Huergo Luciano F, Filipaki Angela, Chubatsu Leda S, Yates M Geoffrey, Steffens Maria Berenice, Pedrosa Fabio O, Souza Emanuel M
Department of Biochemistry and Molecular Biology, Universidade Federal do Paraná, CP 19046, 81531-990, Curitiba, PR, Brazil.
FEMS Microbiol Lett. 2005 Dec 1;253(1):47-54. doi: 10.1016/j.femsle.2005.09.026. Epub 2005 Oct 5.
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.
分别由glnB和glnZ基因编码的巴西固氮螺菌PII和PZ蛋白是具有不同功能的氮水平细胞内传感器。PII蛋白通过控制转录调节因子NifA的活性参与固氮酶调节。PII还参与将主要的氮水平传递至铁蛋白ADP-核糖基化系统。PZ负向调节铵转运并参与固氮酶的再激活。为了进一步研究PII和PZ在固氮调节中的作用,构建了能够在ptac启动子控制下过表达glnB和glnZ基因的广宿主范围质粒,并将其导入巴西固氮螺菌。过表达PII蛋白的巴西固氮螺菌细胞中固氮酶活性和硝酸盐依赖性生长受到损害。通过免疫印迹分析我们观察到,过表达PII的细胞中固氮酶活性的降低是由于在去阻遏条件下铁蛋白的部分ADP-核糖基化以及铁蛋白量的减少。这些结果支持以下假设:未修饰的PII蛋白作为一种信号,使DraT酶在铵冲击时对铁蛋白进行ADP-核糖基化,并且它还抑制固氮酶基因表达。在过表达PZ蛋白的细胞中,铵冲击后的固氮酶再激活延迟,表明PZ蛋白参与DraG活性的调节。