Affiliation:
1. Nitrogen Fixation Laboratory, John Innes Centre, Norwich NR4 7UH, United Kingdom,1 and
2. Unité de Physiologie Cellulaire, Département des Biotechnologies, Institut Pasteur, 75724 Paris Cedex, France2
Abstract
ABSTRACT
In
Klebsiella pneumoniae
, transcription of the nitrogen fixation (
nif
) genes is regulated in response to molecular oxygen or availability of fixed nitrogen by the coordinated activities of the
nifA
and
nifL
gene products. NifA is a
nif
-specific transcriptional activator, the activity of which is inhibited by interaction with NifL. Nitrogen control of NifL occurs at two levels: transcription of the
nifLA
operon is regulated by the global
ntr
system, and the inhibitory activity of NifL is controlled in response to fixed nitrogen by an unknown factor.
K. pneumoniae
synthesizes two P
II
-like signal transduction proteins, GlnB, which we have previously shown not to be involved in the response of NifL to fixed nitrogen, and the recently identified protein GlnK. We have now cloned the
K. pneumoniae glnK
gene, studied its expression, and shown that a null mutation in
glnK
prevents NifL from responding to the absence of fixed nitrogen, i.e., from relieving the inhibition of NifA activity. Hence, GlnK appears to be involved, directly or indirectly, in NifL-dependent regulation of
nif
gene expression in
K. pneumoniae
. Comparison of the GlnB and GlnK amino acid sequences from six species of proteobacteria identifies five residues (residues 3, 5, 52, 54, and 64) which serve to distinguish the GlnB and GlnK proteins.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
96 articles.
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