Cloning and expression of Pseudomonas fluorescens 26-2 lipase gene in Pichia pastoris and characterizing for transesterification

Appl Biochem Biotechnol. 2009 Nov;159(2):355-65. doi: 10.1007/s12010-008-8419-5. Epub 2008 Nov 13.

Abstract

Pseudomonas lipases are important biocatalysts widely used in a variety of industrial fields. An extracellular lipase gene lipA with 1,854-bp open reading frame was cloned from Pseudomonas fluorescens 26-2. The multialignment assay of the putative amino acid and the secondary structure prediction revealed this enzyme could be classified into the lipolytic subfamily I.3 and secreted via adenosine-triphosphate-binding cassette pathway. The lipA gene was integrated into Pichia pastoris GS115, and the methanol-inducible recombinants with Mut(S) and Mut(+) phenotypes were acquired. The characteristics and the transesterification capacity shown by this enzyme suggested it is a useful biocatalyst for biodiesel preparation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cloning, Molecular / methods*
  • Enzyme Activation
  • Enzyme Stability
  • Esterification
  • Esters / chemistry
  • Gene Expression / physiology
  • Lipase / analysis
  • Lipase / chemistry*
  • Lipase / metabolism
  • Pichia / enzymology*
  • Pichia / genetics*
  • Pseudomonas fluorescens / enzymology*
  • Pseudomonas fluorescens / genetics*
  • Recombinant Proteins / chemistry*
  • Recombinant Proteins / metabolism

Substances

  • Esters
  • Recombinant Proteins
  • Lipase