Cloning and expression of a mureinolytic enzyme from the mycobacteriophage TM4

FEMS Microbiol Lett. 2010 Oct;311(2):126-32. doi: 10.1111/j.1574-6968.2010.02080.x. Epub 2010 Aug 19.

Abstract

In this study, we describe the characterization, cloning, expression and purification of the lysin A gene of the mycobacteriophage TM4. The gene TM4_gp29 (gp29) is a 1644-bp gene that codes for a 58.6-kDa protein and contains peptidoglycan recognition protein, Zn-binding and amidase catalytic domains. The gene was cloned into Escherichia coli using the 'His-Tag' pQE60 vector. After affinity chromatography-mediated purification, the protein was concentrated and visualized using sodium dodecyl sulphate polyacrylamide gel electrophoresis. Evidence of peptidoglycan-degrading activity was observed initially by a chloroform assay and later by conventional zymogram analysis.

MeSH terms

  • Amino Acid Sequence
  • Cloning, Molecular*
  • Gene Expression*
  • Molecular Sequence Data
  • Mycobacteriophages / enzymology*
  • Mycobacteriophages / genetics
  • Mycobacteriophages / physiology
  • Peptidoglycan / metabolism
  • Protein Binding
  • Protein Structure, Tertiary
  • Viral Envelope Proteins / chemistry
  • Viral Envelope Proteins / genetics*
  • Viral Envelope Proteins / isolation & purification
  • Viral Envelope Proteins / metabolism

Substances

  • Peptidoglycan
  • Viral Envelope Proteins