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. 1977 Feb;129(2):908–915. doi: 10.1128/jb.129.2.908-915.1977

Effects of galU mutation on flagellar formation in Escherichia coli.

Y Komeda, T Icho, T Iino
PMCID: PMC235029  PMID: 320195

Abstract

Two mutants of Escherichia coli strictly deficient in uridine-diphosphoglucose pyrophosphorylase activity (galU) were found to have very small numbers of flagellar filaments and hooks. In these mutants, both the rate of flagellin (flagellar protein) synthesis and the amount of messenger ribonucleic acid specific for flagellin were considerably lower than in the parental strains. Motile revertants from the galU mutants were isolated and were found to carry a suppressor mutation, which was mapped in the flaH cistron. These strains formed swarms under conditions of catabolite repression; their intracellular concentration of cyclic adenosine 5'-monophosphate was the same as that in the parental strains. These results suggest that the outer membrane affects flagellar formation through the flaH gene product.

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Selected References

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  1. Adler J., Templeton B. The effect of environmental conditions on the motility of Escherichia coli. J Gen Microbiol. 1967 Feb;46(2):175–184. doi: 10.1099/00221287-46-2-175. [DOI] [PubMed] [Google Scholar]
  2. Ames G. F., Spudich E. N., Nikaido H. Protein composition of the outer membrane of Salmonella typhimurium: effect of lipopolysaccharide mutations. J Bacteriol. 1974 Feb;117(2):406–416. doi: 10.1128/jb.117.2.406-416.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Chet I., Henis Y., Mitchell R. Effect of biogenic amines and cannabinoids on bacterial chemotaxis. J Bacteriol. 1973 Sep;115(3):1215–1218. doi: 10.1128/jb.115.3.1215-1218.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. DePamphilis M. L., Adler J. Attachment of flagellar basal bodies to the cell envelope: specific attachment to the outer, lipopolysaccharide membrane and the cyoplasmic membrane. J Bacteriol. 1971 Jan;105(1):396–407. doi: 10.1128/jb.105.1.396-407.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. FUKASAWA T., JOKURA K., KURAHASHI K. A new enzymic defect of galactose metabolism in Escherichia coli K-12 mutants. Biochem Biophys Res Commun. 1962 Apr 3;7:121–125. doi: 10.1016/0006-291x(62)90158-4. [DOI] [PubMed] [Google Scholar]
  6. FUKASAWA T., JOKURA K., KURAHASHI K. MUTATIONS IN ESCHERICHIA COLI THAT AFFECT URIDINE DIPHOSPHATE GLUCOSE PYROPHOSPHORYLASE ACTIVITY AND GALACTOSE FERMENTATION. Biochim Biophys Acta. 1963 Sep 10;74:608–620. doi: 10.1016/0006-3002(63)91412-4. [DOI] [PubMed] [Google Scholar]
  7. Fraenkel D. G., Levisohn S. R. Glucose and gluconate metabolism in an Escherichia coli mutant lacking phosphoglucose isomerase. J Bacteriol. 1967 May;93(5):1571–1578. doi: 10.1128/jb.93.5.1571-1578.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Franklin N. C. Mutation in gal U gene of E. coli blocks phage P1 infection. Virology. 1969 May;38(1):189–191. doi: 10.1016/0042-6822(69)90144-5. [DOI] [PubMed] [Google Scholar]
  9. GOSS W. A., DEITZ W. H., COOK T. M. MECHANISM OF ACTION OF NALIDIXIC ACID ON ESCHERICHIA COLI. J Bacteriol. 1964 Oct;88:1112–1118. doi: 10.1128/jb.88.4.1112-1118.1964. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Guest J. R. Biochemical and genetic studies with nitrate reductase C-gene mutants of Escherichia coli. Mol Gen Genet. 1969;105(4):285–297. doi: 10.1007/BF00277583. [DOI] [PubMed] [Google Scholar]
  11. Harayama S., Iino T. Phototactic response of aerobically cultivated Rhodospirillum rubrum. J Gen Microbiol. 1976 May;94(1):173–179. doi: 10.1099/00221287-94-1-173. [DOI] [PubMed] [Google Scholar]
