Previous Article | Next Article 
Appl Environ Microbiol. 1986 July; 52(1): 86-91
Copyright © 1986, American Society for Microbiology. All Rights Reserved.
Intracellular Conditions Required for Initiation of Solvent Production by Clostridium acetobutylicum
Joseph S. Terracciano and
Eva R. Kashket*
Department of Microbiology, Boston University School of Medicine, Boston, Massachusetts 02118
ABSTRACT
We investigated the intracellular physiological conditions associated with the induction of butanol-producing enzymes in Clostridium acetobutylicum. During the acidogenic phase of growth, the internal pH decreased in parallel with the decrease in the external pH, but the internal pH did not go below 5.5 throughout batch growth. Butanol was found to dissipate the proton motive force of fermenting C. acetobutylicum cells by decreasing the transmembrane pH gradient, whereas the membrane potential was affected only slightly. In growing cells, the switch from acid to solvent production occurred when the internal undissociated butyric acid concentration reached 13 mM and the total intracellular undissociated acid concentration (acetic plus butyric acids) was at least 40 to 45 mM. Similar values were obtained when cultures were supplemented with 50 mM butyric acid initially or when a phosphate-buffered medium was used instead of an acetate-buffered medium. To measure the induction of the enzymes involved in solvent synthesis, we determined the rates of conversion of butyrate to butanol in growing cells. The rate of butanol formation reached a maximum in the mid-solvent phase, when the butanol concentration was 50 mM. Although more solvent accumulated later, de novo enzyme synthesis decreased and then ceased.
FOOTNOTES
* Corresponding author.
Appl Environ Microbiol. 1986 July; 52(1): 86-91
Copyright © 1986, American Society for Microbiology. All Rights Reserved.
This article has been cited by other articles:
-
Borden, J. R., Papoutsakis, E. T.
(2007). Dynamics of Genomic-Library Enrichment and Identification of Solvent Tolerance Genes for Clostridium acetobutylicum. Appl. Environ. Microbiol.
73: 3061-3068
[Abstract]
[Full Text]
-
Chatterjee, I., Somerville, G. A., Heilmann, C., Sahl, H.-G., Maurer, H. H., Herrmann, M.
(2006). Very Low Ethanol Concentrations Affect the Viability and Growth Recovery in Post-Stationary-Phase Staphylococcus aureus Populations. Appl. Environ. Microbiol.
72: 2627-2636
[Abstract]
[Full Text]
-
Lee, J., Mitchell, W. J., Tangney, M., Blaschek, H. P.
(2005). Evidence for the Presence of an Alternative Glucose Transport System in Clostridium beijerinckii NCIMB 8052 and the Solvent-Hyperproducing Mutant BA101. Appl. Environ. Microbiol.
71: 3384-3387
[Abstract]
[Full Text]
-
Wang, F., Kashket, S., Kashket, E. R.
(2005). Maintenance of {Delta}pH by a butanol-tolerant mutant of Clostridium beijerinckii. Microbiology
151: 607-613
[Abstract]
[Full Text]
-
Zhao, Y., Tomas, C. A., Rudolph, F. B., Papoutsakis, E. T., Bennett, G. N.
(2005). Intracellular Butyryl Phosphate and Acetyl Phosphate Concentrations in Clostridium acetobutylicum and Their Implications for Solvent Formation. Appl. Environ. Microbiol.
71: 530-537
[Abstract]
[Full Text]
-
Desmond, C., Fitzgerald, G. F., Stanton, C., Ross, R. P.
(2004). Improved Stress Tolerance of GroESL-Overproducing Lactococcus lactis and Probiotic Lactobacillus paracasei NFBC 338. Appl. Environ. Microbiol.
70: 5929-5936
[Abstract]
[Full Text]
-
Alsaker, K. V., Spitzer, T. R., Papoutsakis, E. T.
(2004). Transcriptional Analysis of spo0A Overexpression in Clostridium acetobutylicum and Its Effect on the Cell's Response to Butanol Stress. J. Bacteriol.
186: 1959-1971
[Abstract]
[Full Text]
-
Tomas, C. A., Beamish, J., Papoutsakis, E. T.
(2004). Transcriptional Analysis of Butanol Stress and Tolerance in Clostridium acetobutylicum. J. Bacteriol.
186: 2006-2018
[Abstract]
[Full Text]
-
Tomas, C. A., Welker, N. E., Papoutsakis, E. T.
(2003). Overexpression of groESL in Clostridium acetobutylicum Results in Increased Solvent Production and Tolerance, Prolonged Metabolism, and Changes in the Cell's Transcriptional Program. Appl. Environ. Microbiol.
69: 4951-4965
[Abstract]
[Full Text]
-
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]
-
Rao, M., Streur, T. L., Aldwell, F. E., Cook, G. M.
(2001). Intracellular pH regulation by Mycobacterium smegmatis and Mycobacterium bovis BCG. Microbiology
147: 1017-1024
[Abstract]
[Full Text]
-
Desai, R. P., Papoutsakis, E. T.
(1999). Antisense RNA Strategies for Metabolic Engineering of Clostridium acetobutylicum. Appl. Environ. Microbiol.
65: 936-945
[Abstract]
[Full Text]
-
Nair, R. V., Green, E. M., Watson, D. E., Bennett, G. N., Papoutsakis, E. T.
(1999). Regulation of the sol Locus Genes for Butanol and Acetone Formation in Clostridium acetobutylicum ATCC 824 by a Putative Transcriptional Repressor. J. Bacteriol.
181: 319-330
[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]
Copyright © 1986 by the American Society for Microbiology. All rights reserved.