Effect of the over-expression of PII and PZ proteins on the nitrogenase activity of Azospirillum brasilense

被引:13
作者
Huergo, LF [1 ]
Filipaki, A [1 ]
Chubatsu, LS [1 ]
Yates, MG [1 ]
Steffens, MB [1 ]
Pedrosa, FO [1 ]
Souza, EM [1 ]
机构
[1] Univ Fed Parana, Dept Biochem & Mol Biol, BR-81531990 Curitiba, Parana, Brazil
关键词
Azospirillum brasilense; PII-like protein; nitrogen fixation regulation; DraT; DraG;
D O I
10.1016/j.femsle.2005.09.026
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The Azospirillum brasilense PII and PZ proteins, encoded by the glnB and glnZ genes respectively, are intracellular transducers of nitrogen levels with distinct functions. The PII protein participates in nif regulation by controlling the activity of the transcriptional regulator NifA. PII is also involved in transducing the prevailing nitrogen levels to the Fe-protein ADP-ribosylation system. PZ regulates negatively ammonium transport and is involved in nitrogenase reactivation. To further investigate the role of PH and PZ in the regulation of nitrogen fixation, broad-host-range plasmids capable of over-expressing the glnB and glnZ genes under control of the ptac promoter were constructed and introduced into A. brasilense. The nitrogenase activity and nitrate-dependent growth was impaired in A. brasilense cells over-expressing the PH protein. Using immunoblot analysis we observed that the reduction of nitrogenase activity in cells over-expressing PH was due to partial ADP-ribosylation of the Fe-protein under derepressing conditions and a reduction in the amount of Fe-protein. These results support the hypothesis that the unmodified PH protein act as a signal to the DraT enzyme to ADP-ribosylate the Fe-protein in response to ammonium shock, and that it also inhibits nif gene expression. In cells over-expressing the PZ protein the nitrogenase reactivation after an ammonium shock was delayed indicating that the PZ protein is involved in regulation of DraG activity. (c) 2005 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:47 / 54
页数:8
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