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(+)-(R)-limonene + H2O2
(R)-limonene trans-1,2-epoxide
-
-
97% of products
-
?
(-)-(S)-limonene + H2O2
(S)-limonene cis-1,2-epoxide
-
-
88% of products
-
?
(10E,12Z,9S)-9-hydroperoxy-octadec-10,12-dienoate + H2O2
(10E,12Z,9S)-9-hydroxyoctadec-10,12-dienoate + H2O
(10E,12Z,9S)-9-hydroxy-octadec-10,12-dienoate + H2O2
(10E,12R,13S,9S)-12,13-epoxy-9-hydroxy-octadec-10-enoate + H2O
(10E,12Z,9S)-9-hydroxyoctadec-10,12-dienoate + H2O2
(10E,12R,13S,9S)-12,13-epoxy-9-hydroxy-octadec-10-enoate + H2O
-
-
-
-
?
(3Z)-hexenal + H2O2
(2E)-4-hydroxy-2-hexenal + H2O
-
-
-
-
?
(3Z)-nonenal + H2O2
(2E)-4-hydroxy-2-nonenal + H2O
-
-
-
-
?
(9Z,12Z,15Z)-octadeca-9,12,15-trienoic acid + tert-butyl hydroperoxide
(12Z,15Z)-9,10-epoxyoctadeca-12,15-dienoic aicd + (9Z,12Z)-15,16-epoxy-9,12-octadecadienoic acid + ?
-
-
-
-
?
10-cis-heptadecenoic acid + cumene hydroperoxide
10,11-epoxyheptadecanoic acid + ?
94% of the activity with oleic acid
-
-
?
10-cis-pentadecenoic acid + cumene hydroperoxide
10,11-epoxypentadecanoic acid + ?
98% of the activity with oleic acid
-
-
?
13-hydroperoxy-9,11-octadecadienoic acid + H2O2
?
-
-
-
?
13-hydroperoxy-9,11E,15Z-octadecatrienoic acid + H2O2
?
-
-
-
?
13-hydroperoxy-9Z,11E-octadecadienoic acid + H2O2
?
-
-
-
?
13-hydroperoxyoctadecatrienoic acid + H2O2
13-hydroxyoctadecatrienoic acid + ?
-
-
-
?
13-hydroxyoctadecatrienoic acid + H2O2
15,16-epoxy-13-hydroperoxyoctadecadienoic acid + ?
-
-
-
?
2 linolenic acid + 3 tert-butyl hydroperoxide
(12Z,15Z)-9-epoxyoctadec-12,15-dienoic acid + (12Z)-9,15-diepoxyoctadec-12-enoic acid + 3 tert-butanol
-
-
-
-
?
2-hydroperoxyoctadecatrienoic acid + H2O2
2-hydroxyoctadecatrienoic acid + ?
-
-
-
?
2-methylhept-1-ene + tert-butyl hydroperoxide
2-methyl-2-pentyloxirane + ?
-
-
-
-
?
4-chloroaniline + H2O2
4-chloronitrosobenzene + ?
-
-
-
-
?
9-cis-hexadecenoic acid + cumene hydroperoxide
9,10-epoxy hexadecanoic acid + ?
89% of the activity with oleic acid
-
-
?
alpha-terpinene + H2O2
cis-1,4-dihydroxy-p-menth-2-ene
-
-
-
-
?
alphax1elinolenic acid + 7-HpHxTrE
?
-
-
-
-
?
aniline + cumene hydroperoxide
?
aniline + cumene hydroperoxide
N-phenylhydroxylamine + H2O
-
-
-
?
aniline + cumene hydroperoxide
nitrosobenzene + ?
-
-
-
-
?
aniline + H2O2
nitrosobenzene + ?
-
-
-
?
arachidonic acid + 7-HpHxTrE
?
-
weak substrate
-
-
?
cis-2-heptene + tert-butyl hydroperoxide
2-butyl-3-methyl-cis-oxirane + ?
-
-
93.9% yield
-
?
cis-3-heptene + tert-butyl hydroperoxide
2-ethyl-3-propyl-cis-oxirane + ?
-
-
72.7% yield
-
?
cyclohexene + tert-butyl hydroperoxide
7-oxabicyclo-[4.1.0]-heptane + ?
-
-
70.5% yield
-
?
gamma-terpinene + H2O2
p-cymene
-
-
in this reaction, hydroperoxide serves as hydrogen acceptor rather than an oxygen donor
-
?
hept-1-ene + tert-butyl hydroperoxide
2-pentyloxirane + ?
