Gene cloning, overexpression, and characterization of the nitrilase from Rhodococcus rhodochrous tg1-A6 in E. coli

Appl Biochem Biotechnol. 2010 Jan;160(2):393-400. doi: 10.1007/s12010-008-8324-y. Epub 2008 Aug 5.

Abstract

A DNA fragment containing the entire coding sequence of nitrilase gene was amplified from Rhodococcus rhodochrous tg1-A6 with high nitrilase activity using PCR and sequenced. The open reading frame of the nitrilase gene contains 1,101 base pairs, which encodes a putative polypeptide of 366 amino acid residues. The nitrilase gene was cloned into an expression vector pET-28a and expressed in an Escherichia coli strain BL21(DE3). The enzymatic activity of nitrilase, which converts various nitriles to the corresponding carboxylic acids, was detected to reach 24.5 U/ml at 9 h in the recombinant bacteria.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aminohydrolases / chemistry
  • Aminohydrolases / genetics*
  • Aminohydrolases / metabolism
  • Bacterial Proteins / chemistry
  • Bacterial Proteins / genetics*
  • Bacterial Proteins / metabolism
  • Cloning, Molecular*
  • Escherichia coli / genetics*
  • Escherichia coli / metabolism
  • Gene Expression*
  • Rhodococcus / chemistry
  • Rhodococcus / enzymology*
  • Rhodococcus / genetics
  • Substrate Specificity

Substances

  • Bacterial Proteins
  • Aminohydrolases
  • nitrilase