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首页> 外文期刊>Applied and Environmental Microbiology >Citrate Synthase Mutants of Sinorhizobium fredii USDA257 Form Ineffective Nodules with Aberrant Ultrastructure
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Citrate Synthase Mutants of Sinorhizobium fredii USDA257 Form Ineffective Nodules with Aberrant Ultrastructure

机译:中华根瘤菌USDA257的柠檬酸合酶突变体形成无效的结节,异常的超微结构

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The tricarboxylic acid (TCA) cycle plays an important role in generating the energy required by bacteroids to fix atmospheric nitrogen. Citrate synthase is the first enzyme that controls the entry of carbon into the TCA cycle. We cloned and determined the nucleotide sequence of the gltA gene that encodes citrate synthase in Sinorhizobium fredii USDA257, a symbiont of soybeans (Glycine max [L.] Merr.) and several other legumes. The deduced citrate synthase protein has a molecular weight of 48,198 and exhibits sequence similarity to citrate synthases from several bacterial species, including Sinorhizobium meliloti and Rhizobium tropici. Southern blot analysis revealed that the fast-growing S. fredii strains and Rhizobium sp. strain NGR234 contained a single copy of the gene located in the bacterial chromosome. S. fredii USDA257 gltA mutant HBK-CS1, which had no detectable citrate synthase activity, had diminished nodulation capacity and produced ineffective nodules on soybean. Light and electron microscopy observations revealed that the nodules initiated by HBK-CS1 contained very few bacteroids. The infected cells contained large vacuoles and prominent starch grains. Within the vacuoles, membrane structures that appeared to be reminiscent of disintegrating bacteroids were detected. The citrate synthase mutant had altered cell surface characteristics and produced three times more exopolysaccarides than the wild type produced. A plasmid carrying the USDA257 gltA gene, when introduced into HBK-CS1, was able to restore all of the defects mentioned above. Our results demonstrate that a functional citrate synthase gene of S. fredii USDA257 is essential for efficient soybean nodulation and nitrogen fixation.
机译:三羧酸(TCA)循环在产生类固醇固定大气氮所需的能量方面起着重要作用。柠檬酸合酶是第一个控制碳进入TCA循环的酶。我们克隆并确定了 Sltorhizobium fredii USDA257(大豆的共生体)中编码柠檬酸合酶的 gltA 基因的核苷酸序列( Glycine max [L 。] Merr。)和其他几种豆类。推导的柠檬酸合酶蛋白的分子量为48,198,与来自几种细菌的柠檬酸合酶具有序列相似性,其中包括 Sinorhizobium meliloti tropicrhizobium tropici 。 Southern印迹分析表明,快速生长的 S。 fredii 菌株和 Rhizobium sp.。 NGR234菌株包含位于细菌染色体上的基因的单个副本。 S。 fredii USDA257 gltA 突变体HBK-CS1没有可检测的柠檬酸合酶活性,减少了结瘤能力,并在大豆上产生了无效的结节。光镜和电子显微镜观察表明,由HBK-CS1引发的结节中几乎没有类杆菌。被感染的细胞含有较大的液泡和突出的淀粉粒。在液泡中,检测到似乎使类细菌崩解的膜结构。柠檬酸合酶突变体具有改变的细胞表面特征,其胞外多糖的产量是野生型的三倍。携带USDA257 gltA 基因的质粒被导入HBK-CS1后,能够修复上述所有缺陷。我们的结果证明了 S的功能性柠檬酸盐合酶基因。 fredii USDA257对于有效的大豆结瘤和固氮至关重要。

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