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荚膜红假单胞菌固氮酶复合物编码结构基因(nifH、D、K)的遗传图谱和物理图谱。

Genetic and physical map of the structural genes (nifH,D,K) coding for the nitrogenase complex of Rhodopseudomonas capsulata.

作者信息

Avtges P, Scolnik P A, Haselkorn R

出版信息

J Bacteriol. 1983 Oct;156(1):251-6. doi: 10.1128/jb.156.1.251-256.1983.

Abstract

Functional genes coding for the structural components of the nitrogenase complex (nifH,D,K) have been cloned on an 11.8-kilobase-pair HindIII fragment of DNA from the photosynthetic bacterium Rhodopseudomonas capsulata. The genes were physically mapped by hybridization of individual cloned nif genes from Klebsiella pneumoniae and Anabaena sp. strain 7120 to Southern blots of HindIII digests of the cloned R. capsulata fragment, after introduction of HindIII sites into the latter at specified locations by insertion of Tn5. Plasmids with the 11.8-kilobase-pair HindIII fragment containing the Tn5 insertions were also used for complementation tests with chromosomal Nif- mutations and for the generation of subfragments to locate those mutations by marker rescue. The R. capsulata nifH,D,K genes comprise a single unit of expression, with the same organization and polarity as found in K. pneumoniae. However, the R. capsulata nifH,D,K fragment did not complement Nif- point mutations in the corresponding Klebsiella genes, and the Klebsiella nif genes did not function in R. capsulata.

摘要

编码固氮酶复合物结构成分(nifH、D、K)的功能基因已被克隆到来自光合细菌荚膜红假单胞菌的一段11.8千碱基对的HindIII DNA片段上。通过将肺炎克雷伯菌和鱼腥藻7120株的单个克隆nif基因与克隆的荚膜红假单胞菌片段的HindIII酶切产物的Southern印迹杂交,对这些基因进行物理定位,此前已通过插入Tn5在特定位置将HindIII位点引入后者。含有Tn5插入片段的11.8千碱基对HindIII片段的质粒也用于与染色体Nif - 突变体的互补试验,并用于产生亚片段以通过标记拯救定位那些突变。荚膜红假单胞菌的nifH、D、K基因构成一个单一的表达单元,其组织和极性与肺炎克雷伯菌中的相同。然而,荚膜红假单胞菌的nifH、D、K片段不能互补肺炎克雷伯菌相应基因中的Nif - 点突变,并且肺炎克雷伯菌的nif基因在荚膜红假单胞菌中不起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7e4/215077/28de49fff357/jbacter00239-0263-a.jpg

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