Metabolic engineering of p‐hydroxybenzylglucosinolate in Arabidopsis by expression of the cyanogenic CYP79A1 from Sorghum bicolor

Summary Glucosinolates are natural products in cruciferous plants, including Arabidopsis thaliana. CYP79A1 is the cytochrome P450 catalysing the conversion of tyrosine to p‐hydroxyphenylacetaldoxime in the biosynthesis of the cyanogenic glucoside dhurrin in sorghum. Both glucosinolates and cyanogeni...

Full description

Saved in:
Bibliographic Details
Published inThe Plant journal : for cell and molecular biology Vol. 20; no. 6; pp. 663 - 671
Main Authors Bak, Søren, Olsen, Carl Erik, Petersen, Bent Larsen, Møller, Birger Lindberg, Halkier, Barbara Ann
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Science Ltd 01.12.1999
Blackwell Science
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Summary Glucosinolates are natural products in cruciferous plants, including Arabidopsis thaliana. CYP79A1 is the cytochrome P450 catalysing the conversion of tyrosine to p‐hydroxyphenylacetaldoxime in the biosynthesis of the cyanogenic glucoside dhurrin in sorghum. Both glucosinolates and cyanogenic glucosides have oximes as intermediates. Expression of CYP79A1 in A. thaliana results in the production of high levels of the tyrosine‐derived glucosinolate p‐hydroxybenzylglucosinolate, which is not a natural constituent of A. thaliana. This provides further evidence that the enzymes have low substrate specificity with respect to the side chain. The ability of the cyanogenic CYP79A1 to integrate itself into the glucosinolate pathway has important implications for an evolutionary relationship between cyanogenic glucosides and glucosinolates, and for the possibility of genetic engineering of novel glucosinolates.
Bibliography:Present address: Department of Plant Sciences, University of Arizona, Forbes 303, PO Box 210036, Tucson, AZ 85721–0036, USA.
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ObjectType-Article-1
ObjectType-Feature-2
ISSN:0960-7412
1365-313X
DOI:10.1046/j.1365-313X.1999.00642.x