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Appl Environ Microbiol. 1993 December; 59(12): 4198-4202
Copyright © 1993, American Society for Microbiology. All Rights Reserved.

Isolation of a Degeneration-Resistant Mutant of Clostridium acetobutylicum NCIMB 8052

Eva R. Kashket* and Zhi-Yi Cao

Department of Microbiology, Boston University School of Medicine, 80 East Concord Street, Boston, Massachusetts 02118-2394

ABSTRACT

Unless periodically grown from germinated spores, Clostridium acetobutylicum tends to degenerate (that is, to spontaneously lose the capacity both to produce solvents and to develop into spores). To obtain mutants that are deficient in degeneration, C. acetobutylicum NCIMB 8052 was mated with Enterococcus faecalis BM4110 harboring transposon Tn1545. We developed a degeneration resistance assay based on a secondary effect of degeneration, the production of toxic levels of acetic and butyric acids. Erythromycin-resistant transconjugant clones were tested individually for longevity by repeated and timely subculturing. One long-lived mutant, A10, survived 18 ± 3 transfers (mean ± standard deviation; n = 20) before extinction, while the wild type (parental cells) survived 6.6 ± 1.5 transfers (n = 11). The three-fold difference in longevity is statistically significant. In a batch culture in a rich medium, the wild-type cells degenerated within 24 h after inoculation with 1% of an overnight culture derived from germinated spores. In contrast, A10 cells were able to switch to solventogenesis and to sporulate. In a minimal medium with greater buffering capacity, both cell types produced solvents and spores. Southern blots of EcoRI and HindIII restriction digests of A10 chromosomal DNA (but not parental DNA) showed that only one copy of Tn1545 was inserted into the clostridial chromosome. Our findings are consistent with the hypothesis that there was an alteration at a regulatory locus that was effected by the insertion of the transposon.

FOOTNOTES

* Corresponding author.

Appl Environ Microbiol. 1993 December; 59(12): 4198-4202
Copyright © 1993, American Society for Microbiology. All Rights Reserved.



This article has been cited by other articles:

  • Liyanage, H., Kashket, S., Young, M., Kashket, E. R. (2001). Clostridium beijerinckii and Clostridium difficile Detoxify Methylglyoxal by a Novel Mechanism Involving Glycerol Dehydrogenase. Appl. Environ. Microbiol. 67: 2004-2010 [Abstract] [Full Text]  
  • Evans, V. J., Liyanage, H., Ravagnani, A., Young, M., Kashket, E. R. (1998). Truncation of Peptide Deformylase Reduces the Growth Rate and Stabilizes Solvent Production in Clostridium beijerinckii NCIMB 8052. Appl. Environ. Microbiol. 64: 1780-1785 [Abstract] [Full Text]  


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