Pseudomonas syringae self-protection from tabtoxinine-β-lactam by ligase TblF and acetylase Ttr

Biochemistry. 2012 Oct 2;51(39):7712-25. doi: 10.1021/bi3011384. Epub 2012 Sep 19.

Abstract

Plant pathogenic Pseudomonas syringae produce the hydroxy-β-lactam antimetabolite tabtoxinine-β-lactam (TβL) as a time-dependent inactivating glutamine analogue of plant glutamine synthetases. The producing pseudomonads use multiple modes of self-protection, two of which are characterized in this study. The first is the dipeptide ligase TblF which converts tabtoxinine-β-lactam to the TβL-Thr dipeptide known as tabtoxin. The dipeptide is not recognized by glutamine synthetase. This represents a Trojan Horse strategy: the dipeptide is secreted, taken up by dipeptide permeases in neighboring cells, and TβL is released by peptidase action. The second self-protection mode is elaboration by the acetyltransferase Ttr, which acetylates the α-amino group of the proximal inactivator TβL, but not the tabtoxin dipeptide.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Acetyltransferases / metabolism*
  • Azetidines / metabolism*
  • Bacterial Toxins / metabolism*
  • Dipeptides / metabolism*
  • Ligases / metabolism*
  • Plants / microbiology
  • Pseudomonas syringae / enzymology*
  • Pseudomonas syringae / metabolism
  • Threonine / metabolism

Substances

  • Azetidines
  • Bacterial Toxins
  • Dipeptides
  • Threonine
  • tabtoxinine beta-lactam
  • Acetyltransferases
  • Ligases
  • tabtoxin