  12. Hilmen M., Silverman M., Simon M. The regulation of flagellar formation and function. J Supramol Struct. 1974;2(2-4):360–371. doi: 10.1002/jss.400020225. [DOI] [PubMed] [Google Scholar]
  13. Iino T., Enomoto M. Genetical studies of non-flagellate mutants of Salmonella. J Gen Microbiol. 1966 Jun;43(3):315–327. doi: 10.1099/00221287-43-3-315. [DOI] [PubMed] [Google Scholar]
  14. Irvin R. T., Chatterjee A. K., Sanderson K. E., Costerton J. W. Comparison of the cell envelope structure of a lipopolysaccharide-defective (heptose-deficient) strain and a smooth strain of Salmonella typhimurium. J Bacteriol. 1975 Nov;124(2):930–941. doi: 10.1128/jb.124.2.930-941.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Komeda Y., Suzuki H., Ishidsu J. I., Iino T. The role of cAMP in flagellation of Salmonella typhimurium. Mol Gen Genet. 1976 Dec 31;142(4):289–298. doi: 10.1007/BF00271253. [DOI] [PubMed] [Google Scholar]
  16. Koplow J., Goldfine H. Alterations in the outer membrane of the cell envelope of heptose-deficient mutants of Escherichia coli. J Bacteriol. 1974 Feb;117(2):527–543. doi: 10.1128/jb.117.2.527-543.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. MEYNELL E. W. A phage, phi chi, which attacks motile bacteria. J Gen Microbiol. 1961 Jun;25:253–290. doi: 10.1099/00221287-25-2-253. [DOI] [PubMed] [Google Scholar]
  18. McGroarty E. J., Koffler H., Smith R. W. Regulation of flagellar morphogenesis by temperature: involvement of the bacterial cell surface in the synthesis of flagellin and the flagellum. J Bacteriol. 1973 Jan;113(1):295–303. doi: 10.1128/jb.113.1.295-303.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Nikaido H. Outer membrane of Salmonella typhimurium. Transmembrane diffusion of some hydrophobic substances. Biochim Biophys Acta. 1976 Apr 16;433(1):118–132. doi: 10.1016/0005-2736(76)90182-6. [DOI] [PubMed] [Google Scholar]
  20. Risse H. J., Lüderitz O., Westphal O. Vergleichende Untersuchungen zur Biosynthese von Nucleotid-Zuckern in S- und R-Formen von Salmonella minnesota und Salmonella ruiru. Eur J Biochem. 1967 Apr;1(2):233–242. doi: 10.1111/j.1432-1033.1967.tb00067.x. [DOI] [PubMed] [Google Scholar]
  21. STOCKER B. A. Transduction of flagellar characters in Salmonella. J Gen Microbiol. 1953 Dec;9(3):410–433. doi: 10.1099/00221287-9-3-410. [DOI] [PubMed] [Google Scholar]
  22. SUNDARARAJAN T. A., RAPIN A. M., KALCKAR H. M. Biochemical observations on E. coli mutants defective in uridine diphosphoglucose. Proc Natl Acad Sci U S A. 1962 Dec 15;48:2187–2193. doi: 10.1073/pnas.48.12.2187. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Silverman M., Simon M. Characterization of Escherichia coli flagellar mutants that are insensitive to catabolite repression. J Bacteriol. 1974 Dec;120(3):1196–1203. doi: 10.1128/jb.120.3.1196-1203.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Silverman M., Simon M. Genetic analysis of flagellar mutants in Escherichia coli. J Bacteriol. 1973 Jan;113(1):105–113. doi: 10.1128/jb.113.1.105-113.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Suzuki H., Iino T. Absence of messenger ribonucleic acid specific for flagellin in non-flagellate mutants of Salmonella. J Mol Biol. 1975 Jul 15;95(4):549–556. doi: 10.1016/0022-2836(75)90316-2. [DOI] [PubMed] [Google Scholar]
  26. Tamaki S., Sato T., Matsuhashi M. Role of lipopolysaccharides in antibiotic resistance and bacteriophage adsorption of Escherichia coli K-12. J Bacteriol. 1971 Mar;105(3):968–975. doi: 10.1128/jb.105.3.968-975.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Yokota T., Gots J. S. Requirement of adenosine 3', 5'-cyclic phosphate for flagella formation in Escherichia coli and Salmonella typhimurium. J Bacteriol. 1970 Aug;103(2):513–516. doi: 10.1128/jb.103.2.513-516.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]

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