植物乳杆菌微细胞的生成和纯化。

IF 2.6 4区 生物学 Q2 MICROBIOLOGY
Journal of Microbiology Pub Date : 2025-05-01 Epub Date: 2025-04-30 DOI:10.71150/jm.2412002
Hyemin Kang, Donghyun Kim, Juhyun Kim
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引用次数: 0

摘要

微细胞是由不规则细胞分裂产生的无核细胞,由于合成生物学的进步,微细胞正在成为有希望的药物传递系统。然而,它们的发展在很大程度上仅限于几种模式细菌,这突出了在替代宿主中探索微型细胞平台的必要性。植物乳杆菌(L. plantarum)是一种公认安全的益生菌,是这种探索的理想候选者。通过质粒介导的同源重组,删除了假定的minD基因,使细胞分裂失活,形成球形小细胞。通过差速离心和过滤分离无核细胞,然后再进行药物处理以完全消除祖细胞。显微镜和流式细胞术分析纯化的样品证实没有祖细胞的DAPI染色。该方案有效地从植物乳杆菌中产生细菌微型细胞,用于各种生物技术应用,包括治疗剂输送。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protocol for the generation and purification of minicells from Lactiplantibacillus plantarum.

Minicells, which are anucleate cells generated by irregular cell division, are emerging as promising drug delivery systems owing to advances in synthetic biology. However, their development is largely limited to a few model bacteria, highlighting the need to explore minicell platforms in alternative hosts. Lactiplantibacillus plantarum (L. plantarum), a probiotic bacterium classified as Generally Recognized as Safe, is an ideal candidate for such exploration. Minicell-producing L. plantarum was engineered by deleting the putative minD gene via plasmid-mediated homologous recombination, which inactivates cell division to form spherical minicells. Anucleate cells were isolated through differential centrifugation and filtration, followed by additional drug treatment to completely eliminate progenitor cells. Microscopy and flow cytometry analyses of the purified sample confirmed the absence of progenitor cells by DAPI staining. This protocol effectively produces bacterial minicells from L. plantarum for use in various biotechnological applications, including therapeutic agent delivery.

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来源期刊
Journal of Microbiology
Journal of Microbiology 生物-微生物学
CiteScore
5.70
自引率
3.30%
发文量
0
审稿时长
3 months
期刊介绍: Publishes papers that deal with research on microorganisms, including archaea, bacteria, yeasts, fungi, microalgae, protozoa, and simple eukaryotic microorganisms. Topics considered for publication include Microbial Systematics, Evolutionary Microbiology, Microbial Ecology, Environmental Microbiology, Microbial Genetics, Genomics, Molecular Biology, Microbial Physiology, Biochemistry, Microbial Pathogenesis, Host-Microbe Interaction, Systems Microbiology, Synthetic Microbiology, Bioinformatics and Virology. Manuscripts dealing with simple identification of microorganism(s), cloning of a known gene and its expression in a microbial host, and clinical statistics will not be considered for publication by JM.
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