Effect of P-II and its homolog GlnK on reversible ADP-ribosylation of dinitrogenase reductase by heterologous expression of the Rhodospirillum rubrumdinitrogenase reductase ADP-ribosyl transferase-dinitrogenase reductase-activating glycohydrolase regulatory system in Klebsiella pneumoniae

Citation
Yp. Zhang et al., Effect of P-II and its homolog GlnK on reversible ADP-ribosylation of dinitrogenase reductase by heterologous expression of the Rhodospirillum rubrumdinitrogenase reductase ADP-ribosyl transferase-dinitrogenase reductase-activating glycohydrolase regulatory system in Klebsiella pneumoniae, J BACT, 183(5), 2001, pp. 1610-1620
Citations number
55
Categorie Soggetti
Microbiology
Journal title
JOURNAL OF BACTERIOLOGY
ISSN journal
00219193 → ACNP
Volume
183
Issue
5
Year of publication
2001
Pages
1610 - 1620
Database
ISI
SICI code
0021-9193(200103)183:5<1610:EOPAIH>2.0.ZU;2-N
Abstract
Reversible ADP-ribosylation of dinitrogenase reductase, catalyzed by the di nitrogenase reductase ADP-ribosyl transferase-dinitrogenase reductase-activ ating 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 gln B 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, Howe ver, the regulation of both DRAT and DRAG activities is altered in a glnB b ackground, Some DRAT escapes regulation and becomes active under N-limiting conditions. The regulation of DRAG activity is also altered in a glnB muta nt, with DRAG being inactivated more slowly in response to NH4+ treatment t han 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 a bolished in the glnK mutant; DRAG remains active even after NH4+ addition, so there is no loss of nitrogenase activity. The results with this heterolo gous expression system have implications for DRAT-DRAG regulation in R. rub rum.