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 D2O.
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 -CHD2 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.
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Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Ito J., Yanofsky C. 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):734–742. doi: 10.1128/jb.97.2.734-742.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Srinivasan P. R. The biosynthesis of anthranilate from [3,4-'+C]glucose in Escherichia coli. Biochemistry. 1965 Dec;4(12):2860–2865. doi: 10.1021/bi00888a043. [DOI] [PubMed] [Google Scholar]
- Tamir H., Srinivasan P. R. Purification and properties of anthranilate synthase from Salmonella typhimurium. J Biol Chem. 1969 Dec 10;244(23):6507–6513. [PubMed] [Google Scholar]
- Zalkin H., Kling D. Anthranilate synthetase. Purification and properties of component I from Salmonella typhimurium. Biochemistry. 1968 Oct;7(10):3566–3573. doi: 10.1021/bi00850a034. [DOI] [PubMed] [Google Scholar]
