Literature DB >> 9785457

Metabolic routing towards polyhydroxyalkanoic acid synthesis in recombinant Escherichia coli (fadR): inhibition of fatty acid beta-oxidation by acrylic acid.

Q Qi1, A Steinbüchel, B H Rehm.   

Abstract

Heterologous expression of the phaC1 gene from Pseudomonas aeruginosa, which encodes one of the polyhydroxyalkanoic acid synthases, in Escherichia coli impaired in fatty acid beta-oxidation results in polyhydroxyalkanoic acid accumulation when cells were cultivated on fatty acids. We evaluated the application of the fatty acid beta-oxidation inhibitor acrylic acid as a tool to channel intermediates of beta-oxidation to polyhydroxyalkanoic acid synthesis. Various E. coli strains affected in fatty acid metabolism and the wild-type strain harboring plasmid pBHR71 were analyzed with respect to polyhydroxyalkanoic acid accumulation in the presence of acrylic acid. The E. coli fadR mutant RS3097 revealed the strongest polyhydroxyalkanoic acid accumulation. The optimum inhibitory concentration of acrylic acid was 0.24 mg ml-1 and caused efficient channeling of intermediates of beta-oxidation to polyhydroxyalkanoic acid synthesis. Under these conditions and grown on decanoate E. coli RS3097 harboring plasmid pBHR71 revealed a polyhydroxyalkanoic acid accumulation contributing to about 60% of cellular dry weight.

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Year:  1998        PMID: 9785457     DOI: 10.1111/j.1574-6968.1998.tb13212.x

Source DB:  PubMed          Journal:  FEMS Microbiol Lett        ISSN: 0378-1097            Impact factor:   2.742


  21 in total

1.  From oil to bioplastics, a dream come true?

Authors:  María A Prieto
Journal:  J Bacteriol       Date:  2006-11-03       Impact factor: 3.490

2.  Properties of engineered poly-3-hydroxyalkanoates produced in recombinant Escherichia coli strains.

Authors:  Q Ren; N Sierro; M Kellerhals; B Kessler; B Witholt
Journal:  Appl Environ Microbiol       Date:  2000-04       Impact factor: 4.792

3.  Engineering of stable recombinant bacteria for production of chiral medium-chain-length poly-3-hydroxyalkanoates.

Authors:  M A Prieto; M B Kellerhals; G B Bozzato; D Radnovic; B Witholt; B Kessler
Journal:  Appl Environ Microbiol       Date:  1999-08       Impact factor: 4.792

4.  FabG, an NADPH-dependent 3-ketoacyl reductase of Pseudomonas aeruginosa, provides precursors for medium-chain-length poly-3-hydroxyalkanoate biosynthesis in Escherichia coli.

Authors:  Q Ren; N Sierro; B Witholt; B Kessler
Journal:  J Bacteriol       Date:  2000-05       Impact factor: 3.490

5.  PhaG-mediated synthesis of Poly(3-hydroxyalkanoates) consisting of medium-chain-length constituents from nonrelated carbon sources in recombinant Pseudomonas fragi.

Authors:  S Fiedler; A Steinbüchel; B H Rehm
Journal:  Appl Environ Microbiol       Date:  2000-05       Impact factor: 4.792

6.  Matrix-assisted in vitro refolding of Pseudomonas aeruginosa class II polyhydroxyalkanoate synthase from inclusion bodies produced in recombinant Escherichia coli.

Authors:  B H Rehm; Q Qi; B B Beermann; H J Hinz; A Steinbüchel
Journal:  Biochem J       Date:  2001-08-15       Impact factor: 3.857

7.  Polyhydroxyalkanoate (PHA) accumulation in sulfate-reducing bacteria and identification of a class III PHA synthase (PhaEC) in Desulfococcus multivorans.

Authors:  Tran Hai; Daniela Lange; Ralf Rabus; Alexander Steinbüchel
Journal:  Appl Environ Microbiol       Date:  2004-08       Impact factor: 4.792

8.  Polyhydroxyalkanoate (PHA) biosynthesis in Thermus thermophilus: purification and biochemical properties of PHA synthase.

Authors:  Anastasia A Pantazaki; Maria G Tambaka; Valerie Langlois; Philippe Guerin; Dimitrios A Kyriakidis
Journal:  Mol Cell Biochem       Date:  2003-12       Impact factor: 3.396

9.  Identification and characterization of a new enoyl coenzyme A hydratase involved in biosynthesis of medium-chain-length polyhydroxyalkanoates in recombinant Escherichia coli.

Authors:  Si Jae Park; Sang Yup Lee
Journal:  J Bacteriol       Date:  2003-09       Impact factor: 3.490

10.  FadD from Pseudomonas putida CA-3 is a true long-chain fatty acyl coenzyme A synthetase that activates phenylalkanoic and alkanoic acids.

Authors:  Aisling R Hume; Jasmina Nikodinovic-Runic; Kevin E O'Connor
Journal:  J Bacteriol       Date:  2009-10-09       Impact factor: 3.490

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