Abstract
Clostridium pasteurianum strain W-5 was selected as an anaerobe which may be grown from large inocula in defined media with sulfate as its primary sulfur source. Since it is important to keep inocula small in minimizing transfer of sulfur sources, culture conditions were optimized. The medium devised decreased lag period and generation time when compared with other media, but growth could not be induced consistently with 6 × 106 cells per ml or less. Addition of trace elements, chelating agents, reducing agents, metabolites, and spent medium from various stages of growth did not stimulate growth from small inocula. Generation time was 85 min on inoculation with 107 or more cells per ml taken from young stocks, but the lag period decreased somewhat with larger inocula. On the other hand, generation time and lag period increased with age of the inoculum. The total yield of cells increased when buffer capacity was increased. Growth of C. pasteurianum W-5 was dependent upon sulfate at relatively low sulfate concentrations, and the organism is thus suitable for study of sulfur metabolism. No evidence of a maintenance requirement for sulfate was detected.
Full text
PDF




Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bohinski R. C., Mallette M. F. Behavior of Escherichia coli B in sulfate-limited medium. Can J Microbiol. 1965 Aug;11(4):663–669. doi: 10.1139/m65-089. [DOI] [PubMed] [Google Scholar]
- CARNAHAN J. E., CASTLE J. E. Some requirements of biological nitrogen fixation. J Bacteriol. 1958 Feb;75(2):121–124. doi: 10.1128/jb.75.2.121-124.1958. [DOI] [PMC free article] [PubMed] [Google Scholar]
- CARNAHAN J. E., MORTENSON L. E., MOWER H. F., CASTLE J. E. Nitrogen fixation in cell-free extracts of Clostridium pasteurianum. Biochim Biophys Acta. 1960 Nov 18;44:520–535. doi: 10.1016/0006-3002(60)91606-1. [DOI] [PubMed] [Google Scholar]
- Daesch G., Mortenson L. E. Effect of ammonia on the synthesis and function of the N 2 -fixing enzyme system in Clostridium pasteurianum. J Bacteriol. 1972 Apr;110(1):103–109. doi: 10.1128/jb.110.1.103-109.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dalton H., Postgate J. R. Growth and physiology of Azotobacter chroococcum in continuous culture. J Gen Microbiol. 1969 Jun;56(3):307–319. doi: 10.1099/00221287-56-3-307. [DOI] [PubMed] [Google Scholar]
- LOVENBERG W., BUCHANAN B. B., RABINOWITZ J. C. STUDIES ON THE CHEMICAL NATURE OF CLOSTRIDIAL FERREDOXIN. J Biol Chem. 1963 Dec;238:3899–3913. [PubMed] [Google Scholar]
- ROSENBLUM E. D., WILSON P. W. Molecular hydrogen and nitrogen fixation by Clostridium. J Bacteriol. 1950 Jan;59(1):83–91. doi: 10.1128/jb.59.1.83-91.1950. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sargeant K., Ford J. W., Longyear V. M. Production of Clostridium pasteurianum in a defined medium. Appl Microbiol. 1968 Feb;16(2):296–300. doi: 10.1128/am.16.2.296-300.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schroeder H. R., Barnes C. J., Bohinski R. C., Mumma R. O., Mallette M. F. Isolation and identification of 5-methylthioribose from Escherichia coli B. Biochim Biophys Acta. 1972 Jul 19;273(2):254–264. doi: 10.1016/0304-4165(72)90215-2. [DOI] [PubMed] [Google Scholar]
- WESTLAKE D. W., WILSON P. W. Molecular hydrogen and nitrogen fixation by Clostridium pasteurianum. Can J Microbiol. 1959 Dec;5:617–620. doi: 10.1139/m59-075. [DOI] [PubMed] [Google Scholar]