Open AccessEffect of the over‐expression of PII and PZ proteins on the nitrogenase activity of Azospirillum brasilense
Author(s) -
Huergo Luciano F.,
Filipaki Angela,
Chubatsu Leda S.,
Yates M. Geoffrey,
Steffens Maria Berenice,
Pedrosa Fabio O.,
Souza Emanuel M.
Publication year - 2005
Publication title -
fems microbiology letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.899
H-Index - 151
eISSN - 1574-6968
pISSN - 0378-1097
DOI - 10.1016/j.femsle.2005.09.026
Subject(s) - azospirillum brasilense , nitrogenase , biochemistry , biology , adp ribosylation , nitrogen fixation , microbiology and biotechnology , enzyme , bacteria , nad+ kinase , genetics
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 PII 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 PII protein. Using immunoblot analysis we observed that the reduction of nitrogenase activity in cells over‐expressing PII 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 PII 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.