Suppr超能文献

日本慢生根瘤菌I110共生固氮必需基因的组织与特性分析

Organization and characterization of genes essential for symbiotic nitrogen fixation from Bradyrhizobium japonicum I110.

作者信息

Noti J D, Folkerts O, Turken A N, Szalay A A

出版信息

J Bacteriol. 1986 Sep;167(3):774-83. doi: 10.1128/jb.167.3.774-783.1986.

Abstract

A total of 96 independent Tn5 insertions within a 39-kilobase-pair (kbp) segment of chromosomal DNA containing the three structural genes for nitrogenase (nifH, nifD, and nifK) from Bradyhizobium japonicum I110 were obtained in Escherichia coli and transferred to the wild-type strain by marker exchange. Individual transconjugants containing a Tn5 insertion were inoculated onto Glycine max cv. Wilkin (soybeans) and analyzed for their effect on symbiotic nitrogen fixation. In addition to the three structural genes, genes essential for nitrogen fixation (fix genes) were located in three separate regions: 9 kbp upstream of the nifDK operon; 1.5 kbp downstream of the nifDK operon; 4.5 kbp upstream of nifH. All of the fix::Tn5 insertion strains formed nodules which contained low or undetectable levels of nitrogenase activity. Bacteroids isolated from these nodules had approximately the same levels of the nifDK and nifH transcripts as those detectable from nodules formed by the wild-type strain. Western blot analysis of bacteroid proteins from nodules formed by the fix::Tn5 mutants or the wild-type strain showed the presence of similar levels of the nitrogenase protein subunits. The region upstream of nifH was characterized further by DNA sequence analysis and was shown to contain the nifB gene. The coding sequence of the nifB gene consisted of 1,494 nucleotides and was preceded by putative promoter (5' GTGG-10 base pairs [bp] TTGCA 3') and upstream activator (5' TGT-4 bp-T-5 bp-ACA 3') sequences.

摘要

在大肠杆菌中获得了共96个独立的Tn5插入,这些插入位于日本慢生根瘤菌I110染色体DNA的一个39千碱基对(kbp)片段内,该片段包含固氮酶的三个结构基因(nifH、nifD和nifK),并通过标记交换转移到野生型菌株中。将含有Tn5插入的单个转接合子接种到大豆品种Wilkin(大豆)上,并分析它们对共生固氮的影响。除了这三个结构基因外,固氮必需基因(fix基因)位于三个独立区域:nifDK操纵子上游9 kbp处;nifDK操纵子下游1.5 kbp处;nifH上游4.5 kbp处。所有fix::Tn5插入菌株都形成了根瘤,其中固氮酶活性水平较低或无法检测到。从这些根瘤中分离出的类菌体中nifDK和nifH转录本的水平与野生型菌株形成的根瘤中可检测到的水平大致相同。对fix::Tn5突变体或野生型菌株形成的根瘤中的类菌体蛋白进行蛋白质免疫印迹分析,结果显示固氮酶蛋白亚基的水平相似。通过DNA序列分析进一步对nifH上游区域进行了表征,结果表明该区域包含nifB基因。nifB基因的编码序列由1494个核苷酸组成,其前面是推定的启动子(5' GTGG - 10个碱基对 [bp] TTGCA 3')和上游激活剂(5' TGT - 4 bp - T - 5 bp - ACA 3')序列。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验