2009
DOI: 10.1016/j.jbiotec.2008.10.009
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A combination of metabolome and transcriptome analyses reveals new targets of the Corynebacterium glutamicum nitrogen regulator AmtR

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Cited by 37 publications
(33 citation statements)
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References 35 publications
(22 reference statements)
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“…Its sevenfold increased expression in glutamine-grown cells might indicate that its activity with glutamine is lower than with ammonia. The pyrG gene could be a novel member of the AmtR regulon, as its expression was also threefold increased in a DamtR mutant compared with the wild-type (Buchinger et al, 2009). …”
Section: Discussionmentioning
confidence: 99%
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“…Its sevenfold increased expression in glutamine-grown cells might indicate that its activity with glutamine is lower than with ammonia. The pyrG gene could be a novel member of the AmtR regulon, as its expression was also threefold increased in a DamtR mutant compared with the wild-type (Buchinger et al, 2009). …”
Section: Discussionmentioning
confidence: 99%
“…Expression of nitrogencontrolled genes is regulated by the TetR-family protein AmtR (Jakoby et al, 2000), which blocks transcription of various genes during growth in nitrogen-rich medium. At least 35 genes are directly controlled by the AmtR repressor (Beckers et al, 2005;Buchinger et al, 2009) and these encode transporters and enzymes for ammonium assimilation (amtA, amtB, glnA, gltBD, dapA), creatinine (codA, crnT) and urea (urtABCDE, ureABCEFGD) metabolism, a number of biochemically uncharacterized enzymes and transport systems, as well as signal transduction proteins (glnD, glnK). In contrast with most TetR-type regulators, the dissociation of AmtR from its target promoters is not triggered by the binding of a low-molecular mass ligand, but by complex formation with the PII-type signal transduction protein GlnK (Beckers et al, 2005).…”
Section: Introductionmentioning
confidence: 99%
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“…Metabolomics can reveal the changes at metabolite level and reflect the phenotype directly, and therefore has been applied in a broad range of studies in various fields (Adamski and Suhre 2012;Putri et al 2013). Although more and more investigations are carried out to reveal the molecular mechanisms of cellular pathways in microbes using metabolomic technologies (Buchinger et al 2009;Yuan et al 2009), the metabolomic profilings of the host bacteria associated with the bacteriophage infection are still unclear.…”
Section: Introductionmentioning
confidence: 99%
“…For a rough microbial phenotyping, it could be sufficient to use qualitative and semiquantitative data if the expected difference in the metabolome of a mutant strain in reference to the parental strain is significant enough [12,13]. Nevertheless, the same information quality is usually not sufficient to serve for mathematical modeling and validation of a mechanistic metabolic model.…”
Section: Introductionmentioning
confidence: 99%