategy for removing nitroaromatics from wastewater and process water is investigated here.	Aniline Compounds	104-112	peroxidase	Glycine max	58-68
12150251-2	2002	Zero-valent iron reduction of nitroaromatics coupled with peroxidase-catalyzed capture of the resulting anilines as a two-step strategy for removing nitroaromatics from wastewater and process water is investigated here.	nitroaromatics	149-163	peroxidase	Glycine max	58-68
12150251-5	2002	The enzymatic treatment following zero-valent iron reduction was carried out in a plug-flow reactor using a crude preparation of the enzyme soybean peroxidase extracted from soybean hulls.	Iron	46-50	peroxidase	Glycine max	148-158
12125206-1	2002	The influence of the allelochemicals ferulic (FA) and vanillic (VA) acids on peroxidase (POD, EC 1.11.1.7) and phenylalanine ammonia-lyase (PAL, EC 4.3.1.5) activities and their relationships with phenolic acid (PhAs) contents and root growth of soybean (Glycine max (L.) Merr.)	Vanillic Acid	64-66	peroxidase	Glycine max	77-87
12125206-1	2002	The influence of the allelochemicals ferulic (FA) and vanillic (VA) acids on peroxidase (POD, EC 1.11.1.7) and phenylalanine ammonia-lyase (PAL, EC 4.3.1.5) activities and their relationships with phenolic acid (PhAs) contents and root growth of soybean (Glycine max (L.) Merr.)	Vanillic Acid	64-66	peroxidase	Glycine max	89-92
11342058-11	2001	The reactions of soybean peroxidase compounds I and II with veratryl alcohol at pH 2.44 give very similar second order rate constants, k(2)=(2.5+/-0.1)x10(4) M(-1) s(-1) and k(3)=(2.2+/-0.1)x10(4) M(-1) s(-1), respectively, which is unusual.	veratryl alcohol	60-76	peroxidase	Glycine max	25-35
11642043-1	2001	Horseradish peroxidase is immobilized by a periodate method on the gold surfaces previously modified with 16-mercapto-hexadecanoic acid or with hydrogen disulfide and soybean trypsin inhibitor.	16-mercaptohexadecanoic acid	106-135	peroxidase	Glycine max	12-22
11642043-1	2001	Horseradish peroxidase is immobilized by a periodate method on the gold surfaces previously modified with 16-mercapto-hexadecanoic acid or with hydrogen disulfide and soybean trypsin inhibitor.	Disulfides	144-162	peroxidase	Glycine max	12-22
11266599-5	2001	This TRIS molecule has hydrogen bonds to active site residues corresponding to the residues that interact with the small phenolic substrate ferulic acid in the horseradish peroxidase C (HRPC):ferulic acid complex.	Tromethamine	5-9	peroxidase	Glycine max	172-182
11266599-5	2001	This TRIS molecule has hydrogen bonds to active site residues corresponding to the residues that interact with the small phenolic substrate ferulic acid in the horseradish peroxidase C (HRPC):ferulic acid complex.	Hydrogen	23-31	peroxidase	Glycine max	172-182
11266599-5	2001	This TRIS molecule has hydrogen bonds to active site residues corresponding to the residues that interact with the small phenolic substrate ferulic acid in the horseradish peroxidase C (HRPC):ferulic acid complex.	ferulic acid	140-152	peroxidase	Glycine max	172-182
11266599-5	2001	This TRIS molecule has hydrogen bonds to active site residues corresponding to the residues that interact with the small phenolic substrate ferulic acid in the horseradish peroxidase C (HRPC):ferulic acid complex.	ferulic acid	192-204	peroxidase	Glycine max	172-182
11266599-7	2001	SBP has one of the most solvent accessible delta-meso haem edge (the site of electron transfer from reducing substrates to the enzymatic intermediates compound I and II) so far described for a plant peroxidase and structural alignment suggests that the volume of Ile74 is a factor that influences the solvent accessibility of this important site.	delta-meso haem	43-58	peroxidase	Glycine max	199-209
