Literature DB >> 21296938

Versatile metabolic adaptations of Ralstonia eutropha H16 to a loss of PdhL, the E3 component of the pyruvate dehydrogenase complex.

Matthias Raberg1, Jan Bechmann, Ulrike Brandt, Jonas Schlüter, Bianca Uischner, Birgit Voigt, Michael Hecker, Alexander Steinbüchel.   

Abstract

A previous study reported that the Tn5-induced poly(3-hydroxybutyric acid) (PHB)-leaky mutant Ralstonia eutropha H1482 showed a reduced PHB synthesis rate and significantly lower dihydrolipoamide dehydrogenase (DHLDH) activity than the wild-type R. eutropha H16 but similar growth behavior. Insertion of Tn5 was localized in the pdhL gene encoding the DHLDH (E3 component) of the pyruvate dehydrogenase complex (PDHC). Taking advantage of the available genome sequence of R. eutropha H16, observations were verified and further detailed analyses and experiments were done. In silico genome analysis revealed that R. eutropha possesses all five known types of 2-oxoacid multienzyme complexes and five DHLDH-coding genes. Of these DHLDHs, only PdhL harbors an amino-terminal lipoyl domain. Furthermore, insertion of Tn5 in pdhL of mutant H1482 disrupted the carboxy-terminal dimerization domain, thereby causing synthesis of a truncated PdhL lacking this essential region, obviously leading to an inactive enzyme. The defined ΔpdhL deletion mutant of R. eutropha exhibited the same phenotype as the Tn5 mutant H1482; this excludes polar effects as the cause of the phenotype of the Tn5 mutant H1482. However, insertion of Tn5 or deletion of pdhL decreases DHLDH activity, probably negatively affecting PDHC activity, causing the mutant phenotype. Moreover, complementation experiments showed that different plasmid-encoded E3 components of R. eutropha H16 or of other bacteria, like Burkholderia cepacia, were able to restore the wild-type phenotype at least partially. Interestingly, the E3 component of B. cepacia possesses an amino-terminal lipoyl domain, like the wild-type H16. A comparison of the proteomes of the wild-type H16 and of the mutant H1482 revealed striking differences and allowed us to reconstruct at least partially the impressive adaptations of R. eutropha H1482 to the loss of PdhL on the cellular level.

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Year:  2011        PMID: 21296938      PMCID: PMC3067459          DOI: 10.1128/AEM.02360-10

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


  53 in total

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  4 in total

1.  Proteomic analysis of the influence of Cu(2+) on the crystal protein production of Bacillus thuringiensis X022.

Authors:  Xuemei Liu; Mingxing Zuo; Ting Wang; Yunjun Sun; Shuang Liu; Shengbiao Hu; Hao He; Qi Yang; Jie Rang; Meifang Quan; Liqiu Xia; Xuezhi Ding
Journal:  Microb Cell Fact       Date:  2015-10-05       Impact factor: 5.328

2.  A closer look on the polyhydroxybutyrate- (PHB-) negative phenotype of Ralstonia eutropha PHB-4.

Authors:  Matthias Raberg; Birgit Voigt; Michael Hecker; Alexander Steinbüchel
Journal:  PLoS One       Date:  2014-05-02       Impact factor: 3.240

3.  Minimal genome encoding proteins with constrained amino acid repertoire.

Authors:  Olga Tsoy; Marina Yurieva; Andrey Kucharavy; Mary O'Reilly; Arcady Mushegian
Journal:  Nucleic Acids Res       Date:  2013-07-19       Impact factor: 16.971

4.  Detection of phase-dependent transcriptomic changes and Rubisco-mediated CO2 fixation into poly (3-hydroxybutyrate) under heterotrophic condition in Ralstonia eutropha H16 based on RNA-seq and gene deletion analyses.

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Journal:  BMC Microbiol       Date:  2013-07-23       Impact factor: 3.605

  4 in total

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