Identification of the in vivo function of the high-efficiency D-mannonate dehydratase in Caulobacter crescentus NA1000 from the enolase superfamily

Biochemistry. 2014 Jul 1;53(25):4087-9. doi: 10.1021/bi500683x. Epub 2014 Jun 20.

Abstract

The d-mannonate dehydratase (ManD) subgroup of the enolase superfamily contains members with varying catalytic activities (high-efficiency, low-efficiency, or no activity) that dehydrate d-mannonate and/or d-gluconate to 2-keto-3-deoxy-d-gluconate [Wichelecki, D. J., et al. (2014) Biochemistry 53, 2722-2731]. Despite extensive in vitro characterization, the in vivo physiological role of a ManD has yet to be established. In this study, we report the in vivo functional characterization of a high-efficiency ManD from Caulobacter crescentus NA1000 (UniProt entry B8GZZ7) by in vivo discovery of its essential role in d-glucuronate metabolism. This in vivo functional annotation may be extended to ~50 additional proteins.

Publication types

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

MeSH terms

  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • Caulobacter crescentus / metabolism*
  • Gene Knockout Techniques
  • Genome, Bacterial
  • Glucuronic Acid / metabolism
  • Hydro-Lyases / genetics
  • Hydro-Lyases / metabolism*
  • Phosphopyruvate Hydratase / genetics
  • Phosphopyruvate Hydratase / metabolism*
  • Stereoisomerism

Substances

  • Bacterial Proteins
  • Glucuronic Acid
  • Hydro-Lyases
  • Phosphopyruvate Hydratase
  • mannonate dehydratase