An engineered eukaryotic protein glycosylation pathway in Escherichia coli

Nat Chem Biol. 2012 Mar 25;8(5):434-6. doi: 10.1038/nchembio.921.

Abstract

We performed bottom-up engineering of a synthetic pathway in Escherichia coli for the production of eukaryotic trimannosyl chitobiose glycans and the transfer of these glycans to specific asparagine residues in target proteins. The glycan biosynthesis was enabled by four eukaryotic glycosyltransferases, including the yeast uridine diphosphate-N-acetylglucosamine transferases Alg13 and Alg14 and the mannosyltransferases Alg1 and Alg2. By including the bacterial oligosaccharyltransferase PglB from Campylobacter jejuni, we successfully transferred glycans to eukaryotic proteins.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Campylobacter jejuni / enzymology
  • Disaccharides / biosynthesis*
  • Escherichia coli / metabolism*
  • Escherichia coli Proteins / metabolism*
  • Glycosylation
  • Hexosyltransferases / metabolism
  • Mannosyltransferases / metabolism
  • Membrane Proteins / metabolism
  • N-Acetylglucosaminyltransferases / metabolism
  • Polysaccharides / biosynthesis*
  • Protein Engineering*
  • Saccharomyces cerevisiae Proteins / metabolism

Substances

  • Disaccharides
  • Escherichia coli Proteins
  • Membrane Proteins
  • Polysaccharides
  • Saccharomyces cerevisiae Proteins
  • chitobiose
  • ALG2 protein, S cerevisiae
  • Alg13 protein, S cerevisiae
  • Alg14 protein, S cerevisiae
  • Hexosyltransferases
  • Mannosyltransferases
  • N-Acetylglucosaminyltransferases
  • chitobiosyldiphosphodolichol beta-mannosyltransferase
  • dolichyl-diphosphooligosaccharide - protein glycotransferase