Carbonetti N H, Williams P H
Infect Immun. 1984 Oct;46(1):7-12. doi: 10.1128/iai.46.1.7-12.1984.
The genetic determinants for the aerobactin iron uptake system of plasmid ColV-K30, cloned as recombinant plasmid pABN1, were mapped by insertional inactivation using Tn1000 (gamma delta). Sites of insertion resulting in loss of aerobactin biosynthesis spanned ca. 5.5 kilobase pairs of cloned ColV-K30 DNA contiguous with a 2-kilobase-pair region in which transposon insertion resulted in loss of the outer membrane ferric-aerobactin receptor protein. Translation products of plasmid pABN1, and of subclones specifying siderophore biosynthesis alone or receptor activity alone, were analyzed by using the maxicell and minicell expression system. Four polypeptides (Mr = 62,000, 35,000, 45,000, and 50,000) are required for biosynthesis of aerobactin. A fifth product (Mr = 74,000) of plasmid pABN1 represents the outer membrane receptor protein. The linear order of genes for these polypeptides was determined by comparing translation products of a series of smaller derivative plasmids and of a number of mutant plasmids carrying Tn1000 at known locations.
作为重组质粒pABN1克隆的质粒ColV-K30的气杆菌素铁摄取系统的遗传决定因素,通过使用Tn1000(γδ)进行插入失活来定位。导致气杆菌素生物合成丧失的插入位点跨越约5.5千碱基对的克隆ColV-K30 DNA,与一个2千碱基对区域相邻,在该区域转座子插入导致外膜铁-气杆菌素受体蛋白丧失。使用大细胞和小细胞表达系统分析了质粒pABN1以及仅指定铁载体生物合成或仅指定受体活性的亚克隆的翻译产物。气杆菌素的生物合成需要四种多肽(Mr = 62,000、35,000、45,000和50,000)。质粒pABN1的第五种产物(Mr = 74,000)代表外膜受体蛋白。通过比较一系列较小的衍生质粒和一些在已知位置携带Tn1000的突变质粒的翻译产物,确定了这些多肽的基因线性顺序。