Conversion of a Mono- and Diacylglycerol Lipase into a Triacylglycerol Lipase by Protein Engineering

Chembiochem. 2015 Jul 6;16(10):1431-4. doi: 10.1002/cbic.201500163. Epub 2015 May 29.

Abstract

Despite the fact that most lipases are believed to be active against triacylglycerides, there is a small group of lipases that are active only on mono- and diacylglycerides. The reason for this difference in substrate scope is not clear. We tried to identify the reasons for this in the lipase from Malassezia globosa. By protein engineering, and with only one mutation, we managed to convert this enzyme into a typical triacylglycerol lipase (the wild-type lipase does not accept triacylglycerides). The variant Q282L accepts a broad spectrum of triacylglycerides, although the catalytic behavior is altered to some extent. From in silico analysis it seems that specific hydrophobic interactions are key to the altered substrate specificity.

Keywords: enzyme catalysis; lipases; protein engineering; steric hindrance; substrate specificity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalytic Domain
  • Lipase / chemistry
  • Lipase / genetics*
  • Lipase / metabolism
  • Lipoprotein Lipase / chemistry
  • Lipoprotein Lipase / genetics*
  • Lipoprotein Lipase / metabolism
  • Malassezia / chemistry
  • Malassezia / enzymology*
  • Malassezia / genetics
  • Malassezia / metabolism
  • Models, Molecular
  • Monoacylglycerol Lipases / chemistry
  • Monoacylglycerol Lipases / genetics*
  • Monoacylglycerol Lipases / metabolism
  • Point Mutation*
  • Protein Engineering*
  • Substrate Specificity

Substances

  • Monoacylglycerol Lipases
  • Lipase
  • Lipoprotein Lipase