Literature DB >> 35930086

Metabolic pathway design for growth-associated phenylalanine production using synthetically designed mutualism.

Ryutaro Kawai1, Yoshihiro Toya1, Hiroshi Shimizu2.   

Abstract

Combination of growth-associated pathway engineering based on flux balance analysis (FBA) and adaptive laboratory evolution (ALE) is a powerful approach to enhance the production of useful compounds. However, the feasibility of such growth-associated pathway designs depends on the type of target compound. In the present study, FBA predicted a set of gene deletions (pykA, pykF, ppc, zwf, and adhE) that leads to growth-associated phenylalanine production in Escherichia coli. The knockout strain is theoretically enforced to produce phenylalanine only at high growth yields, and could not be applied to the ALE experiment because of a severe growth defect. To overcome this challenge, we propose a novel approach for ALE based on mutualistic co-culture for coupling growth and production, regardless of the growth rate. We designed a synthetic mutualism of a phenylalanine-producing leucine-auxotrophic strain (KF strain) and a leucine-producing phenylalanine-auxotrophic strain (KL strain) and performed an ALE experiment for approximately 160 generations. The evolved KF strain (KF-E strain) grew in a synthetic medium (with glucose as the main carbon source) supplemented with leucine, while severe growth defects were observed in the parental KF strain. The phenylalanine yield of the KF-E strain was 2.3 times higher than that of the KF strain.
© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  Flux balance analysis; Metabolic engineering; Mutualistic co-culture

Mesh:

Substances:

Year:  2022        PMID: 35930086     DOI: 10.1007/s00449-022-02762-4

Source DB:  PubMed          Journal:  Bioprocess Biosyst Eng        ISSN: 1615-7591            Impact factor:   3.434


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2.  E. coli genome manipulation by P1 transduction.

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Journal:  Curr Protoc Mol Biol       Date:  2007-07

3.  Modeling the Contribution of Allosteric Regulation for Flux Control in the Central Carbon Metabolism of E. coli.

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