Abstract
The nickel transport system of Clostridium thermoaceticum was investigated with 63NiCl2 and an anaerobic microfiltration transport assay. Transport was optimal at pH 7 to pH 7.5 and 65 degrees C and decreased in the presence of metabolic uncouplers and inhibitors. Exogenous nickel was concentrated 3,000-fold over the apparent nickel concentration gradient during typical transport assays. Stored cellular energy appeared to provide a short-term energy source to power nickel transport, and starvation experiments demonstrated external energy source stimulation of nickel translocation. The apparent Km and Vmax for nickel transport by carbon monoxide-dependent chemolithotrophic cells approximated 3.2 microM Ni and 400 pmol of Ni transported per min per mg of cells (dry weight), respectively. Magnesium, calcium, cobalt, iron, manganese, and zinc did not inhibit the transport of nickel.
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Selected References
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- Baronofsky J. J., Schreurs W. J., Kashket E. R. Uncoupling by Acetic Acid Limits Growth of and Acetogenesis by Clostridium thermoaceticum. Appl Environ Microbiol. 1984 Dec;48(6):1134–1139. doi: 10.1128/aem.48.6.1134-1139.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bradford M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976 May 7;72:248–254. doi: 10.1016/0003-2697(76)90527-3. [DOI] [PubMed] [Google Scholar]
- Bryson M. F., Drake H. L. Energy-dependent transport of nickel by Clostridium pasteurianum. J Bacteriol. 1988 Jan;170(1):234–238. doi: 10.1128/jb.170.1.234-238.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Campbell P. M., Smith G. D. Transport and accumulation of nickel ions in the cyanobacterium Anabaena cylindrica. Arch Biochem Biophys. 1986 Feb 1;244(2):470–477. doi: 10.1016/0003-9861(86)90615-6. [DOI] [PubMed] [Google Scholar]
- Drake H. L. Occurrence of nickel in carbon monoxide dehydrogenase from Clostridium pasteurianum and Clostridium thermoaceticum. J Bacteriol. 1982 Feb;149(2):561–566. doi: 10.1128/jb.149.2.561-566.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hausinger R. P. Nickel utilization by microorganisms. Microbiol Rev. 1987 Mar;51(1):22–42. doi: 10.1128/mr.51.1.22-42.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ivey D. M., Ljungdahl L. G. Purification and characterization of the F1-ATPase from Clostridium thermoaceticum. J Bacteriol. 1986 Jan;165(1):252–257. doi: 10.1128/jb.165.1.252-257.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jarrell K. F., Colvin J. R., Sprott G. D. Spontaneous protoplast formation in Methanobacterium bryantii. J Bacteriol. 1982 Jan;149(1):346–353. doi: 10.1128/jb.149.1.346-353.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jarrell K. F., Sprott G. D. Nickel transport in Methanobacterium bryantii. J Bacteriol. 1982 Sep;151(3):1195–1203. doi: 10.1128/jb.151.3.1195-1203.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kanodia S., Roberts M. F. Methanophosphagen: Unique cyclic pyrophosphate isolated from Methanobacterium thermoautotrophicum. Proc Natl Acad Sci U S A. 1983 Sep;80(17):5217–5221. doi: 10.1073/pnas.80.17.5217. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Keltjens J. T., van Erp R., Mooijaart R. J., van der Drift C., Vogels G. D. Inorganic pyrophosphate synthesis during methanogenesis from methylcoenzyme M by cell-free extracts of Methanobacterium thermoautotrophicum (strain delta H). Eur J Biochem. 1988 Mar 1;172(2):471–476. doi: 10.1111/j.1432-1033.1988.tb13912.x. [DOI] [PubMed] [Google Scholar]
- Ljungdahl L. G. The autotrophic pathway of acetate synthesis in acetogenic bacteria. Annu Rev Microbiol. 1986;40:415–450. doi: 10.1146/annurev.mi.40.100186.002215. [DOI] [PubMed] [Google Scholar]
- Lorowitz W. H., Bryant M. P. Peptostreptococcus productus strain that grows rapidly with CO as the energy source. Appl Environ Microbiol. 1984 May;47(5):961–964. doi: 10.1128/aem.47.5.961-964.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lundie L. L., Jr, Drake H. L. Development of a minimally defined medium for the acetogen Clostridium thermoaceticum. J Bacteriol. 1984 Aug;159(2):700–703. doi: 10.1128/jb.159.2.700-703.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Partridge C. D., Yates M. G. Effect of chelating agents on hydrogenase in Azotobacter chroococcum. Evidence that nickel is required for hydrogenase synthesis. Biochem J. 1982 Apr 15;204(1):339–344. doi: 10.1042/bj2040339. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Savage M. D., Drake H. L. Adaptation of the acetogen Clostridium thermoautotrophicum to minimal medium. J Bacteriol. 1986 Jan;165(1):315–318. doi: 10.1128/jb.165.1.315-318.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Savage M. D., Wu Z. G., Daniel S. L., Lundie L. L., Jr, Drake H. L. Carbon monoxide-dependent chemolithotrophic growth of Clostridium thermoautotrophicum. Appl Environ Microbiol. 1987 Aug;53(8):1902–1906. doi: 10.1128/aem.53.8.1902-1906.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Seely R. J., Fahrney D. E. A novel diphospho-P,P'-diester from Methanobacterium thermoautotrophicum. J Biol Chem. 1983 Sep 25;258(18):10835–10838. [PubMed] [Google Scholar]
- Stults L. W., Mallick S., Maier R. J. Nickel uptake in Bradyrhizobium japonicum. J Bacteriol. 1987 Apr;169(4):1398–1402. doi: 10.1128/jb.169.4.1398-1402.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Terracciano J. S., Schreurs W. J., Kashket E. R. Membrane H Conductance of Clostridium thermoaceticum and Clostridium acetobutylicum: Evidence for Electrogenic Na/H Antiport in Clostridium thermoaceticum. Appl Environ Microbiol. 1987 Apr;53(4):782–786. doi: 10.1128/aem.53.4.782-786.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Webb M. Interrelationships between the utilization of magnesium and the uptake of other bivalent cations by bacteria. Biochim Biophys Acta. 1970 Nov 24;222(2):428–439. doi: 10.1016/0304-4165(70)90133-9. [DOI] [PubMed] [Google Scholar]
- Willecke K., Gries E. M., Oehr P. Coupled transport of citrate and magnesium in Bacillus subtilis. J Biol Chem. 1973 Feb 10;248(3):807–814. [PubMed] [Google Scholar]