Mechanism of 3-Methylanthranilic Acid Derepression of the Tryptophan Operon in Escherichia coli

Author:

Held William A.1,Smith Oliver H.1

Affiliation:

1. Department of Biology, Marquette University, Milwaukee, Wisconsin 53233

Abstract

3-Methylanthranilic acid (3MA) inhibits growth and causes derepression of the tryptophan biosynthetic enzymes in wild-type strains of Escherichia coli . Previous reports attributed this effect to an inhibition of the conversion of 1-( o -carboxyphenylamino)-1-deoxyribulose 5-phosphate to indole-3-glycerol phosphate and a consequent reduction in the concentration of endogenous tryptophan. Our studies have shown that 3MA-resistant mutants linked to the tryptophan operon have a feedback-resistant anthranilate synthetase; mutants with an altered indole-3-glycerol phosphate synthetase were not found. 3MA or 7-methylindole can be metabolized to 7-methyltryptophan, and 3MA, 7-methylindole, and 7-methyltryptophan lead to derepression of the tryptophan operon. Furthermore, 3MA-resistant mutants are also resistant to 7-methylindole derepression. These results strongly suggest that the primary cause of derepression by 3MA is through its conversion to 7-methyltryptophan, which can inhibit anthranilate synthetase, thereby decreasing the concentration of endogenous tryptophan. Unlike 5- or 6-methyltryptophan, 7-methyltryptophan does not appear to function as an active corepressor.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

Reference21 articles.

1. Anthranilate synthetase. Partial purification and some kinetic studies on the enzyme from Escherichia coli;Baker T. I.;J. Biol. Chem.,1966

2. Sur la repression de la synthesis des enzymes intervenant dans la formation du tryptophane chez Escherichia coli;Cohen G. N.;Compt. Rend.,1959

3. Product inhibition of anthranilate synthetase in Salmonella typhimurium;Cordaro J.;Biochem. Biophys. Res. Commun.,1968

4. Mutants of Escherichia coli with an altered tryptophanyl-transfer ribonucleic acid synthetase;Doolittle W. F.;J. Bacteriol.,1968

5. The partial purification and properties of indole-3-glycerol phosphate synthetase from Escherichia coli;Gibson F.;Biochim. Biophys. Acta,1960

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