Muñoz-Centeno M C, Peciña A, Cejudo F J, Paneque A
Instituto de Bioquímica Vegetal y Fotosíntesis, Universidad de Sevilla-Consejo Superior de Investigaciones Científicas, Spain.
FEBS Lett. 1996 Sep 9;393(1):7-12. doi: 10.1016/0014-5793(96)00843-5.
Nitrogen-fixing Azotobacter chroococcum cells, but not ammonium- or nitrate-grown cells, exhibited two polypeptide components of 22 and 35 kDa, respectively, that we termed P22 and P35. Bidimensional polyacrylamide gel electrophoresis analysis of preparations from N2-fixing cells that had been transferred to nitrate medium and then incubated for 2 h revealed that P22 had shifted to a more acidic part of the gel while P35 did not change its electrophoretic pattern. Using [32P]orthophosphoric acid it could be demonstrated that the shift in mobility of P22 was due to the phosphorylation of the polypeptide dependent on nitrate (nitrite). The A. chroococcum TR1 strain, which is unable to use nitrate as a nitrogen source and displays activities of nitrogenase, nitrate reductase and nitrite reductase, exhibited both polypeptides. In contrast, P22 and P35 were absent from A. chroococcum MCD1, a mutant strain that cannot assimilate nitrate and lacks the nitrate-reducing enzymatic system. The results suggest that P22 could act as a sensor protein for nitrate in A. chroococcum.
固氮的褐球固氮菌细胞,而非以铵盐或硝酸盐培养的细胞,分别展现出两种分子量为22 kDa和35 kDa的多肽组分,我们将其命名为P22和P35。对已转移至硝酸盐培养基并随后培养2小时的固氮细胞制备物进行双向聚丙烯酰胺凝胶电泳分析显示,P22已迁移至凝胶更偏酸性的区域,而P35的电泳图谱未发生变化。使用[32P]正磷酸可以证明,P22迁移率的变化是由于该多肽依赖硝酸盐(亚硝酸盐)发生了磷酸化。无法将硝酸盐用作氮源但具有固氮酶、硝酸盐还原酶和亚硝酸盐还原酶活性的褐球固氮菌TR1菌株,同时展现出这两种多肽。相比之下,不能同化硝酸盐且缺乏硝酸盐还原酶系统的突变菌株褐球固氮菌MCD1中不存在P22和P35。结果表明,P22可能作为褐球固氮菌中硝酸盐的传感蛋白。