The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.
Bistability and biofilm formation in Bacillus subtilis
Open accessAbstract
Summary: Biofilms of Bacillus subtilis consist of long chains of cells that are held together in bundles by an extracellular matrix of exopolysaccharide and the protein TasA. The exopolysaccharide is produced by enzymes encoded by the epsA‐O operon and the gene encoding TasA is located in the yqxM‐sipW‐tasA operon. Both operons are under the control of the repressor SinR. Derepression is mediated by the antirepressor SinI, which binds to SinR with a 1:1 stoichiometry. Paradoxically, in medium promoting derepression of the matrix operons, the overall concentration of SinR in the culture greatly exceeded that of SinI. We show that under biofilm‐promoting conditions sinI , which is under the control of the response regulator Spo0A, was expressed only in a small subpopulation of cells, whereas sinR was expressed in almost all cells. Activation of Spo0A is known to be subject to a bistable switch, and we infer that SinI reaches levels sufficient to trigger matrix production only in the subpopulation of cells in which Spo0A is active. Additionally, evidence suggests that sinI is expressed at intermediate, but not low or high, levels of Spo0A activity, which may explain why certain nutritional conditions are more effective in promoting biofilm formation than others.
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Cites
The Involvement of Cell-to-Cell Signals in the Development of a Bacterial Biofilm
Davies, D. G., Parsek, M. R., Pearson, J. P., Iglewski, B. H., Costerton, J. W., & Greenberg, E. P. (1998) · Science · doi:10.1126/science.280.5361.295 · Cited by 3,396
Bacterial Persistence as a Phenotypic Switch
Balaban, N. Q., Merrin, J., Chait, R., Kowalik, L., & Leibler, S. (2004) · Science · doi:10.1126/science.1099390 · Cited by 2,952
Persister cells, dormancy and infectious disease
Lewis, K. (2007) · Nature Reviews Microbiology · doi:10.1038/nrmicro1557 · Cited by 2,052
Fruiting body formation by Bacillus subtilis
Branda, S. S., González-Pastor, J. E., Ben-Yehuda, S., Losick, R., & Kolter, R. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.191384198 · Cited by 1,129
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Cited by
Physiological heterogeneity in biofilms
Stewart, P. S., & Franklin, M. J. (2008) · Nature Reviews Microbiology · doi:10.1038/nrmicro1838 · Cited by 2,327
Lewis, K. (2010) · Annual Review of Microbiology · doi:10.1146/annurev.micro.112408.134306 · Cited by 1,858
The developmental model of microbial biofilms: ten years of a paradigm up for review
Monds, R. D., & O’Toole, G. A. (2009) · Trends in Microbiology · doi:10.1016/j.tim.2008.11.001 · Cited by 532
Spatio-temporal assembly of functional mineral scaffolds within microbial biofilms
Oppenheimer-Shaanan, Y., Sibony-Nevo, O., Bloom-Ackermann, Z., Suissa, R., Steinberg, N., Kartvelishvily, E., Brumfeld, V., & Kolodkin-Gal, I. (2016) · npj Biofilms and Microbiomes · doi:10.1038/npjbiofilms.2015.31 · Cited by 131
“SinI is an antirepressor, antagonising the repressor SinR, and thereby regulates biofilm formation and extracellular matrix production.(37) It is synthesised under the direct control of the master-regulator Spo0A.”
BackgroundMstX and a Putative Potassium Channel Facilitate Biofilm Formation in Bacillus subtilis
Lundberg, M. E., Becker, E. C., & Choe, S. (2013) · PLoS ONE · doi:10.1371/journal.pone.0060993 · Cited by 56
Metadata
- Authors
- Chai, Y., Chu, F., Kolter, R., & Losick, R.
- Venue
- Molecular Microbiology
- Publisher
- Wiley
- Published
- 2007-12-07
- Volume
- 67
- Issue
- 2
- Pages
- 254-263
- ISSN
- 0950-382X (ISSN-L)
- 1365-2958
- OpenAlex
- W2110324548
- Cited by
- 340
- References
- 4
- FWCI
- 6.94
- Type
- journal article
- Language
- en
- Open access
- bronze
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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