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从……到抗转化乳酸杆菌的接合性DNA转移

Conjugative DNA Transfer From to Transformation-Resistant Lactobacilli.

作者信息

Samperio Sara, Guzmán-Herrador Dolores L, May-Cuz Rigoberto, Martín Maria Cruz, Álvarez Miguel A, Llosa Matxalen

机构信息

Instituto de Biomedicina y Biotecnología de Cantabria (IBBTEC), Universidad de Cantabria-CSIC-SODERCAN, Santander, Spain.

Dairy Research Institute (IPLA-CSIC), Villaviciosa, Spain.

出版信息

Front Microbiol. 2021 Feb 11;12:606629. doi: 10.3389/fmicb.2021.606629. eCollection 2021.

Abstract

Lactic acid bacteria (LAB) belonging to the genus classically known as , recently split into 25 different genera, include many relevant species for the food industry. The well-known properties of lactobacilli as probiotics make them an attractive model also for vaccines and therapeutic proteins delivery in humans. However, scarce tools are available to accomplish genetic modification of these organisms, and most are only suitable for laboratory strains. Here, we test bacterial conjugation as a new tool to introduce genetic modifications into many biotechnologically relevant laboratory and wild type lactobacilli. Using mobilizable shuttle plasmids from a donor carrying either RP4 or R388 conjugative systems, we were able to get transconjugants to all tested strains, including many natural isolates, and to several other genera, including , for which no transformation protocol has been reported. Transconjugants were confirmed by the presence of the and 16S rRNA gene sequencing. Serendipitously, we also found transconjugants into researcher-contaminant . Conjugative DNA transfer from to was previously described, but at very low frequencies. We have purified this recipient strain and used it in standard conjugation assays, confirming that both R388 and RP4 conjugative systems mediate mobilization of plasmids into . This protocol could be assayed to introduce DNA into other Gram-positive microorganisms which are resistant to transformation.

摘要

传统上归为同一属的乳酸菌(LAB),最近已分为25个不同的属,其中包括许多与食品工业相关的物种。众所周知,乳酸杆菌作为益生菌的特性使其成为人类疫苗和治疗性蛋白质递送的有吸引力的模型。然而,用于完成这些生物体基因改造的工具很少,而且大多数仅适用于实验室菌株。在这里,我们测试细菌接合作为一种新工具,将基因改造引入许多与生物技术相关的实验室和野生型乳酸杆菌中。使用来自携带RP4或R388接合系统的供体的可移动穿梭质粒,我们能够获得所有测试菌株的转接合子,包括许多天然分离株,以及其他几个属,包括尚未报道转化方案的属。通过存在和16S rRNA基因测序确认转接合子。偶然地,我们还在研究人员污染的中发现了转接合子。先前已描述了从到的接合性DNA转移,但频率非常低。我们已经纯化了这种受体菌株并将其用于标准接合试验,证实R388和RP4接合系统都介导质粒向的转移。该方案可用于将DNA引入其他对转化有抗性的革兰氏阳性微生物中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ef6/7905204/1e377879fa5f/fmicb-12-606629-g001.jpg

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