Abstract
Galactose and other chemotactic attractants have been shown to trigger an apparent hyperpolarization in Escherichia coli (Eisenbach, M., 1982, Biochemistry, 21:6818-6825). The probe used to measure membrane potential in that study, tetraphenylphosphonium (TPP+), may respond also to surface-charge changes in the membrane. The distinction between true changes in membrane potential and changes in the surface charge of the membrane is crucial for the study of this phenomenon in bacterial chemotaxis. To distinguish between these parameters, we compared the response to galactose with different techniques: K+ distribution in the presence of valinomycin (measured with a K+-selective electrode), TPP+ distribution (measured with a TPP+-selective electrode) at different ionic strengths, absorbance changes of bis(3-phenyl-5-oxoisoxazol-4-yl)pentamethineoxonol (oxonol V), and fluorescence changes of three probes with different mechanisms of response. All the techniques revealed stimulation by galactose of transient hyperpolarization, of comparable magnitude. This indicates the involvement of ion currents rather than alterations of local surface properties.
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Selected References
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- Adler J. Chemoreceptors in bacteria. Science. 1969 Dec 26;166(3913):1588–1597. doi: 10.1126/science.166.3913.1588. [DOI] [PubMed] [Google Scholar]
- Ahmed S., Booth I. R. Quantitative measurements of the proton-motive force and its relation to steady state lactose accumulation in Escherichia coli. Biochem J. 1981 Dec 15;200(3):573–581. doi: 10.1042/bj2000573. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Azzi A. The application of fluorescent probes in membrane studies. Q Rev Biophys. 1975 May;8(2):237–316. doi: 10.1017/s0033583500001803. [DOI] [PubMed] [Google Scholar]
- Bakker E. P. Membrane potential in a potassium transport-negative mutant of Escherichia coli K-12. The distribution of rubidium in the presence of valinomycin indicates a higher potential than that of the tetraphenylphosphonium cation. Biochim Biophys Acta. 1982 Sep 15;681(3):474–483. doi: 10.1016/0005-2728(82)90190-6. [DOI] [PubMed] [Google Scholar]
- Bashford C. L., Smith J. C. The use of optical probes to monitor membrane potential. Methods Enzymol. 1979;55:569–586. doi: 10.1016/0076-6879(79)55067-8. [DOI] [PubMed] [Google Scholar]
- Boos W. The properties of the galactose-binding protein, the possible chemoreceptor for galactose chemotaxis in Escherichia coli. Antibiot Chemother (1971) 1974;19:21–54. doi: 10.1159/000395423. [DOI] [PubMed] [Google Scholar]
- Borochov H., Shinitzky M. Vertical displacement of membrane proteins mediated by changes in microviscosity. Proc Natl Acad Sci U S A. 1976 Dec;73(12):4526–4530. doi: 10.1073/pnas.73.12.4526. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Eisenbach M. Changes in membrane potential of Escherichia coli in response to temporal gradients of chemicals. Biochemistry. 1982 Dec 21;21(26):6818–6825. doi: 10.1021/bi00269a030. [DOI] [PubMed] [Google Scholar]
- Eisenbach M., Raz T., Ciobotariu A. A process related to membrane potential involved in bacterial chemotaxis to galactose. Biochemistry. 1983 Jun 21;22(13):3293–3298. doi: 10.1021/bi00282a039. [DOI] [PubMed] [Google Scholar]
- Felle H., Porter J. S., Slayman C. L., Kaback H. R. Quantitative measurements of membrane potential in Escherichia coli. Biochemistry. 1980 Jul 22;19(15):3585–3590. doi: 10.1021/bi00556a026. [DOI] [PubMed] [Google Scholar]
- Ghazi A., Schechter E., Letellier L., Labedan B. Probes of membrane potential in Escherichia coli cells. FEBS Lett. 1981 Mar 23;125(2):197–200. doi: 10.1016/0014-5793(81)80717-x. [DOI] [PubMed] [Google Scholar]
