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首页> 外文期刊>Science in China. Series C, Life sciences >Cloning and sequencing of nifBHDKENX genes of Paenibacillus massiliensis T7 and its nif promoter analysis
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Cloning and sequencing of nifBHDKENX genes of Paenibacillus massiliensis T7 and its nif promoter analysis

机译:马氏芽孢杆菌T7 nifBHDKENX基因的克隆,序列分析及nif启动子分析

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摘要

A 324 bp of nifH fragment was PCR amplified from Paenibacillus massiliensis T7 using the universal degenerate primers. The PCR-amplified nifH fragment was labeled with DIG and then used as a probe in Southern blot analysis. Southern blot result showed that there were two positive signals, indicating that there might be two copies of nifH in P. massiliensis T7. A total of 10254 bp DNA sequence containing purD and nifBHDKENX was obtained by five rounds of inverse-PCR amplification. The predicted proteins of nifBHDKENX had high homology with those from other nitrogen-fixing bacteria. Only one putative σ~(54)-dependent promoter sequence was detected upstream of the nifB gene and nifBHDKENX were likely to be organized in one operon. Assays of ?-galactosidase activity of P. massiliensis T7PB carrying a nifB-lacZ fusion under different concentrations of NH_4~+ and O_2 showed that the expression of nifB-lacZ was strongly inhibited by O_2.
机译:使用通用简并引物从马氏芽孢杆菌T7 PCR扩增出324 bp的nifH片段。 PCR扩增的nifH片段用DIG标记,然后用作Southern印迹分析的探针。 Southern印迹结果表明,存在两个阳性信号,表明在P. massiliensis T7中可能存在两个拷贝的nifH。通过五轮反向PCR扩增,获得了包含purD和nifBHDKENX的总共10254 bp的DNA序列。 nifBHDKENX的预测蛋白与其他固氮细菌的蛋白具有高度同源性。在nifB基因上游仅检测到一个假定的σ〜(54)依赖性启动子序列,而nifBHDKENX可能在一个操纵子中组织。在不同浓度的NH_4〜+和O_2条件下携带nifB-lacZ融合蛋白的马氏疟原虫T7PB的β-半乳糖苷酶活性检测表明,O_2强烈抑制了nifB-lacZ的表达。

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