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首页> 外文期刊>Plasmid: An International Journal Devoted to Extrachromosomal Gene Systems >Characterization of plasmids from human infant Bifidobacterium strains: sequence analysis and construction of E. coli-Bifidobacterium shuttle vectors.
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Characterization of plasmids from human infant Bifidobacterium strains: sequence analysis and construction of E. coli-Bifidobacterium shuttle vectors.

机译:人类婴儿双歧杆菌菌株质粒的表征:大肠杆菌-双歧杆菌穿梭载体的序列分析和构建。

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摘要

A survey of infant fecal Bifidobacterium isolates for plasmid DNA revealed that a significant portion of the strains, 17.6%, carry small plasmids. The majority of plasmid-harboring strains belonged to the Bifidobacterium longum/infantis group. Most of the plasmids could be assigned into two groups based on their sizes and the restriction profiles. Three plasmids, pB44 (3.6 kb) from B. longum, pB80 (4.9 kb) from Bifidobacterium bifidum, and pB21a (5.2kb) from Bifidobacterium breve were sequenced. While the former two plasmids were found to be highly similar to previously characterized rolling-circle replicating pKJ36 and pKJ56, respectively, the third plasmid, pB21a, does not share significant nucleotide homology with known plasmids. However, it might be placed into the pCIBb1-like group of bifidobacterial rolling-plasmids based on the homology of its Rep protein and the overall molecular organization. Two sets of Escherichia coli-Bifidobacterium shuttle vectors constructed based on pB44 and pB80 replicons were capable of transforming B. bifidum and B. breve strains with efficiency up to 3x10(4)cfu/microg DNA. Additionally, an attempt was made to employ a broad host range conjugation element, RP4, in developing of E. coli-Bifidobacterium gene transfer system.
机译:一项针对婴儿粪便双歧杆菌分离株的质粒DNA的调查显示,该菌株的很大一部分(17.6%)带有小质粒。大多数携带质粒的菌株都属于长双歧杆菌/婴儿双歧杆菌组。根据质粒的大小和限制图谱,大多数质粒可分为两组。测序了三个质粒,长双歧杆菌的pB44(3.6 kb),双歧双歧杆菌的pB80(4.9 kb)和短双歧杆菌的pB21a(5.2kb)。虽然发现前两个质粒分别与先前表征的滚环复制pKJ36和pKJ56高度相似,但第三个质粒pB21a与已知质粒没有显着的核苷酸同源性。但是,根据其Rep蛋白的同源性和整体分子结构,可以将其放入双歧杆菌滚动质粒的pCIBb1样组中。基于pB44和pB80复制子构建的两套大肠杆菌-双歧杆菌穿梭载体能够转化双歧双歧杆菌和短双歧杆菌,效率高达3x10(4)cfu / microg DNA。另外,尝试在大肠杆菌-双歧杆菌基因转移系统的开发中采用广泛的宿主范围缀合元件RP4。

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