Literature DB >> 9219997

Regulation of directed motility in Myxococcus xanthus.

M J Ward1, D R Zusman.   

Abstract

Myxococcus xanthus is a Gram-negative bacterium that exhibits a complex life cycle. During vegetative growth, cells move as large swarms. However, when starved, cells aggregate into fruiting bodies and sporulate. Both vegetative swarming and developmental aggregation require gliding motility, which involves the slow movement of cells on a solid surface in the absence of flagella. The frequency of cell reversals controls the direction of movement and is regulated by the frz genes, which encode the 'frizzy' signal-transduction proteins. These proteins contain domains which bear striking similarities to the major chemotaxis proteins of the enteric bacteria: CheA, CheY, CheW, CheR, CheB and Tar. However, significant differences exist between the Myxococcus Frz proteins and the enteric Che/MCP proteins. For example, the Frz system contains three CheY-like response-regulator domains: one is present on FrzE, which also contains a CheA-like domain, and two are present on FrzZ, which is a novel protein required for attractant, but not for repellent, responses. The identification of multiple CheY homologues in this system indicates a more complex regulatory pathway than that found in the enteric bacteria. While responses to repellent stimuli appear to follow the enteric paradigm, responses to attractants during vegetative swarming and development are more complex and may involve self-generated autoattractants. The Frz signal-transduction system regulates directed motility in M. xanthus and is essential for controlling both fruiting-body development and vegetative swarming.

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Year:  1997        PMID: 9219997     DOI: 10.1046/j.1365-2958.1997.4261783.x

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


  25 in total

Review 1.  Signaling components in bacterial locomotion and sensory reception.

Authors:  S I Aizawa; C S Harwood; R J Kadner
Journal:  J Bacteriol       Date:  2000-03       Impact factor: 3.490

2.  A sigma(54) activator protein necessary for spore differentiation within the fruiting body of Myxococcus xanthus.

Authors:  L Gorski; T Gronewold; D Kaiser
Journal:  J Bacteriol       Date:  2000-05       Impact factor: 3.490

3.  The cell surface-associated intercellular C-signal induces behavioral changes in individual Myxococcus xanthus cells during fruiting body morphogenesis.

Authors:  L Jelsbak; L Søgaard-Andersen
Journal:  Proc Natl Acad Sci U S A       Date:  1999-04-27       Impact factor: 11.205

4.  Car: a cytoplasmic sensor responsible for arginine chemotaxis in the archaeon Halobacterium salinarum.

Authors:  K F Storch; J Rudolph; D Oesterhelt
Journal:  EMBO J       Date:  1999-03-01       Impact factor: 11.598

5.  Developmental aggregation of Myxococcus xanthus requires frgA, an frz-related gene.

Authors:  K Cho; A Treuner-Lange; K A O'Connor; D R Zusman
Journal:  J Bacteriol       Date:  2000-12       Impact factor: 3.490

6.  Analyses of mrp genes during Myxococcus xanthus development.

Authors:  H Sun; W Shi
Journal:  J Bacteriol       Date:  2001-12       Impact factor: 3.490

7.  Adaptation of salt-tolerant Myxococcus strains and their motility systems to the ocean conditions.

Authors:  Bing Wang; Wei Hu; Hong Liu; Cui-ying Zhang; Jing-yi Zhao; De-ming Jiang; Zhi-hong Wu; Yue-zhong Li
Journal:  Microb Ecol       Date:  2006-12-22       Impact factor: 4.552

8.  PilJ localizes to cell poles and is required for type IV pilus extension in Pseudomonas aeruginosa.

Authors:  Paul A DeLange; Tracy L Collins; George E Pierce; Jayne B Robinson
Journal:  Curr Microbiol       Date:  2007-08-23       Impact factor: 2.188

9.  An ABC transporter plays a developmental aggregation role in Myxococcus xanthus.

Authors:  M J Ward; K C Mok; D P Astling; H Lew; D R Zusman
Journal:  J Bacteriol       Date:  1998-11       Impact factor: 3.490

10.  Regulation of motility behavior in Myxococcus xanthus may require an extracytoplasmic-function sigma factor.

Authors:  M J Ward; H Lew; A Treuner-Lange; D R Zusman
Journal:  J Bacteriol       Date:  1998-11       Impact factor: 3.490

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