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首页> 外文期刊>Journal of Plant Physiology >Nitrogen fixation in transposon mutants from Bradyrhizobium japonicum USDA110 impaired in nitrate reductase
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Nitrogen fixation in transposon mutants from Bradyrhizobium japonicum USDA110 impaired in nitrate reductase

机译:硝酸根还原酶受损的日本慢生根瘤菌USDA110转座子突变体的固氮作用

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摘要

Tn5 transposon mutagenesis was carried out in Bradyrhizobium japonicum strain USDA110 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, N-2 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 N-2 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 N-2 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 5mmol/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 N-2 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.
机译:在日本根瘤菌(Bradyrhizobium japonicum)菌株USDA110中进行了Tn5转座子诱变,以产生有缺陷的突变体。在来自大豆结核的类杆菌中,与野生菌株相比,在成千上万个表达低水平硝酸盐还原酶活性的克隆中,大约有5%的根瘤,N-2固定或硝酸盐还原酶活性比率与野生菌株显着不同。事先检查了Tn5插入,并将突变体分为四个不同的组。这些组中只有一个被命名为AN,其对N-2的固定作用不如野生株有效,这表明固氮酶和NR共有的结构域发生了突变。其余插入物组成功地被结瘤,并且在N-2固定中与野生株一样有效,但是当用NADH或甲基紫精作为电子供体体外测定时,在结节和分离的类细菌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盐还原酶活性的突变体(CC)类型似乎在两个基因中都具有转座因子。仅在那些表达本构活性低的克隆(AN和AE)中观察到硝酸盐诱导的硝酸盐还原酶活性。包括无效的AN组在内的所有组中,类细菌中硝酸盐还原酶的活性均随结节的增长而降低,AN组的结瘤作用受到5mmol / L N的硝酸盐的高度抑制。寄主-品种相互作用似乎影响类细菌中硝酸盐还原酶活性的调节。与野生菌株相比,不受N-2固定影响的类细菌中硝酸盐还原酶活性的全部或部分抑制(CC,AJ和AE组)提高了芽的根瘤对硝酸盐和N产量的抗性。这些观察结果可能表明,提供给类细菌的一些能量被其组成型NRA浪费了。

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