Abstract
A putative hydrogenase (hydA) gene of Clostridium perfringens encodes a protein with strong identity to Clostridium pasteurianum hydrogenase I. Disruption of the hydA gene abolished H2 productivity, confirming its function. A putative butyrate kinase gene (buk) is adjacent to the hydA gene. When cultures were grown in medium with glucose, 1.8-kb hydA and 2.1-kb buk transcripts and a 3.9-kb transcript hybridized with both hydA and buk-probe were detectable in all the exponential growth phases. In medium without glucose, these transcripts were decreased rapidly after the mid-exponential phase. These results suggest that the transcription of these two genes is probably regulated by a similar mechanism in response to glucose availability. Copyright (C) 1999 Federation of European Microbiological Societies.
Original language | English |
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Pages (from-to) | 329-336 |
Number of pages | 8 |
Journal | FEMS Microbiology Letters |
Volume | 181 |
Issue number | 2 |
DOIs | |
Publication status | Published - Dec 15 1999 |
Externally published | Yes |
Keywords
- Clostridium perfringens
- Fermentation
- Gene disruption
- Hydrogen gas
- Hydrogenase
ASJC Scopus subject areas
- Microbiology
- Molecular Biology
- Genetics