lipases are well-studied, but few studies have examined the mechanisms of lipase expression regulation. As a global regulatory protein, PmrA controls the expression of multiple genes such as the Dot/Icm apparatus, eukaryotic-like proteins, and secreted effectors. In this study, the effect of PmrA on expression of the lipase lipA in PAO1 was investigated by knocking out or overexpressing , and . PmrA regulated the expression of at both the transcriptional and translational level although translation was the pivotal regulatory mechanism for expression. PmrA also regulated the expression of . Using gel mobility shift assay and double gene knock-out model, we showed that PmrA directly bound to the promoter sequence of to regulate expression. Translation of was activated by the PmrA/PmrB system via RsmA. Specifically, the Shine-Dalgarno (SD) sequence located at mRNA was overlapped through combination between RsmA and the AGAUGA sequence, subsequently blocking the 30S ribosomal subunit to the SD sequence, leading to translational inhibition of . Transcriptional repression of RsmY initiated translation of through negative translational regulation of . In conclusion, this study demonstrated that in PAO1, PmrA mainly regulated expression at a translational level to influence expression. RsmY primarily activated translation via negative translational regulation of .
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http://dx.doi.org/10.3389/fmicb.2017.02690 | DOI Listing |
PLoS One
August 2024
Graduate School of Health Sciences, Koç University, Istanbul, Türkiye.
Background: Colistin resistance in Acinetobacter baumannii is an emerging problem that limits antimicrobial therapy options.
Materials & Methods: We isolated two pairs of colistin susceptible and colistin-resistant A. baumannii (K1007/K1006 and K408/K409) from two patients diagnosed with carbapenem-resistant A.
J Glob Antimicrob Resist
September 2024
Division of Infectious Diseases and Tropical Medicine, Department of Internal, Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan. Electronic address:
Objectives: The mechanisms underlying chromosomally encoded colistin resistance in Escherichia coli remain insufficiently investigated. In this study, we investigated the contribution of various pmrB mutations from E. coli clinical isolates to colistin resistance.
View Article and Find Full Text PDFBMC Microbiol
May 2024
Department of Microbiology, School of Medicine, Ardabil University of Medical Sciences, Ardabil, Iran.
J Bacteriol
May 2024
Laboratory of Microbiology and Infection Control, Kyoto Pharmaceutical University, Kyoto, Japan.
BMC Microbiol
April 2024
Division of Infectious Diseases and Tropical Medicine, Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical Center, No. 325, Section 2, Cheng-Kung Road, Neihu 114, Taipei, Taiwan.
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