2008
DOI: 10.1128/jb.00868-08
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A Two-Component Regulatory System Integrates Redox State and Population Density Sensing in Pseudomonas putida

Abstract: A two-component system formed by a sensor histidine kinase and a response regulator has been identified as an element participating in cell density signal transduction in Pseudomonas putida KT2440. It is a homolog of the Pseudomonas aeruginosa RoxS/RoxR system, which in turn belongs to the RegA/RegB family, described in photosynthetic bacteria as a key regulatory element. In KT2440, the two components are encoded by PP_0887 (roxS) and PP_0888 (roxR), which are transcribed in a single unit. Characterization of … Show more

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Cited by 34 publications
(44 citation statements)
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“…The two-component signal transduction system (TCS) is a stimulus–response coupling signal transduction machinery that allows bacteria to respond and adapt to changes in a wide range of environmental conditions, such as nutrient assimilation [32], cellular redox state [33] and bacterial virulence regulation [34]. Chemotaxis, controlled by TCS, is the cells’ response to stressful environments.…”
Section: Discussionmentioning
confidence: 99%
“…The two-component signal transduction system (TCS) is a stimulus–response coupling signal transduction machinery that allows bacteria to respond and adapt to changes in a wide range of environmental conditions, such as nutrient assimilation [32], cellular redox state [33] and bacterial virulence regulation [34]. Chemotaxis, controlled by TCS, is the cells’ response to stressful environments.…”
Section: Discussionmentioning
confidence: 99%
“…The RoxSR regulon of Ps. putida includes genes for respiratory function and maintenance of the redox balance, genes involved in sugar and amino acid metabolism, and the sulfur starvation response (78). These authors also showed that RoxSR participates in cell density signal transduction in Ps.…”
Section: Pseudomonas Species Roxsrmentioning
confidence: 95%
“…To test if the observed activation of ddcA expression by culture supernatants of P. aeruginosa could be mediated by PpoR, the reporter plasmid pME510 was introduced into the strain EU6, a ppoR mutant of KT2440 (Fernández-Piñar et al, 2011b) and b-galactosidase activity analysed both in liquid cultures and using the disc assay described above. In contrast, expression of the ddcA-::lacZ fusion was not activated by culture supernatants or extracts when pME510 was introduced in strain EU58, a roxS transposon insertion mutant (Fernández-Piñar et al, 2008). This indicated that the response of ddcA to interspecies signalling molecules is independent of PpoR.…”
Section: Resultsmentioning
confidence: 95%