-
-
2.8% yield
-
?
indole + H2O2
?
-
-
-
-
?
indole + H2O2
indoxyl + H2O
indole + linoleic acid hydroperoxide
?
-
-
-
-
?
lauric acid + NADPH + H+
?
-
-
-
-
?
linoleate + H2O2
(12Z,9R,10S)-9,10-epoxyoctadec-12-enoate + H2O
linoleate + tert-butyl hydroperoxide
(9Z)-12,13-epoxyoctadec-9-enoate + (12Z)-9,10-epoxyoctadec-12-enoate + 9,10-12,13-diepoxy-octadecanoate + ?
-
-
23.4% yield, 25.4% yield and 46.7% yield, respectively
-
?
linoleate methyl ester + tert-butyl hydroperoxide
methyl 12,13-epoxy-9(Z)-octadecenoate + methyl 9,10-epoxy-12(Z)-octadecenoate + methyl 9,10-12,13-diepoxyoctadecanoate + ?
-
-
17.6% yield, 21.9% yield and 49.5% yield, respectively
-
?
linoleic acid + 13-hydroperoxy-9,11-octadecadienoic acid
?
13-hydroperoxy-9,11-octadecadienoic acid is the most active cosubstrate
-
-
?
linoleic acid + 7-HpHxTrE
?
-
-
-
-
?
linoleic acid + cumene hydroperoxide
?
linoleic acid + H2O2
15,16-epoxy-9,12-octadecadienoic acid + H2O
-
-
25% yield
-
?
linoleic acid + NADPH + H+
12,13-epoxy-octadec-cis-9-enoic acid + NADP+
-
-
-
-
?
linoleic acid + tert-butyl hydroperoxide
9,10-epoxy-octadecanoic acid + tert-butanol
-
-
-
-
?
linolenic acid + 13-hydroperoxy-9,11-octadecadienoic acid
?
13-hydroperoxy-9,11-octadecadienoic acid is the most active cosubstrate
-
-
?
linolenic acid + cumene hydroperoxide
?
-
-
-
?
linolenic acid + cumene hydroperoxide
linolenic acid 9,10-15,16-diepoxide + ?
74% conversion, physiological linoleic and linolenic acids are the preferred substrates for isoform PXG4
major product, (R),(S)-epoxide enantiomers
-
?
linolenic acid + H2O2
?
-
-
-
?
methyl (13Z)-docos-13-enoate + tert-butyl hydroperoxide
methyl behenate 13,14-epoxide + H2O
-
-
26.9% yield
-
?
methyl 4-tolyl sulfide + cumene hydroperoxide
?
myristoleic acid + 7-HpHxTrE
?
-
-
-
-
?
N-iso-butyl-(9Z,12Z,15Z)-octadecatrienamide + tert-butyl hydroperoxide
N-iso-butyl-9,10-15,16-diepoxy-(12Z)-octadecenamide + ?
-
-
-
-
?
nerol + H2O2
nerol-2,3-epoxide
-
-
sole product
-
?
oleate + tert-butyl hydroperoxide
methyl 9,10-epoxyoctadecanoate + ?
-
-
99.8% yield
-
?
oleate methyl ester + tert-butyl hydroperoxide
methyl 9,10-epoxyoctadecanoate + ?
-
-
93.9% yield
-
?
oleic acid + 11-HpHxTrE
?
-
-
-
-
?
oleic acid + 13-HpODE
?
-
-
-
-
?
oleic acid + 13-HpOTrE
?
-
-
-
-
?
oleic acid + 13-hydroperoxy-9,11-octadecadienoic acid
?
13-hydroperoxy-9,11-octadecadienoic acid is the most active cosubstrate
-
-
?
oleic acid + 7-HpHxTrE
?
-
high activity
-
-
?
oleic acid + 9-HpODE
?
-
-
-
-
?
oleic acid + 9-HpOTrE
?
-
-
-
-
?
oleic acid + cumene hydroperoxide
?
oleic acid + cumene hydroperoxide
cis-9,10-epoxystearic acid + ?
oleic acid + fatty acid hydroperoxide
cis-9,10-epoxystearic acid + ?
-
-
-
-
?
oleic acid + H2O2
9,10-epoxyoctadecanoic acid
-
-
15% yield
-
?
oleic acid + H2O2
9,10-epoxystearic acid
-
-
-
-
?
palmitic acid + 11-HpHxTrE
?
