Characterization and function of Mycobacterium tuberculosis H37Rv Lipase Rv1076 (LipU)

Microbiol Res. 2017 Mar:196:7-16. doi: 10.1016/j.micres.2016.12.005. Epub 2016 Dec 15.

Abstract

Lipids and lipases/esterases are essential for Mycobacterium tuberculosis (Mtb) survival and persistence, even virulence. Mycobacterium tuberculosis H37Rv Rv1076 (LipU), a member of lipase family, is homologous to the human Hormone Sensitive Lipase (HSL) based on the presence of conserved motif 'GXSXG'. To define the enzymatic characteristics of rv1076, the gene was cloned, and expressed in Escherichia coli. The protein was purified for enzymatic characterization. LipU showed high specific activity for the hydrolysis of short carbon chain substrates with optimal activity at 40°C/pH 8.0 and stability at low temperature and near-neutral pH. The specific activity, Km and Vmax of LipU was calculated to 176.7U/mg, 1.73μM and 62.24μM/min respectively. Ionic detergents can inhibit its activity. The active-site residues of LipU were determined to be Ser140, Asp244 and His269 by site-directed mutagenesis. The upregulation of Mycobacterium tuberculosis rv1076 under nutritive stress implicates a role in starvation.

Keywords: Characteristics; Lipases/esterases; Mycobacterium tuberculosis; Rv1076; lipU.

MeSH terms

  • Amino Acid Sequence
  • Bacterial Proteins / genetics
  • Bacterial Proteins / isolation & purification
  • Bacterial Proteins / metabolism*
  • Base Sequence
  • Catalytic Domain
  • Cloning, Molecular
  • Enzyme Activation / drug effects
  • Enzyme Induction
  • Enzyme Stability
  • Escherichia coli / genetics
  • Esterases / metabolism
  • Hydrogen-Ion Concentration
  • Lipase / genetics
  • Lipase / isolation & purification
  • Lipase / metabolism*
  • Mutagenesis, Site-Directed
  • Mycobacterium smegmatis / drug effects
  • Mycobacterium smegmatis / growth & development
  • Mycobacterium tuberculosis / enzymology*
  • Mycobacterium tuberculosis / genetics
  • Protein Structure, Secondary
  • Recombinant Proteins / genetics
  • Recombinant Proteins / isolation & purification
  • Recombinant Proteins / metabolism
  • Substrate Specificity

Substances

  • Bacterial Proteins
  • Recombinant Proteins
  • Esterases
  • Lipase