Camacho María, Burgos Araceli, Chamber-Pérez Manuel A
Dpto. Fijación de Nitrógeno, C.I.F.A. Las Torres, Alcalá del Río, E-41200, Sevilla, Spain.
J Plant Physiol. 2003 Apr;160(4):377-86. doi: 10.1078/0176-1617-00647.
Tn5 transposon mutagenesis was carried out in Bradyrhizobium japonicum strain USDA 110 to produce defective mutants. From over one thousand clones expressing low levels of nitrate reductase activity as free-living bacteria, approximately five percent had significantly different ratios of nodulation, N2 fixation or nitrate reductase activity compared to the wild strain when determined in bacteroids from soybean nodules. Tn5 insertions were checked previously and mutants were arranged into four different groups. Only one of these groups, designated AN, was less effective at N2 fixation than the wild strain, suggesting a mutation in a domain shared by nitrogenase and NR. The remaining groups of insertions successfully nodulated and were as effective at N2 fixation as the wild strain, but showed diminished ability to reduce nitrate both in nodules and in the isolated bacteroids when assayed in vitro with NADH or methyl viologen as electron donors. PCR amplification demonstrated that Tn5 insertions took place in different genes on each mutant group and the type of mutant (CC) expressing almost no nitrate reductase activity under all treatments seemed to possess transposable elements in two genes. Induction of nitrate reductase activity by nitrate was observed only in those clones expressing a low constitutive activity (AN and AE). Nitrate reductase activity in bacteroids along nodule growth decreased in all groups including the ineffective AN group, whose nodulation was highly inhibited by nitrate at 5 mmol/L N. Host-cultivar interaction seemed to influence the regulation of nitrate reductase activity in bacteroids. Total or partial repression of nitrate reductase activity in bacteroids unaffected by N2 fixation (CC, AJ and AE groups) improved nodule resistance to nitrate and N yields of shoots over those of the wild strain. These observations may suggest that some of the energy supplied to bacteroids was wasted by its constitutive NRA.
在慢生根瘤菌日本种USDA 110中进行Tn5转座子诱变以产生缺陷型突变体。从超过一千个作为自由生活细菌表达低水平硝酸还原酶活性的克隆中,当在大豆根瘤的类菌体中测定时,约5%的克隆与野生菌株相比,在结瘤、固氮或硝酸还原酶活性方面具有显著不同的比率。先前已检查了Tn5插入情况,并将突变体分为四个不同的组。这些组中只有一组,命名为AN,在固氮方面比野生菌株效率低,这表明在固氮酶和硝酸还原酶共享的结构域中发生了突变。其余插入组成功结瘤,并且在固氮方面与野生菌株一样有效,但当用NADH或甲基紫精作为电子供体在体外测定时,其在根瘤和分离的类菌体中还原硝酸盐的能力减弱。PCR扩增表明,Tn5插入发生在每个突变体组的不同基因中,并且在所有处理下几乎不表达硝酸还原酶活性的突变体类型(CC)似乎在两个基因中具有转座元件。仅在那些组成型活性较低的克隆(AN和AE)中观察到硝酸盐对硝酸还原酶活性的诱导作用。在包括无效的AN组在内的所有组中,随着根瘤生长,类菌体中的硝酸还原酶活性均降低,AN组的结瘤在5 mmol/L N的硝酸盐处理下受到高度抑制。宿主-品种相互作用似乎影响类菌体中硝酸还原酶活性的调节。不受固氮影响的类菌体(CC、AJ和AE组)中硝酸还原酶活性的全部或部分抑制提高了根瘤对硝酸盐的抗性以及地上部的氮产量,超过野生菌株。这些观察结果可能表明,提供给类菌体的一些能量被其组成型硝酸还原酶活性浪费了。