-
-
-
-
?
palmitic acid + 13-HpODE
?
-
-
-
-
?
palmitic acid + 13-HpOTrE
?
-
-
-
-
?
palmitic acid + 7-HpHxTrE
?
-
highest activity
-
-
?
palmitic acid + 9-HpODE
?
-
-
-
-
?
palmitic acid + 9-HpOTrE
?
-
-
-
-
?
palmitic acid + cumene hydroperoxide
?
-
-
-
-
?
palmitic acid + H2O2
?
-
-
-
-
?
palmitoleic acid methyl ester + 7-HpHxTrE
?
-
excellent substrate
-
-
?
parathion ethyl + cumene hydroperoxide
paraoxon + ?
phenylsulfide + H2O2
phenylsulfoxide + ?
-
-
-
-
?
pyrogallol + H2O2
purpurogallin + H2O
-
-
-
-
?
ricinoleate + tert-butyl hydroperoxide
9,10-epoxy-12-hydroxyoctadecanoate + ?
-
-
73.6% yield
-
?
styrene + tert-butyl hydroperoxide
epoxyethyl benzene + ?
-
-
57.4% yield
-
?
thioanisole + H2O2
?
-
-
-
-
?
thiobenzamide + cumene hydroperoxide
?
trans-10,cis-12-linoleic acid + H2O2
12,13-epoxy-10-octadecenoic acid
-
-
epoxidation occurs only at cis-double bond
-
?
trans-2-heptene + tert-butyl hydroperoxide
2-butyl-3-methyl-trans-oxirane + ?
-
-
26.6% yield
-
?
linolenate + tert-butyl hydroperoxide
additional information
-
(10E,12Z,9S)-9-hydroperoxy-octadec-10,12-dienoate + H2O2
(10E,12Z,9S)-9-hydroxyoctadec-10,12-dienoate + H2O
-
-
-
-
?
(10E,12Z,9S)-9-hydroperoxy-octadec-10,12-dienoate + H2O2
(10E,12Z,9S)-9-hydroxyoctadec-10,12-dienoate + H2O
-
-
-
-
?
(10E,12Z,9S)-9-hydroperoxy-octadec-10,12-dienoate + H2O2
(10E,12Z,9S)-9-hydroxyoctadec-10,12-dienoate + H2O
-
-
-
-
?
(10E,12Z,9S)-9-hydroperoxy-octadec-10,12-dienoate + H2O2
(10E,12Z,9S)-9-hydroxyoctadec-10,12-dienoate + H2O
-
-
-
-
?
(10E,12Z,9S)-9-hydroperoxy-octadec-10,12-dienoate + H2O2
(10E,12Z,9S)-9-hydroxyoctadec-10,12-dienoate + H2O
-
-
-
-
?
(10E,12Z,9S)-9-hydroxy-octadec-10,12-dienoate + H2O2
(10E,12R,13S,9S)-12,13-epoxy-9-hydroxy-octadec-10-enoate + H2O
-
-
-
-
?
(10E,12Z,9S)-9-hydroxy-octadec-10,12-dienoate + H2O2
(10E,12R,13S,9S)-12,13-epoxy-9-hydroxy-octadec-10-enoate + H2O
-
-
-
-
?
(10E,12Z,9S)-9-hydroxy-octadec-10,12-dienoate + H2O2
(10E,12R,13S,9S)-12,13-epoxy-9-hydroxy-octadec-10-enoate + H2O
-
-
-
-
?
(10E,12Z,9S)-9-hydroxy-octadec-10,12-dienoate + H2O2
(10E,12R,13S,9S)-12,13-epoxy-9-hydroxy-octadec-10-enoate + H2O
-
-
-
-
?
aniline + cumene hydroperoxide
?
-
-
-
-
?
aniline + cumene hydroperoxide
?
