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干酪乳杆菌噬菌体 phiadh 介导的高频质粒转导

High-Frequency Plasmid Transduction by Lactobacillus gasseri Bacteriophage phiadh.

机构信息

Departments of Food Science and Microbiology, Southeast Dairy Foods Research Center, North Carolina State University, Raleigh, North Carolina 27695-7624.

出版信息

Appl Environ Microbiol. 1992 Jan;58(1):187-93. doi: 10.1128/aem.58.1.187-193.1992.

Abstract

The temperate bacteriophage phiadh mediates plasmid DNA transduction in Lactobacillus gasseri ADH at frequencies in the range of 10 to 10 transductants per PFU. BglII-generated DNA fragments from phage phiadh were cloned into the BclI site of the transducible plasmid vector pGK12 (4.4 kb). Phage phiadh lysates induced from Lactobacillus lysogens harboring pGK12 or the recombinant plasmids were used to transduce strain ADH to chloramphenicol resistance. The transduction frequencies of recombinant plasmids were 10- to 10-fold higher than that of native pGK12. The increase in frequency generally correlated with the extent of DNA-DNA homology between plasmid and phage DNAs. The highest transduction frequency was obtained with plasmid pTRK170 (6.6 kb), a pGK12 derivative containing the 1.4- and 0.8-kb BglII DNA fragments of phiadh. DNA hybridization analysis of pTRK170-transducing phage particles revealed that pTRK170 had integrated into the phiadh genome, suggesting that recombination between homologous sequences present in phage and plasmid DNAs was responsible for the formation of high-frequency transducing phage particles. Plasmid DNA analysis of 13 transductants containing pTRK170 showed that each had acquired intact plasmids, indicating that in the process of transduction a further recombination step was involved in the resolution of plasmid DNA monomers from the recombinant pTRK170::phiadh molecule. In addition to strain ADH, pTRK170 could be transduced via phiadh to eight different L. gasseri strains, including the neotype strain, F. Gasser 63 AM (ATCC 33323).

摘要

温和噬菌体 phiadh 介导了嗜酸乳杆菌 ADH 中质粒 DNA 的转导,其转导频率在每 PFU 10 到 10 个转导子的范围内。来自噬菌体 phiadh 的 BglII 生成的 DNA 片段被克隆到可转导质粒载体 pGK12(4.4kb)的 BclI 位点中。从携带 pGK12 或重组质粒的噬菌体溶源菌中诱导的噬菌体 phiadh 裂解物被用于将 ADH 菌株转导为氯霉素抗性。重组质粒的转导频率比天然 pGK12 高 10 到 100 倍。频率的增加通常与质粒和噬菌体 DNA 之间的 DNA-DNA 同源性程度相关。获得的最高转导频率来自质粒 pTRK170(6.6kb),它是 pGK12 的衍生物,包含 phiadh 的 1.4 和 0.8kb BglII DNA 片段。pTRK170 转导噬菌体颗粒的 DNA 杂交分析表明,pTRK170 已整合到 phiadh 基因组中,这表明噬菌体和质粒 DNA 中同源序列之间的重组是形成高频转导噬菌体颗粒的原因。含有 pTRK170 的 13 个转导子的质粒 DNA 分析表明,每个转导子都获得了完整的质粒,这表明在转导过程中,进一步的重组步骤涉及到从重组 pTRK170::phiadh 分子中分离质粒 DNA 单体。除了 ADH 菌株外,pTRK170 还可以通过 phiadh 转导到包括新的模式菌株 F. Gasser 63 AM(ATCC 33323)在内的 8 种不同的嗜酸乳杆菌菌株中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39b2/195190/151739e3a732/aem00042-0211-a.jpg

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