Engineering of cellobiose phosphorylase for glycoside synthesis

J Biotechnol. 2011 Dec 20;156(4):253-60. doi: 10.1016/j.jbiotec.2011.07.006. Epub 2011 Jul 20.

Abstract

Disaccharide phosphorylases are increasingly applied for glycoside synthesis, since they are very regiospecific and use cheap and easy to obtain donor substrates. A promising enzyme is cellobiose phosphorylase (CP), which was discovered more than 50 years ago. Many other bacterial CP enzymes have since then been characterized, cloned and applied for glycoside synthesis. However, the general application of wild-type CP for glycoside synthesis is hampered by its relatively narrow substrate specificity. Recently we have taken some successful efforts to broaden the substrate specificity of Cellulomonas uda CP by directed evolution and protein engineering. This review will give an overview of the obtained results and address the applicability of the engineered CP enzymes for glycoside synthesis. CP is the first example of an extensively engineered disaccharide phosphorylase, and may provide valuable information for protein engineering of other phosphorylase enzymes.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Bacterial Proteins / chemistry
  • Bacterial Proteins / metabolism
  • Directed Molecular Evolution / methods*
  • Glucosyltransferases / chemistry*
  • Glucosyltransferases / metabolism*
  • Glycosides / biosynthesis*
  • Glycosides / chemistry
  • Protein Engineering / methods*
  • Substrate Specificity / genetics

Substances

  • Bacterial Proteins
  • Glycosides
  • Glucosyltransferases
  • cellobiose phosphorylase