-
-
-
-
?
indole + H2O2
indoxyl + H2O
-
-
-
-
?
indole + H2O2
indoxyl + H2O
-
-
-
-
?
indole + H2O2
indoxyl + H2O
-
-
-
-
?
indole + H2O2
indoxyl + H2O
-
-
-
-
?
indole + H2O2
indoxyl + H2O
-
-
-
-
?
linoleate + H2O2
(12Z,9R,10S)-9,10-epoxyoctadec-12-enoate + H2O
-
-
-
-
?
linoleate + H2O2
(12Z,9R,10S)-9,10-epoxyoctadec-12-enoate + H2O
-
-
-
-
?
linoleate + H2O2
(12Z,9R,10S)-9,10-epoxyoctadec-12-enoate + H2O
-
-
-
-
?
linoleate + H2O2
(12Z,9R,10S)-9,10-epoxyoctadec-12-enoate + H2O
-
-
-
-
?
linoleate + H2O2
(12Z,9R,10S)-9,10-epoxyoctadec-12-enoate + H2O
-
-
-
-
?
linoleic acid + cumene hydroperoxide
?
-
-
-
-
?
linoleic acid + cumene hydroperoxide
?
-
-
-
?
linoleic acid + cumene hydroperoxide
?
-
64% conversion, physiological linoleic and linolenic acids are the preferred substrates for isoform PXG4
-
?
linoleic acid + cumene hydroperoxide
?
-
-
-
-
?
linoleic acid + cumene hydroperoxide
?
47% of the activity with oleic acid
-
-
?
linoleic acid + H2O2
?
-
-
-
?
linoleic acid + H2O2
?
-
-
-
-
?
methyl 4-tolyl sulfide + cumene hydroperoxide
?
-
-
-
-
?
methyl 4-tolyl sulfide + cumene hydroperoxide
?
-
-
-
-
?
oleate + H2O2
?
-
-
-
-
?
oleate + H2O2
?
-
-
-
-
?
oleate + H2O2
?
-
-
-
-
?
oleate + H2O2
?
-
-
-
-
?
oleate + H2O2
?
-
-
-
-
?
oleic acid + cumene hydroperoxide
?
-
-
-
?
oleic acid + cumene hydroperoxide
?
-
-
-
-
?
oleic acid + cumene hydroperoxide
?
preferred substrate
-
-
?
oleic acid + cumene hydroperoxide
?
-
-
-
-
?
oleic acid + cumene hydroperoxide
?
-
-
-
-
?
oleic acid + cumene hydroperoxide
?
-
-
-
-
?
oleic acid + cumene hydroperoxide
cis-9,10-epoxystearic acid + ?
-
-
-
-
?
oleic acid + cumene hydroperoxide
cis-9,10-epoxystearic acid + ?
-
-
-
-
?
oleic acid + H2O2
?
-
-
-
?
oleic acid + H2O2
?
-
-
-
-
?
parathion ethyl + cumene hydroperoxide
paraoxon + ?
-
-
-
-
?
parathion ethyl + cumene hydroperoxide
paraoxon + ?
-
-
-
-
?
parathion ethyl + cumene hydroperoxide
paraoxon + ?
-
-
-
-
?
thiobenzamide + cumene hydroperoxide
?
-
-
-
-
?
thiobenzamide + cumene hydroperoxide
?
-
-
-
-
?
linolenate + tert-butyl hydroperoxide
additional information
-
-
-
0.6% monoepoxy product and 91.6% diepoxy product
-
?
methyl linolenate + tert-butyl hydroperoxide
additional information
-
-
-
14.3% monoepoxy product and 78.3% diepoxy product
-
?
additional information
?
-
enzyme is an efficient fatty acid epoxygenase, catalyzing the oxidation of cis double bonds of unsaturated fatty acids. The C-12,13 double bond of these unsaturated fatty acids is the least favoured. Isoform PXG4 catalyzes exclusively the formation of (R),(S)-epoxide enantiomers, which is the absolute stereochemistry of the epoxides found in planta. Poor substrate: oleic acid methyl ester
-
-
?
additional information
?
-
-
the enzyme does not oxidize diacylglycerol and triacylglycerol
-
-
?
additional information
?
-
isoform PXG1 catalyzes the strictly hydroperoxide-dependent epoxidation of unsaturated fatty acids. It prefers hydroperoxy-trienoic acids over hydroperoxydienoic acids as oxygen donors to oxidize a wide range of unsaturated fatty acids with cis double bonds. Phospholipids and acyl-CoA are not effective substrates and it will only use free fatty acid or fatty acid methyl esters as substrates. Both hydroperoxy-dienoic and hydroperoxy-trienoic acids are effectively utilized as oxygen donors, with hydroperoxy-trienoic acids being more efficiently reduced
-
-
?
additional information
?
