Affiliation:
1. Departments of Bacteriology1 and
2. Biochemistry2 and
3. the Center for the Study of Nitrogen Fixation,3 University of Wisconsin–Madison, Madison, Wisconsin 53706
Abstract
ABSTRACT
Reversible ADP-ribosylation of dinitrogenase reductase, catalyzed by the dinitrogenase reductase ADP-ribosyl transferase–dinitrogenase reductase-activating glycohydrolase (DRAT-DRAG) regulatory system, has been characterized in
Rhodospirillum rubrum
and other nitrogen-fixing bacteria. To investigate the mechanisms for the regulation of DRAT and DRAG activities, we studied the heterologous expression of
R. rubrum draTG
in
Klebsiella pneumoniae glnB
and
glnK
mutants. In
K. pneumoniae
wild type, the regulation of both DRAT and DRAG activity appears to be comparable to that seen in
R. rubrum
. However, the regulation of both DRAT and DRAG activities is altered in a
glnB
background. Some DRAT escapes regulation and becomes active under N-limiting conditions. The regulation of DRAG activity is also altered in a
glnB
mutant, with DRAG being inactivated more slowly in response to NH
4
+
treatment than is seen in wild type, resulting in a high residual nitrogenase activity. In a
glnK
background, the regulation of DRAT activity is similar to that seen in wild type. However, the regulation of DRAG activity is completely abolished in the
glnK
mutant; DRAG remains active even after NH
4
+
addition, so there is no loss of nitrogenase activity. The results with this heterologous expression system have implications for DRAT-DRAG regulation in
R. rubrum
.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
33 articles.
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