10992240-6	2000	Sulfoxidation of thioanisole catalyzed by four other hemoproteins (soybean peroxidase, myoglobin, hemoglobin, and cytochrome c) is also much faster in isopropyl alcohol than in water.	Water	177-182	peroxidase	Glycine max	75-85
10861408-7	2000	Soybean peroxidase, which normally shows only classical peroxidase activity, was transformed into an oxygen-transfer catalyst when coimmobilized with glucose oxidase.	Oxygen	101-107	peroxidase	Glycine max	8-18
10992240-0	2000	Peroxidase-catalyzed asymmetric sulfoxidation in organic solvents versus in water.	Water	76-81	peroxidase	Glycine max	0-10
10992240-1	2000	Peroxidase-catalyzed asymmetric sulfoxidations, while synthetically attractive, suffer from relatively low reaction rates due to poor substrate solubilities in water and from appreciable spontaneous oxidation of substrates (especially aryl alkyl sulfides) with H(2)O(2).	Water	160-165	peroxidase	Glycine max	0-10
10992240-1	2000	Peroxidase-catalyzed asymmetric sulfoxidations, while synthetically attractive, suffer from relatively low reaction rates due to poor substrate solubilities in water and from appreciable spontaneous oxidation of substrates (especially aryl alkyl sulfides) with H(2)O(2).	aryl alkyl sulfides	235-254	peroxidase	Glycine max	0-10
10992240-1	2000	Peroxidase-catalyzed asymmetric sulfoxidations, while synthetically attractive, suffer from relatively low reaction rates due to poor substrate solubilities in water and from appreciable spontaneous oxidation of substrates (especially aryl alkyl sulfides) with H(2)O(2).	Water	261-266	peroxidase	Glycine max	0-10
10992240-4	2000	In addition, the rates of asymmetric sulfoxidation of thioanisole in isopropyl alcohol and in methanol catalyzed by horseradish peroxidase (HRP) were determined to be tens to hundreds of times faster than in water under otherwise identical conditions.	methylphenylsulfide	54-65	peroxidase	Glycine max	128-138
10992240-4	2000	In addition, the rates of asymmetric sulfoxidation of thioanisole in isopropyl alcohol and in methanol catalyzed by horseradish peroxidase (HRP) were determined to be tens to hundreds of times faster than in water under otherwise identical conditions.	2-Propanol	69-86	peroxidase	Glycine max	128-138
10992240-4	2000	In addition, the rates of asymmetric sulfoxidation of thioanisole in isopropyl alcohol and in methanol catalyzed by horseradish peroxidase (HRP) were determined to be tens to hundreds of times faster than in water under otherwise identical conditions.	Methanol	94-102	peroxidase	Glycine max	128-138
10992240-4	2000	In addition, the rates of asymmetric sulfoxidation of thioanisole in isopropyl alcohol and in methanol catalyzed by horseradish peroxidase (HRP) were determined to be tens to hundreds of times faster than in water under otherwise identical conditions.	Water	208-213	peroxidase	Glycine max	128-138
10992240-6	2000	Sulfoxidation of thioanisole catalyzed by four other hemoproteins (soybean peroxidase, myoglobin, hemoglobin, and cytochrome c) is also much faster in isopropyl alcohol than in water.	methylphenylsulfide	17-28	peroxidase	Glycine max	75-85
10992240-6	2000	Sulfoxidation of thioanisole catalyzed by four other hemoproteins (soybean peroxidase, myoglobin, hemoglobin, and cytochrome c) is also much faster in isopropyl alcohol than in water.	2-Propanol	151-168	peroxidase	Glycine max	75-85
10861408-7	2000	Soybean peroxidase, which normally shows only classical peroxidase activity, was transformed into an oxygen-transfer catalyst when coimmobilized with glucose oxidase.	Oxygen	101-107	peroxidase	Glycine max	56-66
10820120-1	2000	The potential of different peroxidase preparations for the N-demethylation of methyl N-methylanthranilate to produce the food flavor methylanthranilate (MA) was investigated.	methyl N-methylanthranilate	78-105	peroxidase	Glycine max	27-37
