Home LiteratureArticle Details
PMID: 11641410 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

The activity of Arabidopsis glycosyltransferases toward salicylic acid, 4-hydroxybenzoic acid, and other benzoates.

The Journal of biological chemistry ·Vol. 277 ·No. 1 ·2002-01-04 ·Pages 586-92

Lim EK, Doucet CJ, Li Y, Elias L, Worrall D, Spencer SP, Ross J, Bowles DJ

Abstract

Benzoates are a class of natural products containing compounds of industrial and strategic importance. In plants, the compounds exist in free form and as conjugates to a wide range of other metabolites such as glucose, which can be attached to the carboxyl group or to specific hydroxyl groups on the benzene ring. These glucosylation reactions have been studied for many years, but to date only one gene encoding a benzoate glucosyltransferase has been cloned. A phylogenetic analysis of sequences in the Arabidopsis genome revealed a large multigene family of putative glycosyltransferases containing a consensus sequence typically found in enzymes transferring glucose to small molecular weight compounds such as secondary metabolites. Ninety of these sequences have now been expressed as recombinant proteins in Escherichia coli, and their in vitro catalytic activities toward benzoates have been analyzed. The data show that only 14 proteins display activity toward 2-hydroxybenzoic acid, 4-hydroxybenzoic acid, and 3,4-dihydroxybenzoic acid. Of these, only two enzymes are active toward 2-hydroxybenzoic acid, suggesting they are the Arabidopsis salicylic acid glucosyltransferases. All of the enzymes forming glucose esters with the metabolites were located in Group L of the phylogenetic tree, whereas those forming O-glucosides were dispersed among five different groups. Catalytic activities were observed toward glucosylation of the 2-, 3-, or 4-hydroxyl group on the ring. To further explore their regioselectivity, the 14 enzymes were analyzed against benzoic acid, 3-hydroxybenzoic acid, 2,3-, 2,4-, 2,5-, and 2,6-dihydroxybenzoic acid. The data showed that glycosylation of specific sites could be positively or negatively influenced by the presence of additional hydroxyl groups on the ring. This study provides new tools for biotransformation reactions in vitro and a basis for engineering benzoate metabolism in plants.

MeSH Terms
Arabidopsis/enzymology Base Sequence Benzoates/metabolism Glycosyltransferases/metabolism Molecular Conformation Molecular Sequence Data Parabens/metabolism Salicylic Acid/metabolism Uridine Diphosphate Glucose/metabolism
Chemicals
Benzoates Parabens Glycosyltransferases 4-hydroxybenzoic acid Salicylic Acid Uridine Diphosphate Glucose
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Lim Eng-Kiat
Centre for Novel Agricultural Products, Department of Biology, University of York, York YO10 SDD, United Kingdom.
Doucet Charlotte J
Li Yi
Elias Luisa
Worrall Dawn
Spencer Steven P
Ross Joe
Bowles Dianna J
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2002-01-04
Epub
2001-00-18
Pages
586-92
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Databases
GENBANK
AB025634, AC002333, AC005106, AC005496, AC006248, AC016662, AC067971, AL161584, AL162751, AL391141, Z97339
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com