-
the enzyme shows null reductase activity towards 9-hydroperoxy-10E,12Z-octadecadienoic and a weak activity towards 9-hydroperoxy-10E,12,15Z-octadecatrienoic acid
-
-
-
additional information
?
-
-
the enzyme shows null reductase activity towards 9-hydroperoxy-10E,12Z-octadecadienoic and a weak activity towards 9-hydroperoxy-10E,12,15Z-octadecatrienoic acid
-
-
-
additional information
?
-
-
peroxygenase exists in nature as a complex with a carotenoid-binding macromolecule
-
-
?
additional information
?
-
-
thiobenzamide and thioacetamide are no substrates
-
-
?
additional information
?
-
-
no substrate: geraniol
-
-
?
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
(9Z,12Z,15Z)-octadeca-9,12,15-trienoic acid + tert-butyl hydroperoxide
(12Z,15Z)-9,10-epoxyoctadeca-12,15-dienoic aicd + (9Z,12Z)-15,16-epoxy-9,12-octadecadienoic acid + ?
-
-
-
-
?
13-hydroperoxyoctadecatrienoic acid + H2O2
13-hydroxyoctadecatrienoic acid + ?
-
-
-
?
13-hydroxyoctadecatrienoic acid + H2O2
15,16-epoxy-13-hydroperoxyoctadecadienoic acid + ?
-
-
-
?
2 linolenic acid + 3 tert-butyl hydroperoxide
(12Z,15Z)-9-epoxyoctadec-12,15-dienoic acid + (12Z)-9,15-diepoxyoctadec-12-enoic acid + 3 tert-butanol
-
-
-
-
?
2-hydroperoxyoctadecatrienoic acid + H2O2
2-hydroxyoctadecatrienoic acid + ?
-
-
-
?
aniline + cumene hydroperoxide
?
aniline + cumene hydroperoxide
nitrosobenzene + ?
-
-
-
-
?
linoleic acid + cumene hydroperoxide
?
linoleic acid + tert-butyl hydroperoxide
9,10-epoxy-octadecanoic acid + tert-butanol
-
-
-
-
?
linolenic acid + cumene hydroperoxide
linolenic acid 9,10-15,16-diepoxide + ?
74% conversion, physiological linoleic and linolenic acids are the preferred substrates for isoform PXG4
major product, (R),(S)-epoxide enantiomers
-
?
methyl 4-tolyl sulfide + cumene hydroperoxide
?
oleic acid + cumene hydroperoxide
?
-
-
-
-
?
oleic acid + cumene hydroperoxide
cis-9,10-epoxystearic acid + ?
oleic acid + fatty acid hydroperoxide
cis-9,10-epoxystearic acid + ?
-
-
-
-
?
thiobenzamide + cumene hydroperoxide
?
additional information
?
-
aniline + cumene hydroperoxide
?
-
-
-
-
?
aniline + cumene hydroperoxide
?
-
-
-
-
?
linoleic acid + cumene hydroperoxide
?
-
-
-
-
?
linoleic acid + cumene hydroperoxide
?
-
64% conversion, physiological linoleic and linolenic acids are the preferred substrates for isoform PXG4
-
?
linoleic acid + cumene hydroperoxide
?
-
-
-
-
?
methyl 4-tolyl sulfide + cumene hydroperoxide
?
-
-
-
-
?
methyl 4-tolyl sulfide + cumene hydroperoxide
?
-
-
-
-
?
oleic acid + cumene hydroperoxide
cis-9,10-epoxystearic acid + ?
-
-
-
-
?
oleic acid + cumene hydroperoxide
cis-9,10-epoxystearic acid + ?
-
-
-
-
?
thiobenzamide + cumene hydroperoxide
?
-
-
-
-
?
thiobenzamide + cumene hydroperoxide
?
-
-
-
-
?
additional information
?
-
enzyme is an efficient fatty acid epoxygenase, catalyzing the oxidation of cis double bonds of unsaturated fatty acids. The C-12,13 double bond of these unsaturated fatty acids is the least favoured. Isoform PXG4 catalyzes exclusively the formation of (R),(S)-epoxide enantiomers, which is the absolute stereochemistry of the epoxides found in planta. Poor substrate: oleic acid methyl ester
-
-
?
additional information
?
-
-
the enzyme does not oxidize diacylglycerol and triacylglycerol
-
-
?
additional information
?
-
-
peroxygenase exists in nature as a complex with a carotenoid-binding macromolecule
-
-
?
