Literature DB >> 8395512

Chemotactic methylesterase promotes adaptation to high concentrations of attractant in Bacillus subtilis.

M L Kirsch1, P D Peters, D W Hanlon, J R Kirby, G W Ordal.   

Abstract

The Bacillus subtilis gene encoding CheB (cheBB), the chemotactic methylesterase, has been sequenced. The 39-kDa protein which resulted from the expression of cheBB, using a T7 expression system was consistent with the predicted open reading frame. CheBB shares 39.5% identity with Escherichia coli CheBE and can complement a cheBE null mutant. CheBB is required for removal of methyl groups from the receptors upon attractant stimulus and appears to play an important role in adaptation to the addition of attractants, whereas CheBE plays an important role in adaptation to the addition of repellents. Unlike the cheBE and cheRE mutants of E. coli, which show extreme flagellar rotational biases, the unstimulated cheBB mutant showed a normal (wild type) bias. Upon addition of attractant, the cheBB null mutant showed a counter-clockwise bias that was higher than for wild type and demonstrated only partial adaptation. In the capillary assay for the attractant azetidine-2-carboxylic acid, the mutant gave a wild type response at low concentrations but a very reduced response at high concentrations. We conclude that B. subtilis has an effective methylation-independent adaptation system but must utilize the methylation system for adaptation to high concentrations of attractant.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8395512

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  16 in total

1.  Cellular stoichiometry of the chemotaxis proteins in Bacillus subtilis.

Authors:  Vincent J Cannistraro; George D Glekas; Christopher V Rao; George W Ordal
Journal:  J Bacteriol       Date:  2011-04-22       Impact factor: 3.490

2.  CheX in the three-phosphatase system of bacterial chemotaxis.

Authors:  Travis J Muff; Richard M Foster; Peter J Y Liu; George W Ordal
Journal:  J Bacteriol       Date:  2007-08-03       Impact factor: 3.490

3.  A complex pattern of traveling stripes is produced by swimming cells of Bacillus subtilis.

Authors:  N H Mendelson; J Lega
Journal:  J Bacteriol       Date:  1998-07       Impact factor: 3.490

4.  Comprehensive DNA microarray analysis of Bacillus subtilis two-component regulatory systems.

Authors:  K Kobayashi; M Ogura; H Yamaguchi; K Yoshida; N Ogasawara; T Tanaka; Y Fujita
Journal:  J Bacteriol       Date:  2001-12       Impact factor: 3.490

5.  Chemotaxis in Bacillus subtilis requires either of two functionally redundant CheW homologs.

Authors:  M M Rosario; K L Fredrick; G W Ordal; J D Helmann
Journal:  J Bacteriol       Date:  1994-05       Impact factor: 3.490

6.  The Mechanism of Bidirectional pH Taxis in Bacillus subtilis.

Authors:  Payman Tohidifar; Matthew J Plutz; George W Ordal; Christopher V Rao
Journal:  J Bacteriol       Date:  2020-01-29       Impact factor: 3.490

7.  Defining network topologies that can achieve biochemical adaptation.

Authors:  Wenzhe Ma; Ala Trusina; Hana El-Samad; Wendell A Lim; Chao Tang
Journal:  Cell       Date:  2009-08-21       Impact factor: 41.582

Review 8.  Diversity in chemotaxis mechanisms among the bacteria and archaea.

Authors:  Hendrik Szurmant; George W Ordal
Journal:  Microbiol Mol Biol Rev       Date:  2004-06       Impact factor: 11.056

Review 9.  The three adaptation systems of Bacillus subtilis chemotaxis.

Authors:  Christopher V Rao; George D Glekas; George W Ordal
Journal:  Trends Microbiol       Date:  2008-09-04       Impact factor: 17.079

10.  Regulators of aerobic and anaerobic respiration in Bacillus subtilis.

Authors:  G Sun; E Sharkova; R Chesnut; S Birkey; M F Duggan; A Sorokin; P Pujic; S D Ehrlich; F M Hulett
Journal:  J Bacteriol       Date:  1996-03       Impact factor: 3.490

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.