Characterization of two glutaminases from the filamentous cyanobacterium Anabaena sp. PCC 7120

FEMS Microbiol Lett. 2008 Dec;289(2):241-9. doi: 10.1111/j.1574-6968.2008.01395.x.

Abstract

The Anabaena genome contains two ORFs that appear to encode glutaminases. The genes were expressed as histidine-tagged fusion proteins in Escherichia coli. The purified proteins possessed glutaminase activity using l-glutamine as the substrate, but differed in biochemical properties. All2934 showed an optimal activity at 20 degrees C and pH 6.0, with a higher affinity for l-glutamine than All4774, which had optimal activity at 37 degrees C and pH 7.5. Remarkably, the glutaminase activity of All2934 was phosphate dependent, while All4774 was phosphate independent. The expression of all2934 and all4774 was analyzed using semi-quantitative reverse transcriptase-PCR. The expression level of all2934 was much higher than that of all4774 under normal and nitrogen-depletion conditions, indicating that All2934 may play an important role in metabolizing glutamine in Anabaena.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Anabaena / chemistry
  • Anabaena / enzymology*
  • Anabaena / genetics
  • Bacterial Proteins / chemistry*
  • Bacterial Proteins / genetics
  • Bacterial Proteins / isolation & purification
  • Bacterial Proteins / metabolism
  • Enzyme Stability
  • Escherichia coli / genetics
  • Escherichia coli / metabolism
  • Glutaminase / chemistry*
  • Glutaminase / genetics
  • Glutaminase / isolation & purification
  • Glutaminase / metabolism
  • Kinetics
  • Molecular Sequence Data
  • Nitrogen / metabolism
  • Sequence Alignment

Substances

  • Bacterial Proteins
  • Glutaminase
  • Nitrogen