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U.S. Department of Energy
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(Genetics of the methanogenic bacterium Methanococcus voltae with attention to genetic control mechanisms): Progress report

Technical Report ·
OSTI ID:6703730
The development of methanogen plasmid gene vectors would be greatly expedited by knowledge of the structure of methanogen transcription and translation signals. This would allow the directed insertion of a gene of choice downstream of the appropriate DNA sequences so as to bring about expression of that gene in the methanogen. The cloning of a Mc. voltae gene which complemented a hisA mutation in both E. coli and S. typhimurium has been reported. Characterization of the cloned gene indicated that both transcription and translation of the methanogen gene were initiated on the cloned methanogen DNA fragment. The methanogen hisA gene was sequenced and its sequence compared to a hisA-complementing gene isolated from Mc. vannielii. These studies demonstrated that each of these genes contained a eubacterial-like ribosome binding site (G-G-T-G) immediately upstream of the translation initiation codon which strongly suggests that methanogen messenger RNA can be recognized and translated by E. coli ribosomes and, perhaps, vice versa. 5 refs.
Research Organization:
Illinois Univ., Urbana (USA). Dept. of Microbiology
DOE Contract Number:
FG02-84ER13241
OSTI ID:
6703730
Report Number(s):
DOE/ER/13241-1; ON: DE87007064
Country of Publication:
United States
Language:
English