Literature DB >> 24102920

The putative Poc complex controls two distinct Pseudomonas aeruginosa polar motility mechanisms.

Kimberly N Cowles1, Theresa S Moser, Albert Siryaporn, Natsai Nyakudarika, William Dixon, Jonathan J Turner, Zemer Gitai.   

Abstract

Each Pseudomonas aeruginosa cell localizes two types of motility structures, a single flagellum and one or two clusters of type IV pili, to the cell poles. Previous studies suggested that these motility structures arrive at the pole through distinct mechanisms. Here we performed a swimming motility screen to identify polar flagellum localization factors and discovered three genes homologous to the TonB/ExbB/ExbD complex that have defects in both flagella-mediated swimming and pilus-mediated twitching motility. We found that deletion of tonB3, PA2983 or PA2982 led to non-polar localization of the flagellum and FlhF, which was thought to sit at the top of the flagellar localization hierarchy. Surprisingly, these mutants also exhibited pronounced changes in pilus formation or localization, indicating that these proteins may co-ordinate both the pilus and flagellum motility systems. Thus, we have renamed PA2983 and PA2982, pocA and pocB, respectively, for polar organelle co-ordinator to reflect this function. Our results suggest that TonB3, PocA and PocB may form a membrane-associated complex, which we term the Poc complex. These proteins do not exhibit polar localization themselves, but are required for increased expression of pilus genes upon surface association, indicating that they regulate motility structures through either localization or transcriptional mechanisms.
© 2013 John Wiley & Sons Ltd.

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Year:  2013        PMID: 24102920      PMCID: PMC4666538          DOI: 10.1111/mmi.12403

Source DB:  PubMed          Journal:  Mol Microbiol        ISSN: 0950-382X            Impact factor:   3.501


  30 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  2003-11-14       Impact factor: 11.205

Review 3.  TonB-dependent energy transduction between outer and cytoplasmic membranes.

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Authors:  Thomas S Murray; Barbara I Kazmierczak
Journal:  J Bacteriol       Date:  2006-10       Impact factor: 3.490

5.  Two different Pseudomonas aeruginosa chemosensory signal transduction complexes localize to cell poles and form and remould in stationary phase.

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Journal:  Mol Microbiol       Date:  2006-07       Impact factor: 3.501

6.  The Pseudomonas aeruginosa ribbon-helix-helix DNA-binding protein AlgZ (AmrZ) controls twitching motility and biogenesis of type IV pili.

Authors:  Patricia J Baynham; Deborah M Ramsey; Borys V Gvozdyev; Ellen M Cordonnier; Daniel J Wozniak
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7.  Broad-host-range expression vectors that carry the L-arabinose-inducible Escherichia coli araBAD promoter and the araC regulator.

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8.  Flagellar and twitching motility are necessary for Pseudomonas aeruginosa biofilm development.

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4.  Synthetic Antimicrobial Peptide Tuning Permits Membrane Disruption and Interpeptide Synergy.

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Journal:  ACS Pharmacol Transl Sci       Date:  2020-02-21

5.  A Short Protocol for Gene Knockout and Complementation in Xylella fastidiosa Shows that One of the Type IV Pilin Paralogs (PD1926) Is Needed for Twitching while Another (PD1924) Affects Pilus Number and Location.

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Review 6.  Sensational biofilms: surface sensing in bacteria.

Authors:  George A O'Toole; Gerard Cl Wong
Journal:  Curr Opin Microbiol       Date:  2016-03-08       Impact factor: 7.934

7.  Penicillin-Binding Protein 3 Is Essential for Growth of Pseudomonas aeruginosa.

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9.  The Type IVa Pilus Machinery Is Recruited to Sites of Future Cell Division.

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10.  Ras GTPase-like protein MglA, a controller of bacterial social-motility in Myxobacteria, has evolved to control bacterial predation by Bdellovibrio.

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Journal:  PLoS Genet       Date:  2014-04-10       Impact factor: 5.917

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