Previous Article | Next Article ![]()
J. Bacteriol., 12 1995, 7238-7244, Vol 177, No. 24
J Nolling, TD Pihl and JN Reeve
The mer genes, which encode the coenzyme F420-dependent N5,N10-
methylenetetrahydromethanopterin reductases (CH2 = H4MPT reductases), and
their flanking regions have been cloned from Methanobacterium
thermoautotrophicum delta H and Methanopyrus kandleri and sequenced. The
mer genes have DNA sequences that are 57% identical and encode polypeptides
with amino acid sequences that are 57% identical and 71% similar, with
calculated molecular masses of 33.6 and 37.5 kDa, respectively. In M.
thermoautotrophicum, mer transcription has been shown to initiate 10 bp
upstream from the ATG translation initiating codon and to generate a
monocistronic transcript approximately 1 kb in length. This transcript was
synthesized at all stages of M. thermoautotrophicum delta H growth in batch
cultures but was found to increase in abundance from the earliest stages of
exponential growth, reaching a maximum level at the mid-exponential growth
phase. For comparison, transcription of the ftr gene from M.
thermoautotrophicum delta H that encodes the
formylmethanofuran:tetrahydromethanopterin formyltransferase (A. A.
DiMarco, K. A. Sment, J. Konisky, and R. S. Wolfe, J. Biol. Chem.
265:472-476, 1990) was included in this study. The ftr transcript was found
similarly to be monocistronic and to be approximately 1 kb in length, but,
in contrast to the mer transcript, the ftr transcript was present at
maximum levels at both the early and the mid-exponential growth stages.
Copyright © 1995, American Society for Microbiology
Cloning, sequencing, and growth phase-dependent transcription of the coenzyme F420-dependent N5,N10-methylenetetrahydromethanopterin reductase-encoding genes from Methanobacterium thermoautotrophicum delta H and Methanopyrus kandleri
Department of Microbiology, Ohio State University, Columbus 43210, USA.
This article has been cited by other articles:
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»