Literature DB >> 22636005

Genetically modified strains of Ralstonia eutropha H16 with β-ketothiolase gene deletions for production of copolyesters with defined 3-hydroxyvaleric acid contents.

Nicole Lindenkamp1, Elena Volodina, Alexander Steinbüchel.   

Abstract

β-Ketothiolases catalyze the first step of poly(3-hydroxybutyrate) [poly(3HB)] biosynthesis in bacteria by condensation of two acetyl coenzyme A (acetyl-CoA) molecules to acetoacetyl-CoA and also take part in the degradation of fatty acids. During growth on propionate or valerate, Ralstonia eutropha H16 produces the copolymer poly(3-hydroxybutyrate-co-3-hydroxyvalerate) [poly(3HB-co-3HV)]. In R. eutropha, 15 β-ketothiolase homologues exist. The synthesis of 3-hydroxybutyryl-CoA (3HB-CoA) could be significantly reduced in an 8-fold mutant (Lindenkamp et al., Appl. Environ. Microbiol. 76:5373-5382, 2010). In this study, a 9-fold mutant deficient in nine β-ketothiolase gene homologues (phaA, bktB, H16_A1713, H16_B1771, H16_A1528, H16_B0381, H16_B1369, H16_A0170, and pcaF) was generated. In order to examine the polyhydroxyalkanoate production capacity when short- or long-chain and even- or odd-chain-length fatty acids were provided as carbon sources, the growth and storage behavior of several mutants from the previous study and the newly generated 9-fold mutant were analyzed. Propionate, valerate, octanoate, undecanoic acid, or oleate was chosen as the sole carbon source. On octanoate, no significant differences in growth or storage behavior were observed between wild-type R. eutropha and the mutants. In contrast, during the growth on oleate of a multiple mutant lacking phaA, bktB, and H16_A0170, diminished poly(3HB) accumulation occurred. Surprisingly, the amount of accumulated poly(3HB) in the multiple mutants grown on gluconate differed; it was much lower than that on oleate. The β-ketothiolase activity toward acetoacetyl-CoA in H16ΔphaA and all the multiple mutants remained 10-fold lower than the activity of the wild type, regardless of which carbon source, oleate or gluconate, was employed. During growth on valerate as a sole carbon source, the 9-fold mutant accumulated almost a poly(3-hydroxyvalerate) [poly(3HV)] homopolyester with 99 mol% 3HV constituents.

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Year:  2012        PMID: 22636005      PMCID: PMC3416435          DOI: 10.1128/AEM.00824-12

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  33 in total

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Journal:  Microbiology       Date:  2010-04-15       Impact factor: 2.777

5.  Elucidation of beta-oxidation pathways in Ralstonia eutropha H16 by examination of global gene expression.

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7.  Impact of multiple beta-ketothiolase deletion mutations in Ralstonia eutropha H16 on the composition of 3-mercaptopropionic acid-containing copolymers.

Authors:  Nicole Lindenkamp; Katja Peplinski; Elena Volodina; Armin Ehrenreich; Alexander Steinbüchel
Journal:  Appl Environ Microbiol       Date:  2010-07-02       Impact factor: 4.792

8.  Influence of homologous phasins (PhaP) on PHA accumulation and regulation of their expression by the transcriptional repressor PhaR in Ralstonia eutropha H16.

Authors:  Markus Pötter; Helena Müller; Alexander Steinbüchel
Journal:  Microbiology (Reading)       Date:  2005-03       Impact factor: 2.777

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  8 in total

1.  Haloarchaeal-type β-ketothiolases involved in Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) synthesis in Haloferax mediterranei.

Authors:  Jing Hou; Bo Feng; Jing Han; Hailong Liu; Dahe Zhao; Jian Zhou; Hua Xiang
Journal:  Appl Environ Microbiol       Date:  2013-06-21       Impact factor: 4.792

Review 2.  Genome characteristics dictate poly-R-(3)-hydroxyalkanoate production in Cupriavidus necator H16.

Authors:  Gurusamy Kutralam-Muniasamy; Fermín Peréz-Guevara
Journal:  World J Microbiol Biotechnol       Date:  2018-05-24       Impact factor: 3.312

3.  Impact of various β-ketothiolase genes on PHBHHx production in Cupriavidus necator H16 derivatives.

Authors:  Hisashi Arikawa; Shunsuke Sato
Journal:  Appl Microbiol Biotechnol       Date:  2022-04-22       Impact factor: 4.813

4.  Insights into the Degradation of Medium-Chain-Length Dicarboxylic Acids in Cupriavidus necator H16 Reveal β-Oxidation Differences between Dicarboxylic Acids and Fatty Acids.

Authors:  Carl Simon Strittmatter; Jessica Eggers; Vanessa Biesgen; Jan-Niklas Hengsbach; Akihiro Sakatoku; Dirk Albrecht; Katharina Riedel; Alexander Steinbüchel
Journal:  Appl Environ Microbiol       Date:  2021-11-03       Impact factor: 5.005

5.  (S)-3-hydroxyacyl-CoA dehydrogenase/enoyl-CoA hydratase (FadB') from fatty acid degradation operon of Ralstonia eutropha H16.

Authors:  Elena Volodina; Alexander Steinbüchel
Journal:  AMB Express       Date:  2014-08-28       Impact factor: 3.298

6.  Production of (R)-3-hydroxybutyric acid by Arxula adeninivorans.

Authors:  Mateusz Biernacki; Jan Riechen; Urs Hähnel; Thomas Roick; Kim Baronian; Rüdiger Bode; Gotthard Kunze
Journal:  AMB Express       Date:  2017-01-03       Impact factor: 3.298

Review 7.  Challenges and Advances for Genetic Engineering of Non-model Bacteria and Uses in Consolidated Bioprocessing.

Authors:  Qiang Yan; Stephen S Fong
Journal:  Front Microbiol       Date:  2017-10-24       Impact factor: 5.640

Review 8.  Microbial production of lactate-containing polyesters.

Authors:  Jung Eun Yang; So Young Choi; Jae Ho Shin; Si Jae Park; Sang Yup Lee
Journal:  Microb Biotechnol       Date:  2013-05-29       Impact factor: 5.813

  8 in total

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