Affiliation:
1. Department of Microbiology, Cornell University, Ithaca, New York 14853
Abstract
ABSTRACT
Methanosarcina barkeri
227 possesses two clusters of genes potentially encoding nitrogenases. We have previously demonstrated that one cluster, called
nif2
, is expressed under molybdenum (Mo)-sufficient conditions, and the deduced amino acid sequences for nitrogenase structural genes in that cluster most closely resemble those for the Mo nitrogenase of the gram-positive eubacterium
Clostridium pasteurianum
. The previously cloned
nifH1
from
M. barkeri
shows phylogenetic relationships with genes encoding components of eubacterial Mo-independent eubacterial alternative nitrogenases and other methanogen nitrogenases. In this study, we cloned and sequenced
nifD1
and part of
nifK1
from
M. barkeri
227. The deduced amino acid sequence encoded by
nifD1
from
M. barkeri
showed great similarity with
vnfD
gene products from vanadium (V) nitrogenases, with an 80% identity at the amino acid level with the
vnfD
gene product from
Anabaena variabilis
. Moreover, there was a small open reading frame located between
nifD1
and
nifK1
with clear homology to
vnfG
, a hallmark of eubacterial alternative nitrogenases. Stimulation of diazotrophic growth of
M. barkeri
227 by V in the absence of Mo was demonstrated. The unusual complement of
nif
genes in
M. barkeri
227, with one cluster resembling that from a gram-positive eubacterium and the other resembling a eubacterial V nitrogenase gene cluster, suggests horizontal genetic transfer of those genes.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
34 articles.
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