4.5 Article

4-Nitrotryptophan is a substrate for the non-ribosomal peptide synthetase TxtB in the thaxtomin A biosynthetic pathway

期刊

MOLECULAR MICROBIOLOGY
卷 73, 期 3, 页码 409-418

出版社

WILEY
DOI: 10.1111/j.1365-2958.2009.06780.x

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资金

  1. National Research Initiative of the United States Department of Agriculture (USDA) Cooperative State Research, Education, and Extension Service [2005-35319-19202]
  2. Robert A. Welch Foundation [C-0729]
  3. USDA Cooperative State Research, Education, and Extension Service [2001-52104-11484]
  4. National Institutes of Health (NIH) Chemistry of Biological Systems Training Grant at Cornell University

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Thaxtomin A, a cyclic dipeptide with a nitrated tryptophan moiety, is a phytotoxic pathogenicity determinant in scab-causing Streptomyces species that inhibits cellulose synthesis by an unknown mechanism. Thaxtomin A is produced by the action of two non-ribosomal peptide synthetase modules (TxtA and TxtB) and a complement of modifying enzymes, although the order of biosynthesis has not yet been determined. Analysis of a thaxtomin dual module knockout mutant and single module knockout mutants revealed that 4-nitrotryptophan is an intermediate in thaxtomin A biosynthesis prior to backbone assembly. The 4-nitrotryptophan represents a novel substrate for non-ribosomal peptide synthetases. Through identification of N-methyl-4-nitrotryptophan in a single module knockout and the use of adenylation domain specificity prediction software, TxtB was identified as the non-ribosomal peptide synthetase module specific for 4-nitrotryptophan.

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