10942299-0	2000	Purification of soybean peroxidase (Glycine max) by metal affinity partitioning in aqueous two-phase systems.	Metals	52-57	peroxidase	Glycine max	24-34
10942299-1	2000	Combining two concepts in downstream processing, this work investigates the partitioning of a crude soybean peroxidase (Glycine max) in an aqueous two-phase system by metal affinity.	Metals	167-172	peroxidase	Glycine max	108-118
10942299-2	2000	A liquid-liquid extraction process using metal ligands was developed in two steps with the aim of purifying the enzyme peroxidase.	Metals	41-46	peroxidase	Glycine max	119-129
10942299-5	2000	In the second step, a system formed by 14% PEG 4000 and 10% phosphate was used to revert the value of the partition coefficient of peroxidase to the bottom salt-rich phase (K = 0.05), thereby achieving a recovery of 64% of the purified enzyme.	Polyethylene Glycols	43-46	peroxidase	Glycine max	131-141
10942299-5	2000	In the second step, a system formed by 14% PEG 4000 and 10% phosphate was used to revert the value of the partition coefficient of peroxidase to the bottom salt-rich phase (K = 0.05), thereby achieving a recovery of 64% of the purified enzyme.	Phosphates	60-69	peroxidase	Glycine max	131-141
10942299-5	2000	In the second step, a system formed by 14% PEG 4000 and 10% phosphate was used to revert the value of the partition coefficient of peroxidase to the bottom salt-rich phase (K = 0.05), thereby achieving a recovery of 64% of the purified enzyme.	Salts	156-160	peroxidase	Glycine max	131-141
10785362-1	2000	Homovanillic acid is the most extensively employed reagent for the fluorometric detection of peroxidase.	Homovanillic Acid	0-17	peroxidase	Glycine max	93-103
10785362-8	2000	It can be affirmed that possible interference by other oxidative systems - that could be present in the biological materials tested - should be considered in assays of peroxidase activity based on the detection of the dimer of homovanillic acid.	Homovanillic Acid	227-244	peroxidase	Glycine max	168-178
10835257-1	2000	Phenolic polymers were synthesized via soybean hull peroxidase catalysis and used as metal-based sensor components in a polymer array.	Polymers	9-17	peroxidase	Glycine max	52-62
10835257-1	2000	Phenolic polymers were synthesized via soybean hull peroxidase catalysis and used as metal-based sensor components in a polymer array.	Metals	85-90	peroxidase	Glycine max	52-62
10835257-1	2000	Phenolic polymers were synthesized via soybean hull peroxidase catalysis and used as metal-based sensor components in a polymer array.	Polymers	9-16	peroxidase	Glycine max	52-62
10820120-1	2000	The potential of different peroxidase preparations for the N-demethylation of methyl N-methylanthranilate to produce the food flavor methylanthranilate (MA) was investigated.	methyl anthranilate	87-105	peroxidase	Glycine max	27-37
10361493-0	1999	Sol-gel thin-film immobilized soybean peroxidase biosensor for the amperometric determination of hydrogen peroxide in acid medium.	Hydrogen Peroxide	97-114	peroxidase	Glycine max	38-48
10731690-5	2000	The highest yields of conjugate were obtained with a 15-fold excess of peroxidase in phosphate buffer, pH 7.0.	Phosphates	85-94	peroxidase	Glycine max	71-81
16228440-4	2000	The other effects of O(3) treatment were decrease in seed yield, loss of total sulfhydryl groups, reduction of soluble protein content, and increase in guaiacol peroxidase activity in leaves of both cultivars.	Ozone	21-25	peroxidase	Glycine max	161-171
16228440-5	2000	The O(3)-induced increase in guaiacol peroxidase activity was much smaller in cv.	Ozone	4-8	peroxidase	Glycine max	38-48
10647213-0	1999	Effectiveness of ascorbate and ascorbate peroxidase in promoting nitrogen fixation in model systems.	Nitrogen	65-73	peroxidase	Glycine max	41-51
