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Role of AcsR in expression of the acetyl-CoA synthetase gene in Vibrio vulnificus.

Authors :
Min Jung Kim
Juri Kim
Hye-Yeon Lee
Hyeon Jin Noh
Kyu-Ho Lee
Soon-Jung Park
Source :
BMC Microbiology. 2015, Vol. 15 Issue 1, p1-16. 16p.
Publication Year :
2015

Abstract

Background: VarS/VarA is one of the global factors regulating diverse aspects of the metabolism and virulence of bacteria including pathogenic Vibrio spp. An experiment to identify the VarS/VarA-regulon in V. vulnificus revealed that a putative LuxR-type transcriptional regulator was down-regulated in ΔvarA mutant. To investigate the roles of this regulatory cascade, the target gene regulated by a LuxR-regulator was identified and its expression was characterized. Results: Transcriptomic analysis of the mutant deficient in this LuxR-type regulator showed that the acsA gene encoding acetyl-CoA synthetase was down-regulated. Thus, this regulator was named AcsR for "regulator of acetyl-CoA synthetase". A putative histidine kinase gene, acsS, was located five ORFs downstream of the acsR gene. Expression of an acsA::luxAB transcriptional fusion was decreased in both ΔacsR and AacsS mutants. Similar to a AacsA mutant, strains carrying deletions either in acsR or acsS grew slowly than wild type in a minimal medium with acetate as a sole carbon source. Growth defect of the ΔacsR strain in acetate-minimal medium was restored by complementation. To investigate if AcsR directly regulates acsA expression, in vitro-gel shift assays were performed using the recombinant AcsR and the regulatory region of the acsA gene, showing that AcsR specifically bound the upstream region of the acsA ORF. Conclusion: This study indicates that the VarS/VarA system plays a role in V. vulnificus metabolism via regulating AcsR, which in turn controls acetate metabolism by activating the transcription of the acetyl-CoA synthetase gene. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14712180
Volume :
15
Issue :
1
Database :
Academic Search Index
Journal :
BMC Microbiology
Publication Type :
Academic Journal
Accession number :
102596890
Full Text :
https://doi.org/10.1186/s12866-015-0418-4