In-silico-driven metabolic engineering of Pseudomonas putida for enhanced production of poly-hydroxyalkanoates

I. Poblete-Castro, D. Binger, A. Rodrigues, J. Becker, V.A.P. Martins Dos Santos, C. Wittmann

Research output: Contribution to journalArticleAcademicpeer-review

89 Citations (Scopus)

Abstract

Here, we present systems metabolic engineering driven by in-silico modeling to tailor Pseudomonas putida for synthesis of medium chain length PHAs on glucose. Using physiological properties of the parent wild type as constraints, elementary flux mode analysis of a large-scale model of the metabolism of P. putida was used to predict genetic targets for strain engineering. Among a set of priority ranked targets, glucose dehydrogenase (encoded by gcd) was predicted as most promising deletion target. The mutant P. putida ¿gcd, generated on basis of the computational design, exhibited 100% increased PHA accumulation as compared to the parent wild type, maintained a high specific growth rate and exhibited an almost unaffected gene expression profile, which excluded detrimental side effects of the modification. A second mutant strain, P. putida ¿pgl, that lacked 6-phosphogluconolactonase, exhibited a substantially decreased PHA synthesis, as was also predicted by the model. The production potential of P. putida ¿gcd was assessed in batch bioreactors. The novel strain showed an increase of the PHA yield (+80%), the PHA titer (+100%) and cellular PHA content (+50%) and revealed almost unaffected growth and diminished by-product formation. It was thus found superior in all relevant criteria towards industrial production. Beyond the contribution to more efficient PHA production processes at reduced costs that might replace petrochemical plastics in the future, the study illustrates the power of computational prediction to tailor microbial strains for enhanced biosynthesis of added-value compounds
Original languageEnglish
Pages (from-to)113-123
JournalMetabolic Engineering
Volume15
DOIs
Publication statusPublished - 2013

Keywords

  • chain-length polyhydroxyalkanoates
  • gram-negative bacteria
  • fed-batch culture
  • genome sequence
  • escherichia-coli
  • kt2440
  • pathways
  • acid
  • poly(3-hydroxyalkanoates)
  • biosynthesis

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