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. 1985 Dec;164(3):1294–1300. doi: 10.1128/jb.164.3.1294-1300.1985

Calcium transport in membrane vesicles of Bacillus subtilis.

W de Vrij, R Bulthuis, E Postma, W N Konings
PMCID: PMC219329  PMID: 3934142

Abstract

Right-side-out membrane vesicles of Bacillus subtilis W23 grown on tryptone-citrate medium accumulated Ca2+ under aerobic conditions in the presence of a suitable electron donor. Ca2+ uptake was an electrogenic process which was completely inhibited by carbonyl cyanide m-chlorophenylhydrazone or valinomycin and not by nigericin. This electrogenic uptake of calcium was strongly dependent on the presence of phosphate and magnesium ions. The system had a low affinity for Ca2+. The kinetic constants in membrane vesicles were Km = 310 microM Ca2+ and Vmax = 16 nmol/mg of protein per min. B. subtilis also possesses a Ca2+ extrusion system. Right-side-out-oriented membrane vesicles accumulated Ca2+ upon the artificial imposition of a pH-gradient, inside acid. This system had a high affinity for Ca2+; Km = 17 microM Ca2+ and Vmax = 3.3 nmol/mg of protein per min. Also, a membrane potential, inside positive, drove Ca2+ transport via this Ca2+ extrusion system. Evidence for a Ca2+ extrusion system was also supplied by studies of inside-out-oriented membrane vesicles in which Ca2+ uptake was energized by respiratory chain-linked oxidation of NADH or ascorbate-phenazine methosulfate. Both components of the proton motive force, the pH gradient and the membrane potential, drove Ca2+ transport via the Ca2+ extrusion system, indicating a proton-calcium antiport system with a H+ to Ca2+ stoichiometry larger than 2. The kinetic parameters of this Ca2+ extrusion system in inside-out-oriented membranes were Km = 25 microM and Vmax = 0.7 nmol/mg of protein per min.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Ambudkar S. V., Zlotnick G. W., Rosen B. P. Calcium efflux from Escherichia coli. Evidence for two systems. J Biol Chem. 1984 May 25;259(10):6142–6146. [PubMed] [Google Scholar]
  2. Ando A., Yabuki M., Kusaka I. Na+-driven Ca2+ transport in alkalophilic Bacillus. Biochim Biophys Acta. 1981 Jan 8;640(1):179–184. doi: 10.1016/0005-2736(81)90543-5. [DOI] [PubMed] [Google Scholar]
  3. BURSTONE M. S. New histochemical techniques for the demonstration of tissue oxidase (cytochrome oxidase). J Histochem Cytochem. 1959 Mar;7(2):112–122. doi: 10.1177/7.2.112. [DOI] [PubMed] [Google Scholar]
  4. Bergsma J., Konings W. N. The properties of citrate transport in membrane vesicles from Bacillus subtilis. Eur J Biochem. 1983 Jul 15;134(1):151–156. doi: 10.1111/j.1432-1033.1983.tb07545.x. [DOI] [PubMed] [Google Scholar]
  5. Bergsma J., Strijker R., Alkema J. Y., Seijen H. G., Konings W. N. NADH dehydrogenase and NADH oxidation in membrane vesicle from Bacillus subtilis. Eur J Biochem. 1981 Dec;120(3):599–606. doi: 10.1111/j.1432-1033.1981.tb05742.x. [DOI] [PubMed] [Google Scholar]
  6. Bishop D. G., Op den Kamp J. A., van Deenen L. L. The distribution of lipids in the protoplast membranes of Bacillus subtilis. A study with phospholipase C and trinitrobenzenesulphonic acid. Eur J Biochem. 1977 Nov 1;80(2):381–391. doi: 10.1111/j.1432-1033.1977.tb11893.x. [DOI] [PubMed] [Google Scholar]
  7. Bisschop A., Doddema H., Konings W. N. Dicarboxylic acid transport in membrane vesicles from Bacillus subtilis. J Bacteriol. 1975 Nov;124(2):613–622. doi: 10.1128/jb.124.2.613-622.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. GEST H. Metabolic patterns in photosynthetic bacteria. Bacteriol Rev. 1951 Dec;15(4):183–210. doi: 10.1128/br.15.4.183-210.1951. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Golub E. E., Bronner F. Bacterial calcium transport: energy-dependent calcium uptake by membrane vesicles from Bacillus megaterium. J Bacteriol. 1974 Sep;119(3):840–843. doi: 10.1128/jb.119.3.840-843.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Haug A., Larsen B. Biosynthesis of alginate. II. Polymannuronic acid C-5-epimerase from Azotobacter vinelandii (Lipman). Carbohydr Res. 1971 Apr;17(2):297–308. doi: 10.1016/s0008-6215(00)82537-9. [DOI] [PubMed] [Google Scholar]
  11. Hellingwerf K. J., van Hoorn P. A polyvinylchloride-membrane based anion selective electrode for continuous registration of delta pH (interior alkaline) with salicylate as the indicator probe. J Biochem Biophys Methods. 1985 Aug;11(2-3):83–93. doi: 10.1016/0165-022x(85)90044-2. [DOI] [PubMed] [Google Scholar]
