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Title: Structure and regulation of methanogen genes: Progress report, March 1, 1988--February 15, 1989

Technical Report ·
OSTI ID:6378777

The goals of this project were initially to obtain the primary structures of several cloned methanogen genes and subsequently to determine the mechanism(s) by which these genes are transcribed and how their expression is regulated. Studies have focused on both housekeeping genes encoding enzymes involved in the biosynthesis of amino acids (hisA, hisI, argG) and purines (purE) and on methane genes (mcrBDCGA; mvhDGAB) which encode enzymes (methyl coenzyme M reductase, methyl viologen-reducing hydrogenase) directly involved in the biosynthesis of methane. DNA-dependent-RNA-polymerases (RNAPs) have been purified from Methanococcus vannielii and Methanobacterium thermoautotrophicum and used in DNA-binding and footprinting studies to identify promoter sequences. Sites of transcription initiation in vivo have been shown to correlate well with the sites identified in vitro as RNAP binding sites. The mcr and mvh gene clusters contain open-reading frames (ORFs) which presumably encode polypeptides important in methyl reduction (mcrD and mcrC) and hydrogenase (mvhB) activity, which have yet to be identified in methanogenic cells. The mvhB gene appears to encode a new type of electron-transport protein, a poly-ferredoxin. 18 refs., 1 fig.

Research Organization:
Ohio State Univ., Columbus (USA). Dept. of Microbiology
DOE Contract Number:
FG02-87ER13731
OSTI ID:
6378777
Report Number(s):
DOE/ER/13731-T2; ON: DE89008268
Resource Relation:
Other Information: Portions of this document are illegible in microfiche products
Country of Publication:
United States
Language:
English