Difference between revisions of "Motility and chemotaxis"
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+ | Motility and chemotaxis facilitate swimming and swarming of ''B. subtilis'' {{PubMed|20694026}}. Motility, chemotaxis and aerotaxis facilitate pellicle [[biofilm formation]] in ''B. subtilis'' {{PubMed|26122431}}. Production of flagella is a costly process in ''B. subtilis'' {{PubMed|26122431}}. | ||
+ | |||
{{CategoryTree | {{CategoryTree | ||
|Parents= | |Parents= | ||
Line 5: | Line 7: | ||
|Neighbours= | |Neighbours= | ||
* 4.1.1. [[Motility and chemotaxis]] | * 4.1.1. [[Motility and chemotaxis]] | ||
− | * 4.1.2. [[Biofilm formation]] | + | * 4.1.2. [[Swarming]] |
− | * 4.1. | + | * 4.1.3. [[Sliding]] |
+ | * 4.1.4. [[Biofilm formation]] | ||
+ | * 4.1.5. [[Genetic competence]] | ||
|Related= | |Related= | ||
* {{SubtiWiki regulon|[[SigD regulon]]}} | * {{SubtiWiki regulon|[[SigD regulon]]}} | ||
* {{SubtiWiki regulon|[[SlrR regulon]]}} | * {{SubtiWiki regulon|[[SlrR regulon]]}} | ||
+ | * [[fla-che operon]] | ||
|}} | |}} | ||
+ | |||
+ | ==Labs working on motility and chemotaxis == | ||
+ | * [[Gert Bange]] | ||
+ | * [[Daniel Kearns]] | ||
+ | * [[Akos T Kovacs]] | ||
+ | |||
+ | == Regulation of flagellation == | ||
+ | * number of flagellar hooks per micrometer of cell length | ||
+ | ** in swimming cells: 4 +/- 1 {{PubMed|25538299}} | ||
+ | ** in swarming cells: 9 +/- 2 {{PubMed|25538299}} | ||
== Genes in this functional category == | == Genes in this functional category == | ||
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* ''[[flgM]]'' | * ''[[flgM]]'' | ||
* ''[[fliY]]'' | * ''[[fliY]]'' | ||
+ | * ''[[lonA]]'' | ||
* ''[[luxS]]'' | * ''[[luxS]]'' | ||
+ | * ''[[pdeH]]'' | ||
* ''[[sigD]]'' | * ''[[sigD]]'' | ||
+ | * ''[[smiA]]'' | ||
* ''[[swrAA/1]]'' | * ''[[swrAA/1]]'' | ||
* ''[[swrAA/2]]'' | * ''[[swrAA/2]]'' | ||
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* ''[[flgK]]'' | * ''[[flgK]]'' | ||
* ''[[flgL]]'' | * ''[[flgL]]'' | ||
+ | * ''[[flgN]]'' | ||
* ''[[flhA]]'' | * ''[[flhA]]'' | ||
* ''[[flhB]]'' | * ''[[flhB]]'' | ||
Line 95: | Line 114: | ||
* ''[[yvyC]]'' | * ''[[yvyC]]'' | ||
* ''[[yvyF]]'' | * ''[[yvyF]]'' | ||
− | + | ||
* ''[[yvzB]]'' | * ''[[yvzB]]'' | ||
=== Motility and chemotaxis/ other === | === Motility and chemotaxis/ other === | ||
* ''[[lytC]]'' | * ''[[lytC]]'' | ||
− | |||
* ''[[ycdA]]'' | * ''[[ycdA]]'' | ||
+ | * ''[[yhbE]]'' | ||
+ | * ''[[yhbF]]'' | ||
+ | |||
+ | ==Key original publications== | ||
+ | <pubmed>26122431, 24256735 25035996 25538299 27508446 </pubmed> | ||
==Key reviews== | ==Key reviews== | ||
− | <pubmed> 15187186 18774298 8604438 22092493 </pubmed> | + | <pubmed> 15187186 18774298 8604438 22092493 25251856 26195616 26490009 26731482</pubmed> |
=Back to [[categories]]= | =Back to [[categories]]= |
Latest revision as of 17:49, 14 August 2016
Motility and chemotaxis facilitate swimming and swarming of B. subtilis PubMed. Motility, chemotaxis and aerotaxis facilitate pellicle biofilm formation in B. subtilis PubMed. Production of flagella is a costly process in B. subtilis PubMed.
Parent categories | |
Neighbouring categories |
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Related categories | |
Contents
- 1 Labs working on motility and chemotaxis
- 2 Regulation of flagellation
- 3 Genes in this functional category
- 4 Key original publications
- 5 Key reviews
- 6 Back to categories
Labs working on motility and chemotaxis
Regulation of flagellation
- number of flagellar hooks per micrometer of cell length
Genes in this functional category
Signal transduction in motility and chemotaxis
Soluble signalling proteins
Coupling proteins
Soluble chemoreceptors
Membrane-bound chemoreceptors
Additional chemotaxis signal transduction and regulatory proteins
Flagellar proteins
- flgB
- flgC
- flgD
- flgE
- flgK
- flgL
- flgN
- flhA
- flhB
- flhF
- flhG
- flhO
- flhP
- fliD
- fliE
- fliF
- fliG
- fliH
- fliI
- fliJ
- fliK
- fliL
- fliM
- fliP
- fliQ
- fliR
- fliS
- fliT
- fliW
- fliY
- fliZ
- hag
- motA
- motB
- motP
- motS
Flagellar proteins/ based on similarity
Motility and chemotaxis/ other
Key original publications
Linda Turner, Liam Ping, Marianna Neubauer, Howard C Berg
Visualizing Flagella while Tracking Bacteria.
Biophys J: 2016, 111(3);630-639
[PubMed:27508446]
[WorldCat.org]
[DOI]
(I p)
Theresa Hölscher, Benjamin Bartels, Yu-Cheng Lin, Ramses Gallegos-Monterrosa, Alexa Price-Whelan, Roberto Kolter, Lars E P Dietrich, Ákos T Kovács
Motility, Chemotaxis and Aerotaxis Contribute to Competitiveness during Bacterial Pellicle Biofilm Development.
J Mol Biol: 2015, 427(23);3695-3708
[PubMed:26122431]
[WorldCat.org]
[DOI]
(I p)
Sampriti Mukherjee, Anna C Bree, Jing Liu, Joyce E Patrick, Peter Chien, Daniel B Kearns
Adaptor-mediated Lon proteolysis restricts Bacillus subtilis hyperflagellation.
Proc Natl Acad Sci U S A: 2015, 112(1);250-5
[PubMed:25538299]
[WorldCat.org]
[DOI]
(I p)
Hiraku Takada, Masato Morita, Yuh Shiwa, Ryoma Sugimoto, Shota Suzuki, Fujio Kawamura, Hirofumi Yoshikawa
Cell motility and biofilm formation in Bacillus subtilis are affected by the ribosomal proteins, S11 and S21.
Biosci Biotechnol Biochem: 2014, 78(5);898-907
[PubMed:25035996]
[WorldCat.org]
[DOI]
(I p)
Thomas M Norman, Nathan D Lord, Johan Paulsson, Richard Losick
Memory and modularity in cell-fate decision making.
Nature: 2013, 503(7477);481-486
[PubMed:24256735]
[WorldCat.org]
[DOI]
(I p)
Key reviews