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Biology and Biochemistry of Glucosinolates

Annual review of plant biology, 2006-01, Vol.57 (1), p.303-333

2006

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Camalexin is synthesized from indole-3-acetaldoxime, a key branching point between primary and secondary metabolism in Arabidopsis

Proceedings of the National Academy of Sciences - PNAS, 2004-05, Vol.101 (21), p.8245-8250

2004

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Cytochrome P450 CYP79A2 from Arabidopsis thaliana L. Catalyzes the Conversion of l-Phenylalanine to Phenylacetaldoxime in the Biosynthesis of Benzylglucosinolate

The Journal of biological chemistry, 2000-05, Vol.275 (19), p.14659-14666

2000

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CYP83A1 and CYP83B1, two nonredundant cytochrome P450 enzymes metabolizing oximes in the biosynthesis of glucosinolates in Arabidopsis

Plant physiology (Bethesda), 2003-09, Vol.133 (1), p.63-72

2003

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Functional Expression and Characterization of Plant ABC Transporters in Xenopus laevis Oocytes for Transport Engineering Purposes

Methods in enzymology, 2016, Vol.576, p.207-224

2016

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New insight into the biosynthesis and regulation of indole compounds in Arabidopsis thaliana

Planta, 2005-07, Vol.221 (5), p.603-606

2005

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Functional analysis of the tandem-duplicated P450 genes SPS/BUS/CYP79F1 and CYP79F2 in glucosinolate biosynthesis and plant development by Ds transposition-generated double mutants

Plant physiology (Bethesda), 2004-06, Vol.135 (2), p.840-848

2004

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Mineralization of benzyl glucosinolate and its hydrolysis product the biofumigant benzyl isothiocyanate in soil

Soil biology & biochemistry, 2008, Vol.40 (1), p.135-141

2008

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The presence of CYP79 homologues in glucosinolate-producing plants shows evolutionary conservation of the enzymes in the conversion of amino acid to aldoxime in the biosynthesis of cyanogenic glucosides and glucosinolates

Plant molecular biology, 1998-11, Vol.38 (5), p.725-734

1998

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Cytochrome P-450(TYR) is a multifunctional heme-thiolate enzyme catalyzing the conversion of L-tyrosine to p-hydroxyphenylacetaldehyde oxime in the biosynthesis of the cyanogenic glucoside dhurrin in Sorghum bicolor (L.) Moench

The Journal of biological chemistry, 1995-02, Vol.270 (8), p.3506

1995

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Purification and Characterization of Recombinant Cytochrome P450TYR Expressed at High Levels in Escherichia coli

Archives of biochemistry and biophysics, 1995-10, Vol.322 (2), p.369-377

1995

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Involvement of cytochrome P450 in oxime production in glucosinolate biosynthesis as demonstrated by an in vitro microsomal enzyme system isolated from jasmonic acid-induced seedlings of Sinapis alba L

Proceedings of the National Academy of Sciences - PNAS, 1995-12, Vol.92 (26), p.12505-12509

1995

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Isolation of a microsomal enzyme system involved in glucosinolate biosynthesis from seedlings of Tropaeolum majus L

Plant physiology (Bethesda), 1996-07, Vol.111 (3), p.831-837

1996

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The biosynthesis of cyanogenic glucosides in seedlings of cassava ( Manihot esculenta Crantz)

Archives of biochemistry and biophysics, 1992, Vol.292 (1), p.141-150

1992

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The biosynthesis of cyanogenic glucosides in higher plants. The (E)- and (Z)-isomers of p-hydroxyphenylacetaldehyde oxime as intermediates in the biosynthesis of dhurrin in Sorghum bicolor (L.) Moench

The Journal of biological chemistry, 1989-11, Vol.264 (33), p.19487-19494

1989

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POSSIBLE USE OF A BIOTECHNOLOGICAL APPROACH TO OPTIMIZE AND REGULATE THE CONTENT AND DISTRIBUTION OF CYANOGENIC GLUCOSIDES IN CASSAVA TO INCREASE FOOD SAFETY

Acta horticulturae, 1994-11 (375), p.45-60

1994

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Molecular characterization of laccase genes from the basidiomycete Coprinus cinereus and heterologous expression of the laccase Lcc1

Applied and Environmental Microbiology, 1999-11, Vol.65 (11), p.4943-4948

1999

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Biology and Biochemistry of Glucosinolates

Camalexin is synthesized from indole-3-acetaldoxime, a key branching point between primary and secondary metabolism in Arabidopsis

Cytochrome P450 CYP79A2 from Arabidopsis thaliana L. Catalyzes the Conversion of l-Phenylalanine to Phenylacetaldoxime in the Biosynthesis of Benzylglucosinolate

CYP83A1 and CYP83B1, two nonredundant cytochrome P450 enzymes metabolizing oximes in the biosynthesis of glucosinolates in Arabidopsis

Functional Expression and Characterization of Plant ABC Transporters in Xenopus laevis Oocytes for Transport Engineering Purposes

New insight into the biosynthesis and regulation of indole compounds in Arabidopsis thaliana

Functional analysis of the tandem-duplicated P450 genes SPS/BUS/CYP79F1 and CYP79F2 in glucosinolate biosynthesis and plant development by Ds transposition-generated double mutants

Mineralization of benzyl glucosinolate and its hydrolysis product the biofumigant benzyl isothiocyanate in soil

The presence of CYP79 homologues in glucosinolate-producing plants shows evolutionary conservation of the enzymes in the conversion of amino acid to aldoxime in the biosynthesis of cyanogenic glucosides and glucosinolates

Cytochrome P-450(TYR) is a multifunctional heme-thiolate enzyme catalyzing the conversion of L-tyrosine to p-hydroxyphenylacetaldehyde oxime in the biosynthesis of the cyanogenic glucoside dhurrin in Sorghum bicolor (L.) Moench

Purification and Characterization of Recombinant Cytochrome P450TYR Expressed at High Levels in Escherichia coli

Involvement of cytochrome P450 in oxime production in glucosinolate biosynthesis as demonstrated by an in vitro microsomal enzyme system isolated from jasmonic acid-induced seedlings of Sinapis alba L

Isolation of a microsomal enzyme system involved in glucosinolate biosynthesis from seedlings of Tropaeolum majus L

The biosynthesis of cyanogenic glucosides in seedlings of cassava ( Manihot esculenta Crantz)

The biosynthesis of cyanogenic glucosides in higher plants. The (E)- and (Z)-isomers of p-hydroxyphenylacetaldehyde oxime as intermediates in the biosynthesis of dhurrin in Sorghum bicolor (L.) Moench

POSSIBLE USE OF A BIOTECHNOLOGICAL APPROACH TO OPTIMIZE AND REGULATE THE CONTENT AND DISTRIBUTION OF CYANOGENIC GLUCOSIDES IN CASSAVA TO INCREASE FOOD SAFETY

Molecular characterization of laccase genes from the basidiomycete Coprinus cinereus and heterologous expression of the laccase Lcc1

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