Abstract
Tetracycline accumulation by the phototrophic bacterium Rhodopseudomonas sphaeroides has been studied, using the fluorescence properties of the antibiotic and measuring uptake of [7- 3H]tetracycline. Accumulation was carrier mediated, with a Km of approximately 300 micronM. Efflux also appeared to be carried mediated, with a Km of 25 mM. Chlorotetracycline competitively inhibited tetracycline transport. The transport was energy dependent. Efflux occurred during the influx process, and an energy-requiring steady state was reached when influx balanced efflux. Transport was inhibited by metabolic inhibitors such as antimycin A, cyanide, and iodoacetate. Proton conductors such as carbonylcyanide m-chlorophenyl hydrazone were strongly inhibitory. Efflux was not energy dependent. Efflux is partially blocked by mercuric ions and completely blocked by an external pH of 9 to 11. Although efflux rates increased continuously with lowering of the pH, influx rates have a sharp maximum at pH 7.
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Selected References
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- Dockter M. E., Magnuson J. A. Characterization of the active transport of chlorotetracycline in staphylococcus aureus by a fluorescence technique. J Supramol Struct. 1974;2(1):32–44. doi: 10.1002/jss.400020105. [DOI] [PubMed] [Google Scholar]
- Dockter M. E., Trumble W. R., Magnuson J. A. Membrane lateral phase separations and chlortetracycline transport by Bacillus megaterium. Proc Natl Acad Sci U S A. 1978 Mar;75(3):1319–1323. doi: 10.1073/pnas.75.3.1319. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Harold F. M., Pavlasová E., Baarda J. R. A transmembrane pH gradient in Streptococcus faecalis: origin, and dissipation by proton conductors and N,N'-dicyclohexylcarbodimide. Biochim Biophys Acta. 1970;196(2):235–244. doi: 10.1016/0005-2736(70)90011-8. [DOI] [PubMed] [Google Scholar]
- Harold F. M., Spitz E. Accumulation of arsenate, phosphate, and aspartate by Sreptococcus faecalis. J Bacteriol. 1975 Apr;122(1):266–277. doi: 10.1128/jb.122.1.266-277.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hellingwerf K. J., Michels P. A., Dorpema J. W., Konings W. N. Transport of amino acids in membrane vesicles of Rhodopseudomonas spheroides energized by respiratory and cyclic electron flow. Eur J Biochem. 1975 Jul 1;55(2):397–406. doi: 10.1111/j.1432-1033.1975.tb02175.x. [DOI] [PubMed] [Google Scholar]
- Kanner B. I., Racker E. Light-dependent proton and rubidium translocation in membrane vesicles from Halobacterium halobium. Biochem Biophys Res Commun. 1975 Jan 2;64(3):1054–1061. doi: 10.1016/0006-291x(75)90154-0. [DOI] [PubMed] [Google Scholar]
- Kerwar G. K., Gordon A. S., Kaback H. R. Mechanisms of active transport in isolated membrane vesicles. IV. Galactose transport by isolated membrane vesicles from Escherichia coli. J Biol Chem. 1972 Jan 10;247(1):291–297. [PubMed] [Google Scholar]
- Klein W. L., Boyer P. D. Energization of active transport by Escherichia coli. J Biol Chem. 1972 Nov 25;247(22):7257–7265. [PubMed] [Google Scholar]
- Lanyi J. K., Renthal R., MacDonald R. E. Light-induced glutamate transport in Halobacterium halobium envelope vesicles. II. Evidence that the driving force is a light-dependent sodium gradient. Biochemistry. 1976 Apr 20;15(8):1603–1610. doi: 10.1021/bi00653a002. [DOI] [PubMed] [Google Scholar]
- Lanyi J. K., Yearwood-Drayton V., MacDonald R. E. Light-induced glutamate transport in Halobacterium halobium envelope vesicles. I. Kinetics of the light-dependent and the sodium-gradient-dependent uptake. Biochemistry. 1976 Apr 20;15(8):1595–1603. doi: 10.1021/bi00653a001. [DOI] [PubMed] [Google Scholar]
- Levine M., Oxender D. L., Stein W. D. The substrate-facilitated transport of the glucose carrier across the human erythrocyte membrane. Biochim Biophys Acta. 1965 Sep 27;109(1):151–163. doi: 10.1016/0926-6585(65)90099-3. [DOI] [PubMed] [Google Scholar]
- MacDonald R. E., Lanyi L. K. Light-induced leucine transport in Halobacterium halobium envelope vesicles: a chemiosmotic system. Biochemistry. 1975 Jul;14(13):2882–2889. doi: 10.1021/bi00684a014. [DOI] [PubMed] [Google Scholar]
- Renthal R., Lanyi J. K. Light-induced membrane potential and pH gradient in Halobacterium halobium envelope vesicles. Biochemistry. 1976 May 18;15(10):2136–2143. doi: 10.1021/bi00655a017. [DOI] [PubMed] [Google Scholar]
- Reynard A. M., Nellis L. F. Uptake of tetracycline by Escherichia coli: lack of binding of tetracycline to the uptake system. Biochem Biophys Res Commun. 1972 Sep 5;48(5):1129–1132. doi: 10.1016/0006-291x(72)90827-3. [DOI] [PubMed] [Google Scholar]
- Shipley P. L., Olsen R. H. Characteristics and expression of tetracycline resistance in gram-negative bacteria carrying the Pseudomonas R factor RP1. Antimicrob Agents Chemother. 1974 Aug;6(2):183–190. doi: 10.1128/aac.6.2.183. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Weckesser J., Magnuson J. A. Freie Vorträge aus der naturwissenschaftlichen Mikrobiologie. Zentralbl Bakteriol Orig A. 1976 Aug;235(1-3):153–156. [PubMed] [Google Scholar]
- Weckesser J., Magnuson J. A. Light-induced tetracycline accumulation by Rhodopseudomonas sphaeroides. J Supramol Struct. 1976;4(4):515–520. doi: 10.1002/jss.400040411. [DOI] [PubMed] [Google Scholar]
