Bishop P E, Rizzo T M, Bott K F
J Bacteriol. 1985 Apr;162(1):21-8. doi: 10.1128/jb.162.1.21-28.1985.
Two clones which contained nif DNA were isolated from a clone bank of total EcoRI-digested Azotobacter vinelandii DNA. The clones carrying the recombinant plasmids were identified by use of the 32P-labeled 6.2-kilobase (kb) nif insert from pSA30 (which contains the Klebsiella pneumoniae nifK, nifD, and nifH genes) as a hybridization probe. Hybridization analysis with fragments derived from the nif insert of pSA30 showed that the 2.6-kb insert from one of the plasmids (pLB1) contains nifK whereas the 1.4-kb insert from the other plasmid (pLB3) contains nifD. Marker rescue tests using genetic transformation indicated that the 2.6-kb A. vinelandii nif fragment contains the wild-type alleles for the nif-6 and nif-38 mutations carried by Nif- strains UW6 and UW38. The 1.4-kb insert contains the wild-type allele for the nif-10 mutation carried by Nif- strain UW10.
从用EcoRI完全酶切的维涅兰德固氮菌DNA克隆文库中分离出两个含有固氮基因(nif)DNA的克隆。携带重组质粒的克隆通过使用来自pSA30(含有肺炎克雷伯氏菌nifK、nifD和nifH基因)的32P标记的6.2千碱基(kb)nif插入片段作为杂交探针来鉴定。用源自pSA30的nif插入片段的片段进行杂交分析表明,其中一个质粒(pLB1)的2.6-kb插入片段含有nifK,而另一个质粒(pLB3)的1.4-kb插入片段含有nifD。使用基因转化的标记拯救试验表明,2.6-kb的维涅兰德固氮菌nif片段包含Nif-菌株UW6和UW38携带的nif-6和nif-38突变的野生型等位基因。1.4-kb插入片段包含Nif-菌株UW10携带的nif-10突变的野生型等位基因。