9464451-3	1997	In this report, it was observed that an acidic methanolic extract of soybeans contains compounds that inhibit thyroid peroxidase- (TPO) catalyzed reactions essential to thyroid hormone synthesis.	methanolic	47-57	peroxidase	Glycine max	118-128
10103001-4	1999	Here we show that horseradish peroxidase can also catalyze a third type of reaction that results in the production of hydroxyl radicals (.OH) from H2O2 in the presence of O2.-.	Hydroxyl Radical	118-135	peroxidase	Glycine max	30-40
10103001-4	1999	Here we show that horseradish peroxidase can also catalyze a third type of reaction that results in the production of hydroxyl radicals (.OH) from H2O2 in the presence of O2.-.	Hydrogen Peroxide	147-151	peroxidase	Glycine max	30-40
10103001-4	1999	Here we show that horseradish peroxidase can also catalyze a third type of reaction that results in the production of hydroxyl radicals (.OH) from H2O2 in the presence of O2.-.	Oxygen	149-151	peroxidase	Glycine max	30-40
10103001-5	1999	We provide evidence that to mediate this reaction, the ferric form of horseradish peroxidase must be converted by O2.- into the perferryl form (Compound III), in which the haem iron can assume the ferrous state.	Oxygen	114-116	peroxidase	Glycine max	82-92
10103001-5	1999	We provide evidence that to mediate this reaction, the ferric form of horseradish peroxidase must be converted by O2.- into the perferryl form (Compound III), in which the haem iron can assume the ferrous state.	Iron	177-181	peroxidase	Glycine max	82-92
10103001-6	1999	It is concluded that the ferric/perferryl peroxidase couple constitutes an effective biochemical catalyst for the production of .OH from O2.- and H2O2 (iron-catalyzed Haber-Weiss reaction).	Oxygen	137-139	peroxidase	Glycine max	42-52
10103001-6	1999	It is concluded that the ferric/perferryl peroxidase couple constitutes an effective biochemical catalyst for the production of .OH from O2.- and H2O2 (iron-catalyzed Haber-Weiss reaction).	Hydrogen Peroxide	146-150	peroxidase	Glycine max	42-52
10103001-8	1999	O2.- and H2O2 can be produced by the oxidase reaction of horseradish peroxidase in the presence of NADH.	Oxygen	0-2	peroxidase	Glycine max	69-79
12114996-4	1999	In the presence of cellobiose, CDH could reduce many oxidized products catalyzed by soybean hull peroxidase (SHP).	Cellobiose	19-29	peroxidase	Glycine max	97-107
10103001-8	1999	O2.- and H2O2 can be produced by the oxidase reaction of horseradish peroxidase in the presence of NADH.	Hydrogen Peroxide	9-13	peroxidase	Glycine max	69-79
10103001-8	1999	O2.- and H2O2 can be produced by the oxidase reaction of horseradish peroxidase in the presence of NADH.	NAD	99-103	peroxidase	Glycine max	69-79
10103001-9	1999	The .OH-producing activity of horseradish peroxidase can be inhibited by inactivators of haem iron or by various O2.- and .OH scavengers.	Iron	94-98	peroxidase	Glycine max	42-52
10103001-9	1999	The .OH-producing activity of horseradish peroxidase can be inhibited by inactivators of haem iron or by various O2.- and .OH scavengers.	Oxygen	113-115	peroxidase	Glycine max	42-52
10103001-10	1999	On an equimolar Fe basis, horseradish peroxidase is 1-2 orders of magnitude more active than Fe-EDTA, an inorganic catalyst of the Haber-Weiss reaction.	Iron	16-18	peroxidase	Glycine max	38-48
10103001-10	1999	On an equimolar Fe basis, horseradish peroxidase is 1-2 orders of magnitude more active than Fe-EDTA, an inorganic catalyst of the Haber-Weiss reaction.	Fe(III)-EDTA	93-100	peroxidase	Glycine max	38-48
9367883-3	1997	This similarity suggests that the active site in the resting form of soybean peroxidase contains a ferric iron, is a high-spin 5-coordinate heme binding His as a fifth axial ligand.	ferric sulfate	99-110	peroxidase	Glycine max	77-87
