Literature DB >> 16239079

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

Luciano F Huergo1, Angela Filipaki, Leda S Chubatsu, M Geoffrey Yates, Maria Berenice Steffens, Fabio O Pedrosa, Emanuel M Souza.   

Abstract

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.

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Year:  2005        PMID: 16239079     DOI: 10.1016/j.femsle.2005.09.026

Source DB:  PubMed          Journal:  FEMS Microbiol Lett        ISSN: 0378-1097            Impact factor:   2.742


  4 in total

1.  Adenosine diphosphate ribosylation of dinitrogenase reductase and adenylylation of glutamine synthetase control ammonia excretion in ethylenediamine-resistant mutants of Azospirillum brasilense Sp7.

Authors:  A Srivastava; A K Tripathi
Journal:  Curr Microbiol       Date:  2006-09-12       Impact factor: 2.188

2.  The nitrogenase regulatory enzyme dinitrogenase reductase ADP-ribosyltransferase (DraT) is activated by direct interaction with the signal transduction protein GlnB.

Authors:  Vivian R Moure; Karamatullah Danyal; Zhi-Yong Yang; Shannon Wendroth; Marcelo Müller-Santos; Fabio O Pedrosa; Marcelo Scarduelli; Edileusa C M Gerhardt; Luciano F Huergo; Emanuel M Souza; Lance C Seefeldt
Journal:  J Bacteriol       Date:  2012-11-09       Impact factor: 3.490

3.  In vitro interactions between the PII proteins and the nitrogenase regulatory enzymes dinitrogenase reductase ADP-ribosyltransferase (DraT) and dinitrogenase reductase-activating glycohydrolase (DraG) in Azospirillum brasilense.

Authors:  Luciano F Huergo; Mike Merrick; Rose A Monteiro; Leda S Chubatsu; Maria B R Steffens; Fábio O Pedrosa; Emanuel M Souza
Journal:  J Biol Chem       Date:  2009-01-08       Impact factor: 5.157

4.  Characterization of the DraT/DraG system for posttranslational regulation of nitrogenase in the endophytic betaproteobacterium Azoarcus sp. strain BH72.

Authors:  Janina Oetjen; Barbara Reinhold-Hurek
Journal:  J Bacteriol       Date:  2009-04-03       Impact factor: 3.490

  4 in total

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