Literature DB >> 3076074

A physicist looks at bacterial chemotaxis.

H C Berg1.   

Abstract

What is distinctive about bacterial chemotaxis, as compared to, for example, taste in the elephant, is the time over which decisions must be made. The lower limit is set by diffusion of chemicals to and from the cell surface, which demands long times for statistically significant counts. The upper limit is set by diffusion of the cell itself, which demands short times for well-defined swimming paths. For an organism the size of E. coli, temporal comparisons of the concentrations of chemicals in the environment must be made within a few seconds. Although such short time spans might be difficult for the biochemist, they are not so difficult for E. coli, because diffusion can carry a small molecule across the cell in about 1 msec. E. coli has the opposite problem: How does it integrate inputs from many receptors over periods 1000 times as long? The mechanisms for this signal processing are beginning to be understood. We know how most chemical attractants are identified, how temporal comparisons might be made, and how the behavioral output is effected. We know less about how sensory information crosses the cytoplasmic membrane, how the reactions that link the receptors to the flagella generate such high gain, and what actually controls the direction of flagellar rotation. One thing is quite clear: E. coli demands our admiration and respect.

Entities:  

Mesh:

Year:  1988        PMID: 3076074     DOI: 10.1101/sqb.1988.053.01.003

Source DB:  PubMed          Journal:  Cold Spring Harb Symp Quant Biol        ISSN: 0091-7451


  26 in total

Review 1.  Chemotaxis: signalling modules join hands at front and tail.

Authors:  Marten Postma; Leonard Bosgraaf; Harriët M Loovers; Peter J M Van Haastert
Journal:  EMBO Rep       Date:  2004-01       Impact factor: 8.807

2.  Experimental and theoretical bases of specific affinity, a cytoarchitecture-based formulation of nutrient collection proposed to supercede the Michaelis-Menten paradigm of microbial kinetics.

Authors:  D K Button; Betsy Robertson; Elizabeth Gustafson; Xiaoming Zhao
Journal:  Appl Environ Microbiol       Date:  2004-09       Impact factor: 4.792

3.  Chemotaxis of bacteria in glass capillary arrays. Escherichia coli, motility, microchannel plate, and light scattering.

Authors:  H C Berg; L Turner
Journal:  Biophys J       Date:  1990-10       Impact factor: 4.033

4.  Mutations in the two flagellin genes of Rhizobium meliloti.

Authors:  K Bergman; E Nulty; L H Su
Journal:  J Bacteriol       Date:  1991-06       Impact factor: 3.490

5.  Chemotactic patterns without chemotaxis.

Authors:  Michael P Brenner
Journal:  Proc Natl Acad Sci U S A       Date:  2010-06-18       Impact factor: 11.205

Review 6.  Size structures sensory hierarchy in ocean life.

Authors:  Erik A Martens; Navish Wadhwa; Nis S Jacobsen; Christian Lindemann; Ken H Andersen; André Visser
Journal:  Proc Biol Sci       Date:  2015-09-22       Impact factor: 5.349

7.  Role of CheW protein in coupling membrane receptors to the intracellular signaling system of bacterial chemotaxis.

Authors:  J D Liu; J S Parkinson
Journal:  Proc Natl Acad Sci U S A       Date:  1989-11       Impact factor: 11.205

8.  Highly designable phenotypes and mutational buffers emerge from a systematic mapping between network topology and dynamic output.

Authors:  Yigal D Nochomovitz; Hao Li
Journal:  Proc Natl Acad Sci U S A       Date:  2006-03-03       Impact factor: 11.205

9.  Chemotaxis: the role of internal delays.

Authors:  P-G de Gennes
Journal:  Eur Biophys J       Date:  2004-07-15       Impact factor: 1.733

10.  Network Topologies That Can Achieve Dual Function of Adaptation and Noise Attenuation.

Authors:  Lingxia Qiao; Wei Zhao; Chao Tang; Qing Nie; Lei Zhang
Journal:  Cell Syst       Date:  2019-09-18       Impact factor: 10.304

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