9367883-3	1997	This similarity suggests that the active site in the resting form of soybean peroxidase contains a ferric iron, is a high-spin 5-coordinate heme binding His as a fifth axial ligand.	Heme	140-144	peroxidase	Glycine max	77-87
9254049-0	1997	The N-glycosylation sites of soybean seed coat peroxidase.	Nitrogen	4-5	peroxidase	Glycine max	47-57
8620022-1	1996	Oscillatory kinetics in the peroxidase-oxidase reaction catalyzed by structurally different peroxidases were investigated using NADH as a substrate.	NAD	128-132	peroxidase	Glycine max	28-38
9075402-0	1997	Electrochemical glucose and lactate sensors based on "wired" thermostable soybean peroxidase operating continuously and stably at 37 degrees C. Following a recent report from our laboratory on a thermostable amperometric H2O2 sensor based on "wiring" soybean peroxidase, glucose and lactate sensors maintaining stable output under continuous operation at 37 degrees C for 12 and 8 days, respectively, were built.	Glucose	16-23	peroxidase	Glycine max	82-92
9075402-0	1997	Electrochemical glucose and lactate sensors based on "wired" thermostable soybean peroxidase operating continuously and stably at 37 degrees C. Following a recent report from our laboratory on a thermostable amperometric H2O2 sensor based on "wiring" soybean peroxidase, glucose and lactate sensors maintaining stable output under continuous operation at 37 degrees C for 12 and 8 days, respectively, were built.	Lactic Acid	28-35	peroxidase	Glycine max	82-92
9075402-0	1997	Electrochemical glucose and lactate sensors based on "wired" thermostable soybean peroxidase operating continuously and stably at 37 degrees C. Following a recent report from our laboratory on a thermostable amperometric H2O2 sensor based on "wiring" soybean peroxidase, glucose and lactate sensors maintaining stable output under continuous operation at 37 degrees C for 12 and 8 days, respectively, were built.	Lactic Acid	28-35	peroxidase	Glycine max	259-269
9075402-0	1997	Electrochemical glucose and lactate sensors based on "wired" thermostable soybean peroxidase operating continuously and stably at 37 degrees C. Following a recent report from our laboratory on a thermostable amperometric H2O2 sensor based on "wiring" soybean peroxidase, glucose and lactate sensors maintaining stable output under continuous operation at 37 degrees C for 12 and 8 days, respectively, were built.	Hydrogen Peroxide	221-225	peroxidase	Glycine max	82-92
9075402-0	1997	Electrochemical glucose and lactate sensors based on "wired" thermostable soybean peroxidase operating continuously and stably at 37 degrees C. Following a recent report from our laboratory on a thermostable amperometric H2O2 sensor based on "wiring" soybean peroxidase, glucose and lactate sensors maintaining stable output under continuous operation at 37 degrees C for 12 and 8 days, respectively, were built.	Hydrogen Peroxide	221-225	peroxidase	Glycine max	259-269
9075402-0	1997	Electrochemical glucose and lactate sensors based on "wired" thermostable soybean peroxidase operating continuously and stably at 37 degrees C. Following a recent report from our laboratory on a thermostable amperometric H2O2 sensor based on "wiring" soybean peroxidase, glucose and lactate sensors maintaining stable output under continuous operation at 37 degrees C for 12 and 8 days, respectively, were built.	Glucose	271-278	peroxidase	Glycine max	82-92
9075402-0	1997	Electrochemical glucose and lactate sensors based on "wired" thermostable soybean peroxidase operating continuously and stably at 37 degrees C. Following a recent report from our laboratory on a thermostable amperometric H2O2 sensor based on "wiring" soybean peroxidase, glucose and lactate sensors maintaining stable output under continuous operation at 37 degrees C for 12 and 8 days, respectively, were built.	Lactic Acid	283-290	peroxidase	Glycine max	82-92
