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质粒RK2的广宿主特性:编码质粒复制起始蛋白TrfA的重叠基因的重要性。

Broad-host-range properties of plasmid RK2: importance of overlapping genes encoding the plasmid replication initiation protein TrfA.

作者信息

Fang F C, Helinski D R

机构信息

Center for Molecular Genetics, University of California, San Diego, La Jolla 92093-0634.

出版信息

J Bacteriol. 1991 Sep;173(18):5861-8. doi: 10.1128/jb.173.18.5861-5868.1991.

Abstract

The trfA gene, encoding the essential replication initiation protein of the broad-host-range plasmid RK2, possesses an in-frame overlapping arrangement. This results in the production of TrfA proteins of 33 and 44 kDa, respectively. Utilizing deletion and site-specific mutagenesis to alter the trfA operon, we compared the replication of an RK2-origin plasmid in several distantly related gram-negative bacteria when supported by both TrfA-44 and TrfA-33, TrfA-33 alone, or TrfA-44/98L (a mutant form of the TrfA-44 protein) alone. TrfA-44/98L is identical to wild-type TrfA-44 with the exception of a single conservative amino acid alteration from methionine to leucine at codon 98; this alteration removes the translational start codon for the TrfA-33 protein. Copy number and stability were virtually identical for plasmids containing both TrfA-44 and TrfA-33 proteins or TrfA-44/98L alone in Pseudomonas aeruginosa and Agrobacterium tumefaciens, two unrelated bacteria in which TrfA-33 is poorly functional. This, along with recent in vitro studies comparing TrfA-44, TrfA-33, and TrfA-44/98L, suggests that the functional activity of TrfA-44 is not significantly affected by the 98L mutation. Analysis of minimal RK2 derivatives in certain gram-negative bacterial hosts suggests a role of the overlapping arrangement of trfA in facilitating the broad host range of RK2. RK2 derivatives encoding TrfA-44/98L alone demonstrated decreased copy number and stability in Escherichia coli and Azotobacter vinelandii when compared with derivatives specifying both TrfA-44 and TrfA-33. A strategy employing the trfA-44/98L mutant gene and in vivo homologous recombination was used to eliminate the internal translational start codon of trfA in the intact RK2 plasmid. The mutant intact RK2 plasmid produced only TrfA-44/98L. A small reduction in copy number and beta-lactamase expression resulted in E. coli, suggesting that overlapping trfA genes also enhance the efficiency of replication of the intact RK2 plasmid.

摘要

trfA基因编码广宿主范围质粒RK2的必需复制起始蛋白,其具有读码框内重叠排列。这导致分别产生33 kDa和44 kDa的TrfA蛋白。利用缺失和位点特异性诱变来改变trfA操纵子,我们比较了在TrfA - 44和TrfA - 33、单独的TrfA - 33或单独的TrfA - 44/98L(TrfA - 44蛋白的一种突变形式)的支持下,RK2起源质粒在几种远缘革兰氏阴性细菌中的复制情况。TrfA - 44/98L与野生型TrfA - 44相同,只是在第98密码子处有一个从甲硫氨酸到亮氨酸的单一保守氨基酸改变;这种改变去除了TrfA - 33蛋白的翻译起始密码子。在铜绿假单胞菌和根癌土壤杆菌这两种不相关细菌中,单独含有TrfA - 44和TrfA - 33蛋白或单独含有TrfA - 44/98L的质粒的拷贝数和稳定性几乎相同,在这两种细菌中TrfA - 33功能不佳。这一点,连同最近比较TrfA - 44、TrfA - 33和TrfA - 44/98L的体外研究表明,98L突变对TrfA - 44的功能活性没有显著影响。对某些革兰氏阴性细菌宿主中最小RK2衍生物的分析表明,trfA的重叠排列在促进RK2的广泛宿主范围方面发挥作用。与指定同时含有TrfA - 44和TrfA - 33的衍生物相比,单独编码TrfA - 44/98L的RK2衍生物在大肠杆菌和棕色固氮菌中显示出拷贝数和稳定性降低。采用trfA - 44/98L突变基因和体内同源重组的策略来消除完整RK2质粒中trfA的内部翻译起始密码子。突变的完整RK2质粒仅产生TrfA - 44/98L。在大肠杆菌中导致拷贝数和β - 内酰胺酶表达略有降低,表明重叠的trfA基因也提高了完整RK2质粒的复制效率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/399e/208320/56b613ae5f5b/jbacter00108-0279-a.jpg

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