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PMID: 15175311 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Genes involved in formation of structured multicellular communities by Bacillus subtilis.

Journal of bacteriology ·Vol. 186 ·No. 12 ·2004-06-00 ·Pages 3970-9

Branda SS, González-Pastor JE, Dervyn E, Ehrlich SD, Losick R, Kolter R

Abstract

The spore-forming bacterium Bacillus subtilis is capable of assembling multicellular communities (biofilms) that display a high degree of spatiotemporal organization. Wild strains that have not undergone domestication in the laboratory produce particularly robust biofilms with complex architectural features, such as fruiting-body-like aerial projections whose tips serve as preferential sites for sporulation. To discover genes involved in this multicellular behavior and to do so on a genome-wide basis, we took advantage of a large collection of mutants which have disruptions of most of the uncharacterized genes in the B. subtilis genome. This collection, which was generated with a laboratory strain, was screened for mutants that were impaired in biofilm formation. This subset of mutated genes was then introduced into the wild strain NCIB 3610 to study their effects on biofilm formation in liquid and solid media. In this way we identified six genes that are involved in the development of multicellular communities. These are yhxB (encoding a putative phosphohexomutase that may mediate exopolysaccharide synthesis), sipW (encoding a signal peptidase), ecsB (encoding an ABC transporter subunit), yqeK (encoding a putative phosphatase), ylbF (encoding a regulatory protein), and ymcA (a gene of unknown function). Further analysis revealed that these six genes play different roles in B. subtilis community development.

MeSH Terms
Bacillus subtilis/genetics,growth & development,metabolism Bacterial Proteins/genetics,metabolism Biofilms/growth & development Computational Biology/methods Ecosystem Gene Deletion Gene Expression Regulation, Bacterial Mutation
Chemicals
Bacterial Proteins
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Branda Steven S
Department of Microbiology and Molecular Genetics, Harvard Medical School, 200 Longwood Ave., Boston, MA 02115, USA.
González-Pastor José Eduardo
Dervyn Etienne
Ehrlich S Dusko
Losick Richard
Kolter Roberto
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Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
2004-06-00
Pages
3970-9
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC419949
Subset
IM
Grants
NIGMS NIH HHS · R01 GM018568 · United States
NIGMS NIH HHS · GM18568 · United States
NIGMS NIH HHS · R37 GM018568 · United States
NIGMS NIH HHS · GM58213 · United States
NIGMS NIH HHS · R01 GM058213 · United States
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