- Grinius L. L., Jasaitis A. A., Kadziauskas Y. P., Liberman E. A., Skulachev V. P., Topali V. P., Tsofina L. M., Vladimirova M. A. Conversion of biomembrane-produced energy into electric form. I. Submitochondrial particles. Biochim Biophys Acta. 1970 Aug 4;216(1):1–12. doi: 10.1016/0005-2728(70)90153-2. [DOI] [PubMed] [Google Scholar]
- Grinvald A., Hildesheim R., Farber I. C., Anglister L. Improved fluorescent probes for the measurement of rapid changes in membrane potential. Biophys J. 1982 Sep;39(3):301–308. doi: 10.1016/S0006-3495(82)84520-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Haynes D. H. 1-Anilino-8-naphthalenesulfonate: a fluorescent indicator of ion binding electrostatic potential on the membrane surface. J Membr Biol. 1974 Jul 12;17(3):341–366. doi: 10.1007/BF01870191. [DOI] [PubMed] [Google Scholar]
- Hazelbauer G. L., Adler J. Role of the galactose binding protein in chemotaxis of Escherichia coli toward galactose. Nat New Biol. 1971 Mar 24;230(12):101–104. doi: 10.1038/newbio230101a0. [DOI] [PubMed] [Google Scholar]
- Kell D. B. On the functional proton current pathway of electron transport phosphorylation. An electrodic view. Biochim Biophys Acta. 1979 Jul 3;549(1):55–99. doi: 10.1016/0304-4173(79)90018-1. [DOI] [PubMed] [Google Scholar]
- Leive L. Release of lipopolysaccharide by EDTA treatment of E. coli. Biochem Biophys Res Commun. 1965 Nov 22;21(4):290–296. doi: 10.1016/0006-291x(65)90191-9. [DOI] [PubMed] [Google Scholar]
- Letellier L., Shechter E. Cyanine dye as monitor of membrane potentials in Escherichia coli cells and membrane vesicles. Eur J Biochem. 1979 Dec 17;102(2):441–447. doi: 10.1111/j.1432-1033.1979.tb04259.x. [DOI] [PubMed] [Google Scholar]
- Loew L. M., Simpson L. L. Charge-shift probes of membrane potential: a probable electrochromic mechanism for p-aminostyrylpyridinium probes on a hemispherical lipid bilayer. Biophys J. 1981 Jun;34(3):353–365. doi: 10.1016/S0006-3495(81)84854-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ordal G. W., Adler J. Properties of mutants in galactose taxis and transport. J Bacteriol. 1974 Feb;117(2):517–526. doi: 10.1128/jb.117.2.517-526.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Padan E., Zilberstein D., Rottenberg H. The proton electrochemical gradient in Escherichia coli cells. Eur J Biochem. 1976 Apr 1;63(2):533–541. doi: 10.1111/j.1432-1033.1976.tb10257.x. [DOI] [PubMed] [Google Scholar]
- Rottenberg H. The measurement of membrane potential and deltapH in cells, organelles, and vesicles. Methods Enzymol. 1979;55:547–569. doi: 10.1016/0076-6879(79)55066-6. [DOI] [PubMed] [Google Scholar]
- Skulachev V. P. Membrane electricity as a convertible energy currency for the cell. Can J Biochem. 1980 Mar;58(3):161–175. doi: 10.1139/o80-023. [DOI] [PubMed] [Google Scholar]
- Szmelcman S., Adler J. Change in membrane potential during bacterial chemotaxis. Proc Natl Acad Sci U S A. 1976 Dec;73(12):4387–4391. doi: 10.1073/pnas.73.12.4387. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Waggoner A. S. The use of cyanine dyes for the determination of membrane potentials in cells, organelles, and vesicles. Methods Enzymol. 1979;55:689–695. doi: 10.1016/0076-6879(79)55077-0. [DOI] [PubMed] [Google Scholar]
- Wang E. A., Koshland D. E., Jr Receptor structure in the bacterial sensing system. Proc Natl Acad Sci U S A. 1980 Dec;77(12):7157–7161. doi: 10.1073/pnas.77.12.7157. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zaritsky A., Kihara M., Macnab R. M. Measurement of membrane potential in Bacillus subtilis: a comparison of lipophilic cations, rubidium ion, and a cyanine dye as probes. J Membr Biol. 1981;63(3):215–231. doi: 10.1007/BF01870983. [DOI] [PubMed] [Google Scholar]
