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PMID: 5271179 Published · ppublish English Journal Article

Studies of the mechanism of anthranilate synthase reaction.

Tamir H, Srinivasan PR

Abstract

The enzyme anthranilate synthase catalyzes the formation of anthranilate form either chorismate and glutamine or chorismate and ammonia. In the aromatization of chorismate, a hydroxyl group and an enolpyruvyl group must be eliminated. Elimination of the enolpyruvyl group of chorismate is accompanied by protonation to form pyruvate. The source of this proton was investigated by performing the enzymatic reaction in 99.7 per cent D(2)O. The isolated pyruvate contained close to an atom of deuterium in the methyl group. High resolution mass spectra also revealed that about 6 per cent of the deuterio pyruvate contains a -CHD(2) species. Thus, the results obtained conclusively demonstrate that in the formation of the pyruvate, the third hydrogen of the methyl group arises from water and not by intramolecular shift of a hydrogen from the ring of chorismate.

MeSH Terms
Chemical Phenomena Chemistry Cyclohexanecarboxylic Acids/metabolism,pharmacology Deuterium/pharmacology Pyruvates/analysis,biosynthesis Spectrum Analysis Transaminases/metabolism ortho-Aminobenzoates/metabolism
Chemicals
Cyclohexanecarboxylic Acids Pyruvates ortho-Aminobenzoates Deuterium Transaminases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Tamir H
Srinivasan P R
References (4)
4 references, click to expand
  1. The biosynthesis of anthranilate from [3,4-'+C]glucose in Escherichia coli.
    Biochemistry. 1965 Dec;4(12):2860-5 PMID: 5326358
  2. Anthranilate synthetase. Purification and properties of component I from Salmonella typhimurium.
    Biochemistry. 1968 Oct;7(10):3566-73 PMID: 4878701
  3. Anthranilate synthetase, an enzyme specified by the tryptophan operon of Escherichia coli: Comparative studies on the complex and the subunits.
    J Bacteriol. 1969 Feb;97(2):734-42 PMID: 4886290
  4. Purification and properties of anthranilate synthase from Salmonella typhimurium.
    J Biol Chem. 1969 Dec 10;244(23):6507-13 PMID: 4901372
Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1970-06-00
Pages
547-51
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC283079
Subset
IM
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