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. 1979 Dec;140(3):798–804. doi: 10.1128/jb.140.3.798-804.1979

Response to a metal ion-citrate complex in bacterial sensing.

T D Ingolia, D E Koshland Jr
PMCID: PMC216717  PMID: 160411

Abstract

Salmonella typhimurium responds chemotactically to gradients of divalent cations in the presence of citrate ions. The actual chemoeffector is the citrate-metal ion complex, which acts as an attractant. Citrate (which is also a chemoeffector for Salmonella) and the citrate-metal ion complex are recognized by different receptors. The response of Salmonells, which can transport citrate through its membrane, is quite different than that of Escherichia coli, which cannot.

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Selected References

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  1. Adler J. A method for measuring chemotaxis and use of the method to determine optimum conditions for chemotaxis by Escherichia coli. J Gen Microbiol. 1973 Jan;74(1):77–91. doi: 10.1099/00221287-74-1-77. [DOI] [PubMed] [Google Scholar]
  2. Adler J. Chemotaxis in bacteria. Annu Rev Biochem. 1975;44:341–356. doi: 10.1146/annurev.bi.44.070175.002013. [DOI] [PubMed] [Google Scholar]
  3. 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]
  4. Aksamit R. R., Koshland D. E., Jr Identification of the ribose binding protein as the receptor for ribose chemotaxis in Salmonella typhimurium. Biochemistry. 1974 Oct 22;13(22):4473–4478. doi: 10.1021/bi00719a001. [DOI] [PubMed] [Google Scholar]
  5. Aksamit R., Koshland D. E., Jr A ribose binding protein of Salmonella typhimurium. Biochem Biophys Res Commun. 1972 Sep 26;48(6):1348–1353. doi: 10.1016/0006-291x(72)90860-1. [DOI] [PubMed] [Google Scholar]
  6. Aswad D. W., Koshland D. E., Jr Evidence for an S-adenosylmethionine requirement in the chemotactic behavior of Salmonella typhimurium. J Mol Biol. 1975 Sep 15;97(2):207–223. doi: 10.1016/s0022-2836(75)80035-0. [DOI] [PubMed] [Google Scholar]
  7. Berg H. C. Chemotaxis in bacteria. Annu Rev Biophys Bioeng. 1975;4(00):119–136. doi: 10.1146/annurev.bb.04.060175.001003. [DOI] [PubMed] [Google Scholar]
  8. Butlin J. D., Cox G. B., Gibson F. Oxidative phosphorylation in Escherichia coli K12. Mutations affecting magnesium ion- or calcium ion-stimulated adenosine triphosphatase. Biochem J. 1971 Aug;124(1):75–81. doi: 10.1042/bj1240075. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. DeFranco A. L., Parkinson J. S., Koshland D. E., Jr Functional homology of chemotaxis genes in Escherichia coli and Salmonella typhimurium. J Bacteriol. 1979 Jul;139(1):107–114. doi: 10.1128/jb.139.1.107-114.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Evans D. J., Jr Membrane adenosine triphosphatase of Escherichia coli: activation by calcium ion and inhibition by monovalent cations. J Bacteriol. 1969 Nov;100(2):914–922. doi: 10.1128/jb.100.2.914-922.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Imai K., Iijima T., Hasegawa T. Transport of tricarboxylic acids in Salmonella typhimurium. J Bacteriol. 1973 Jun;114(3):961–965. doi: 10.1128/jb.114.3.961-965.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Kim I. C., Bragg P. D. Some properties of the succinate dehydrogenase of Escherichia coli. Can J Biochem. 1971 Oct;49(10):1098–1104. doi: 10.1139/o71-159. [DOI] [PubMed] [Google Scholar]
  13. Koshland D. E., Jr A response regulator model in a simple sensory system. Science. 1977 Jun 3;196(4294):1055–1063. doi: 10.1126/science.870969. [DOI] [PubMed] [Google Scholar]
  14. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  15. Macnab R. M. Bacterial motility and chemotaxis: the molecular biology of a behavioral system. CRC Crit Rev Biochem. 1978;5(4):291–341. doi: 10.3109/10409237809177145. [DOI] [PubMed] [Google Scholar]
  16. Macnab R. M., Koshland D. E., Jr The gradient-sensing mechanism in bacterial chemotaxis. Proc Natl Acad Sci U S A. 1972 Sep;69(9):2509–2512. doi: 10.1073/pnas.69.9.2509. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Melton T., Hartman P. E., Stratis J. P., Lee T. L., Davis A. T. Chemotaxis of Salmonella typhimurium to amino acids and some sugars. J Bacteriol. 1978 Feb;133(2):708–716. doi: 10.1128/jb.133.2.708-716.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Miller J. B., Koshland D. E., Jr Sensory electrophysiology of bacteria: relationship of the membrane potential to motility and chemotaxis in Bacillus subtilis. Proc Natl Acad Sci U S A. 1977 Nov;74(11):4752–4756. doi: 10.1073/pnas.74.11.4752. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Parkinson J. S. Behavioral genetics in bacteria. Annu Rev Genet. 1977;11:397–414. doi: 10.1146/annurev.ge.11.120177.002145. [DOI] [PubMed] [Google Scholar]
  20. Pollack J. R., Ames B. N., Neilands J. B. Iron transport in Salmonella typhimurium: mutants blocked in the biosynthesis of enterobactin. J Bacteriol. 1970 Nov;104(2):635–639. doi: 10.1128/jb.104.2.635-639.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Strange P. G., Koshland D. E., Jr Receptor interactions in a signalling system: competition between ribose receptor and galactose receptor in the chemotaxis response. Proc Natl Acad Sci U S A. 1976 Mar;73(3):762–766. doi: 10.1073/pnas.73.3.762. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Tsang N., Macnab R., Koshland D. E., Jr Common mechanism for repellents and attractants in bacterial chemotaxis. Science. 1973 Jul 6;181(4094):60–63. doi: 10.1126/science.181.4094.60. [DOI] [PubMed] [Google Scholar]
  23. Tso W. W., Adler J. Negative chemotaxis in Escherichia coli. J Bacteriol. 1974 May;118(2):560–576. doi: 10.1128/jb.118.2.560-576.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Woodrow G. C., Langman L., Young I. G., Gibson F. Mutations affecting the citrate-dependent iron uptake system in Escherichia coli. J Bacteriol. 1978 Mar;133(3):1524–1526. doi: 10.1128/jb.133.3.1524-1526.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Zukin R. S., Koshland D. E., Jr Mg2+, Ca2+-dependent adenosine triphosphatase as receptor for divalent cations in bacterial sensing. Science. 1976 Jul 30;193(4251):405–408. doi: 10.1126/science.132702. [DOI] [PubMed] [Google Scholar]
  26. Zukin R. S., Strange P. G., Heavey R., Koshland D. E. Properties of the galactose binding protein of Salmonella typhimurium and Escherichia coli. Biochemistry. 1977 Feb 8;16(3):381–386. doi: 10.1021/bi00622a007. [DOI] [PubMed] [Google Scholar]

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