Motility behavior of rpoS-deficient Escherichia coli analyzed by individual cell tracking

Journal of Bioscience and Bioengineering

Volumn 114, Issue 6, 2012, Pages 652-656

  Ojima, Yoshihiro ^a   Hakamada, Kazumi ^a   Nishinoue, Yosuke ^a   Nguyen, Minh Hong ^a   Miyake, Jun ^a   Taya, Masahito ^a  

^a OSAKA UNIVERSITY   (Japan)

Author keywords

Escherichia coli; Flagellum; Individual cells; Motility; RpoS gene

Indexed keywords

AGAR PLATES; CELLULAR EVENTS; E. COLI; FLAGELLUM; INDIVIDUAL CELLS; MOTILITY; UP-REGULATION; WILD TYPES;

CYTOLOGY; ESCHERICHIA COLI; GENES;

CELLS;

MESSENGER RNA; RNA 16S; SIGMA FACTOR RPOS;

ARTICLE; BACTERIAL CELL; CELL GROWTH; CELL MOTILITY; CELL POPULATION; ESCHERICHIA COLI; FLAGELLUM; GENE EXPRESSION; NONHUMAN; UPREGULATION; WILD TYPE;

BACTERIAL PROTEINS; BIOLOGICAL ASSAY; CELL TRACKING; ESCHERICHIA COLI; ESCHERICHIA COLI PROTEINS; FLAGELLA; GENE DELETION; GENE EXPRESSION REGULATION, BACTERIAL; MOVEMENT; SIGMA FACTOR; UP-REGULATION;

ESCHERICHIA COLI;

EID: 84868139700     PISSN: 13891723     EISSN: 13474421     Source Type: Journal    
DOI: 10.1016/j.jbiosc.2012.06.014     Document Type: Article

References (23)

1. Berg H.C. E. coli in motion 2004, Springer, New York.
2. Macnab R.M. How bacteria assemble flagella. Annu. Rev. Microbiol. 2003, 57:77-100.
3. Liu X., Matsumura P. The FlhD/FlhC complex, a transcriptional activator of the Escherichia coli flagella class II operons. J. Bacteriol. 1994, 176:7345-7351.
4. Farewell A., Kvint K., Nystöm T. Negative regulation by rpoS: a case of sigma factor competition. Mol. Microbiol. 1998, 29:1039-1051.
5. Patten C.L., Kirchhof M.G., Schertzberg M.R., Morton R.A., Schellhorn H.E. Microarray analysis of rpoS-mediated gene expression in Escherichia coli K-12. Mol. Genet. Genomics 2004, 272:580-591.
6. Dong T., Kirchhof M.G., Schellhorn H.E. RpoS regulation of gene expression during exponential growth of Escherichia coli K12. Mol. Genet. Genomics 2008, 273:267-277.
7. Dong T., Schellhorn H.E. Control of rpoS in global gene expression of Escherichia coli in minimal media. Mol. Genet. Genomics 2009, 281:19-33.
8. Dong T., Yu R., Schellhorn H. Antagonistic regulation of motility and transcriptome expression by rpoN and rpoS in Escherichia coli. Mol. Microbiol. 2011, 79:375-386.
9. Wood T.K., Andrés F., Barrios G., Herzberg M., Lee J. Motility influences biofilm architecture in Escherichia coli. Appl. Microbiol. Biotechnol. 2006, 72:361-367.
10. Baba T., Ara T., Hasegawa M., Takai Y., Okumura Y., Baba M., Datsenko K.A., Tomita M., Wanner B.L., Mori H. Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants: the Keio collection. Mol. Syst. Biol. 2006, 2:E1-E11.
11. Berg H.C., Brown D.A. Chemotaxis in Escherichia coli analysed by three-dimensional tracking. Nature 1972, 239:500-504.
12. Hirota N. Chemotaxis in thermophilic bacterium PS-3. J. Biochem. (Tokyo) 1984, 96:645-650.
13. Maeda K., Imae Y., Shioi J.I., Oosawa F. Effect of temperature on motility and chemotaxis of Escherichia coli. J. Bacteriol. 1976, 127:1039-1046.
14. Banks G., Schaefer D.W., Alpertm S.S. Light-scattering study of the temperature dependence of Escherichia coli motility. Biophys. J. 1975, 15:253-261.
15. Gluch M.F., Typke D., Baumeister W. Motility and thermotactic response of Thermotoga maritima. J. Bacteriol. 1995, 177:5473-5479.
16. Jasuja R., Lin Y., Trentham D.R., Khan S. Response tuning in bacterial chemotaxis. Proc. Natl. Acad. Sci. USA 1999, 96:11346-11351.
17. Miller J.H. A short course in bacterial genetics: A laboratory manual and handbook for Escherichia coli and related bacteria 1992, Cold Spring Harbor Laboratory Press, Cold Spring Harbor.
18. Zwietering M.H., Jongenburger I., Rombouts F.M., van't Riet K. Modeling of the bacterial growth curve. Appl. Environ. Microbiol. 1990, 56:1875-1881.
19. Ojima Y., Nishioka M., Taya M. Metabolic alternations in SOD-deficient Escherichia coli cells when cultivated under oxidative stress from photoexcited titanium dioxide. Biotechnol. Lett. 2008, 30:1107-1113.
20. Ojima Y., Kawase D., Nishioka M., Taya M. Functionally undefined gene, yggE, alleviates oxidative stress generated by monoamine oxidase in recombinant Escherichia coli. Biotechnol. Lett. 2009, 31:139-145.
21. Terashima H., Kojima S., Homma M. Flagella motility in bacteria: structure and function of flagella motor. Int. Rev. Cell Mol. Biol. 2008, 270:39-85.
22. Foladori P., Bruni L., Tamburini S., Ziglio G. Direct quantification of bacterial biomass in influent, effluent and activated sludge of wastewater treatment plants by using flow cytometry. Water Res. 2010, 44:3807-3818.
23. Ozbudak E.M., Thattai M., Lim H.N., Shraiman B.I., van Oudenaarden A. Multistability in the lactose utilization network of Escherichia coli. Nature 2004, 427:737-740.