| Literature DB >> 31018087 |
Jonghyeok Shin1, Jiwon Yu1, Myungseo Park1, Chakhee Kim1, Hooyeon Kim1, Yunjeong Park1, Choongjin Ban1,2, Emine Seydametova1, Young-Ha Song3, Chul-Soo Shin3, Kyung-Hwun Chung4, Ji-Min Woo5, Hyunwoo Chung5, Jin-Byung Park5, Dae-Hyuk Kweon1,2,6.
Abstract
Whole cell biocatalysts can be used to convert fatty acids into various value-added products. However, fatty acid transport across cellular membranes into the cytosol of microbial cells limits substrate availability and impairs membrane integrity, which in turn decreases cell viability and bioconversion activity. Because these problems are associated with the mechanism of fatty acid transport through membranes, a whole-cell biocatalyst that can form caveolae-like structures was generated to promote substrate endocytosis. Caveolin-1 ( CAV1) expression in Escherichia coli increased both the fatty acid transport rate and intracellular fatty acid concentrations via endocytosis of the supplemented substrate. Furthermore, fatty-acid endocytosis alleviated substrate cytotoxicity in E. coli. These traits attributed to bacterial endocytosis resulted in dramatically elevated biotransformation efficiencies in fed-batch and cell-recycle reaction systems when caveolae-forming E. coli was used for the bioconversion of ricinoleic acid (12-hydroxyoctadec-9-enoic acid) to ( Z)-11-(heptanoyloxy) undec-9-enoic acid. We propose that CAV1-mediated endocytosing E. coli represents a versatile tool for the biotransformation of hydrophobic substrates.Entities:
Keywords: biotransformation; caveolin-1; endocytosis; fatty acid; heterologous caveolae
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Year: 2019 PMID: 31018087 DOI: 10.1021/acssynbio.8b00519
Source DB: PubMed Journal: ACS Synth Biol ISSN: 2161-5063 Impact factor: 5.110