In silico prediction and validation of the importance of the Entner-Doudoroff pathway in poly(3-hydroxybutyrate) production by metabolically engineered Escherichia coli

Soon Ho Hong, Si Jae Park, Soo Yun Moon, Jong Pil Park, Sang Yup Lee

Research output: Contribution to journalArticlepeer-review

39 Scopus citations

Abstract

The metabolic network of Escherichia coli was constructed and was used to simulate the distribution of metabolic fluxes in wild-type E. coli and recombinant E. coli producing poly(3-hydroxybutyrate) [P(3HB)]. The flux of acetyl-CoA into the tricarboxylic acid (TCA) cycle, which competes with the P(3HB) biosynthesis pathway, decreased significantly during P(3HB) production. It was notable to find from in silico analysis that the Entner-Doudoroff (ED) pathway flux increased significantly under P(3HB)-accumulating conditions. To prove the role of ED pathway on P(3HB) production, a mutant E. coli strain, KEDA, which is defective in the activity of 2-keto-3-deoxy-6-phosphogluconate aldolase (Eda), was examined as a host strain for the production of P(3HB) by transforming it with pJC4, a plasmid containing the Alcaligenes latus P(3HB) biosynthesis operon. The P(3HB) content obtained with KEDA (pJC4) was lower than that obtained with its parent strain KS272 (pJC4). The reduced P(3HB) biosynthetic capacity of KEDA (pJC4) could be restored by the co-expression of the E. coli eda gene, which proves the important role of ED pathway on P(3HB) synthesis in recombinant E. coli as predicted by metabolic flux analysis.

Original languageEnglish
Pages (from-to)854-863
Number of pages10
JournalBiotechnology and Bioengineering
Volume83
Issue number7
DOIs
StatePublished - 30 Sep 2003

Keywords

  • 2-keto-3-deoxy-6-phosphogluconate aldolase
  • Entner-Doudoroff pathway
  • Escherichia coli
  • Metabolic flux analysis
  • Poly(3-hydroxybutyrate)

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