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Bradyrhizobium diazoefficiens USDA110 PhaR functions for pleiotropic regulation of cellular processes besides PHB accumulation.
Nishihata, Shogo; Kondo, Takahiko; Tanaka, Kosei; Ishikawa, Shu; Takenaka, Shinji; Kang, Choong-Min; Yoshida, Ken-Ichi.
Afiliação
  • Nishihata S; Department of Agrobioscience, Kobe University, 1-1 Rokkodai, Nada, Kobe, 657 8501, Japan.
  • Kondo T; Department of Science, Technology and Innovation, Kobe University, 1-1 Rokkodai, Nada, Kobe, 657 8501, Japan.
  • Tanaka K; Department of Science, Technology and Innovation, Kobe University, 1-1 Rokkodai, Nada, Kobe, 657 8501, Japan.
  • Ishikawa S; Department of Science, Technology and Innovation, Kobe University, 1-1 Rokkodai, Nada, Kobe, 657 8501, Japan.
  • Takenaka S; Department of Agrobioscience, Kobe University, 1-1 Rokkodai, Nada, Kobe, 657 8501, Japan.
  • Kang CM; Department of Biological Science, California State University, Stanislaus, Turlock, CA, 95382, USA.
  • Yoshida KI; Department of Science, Technology and Innovation, Kobe University, 1-1 Rokkodai, Nada, Kobe, 657 8501, Japan. kenyoshi@kobe-u.ac.jp.
BMC Microbiol ; 18(1): 156, 2018 10 24.
Article em En | MEDLINE | ID: mdl-30355296
BACKGROUND: Bradyrhizobium diazoefficiens USDA110 nodulates soybeans for nitrogen fixation. It accumulates poly-3-hydroxybutyrate (PHB), which is of physiological importance as a carbon/energy source for survival during starvation, infection, and nitrogen fixation conditions. PHB accumulation is orchestrated by not only the enzymes for PHB synthesis but also PHB-binding phasin proteins (PhaPs) stabilizing the PHB granules. The transcription factor PhaR controls the phaP genes. RESULTS: Inactivation of phaR led to decreases in PHB accumulation, less cell yield, increases in exopolysaccharide (EPS) production, some improvement in heat stress tolerance, and slightly better growth under microaerobic conditions. Changes in the transcriptome upon phaR inactivation were analyzed. PhaR appeared to be involved in the repression of various target genes, including some PHB-degrading enzymes and others involved in EPS production. Furthermore, in vitro gel shift analysis demonstrated that PhaR bound to the promoter regions of representative targets. For the phaP1 and phaP4 promoter regions, PhaR-binding sites were determined by DNase I footprinting, allowing us to deduce a consensus sequence for PhaR-binding as TGCRNYGCASMA (R: A or G, Y: C or T, S: C or G, M: A or C). We searched for additional genes associated with a PhaR-binding sequence and found that some genes involved in central carbon metabolism, such as pdhA for pyruvate dehydrogenase and pckA for phosphoenolpyruvate carboxykinase, may be regulated positively and directly by PhaR. CONCLUSIONS: These results suggest that PhaR could regulate various genes not only negatively but also positively to coordinate metabolism holistically in response to PHB accumulation.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Poliésteres / Proteínas de Bactérias / Regulação Bacteriana da Expressão Gênica / Bradyrhizobium / Hidroxibutiratos Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Poliésteres / Proteínas de Bactérias / Regulação Bacteriana da Expressão Gênica / Bradyrhizobium / Hidroxibutiratos Idioma: En Ano de publicação: 2018 Tipo de documento: Article