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
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Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
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Henriksen, A.; Mirza, O.; Indiani, C.; Teilum, K.; Smulevich, G.; Welinder, K.G.; Gajhede, M.
Structure of soybean seed coat peroxidase: a plant peroxidase with unusual stability and haem-apoprotein interactions
Protein Sci.
10
108-115
2001
Soja hispida
brenda
Magri, M.; Miranda, M.; Cascone, O.
Immobilization of soybean seed coat peroxidase on polyaniline: Synthesis optimization and catalytic properties
Biocatal. Biotransform.
23
339-346
2005
Glycine max
-
brenda
Doerge, D.R.; Corbett, M.D.
Oxidation of organosulfur compounds by the microsomal fraction of germinating pea seeds (Pisum sativum)
Biochem. Biophys. Res. Commun.
121
1001-1005
1984
Pisum sativum
brenda
Takamura, H.; Gardner, H.W.
Oxygenation of (3Z)-alkenal to (2E)-4-hydroxy-2-alkenal in soybean seed (Glycine max L.)
Biochim. Biophys. Acta
1303
83-91
1996
Glycine max
brenda
Piazza, G.J.; Foglia, T.A.
Synthesis of a fatty tetrahydroxyamide using peroxygenase from oat seeds
J. Am. Oil Chem. Soc.
81
933-937
2004
Avena sativa
brenda
Piazza, G.J.; Foglia, T.A.
One-pot synthesis of fatty acid epoxides from triacylglycerols using enzymes present in oat seeds
J. Am. Oil Chem. Soc.
83
1021-1025
2006
Avena sativa
brenda
Ishimaru, A.
Purification and characterization of solubilized peroxygenase from microsomes of pea seeds
J. Biol. Chem.
254
8427-8433
1979
Pisum sativum
brenda
Kandel, S.; Morant, M.; Benveniste, I.; Blee, E.; Werck-Reichhart, D.; Pinot, F.
Cloning, functional expression, and characterization of CYP709C1, the first sub-terminal hydroxylase of long chain fatty acid in plants. Induction by chemicals and methyl jasmonate
J. Biol. Chem.
280
35881-35889
2005
Triticum aestivum
brenda
Hanano, A.; Burcklen, M.; Flenet, M.; Ivancich, A.; Louwagie, M.; Garin, J.; Blee, E.
Plant seed peroxygenase is an original heme-oxygenase with an EF-hand calcium binding motif
J. Biol. Chem.
281
33140-33151
2006
Arabidopsis thaliana, Avena sativa
brenda
Piazza, G.J.; Nunez, A.; Foglia, T.A.
Epoxidation of fatty acids, fatty methyl esters, and alkenes by immobilized oat seed peroxygenase
J. Mol. Catal. B
21
143-151
2003
Avena sativa
-
brenda
Lequeu, J.; Fauconnier, M.L.; Chammai, A.; Bronner, R.; Blee, E.
Formation of plant cuticle: evidence for the occurrence of the peroxygenase pathway
Plant J.
36
155-164
2003
Avena sativa, Glycine max, Zea mays
brenda
Partridge, M.; Murphy, D.J.
Roles of a membrane-bound caleosin and putative peroxygenase in biotic and abiotic stress responses in Arabidopsis
Plant Physiol. Biochem.
47
796-806
2009
Arabidopsis thaliana
brenda
Hamberg, M.; Hamberg, G.
Peroxygenase-catalyzed fatty acid epoxidation in cereal seeds. Sequential oxidation of linoleic acid into 9(S),12(S),13(S)-trihydroxy-10(E)-octadecenoic acid
Plant Physiol.
110
807-815
1996
Avena sativa, Hordeum vulgare, Hordeum vulgare subsp. vulgare, Secale cereale, Triticum aestivum
brenda
Blee, E.; Flenet, M.; Boachon, B.; Fauconnier, M.L.
A non-canonical caleosin from Arabidopsis efficiently epoxidizes physiological unsaturated fatty acids with complete stereoselectivity
FEBS J.
279
3981-3995
2012
Arabidopsis thaliana (Q9CAB7)
brenda
Fuchs, C.; Schwab, W.
Epoxidation, hydroxylation and aromatization is catalyzed by a peroxygenase from Solanum lycopersicum
J. Mol. Catal. B
96
52-60
2013
Solanum lycopersicum
-
brenda
Kim, Y.Y.; Jung, K.W.; Yoo, K.S.; Jeung, J.U.; Shin, J.S.
