Effect of T- and C-loop mutations on the Herbaspirillum seropedicae GlnB protein in nitrogen signalling

Res Microbiol. 2005 Jun-Jul;156(5-6):634-40. doi: 10.1016/j.resmic.2005.01.015. Epub 2005 Feb 26.

Abstract

Proteins of the PII family are found in species of all kingdoms. Although these proteins usually share high identity, their functions are specific to the different organisms. Comparison of structural data from Escherichia coli GlnB and GlnK and Herbaspirillum seropedicae GlnB showed that the T-loop and C-terminus were variable regions. To evaluate the role of these regions in signal transduction by the H. seropedicae GlnB protein, four mutants were constructed: Y51F, G108A/P109a, G108W and Q3R/T5A. The activities of the native and mutated proteins were assayed in an E. coli background constitutively expressing the Klebsiella pneumoniae nifLA operon. The results suggested that the T-loop and C-terminus regions of H. seropedicae GlnB are involved in nitrogen signal transduction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Amino Acid Substitution
  • Artificial Gene Fusion
  • Bacterial Proteins / chemistry
  • Bacterial Proteins / genetics*
  • Bacterial Proteins / metabolism*
  • Escherichia coli / genetics
  • Escherichia coli / metabolism
  • Gene Expression Regulation, Bacterial
  • Genes, Reporter
  • Herbaspirillum / genetics*
  • Herbaspirillum / metabolism*
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • Mutation*
  • Nitrogen / metabolism*
  • PII Nitrogen Regulatory Proteins
  • Protein Structure, Secondary
  • Sequence Homology, Amino Acid
  • Signal Transduction
  • beta-Galactosidase / analysis

Substances

  • Bacterial Proteins
  • PII Nitrogen Regulatory Proteins
  • PIID regulatory protein, Bacteria
  • beta-Galactosidase
  • Nitrogen