Regulation of pho regulon gene expression by the carbon control protein A, CcpA, in Bacillus subtilis

J Mol Microbiol Biotechnol. 2005;10(1):40-50. doi: 10.1159/000090347.

Abstract

Bacterial regulons involved in carbon, nitrogen and phosphorus metabolism must interact for purposes of coordination, but the mechanisms involved are not understood. We here report that the carbon control pro-tein-A (CcpA) of Bacillus subtilis, primarily concerned with carbon metabolism, influences expression of various phosphorus (pho) regulon genes including the two alkaline phosphatase structural genes, phoA and phoB. The directions and magnitudes of the effects of glucose and the loss of CcpA on these two genes depend on growth conditions, but they always correlate inversely. Absolute expression levels of phoA and phoB depend on a rich nitrogen source, and gene activation by a fermentable substrate such as glucose depends on the presence of a respiratory substrate such as succinate. We show that these CcpA-dependent glucose effects can be explained by the effects of glucose and CcpA acting on the phoPR operon. Although a good CcpA-binding site (CRE) is found in the control region of the phoPR operon, direct regulation of phoPR gene expression by CcpA via this CRE could not account for the effects of glucose and CcpA on phoA and phoB gene expression. We conclude that CcpA exerts indirect control over the pho regulon by a mechanism that involves CcpA and PhoRP but does not involve the phoPR operon CRE.

Publication types

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

MeSH terms

  • Alkaline Phosphatase
  • Bacillus subtilis / genetics*
  • Bacillus subtilis / metabolism
  • Bacterial Proteins / biosynthesis
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • Binding Sites
  • Carbon / metabolism*
  • Cyclin-Dependent Kinases / biosynthesis
  • Cyclin-Dependent Kinases / genetics
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Gene Expression Regulation, Bacterial
  • Genes, Reporter
  • Glucose / pharmacology
  • Glutamic Acid / pharmacology
  • Lac Operon
  • Mutation
  • Operon
  • Regulon / genetics*
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism*
  • Staphylococcal Protein A / genetics
  • Staphylococcal Protein A / metabolism*
  • Succinic Acid / pharmacology
  • Transcriptional Activation

Substances

  • Bacterial Proteins
  • DNA-Binding Proteins
  • Repressor Proteins
  • Staphylococcal Protein A
  • catabolite control proteins, bacteria
  • PhoB protein, Bacteria
  • Glutamic Acid
  • Carbon
  • Succinic Acid
  • Cyclin-Dependent Kinases
  • Alkaline Phosphatase
  • Glucose