Enhancement of cytidine production by coexpression of gnd, zwf, and prs genes in recombinant Escherichia coli CYT15

Biotechnol Lett. 2013 Feb;35(2):245-51. doi: 10.1007/s10529-012-1068-3. Epub 2012 Oct 16.

Abstract

Cytidine is a precursor of several antiviral drugs. The pentose phosphate pathway (PPP) is primarily responsible for NADPH and 5-phospho-α-D-ribose 1-diphosphate as an important precursor of cytidine biosynthesis in Escherichia coli. To enhance cytidine production, we obtained the recombinant E. coli CYT15-gnd-prs-zwf that co-expressed the prs, zwf, and gnd genes encoding phosphoribosylpyrophosphate synthetase, glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase (three key enzymes in PPP) respectively. In fermentation experiments, strain CYT15-gnd-prs-zwf produced 735 mg cytidine/l using glucose as substrate, which was approx. 128 % higher than the cytidine production by the parental strain (CYT15). Co-expression of zwf, gnd, and prs decreased growth (3.2 %) slightly and increased glucose uptake (72 %). This is the first study to report increased cytidine production by increasing metabolic flux through the PPP in E. coli.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cytidine / biosynthesis*
  • Escherichia coli / genetics*
  • Escherichia coli / metabolism*
  • Fermentation
  • Gene Expression
  • Glucosephosphate Dehydrogenase / genetics
  • Glucosephosphate Dehydrogenase / metabolism
  • Metabolic Engineering*
  • Metabolic Networks and Pathways / genetics*
  • Phosphogluconate Dehydrogenase / genetics
  • Phosphogluconate Dehydrogenase / metabolism
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Ribose-Phosphate Pyrophosphokinase / genetics
  • Ribose-Phosphate Pyrophosphokinase / metabolism

Substances

  • Recombinant Proteins
  • Cytidine
  • Phosphogluconate Dehydrogenase
  • Glucosephosphate Dehydrogenase
  • Ribose-Phosphate Pyrophosphokinase