  12. Inesi G. Active transport of calcium ion in sarcoplasmic membranes. Annu Rev Biophys Bioeng. 1972;1:191–210. doi: 10.1146/annurev.bb.01.060172.001203. [DOI] [PubMed] [Google Scholar]
  13. Jasper P., Silver S. Divalent cation transport systems of Rhodopseudomonas capsulata. J Bacteriol. 1978 Mar;133(3):1323–1328. doi: 10.1128/jb.133.3.1323-1328.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Kaback H. R. Transport in isolated bacterial membrane vesicles. Methods Enzymol. 1974;31:698–709. doi: 10.1016/0076-6879(74)31075-0. [DOI] [PubMed] [Google Scholar]
  15. Kobayashi H., Van Brunt J., Harold F. M. ATP-linked calcium transport in cells and membrane vesicles of Streptococcus faecalis. J Biol Chem. 1978 Apr 10;253(7):2085–2092. [PubMed] [Google Scholar]
  16. Kojima M., Suda S., Hotta S., Hamada K. Induction of pleomorphy and calcium ion deficiency in Lactobacillus bifidus. J Bacteriol. 1970 Apr;102(1):217–220. doi: 10.1128/jb.102.1.217-220.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Konings W. N. Active transport of solutes in bacterial membrane vesicles. Adv Microb Physiol. 1977;15:175–251. doi: 10.1016/s0065-2911(08)60317-3. [DOI] [PubMed] [Google Scholar]
  18. Konings W. N., Bisschop A., Daatselaar M. C.C. Transport of L-glutamate and L-aspartate by membrane vesicles of Bacillus subtilis W 23. FEBS Lett. 1972 Aug 15;24(3):260–264. doi: 10.1016/0014-5793(72)80368-5. [DOI] [PubMed] [Google Scholar]
  19. Konings W. N., Bisschop A., Veenhuis M., Vermeulen C. A. New procedure for the isolation of membrane vesicles of Bacillus subtilis and an electron microscopy study of their ultrastructure. J Bacteriol. 1973 Dec;116(3):1456–1465. doi: 10.1128/jb.116.3.1456-1465.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Konings W. N., Freese E. Amino acid transport in membrane vesicles of Bacillus subtilis. J Biol Chem. 1972 Apr 25;247(8):2408–2418. [PubMed] [Google Scholar]
  21. Konings W. N., Robillard G. T. Physical mechanism for regulation of proton solute symport in Escherichia coli. Proc Natl Acad Sci U S A. 1982 Sep;79(18):5480–5484. doi: 10.1073/pnas.79.18.5480. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. 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]
  23. Lehninger A. L., Carafoli E., Rossi C. S. Energy-linked ion movements in mitochondrial systems. Adv Enzymol Relat Areas Mol Biol. 1967;29:259–320. doi: 10.1002/9780470122747.ch6. [DOI] [PubMed] [Google Scholar]
  24. Matin A., Konings W. N. Transport of lactate and succinate by membrane vesicles of Escherichia coli, Bacillus subtilis and a pseudomonas species. Eur J Biochem. 1973 Apr 2;34(1):58–67. doi: 10.1111/j.1432-1033.1973.tb02728.x. [DOI] [PubMed] [Google Scholar]
  25. Owen P., Kaback H. R. Molecular structure of membrane vesicles from Escherichia coli. Proc Natl Acad Sci U S A. 1978 Jul;75(7):3148–3152. doi: 10.1073/pnas.75.7.3148. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Shinbo T., Kamo N., Kurihara K., Kobatake Y. A PVC-based electrode sensitive to DDA+ as a device for monitoring the membrane potential in biological systems. Arch Biochem Biophys. 1978 Apr 30;187(2):414–422. doi: 10.1016/0003-9861(78)90052-8. [DOI] [PubMed] [Google Scholar]
  27. Silver S., Toth K., Scribner H. Facilitated transport of calcium by cells and subcellular membranes of Bacillus subtilis and Escherichia coli. J Bacteriol. 1975 Jun;122(3):880–885. doi: 10.1128/jb.122.3.880-885.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Smyth C. J., Siegel J., Salton M. R., Owen P. Immunochemical analysis of inner and outer membranes of Escherichia coli by crossed immunoelectrophoresis. J Bacteriol. 1978 Jan;133(1):306–319. doi: 10.1128/jb.133.1.306-319.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Tsuchiya T., Rosen B. P. Characterization of an active transport system for calcium in inverted membrane vesicles of Escherichia coli. J Biol Chem. 1975 Oct 10;250(19):7687–7692. [PubMed] [Google Scholar]
  30. Zimniak P., Barnes E. M., Jr Characterization of a calcium/proton antiporter and an electrogenic calcium transporter in membrane vesicles from Azotobacter vinelandii. J Biol Chem. 1980 Nov 10;255(21):10140–10143. [PubMed] [Google Scholar]

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