A stress-responsive caleosin-like protein, AtCLO4, acts as a negative regulator of ABA responses in Arabidopsis
Plant Cell Physiol.
52
874-884
2011
Arabidopsis thaliana (Q9CAB7)
brenda
Meesapyodsuk, D.; Qiu, X.
A peroxygenase pathway involved in the biosynthesis of epoxy fatty acids in oat
Plant Physiol.
157
454-463
2011
Avena sativa (G1JSL4)
brenda
Shimada, T.L.; Hara-Nishimura, I.
Leaf oil bodies are subcellular factories producing antifungal oxylipins
Curr. Opin. Plant Biol.
25
145-150
2015
Arabidopsis thaliana (O22788)
brenda
Blee, E.; Boachon, B.; Burcklen, M.; Le Guedard, M.; Hanano, A.; Heintz, D.; Ehlting, J.; Herrfurth, C.; Feussner, I.; Bessoule, J.J.
The reductase activity of the Arabidopsis caleosin RESPONSIVE TO DESSICATION20 mediates gibberellin-dependent flowering time, abscisic acid sensitivity, and tolerance to oxidative stress
Plant Physiol.
166
109-124
2014
Arabidopsis thaliana (O22788)
brenda
Hanano, A.; Bessoule, J.J.; Heitz, T.; Blee, E.
Involvement of the caleosin/peroxygenase RD20 in the control of cell death during Arabidopsis responses to pathogens
Plant Signal. Behav.
10
e991574
2015
Arabidopsis thaliana (O22788)
brenda
Rahman, F.; Hassan, M.; Hanano, A.; Fitzpatrick, D.A.; McCarthy, C.G.P.; Murphy, D.J.
Evolutionary, structural and functional analysis of the caleosin/peroxygenase gene family in the Fungi
BMC Genomics
19
976
2018
Aspergillus flavus, Aspergillus flavus NRRL3357
brenda
Hanano, A.; Shaban, M.; Murphy, D.J.
Functional involvement of caleosin/peroxygenase PdPXG4 in the accumulation of date palm leaf lipid droplets after exposure to dioxins
Environ. Pollut.
281
116966
2021
Phoenix dactylifera (A0A8B7BGA2), Phoenix dactylifera
brenda
Brunetti, S.C.; Arseneault, M.K.M.; Wright, J.A.; Wang, Z.; Ehdaeivand, M.R.; Lowden, M.J.; Rivoal, J.; Khalil, H.B.; Garg, G.; Gulick, P.J.
The stress induced caleosin, RD20/CLO3, acts as a negative regulator of GPA1 in Arabidopsis
Plant Mol. Biol.
107
159-175
2021
Arabidopsis thaliana
brenda
Pineau, E.; Sauveplane, V.; Grienenberger, E.; Bassard, J.E.; Beisson, F.; Pinot, F.
CYP77B1 a fatty acid epoxygenase specific to flowering plants
Plant Sci.
307
110905
2021
Arabidopsis thaliana
brenda
Pasaribu, B.; Fu, J.H.; Jiang, P.L.
Identification and characterization of caleosin in Cycas revoluta pollen
Plant Signal. Behav.
15
1779486
2020
Cycas revoluta (B8XX15), Cycas revoluta
brenda
Rahman, F.; Hassan, M.; Rosli, R.; Almousally, I.; Hanano, A.; Murphy, D.J.
Evolutionary and genomic analysis of the caleosin/peroxygenase (CLO/PXG) gene/protein families in the Viridiplantae
PLoS ONE
13
e0196669
2018
Arabidopsis thaliana, Chlamydomonas reinhardtii, Auxenochlorella protothecoides, Chlorella vulgaris, Marchantia polymorpha, Oryza sativa, Phoenix dactylifera, Physcomitrium patens, Volvox carteri, Zea mays, Sorangium cellulosum, Selaginella moellendorffii, Gonium pectorale, Chlorella variabilis, Capsaspora owczarzaki, Coccomyxa subellipsoidea, Monoraphidium neglectum, Klebsormidium nitens
brenda
Hanano, A.; Shaban, M.; Almousally, I.; Murphy, D.J.
Identification of a dioxin-responsive oxylipin signature in roots of date palm involvement of a 9-hydroperoxide fatty acid reductase, caleosin/peroxygenase PdPXG2
Sci. Rep.
8
13181
2018
Phoenix dactylifera
brenda