Glucomannan utilization operon of Bacillus subtilis

FEMS Microbiol Lett. 2008 Feb;279(1):103-9. doi: 10.1111/j.1574-6968.2007.01018.x.

Abstract

This study characterizes the glucomannan utilization operon (gmuBACDREFG, formerly ydhMNOPQRST) of Bacillus subtilis. Transcription of the operon is induced by konjac glucomannan and requires the last mannanase gene (gmuG). Cellobiose and mannobiose, possible degradation products of glucomannan by GmuG, are strong inducers of transcription. It is shown that an internal regulator gene (gmuR) encodes a repressor of the operon, as disruption of this gene enhances transcription of the operon in the absence of inducers. The expression of the glucomannan utilizing operon of B. subtilis is thus induced by degraded glucomannan products, and repressed by an internal repressor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacillus subtilis / genetics*
  • Bacillus subtilis / metabolism
  • Bacterial Proteins / genetics
  • Base Sequence
  • Cellobiose / metabolism
  • Gene Deletion
  • Gene Expression Regulation, Bacterial
  • Mannans / metabolism*
  • Metabolic Networks and Pathways*
  • Models, Biological
  • Molecular Sequence Data
  • Mutagenesis, Insertional
  • Operon
  • Repressor Proteins / genetics
  • Transcription, Genetic

Substances

  • Bacterial Proteins
  • Mannans
  • Repressor Proteins
  • mannobiose
  • Cellobiose
  • (1-6)-alpha-glucomannan