8620022-7	1996	Substituting NADH with dihydroxyfumaric acid as a substrate, oscillations in the oxygen concentration were observed for about 1.5 h when a concentrated solution of this substrate was continuously fed to a solution containing horseradish peroxidase.	Oxygen	81-87	peroxidase	Glycine max	237-247
8620022-5	1996	Also, the phase plot of the signal for compound III versus the oxygen concentration for Coprinus peroxidase differs from the corresponding phase plots obtained using other peroxidases.	Oxygen	63-69	peroxidase	Glycine max	97-107
8620022-7	1996	Substituting NADH with dihydroxyfumaric acid as a substrate, oscillations in the oxygen concentration were observed for about 1.5 h when a concentrated solution of this substrate was continuously fed to a solution containing horseradish peroxidase.	NAD	13-17	peroxidase	Glycine max	237-247
8620022-7	1996	Substituting NADH with dihydroxyfumaric acid as a substrate, oscillations in the oxygen concentration were observed for about 1.5 h when a concentrated solution of this substrate was continuously fed to a solution containing horseradish peroxidase.	dihydroxyfumarate	23-44	peroxidase	Glycine max	237-247
12244231-4	1994	Moreover, the induced loss of protoplasts could be prevented by preincubation with DTT, which also blocks peroxidase-mediated oxidative cross-linking.	Dithiothreitol	83-86	peroxidase	Glycine max	106-116
8638916-1	1996	Ascorbate peroxidase is a widespread plant enzyme that catalyzes the removal of potentially harmful H2O2.	Hydrogen Peroxide	100-104	peroxidase	Glycine max	10-20
8991505-0	1996	The glycans of soybean peroxidase.	Polysaccharides	4-11	peroxidase	Glycine max	23-33
16652965-4	1992	The possible involvement of peroxide-like intermediates in the FLbR-catalyzed reactions was analyzed by measuring the effects of peroxidase and catalase on FLbR activities; both enzymes at low concentrations (about 2 mug/mL) stimulated the FLbR-catalyzed NADH oxidation and Lb(+3) reduction.	Peroxides	28-36	peroxidase	Glycine max	129-139
12232000-6	1993	In seed coat extracts, peroxidase was the most abundant soluble protein in EpEp cultivars, whereas this enzyme was present only in trace amounts in epep genotypes, as determined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis.	polyacrylamide	204-218	peroxidase	Glycine max	23-33
7763597-4	1993	This technique has been used to purify the peroxidase from soybean hulls using the lectin concanavalin A (con A) as a sugar-binding affinity ligand.	Sugars	118-123	peroxidase	Glycine max	43-53
7763597-5	1993	A purification factor of 30 is achieved to provide a nearly pure peroxidase solution (as determined by HPLC and SDS-PAGE) with nearly complete regeneration of the con A ligand.	Sodium Dodecyl Sulfate	112-115	peroxidase	Glycine max	65-75
8396932-3	1993	Partial amino acid sequence information confirms the identity of the enzyme as a peroxidase but shows significant deviation from other plant peroxidases in the distal histidine box.	Histidine	167-176	peroxidase	Glycine max	81-91
34121354-0	2021	Asymmetric sulfoxidation of thioether catalyzed by soybean pod shell peroxidase to form enantiopure sulfoxide in water-in-oil microemulsions:kinetic model.	Sulfides	28-37	peroxidase	Glycine max	69-79
32797626-7	2021	Acetic acid-sprayed plants suffered less oxidative stress due to the enhancement of antioxidant defense mechanisms, as evidenced by the increased activities of superoxide dismutase, ascorbate peroxidase, catalase, glutathione peroxidase and glutathione S-transferase.	Acetic Acid	0-11	peroxidase	Glycine max	192-202
24178068-5	1992	In "effective", nitrogen-fixing nodules, colonized by wild-type bacteria, chitinase and peroxidase activities had low levels in the central infected zone and were enhanced primarily in the nodule cortex.	Nitrogen	16-24	peroxidase	Glycine max	88-98
1648400-2	1991	The activities of the enzymes involved in hydroperoxide metabolism, e.g., superoxide dismutase, catalase, peroxidase and glutathione and ascorbate peroxidases, markedly changed during the germination of soybean embryonic axes.	Hydrogen Peroxide	42-55	peroxidase	Glycine max	106-116
1648400-8	1991	Cell wall peroxidase activity increased from 10 to 300 mumol/min per mg protein and appears as a potentially important pathway for H2O2 utilization.	Hydrogen Peroxide	131-135	peroxidase	Glycine max	10-20
16668258-6	1991	Treatment of nodulated plants with fixed nitrogen (urea) led to concomitant decreases in acetylene reduction activity, in leghemoglobin content, and in activities of ASC peroxidase, DHA reductase, and GSSG reductase.	Nitrogen	41-49	peroxidase	Glycine max	170-180
16668258-6	1991	Treatment of nodulated plants with fixed nitrogen (urea) led to concomitant decreases in acetylene reduction activity, in leghemoglobin content, and in activities of ASC peroxidase, DHA reductase, and GSSG reductase.	Urea	51-55	peroxidase	Glycine max	170-180
34495993-14	2021	ZnO NPs induced the activity of antioxidant enzymes, including peroxidase and catalase by averages of 48.3% and 41%, respectively.	Zinc Oxide	0-3	peroxidase	Glycine max	63-73
34121354-0	2021	Asymmetric sulfoxidation of thioether catalyzed by soybean pod shell peroxidase to form enantiopure sulfoxide in water-in-oil microemulsions:kinetic model.	sulfoxide	100-109	peroxidase	Glycine max	69-79
34121354-0	2021	Asymmetric sulfoxidation of thioether catalyzed by soybean pod shell peroxidase to form enantiopure sulfoxide in water-in-oil microemulsions:kinetic model.	Water	113-118	peroxidase	Glycine max	69-79
34121354-0	2021	Asymmetric sulfoxidation of thioether catalyzed by soybean pod shell peroxidase to form enantiopure sulfoxide in water-in-oil microemulsions:kinetic model.	Oils	122-125	peroxidase	Glycine max	69-79
34234933-7	2021	The activity of major antioxidant enzymes such as superoxide dismutase, catalase, polyphenol oxidase, peroxidase and ascorbate peroxidase was stimulated by melatonin application.	Melatonin	156-165	peroxidase	Glycine max	102-112
34234933-7	2021	The activity of major antioxidant enzymes such as superoxide dismutase, catalase, polyphenol oxidase, peroxidase and ascorbate peroxidase was stimulated by melatonin application.	Melatonin	156-165	peroxidase	Glycine max	127-137
35173752-5	2021	The results showed that with a decrease in soil moisture content, the content of malondialdehyde (MDA) in soybean leaves increased significantly; the activities of peroxidase (POD), catalase (CAT), and ascorbic acid peroxidase (APX) increased first and then decreased; the content of proline, soluble sugar, and soluble protein increased; and the total antioxidant capacity (T-AOC) increased significantly.	Malondialdehyde	81-96	peroxidase	Glycine max	164-174
35424610-4	2022	Compared to UV-B treatment alone, soybean treated with GABA (5 mM) in combination with UV-B significantly increased sprout length, fresh weight, Ca2+ inward flow and peroxidase and catalase activities, and decreased malondialdehyde and H2O2 and O2 - fluorescence intensity, while soybean treated with GABA inhibitor showed the opposite trend.	gamma-Aminobutyric Acid	55-59	peroxidase	Glycine max	166-176
35326148-9	2022	Moreover, the reactive oxygen species accumulation was accompanied by improved enzymatic antioxidant activity, such as that of superoxide dismutase, peroxidase, catalase, and ascorbate peroxidase.	Reactive Oxygen Species	14-37	peroxidase	Glycine max	149-159
35326148-9	2022	Moreover, the reactive oxygen species accumulation was accompanied by improved enzymatic antioxidant activity, such as that of superoxide dismutase, peroxidase, catalase, and ascorbate peroxidase.	Reactive Oxygen Species	14-37	peroxidase	Glycine max	185-195
35173752-5	2021	The results showed that with a decrease in soil moisture content, the content of malondialdehyde (MDA) in soybean leaves increased significantly; the activities of peroxidase (POD), catalase (CAT), and ascorbic acid peroxidase (APX) increased first and then decreased; the content of proline, soluble sugar, and soluble protein increased; and the total antioxidant capacity (T-AOC) increased significantly.	Malondialdehyde	98-101	peroxidase	Glycine max	216-226
35173752-5	2021	The results showed that with a decrease in soil moisture content, the content of malondialdehyde (MDA) in soybean leaves increased significantly; the activities of peroxidase (POD), catalase (CAT), and ascorbic acid peroxidase (APX) increased first and then decreased; the content of proline, soluble sugar, and soluble protein increased; and the total antioxidant capacity (T-AOC) increased significantly.	Malondialdehyde	81-96	peroxidase	Glycine max	176-179
35173752-5	2021	The results showed that with a decrease in soil moisture content, the content of malondialdehyde (MDA) in soybean leaves increased significantly; the activities of peroxidase (POD), catalase (CAT), and ascorbic acid peroxidase (APX) increased first and then decreased; the content of proline, soluble sugar, and soluble protein increased; and the total antioxidant capacity (T-AOC) increased significantly.	Proline	284-291	peroxidase	Glycine max	176-179
35173752-5	2021	The results showed that with a decrease in soil moisture content, the content of malondialdehyde (MDA) in soybean leaves increased significantly; the activities of peroxidase (POD), catalase (CAT), and ascorbic acid peroxidase (APX) increased first and then decreased; the content of proline, soluble sugar, and soluble protein increased; and the total antioxidant capacity (T-AOC) increased significantly.	Sugars	301-306	peroxidase	Glycine max	176-179
35161252-7	2022	In contrast, ethanol treatment of salt-treated soybean plants boosted ROS-detoxification mechanisms by enhancing the activities of antioxidant enzymes, including peroxidase, ascorbate peroxidase, catalase, and glutathione S-transferase.	Salts	34-38	peroxidase	Glycine max	162-172
35161252-7	2022	In contrast, ethanol treatment of salt-treated soybean plants boosted ROS-detoxification mechanisms by enhancing the activities of antioxidant enzymes, including peroxidase, ascorbate peroxidase, catalase, and glutathione S-transferase.	Salts	34-38	peroxidase	Glycine max	184-194
35161252-7	2022	In contrast, ethanol treatment of salt-treated soybean plants boosted ROS-detoxification mechanisms by enhancing the activities of antioxidant enzymes, including peroxidase, ascorbate peroxidase, catalase, and glutathione S-transferase.	Reactive Oxygen Species	70-73	peroxidase	Glycine max	162-172
35161252-7	2022	In contrast, ethanol treatment of salt-treated soybean plants boosted ROS-detoxification mechanisms by enhancing the activities of antioxidant enzymes, including peroxidase, ascorbate peroxidase, catalase, and glutathione S-transferase.	Reactive Oxygen Species	70-73	peroxidase	Glycine max	184-194
35161252-7	2022	In contrast, ethanol treatment of salt-treated soybean plants boosted ROS-detoxification mechanisms by enhancing the activities of antioxidant enzymes, including peroxidase, ascorbate peroxidase, catalase, and glutathione S-transferase.	Ethanol	13-20	peroxidase	Glycine max	162-172
35161252-7	2022	In contrast, ethanol treatment of salt-treated soybean plants boosted ROS-detoxification mechanisms by enhancing the activities of antioxidant enzymes, including peroxidase, ascorbate peroxidase, catalase, and glutathione S-transferase.	Ethanol	13-20	peroxidase	Glycine max	184-194