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新型遗传模块可在益生菌乳杆菌中实现高水平抗生素蛋白表达。

Novel genetic modules encoding high-level antibiotic-free protein expression in probiotic lactobacilli.

机构信息

Bioprogrammable Materials, INM - Leibniz Institute for New Materials, Saarbrücken, Germany.

出版信息

Microb Biotechnol. 2023 Jun;16(6):1264-1276. doi: 10.1111/1751-7915.14228. Epub 2023 Feb 1.

DOI:10.1111/1751-7915.14228
PMID:36722614
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10221531/
Abstract

Lactobacilli are ubiquitous in nature, often beneficially associated with animals as commensals and probiotics, and are extensively used in food fermentation. Due to this close-knit association, there is considerable interest to engineer them for healthcare applications in both humans and animals, for which high-performance and versatile genetic parts are greatly desired. For the first time, we describe two genetic modules in Lactiplantibacillus plantarum that achieve high-level gene expression using plasmids that can be retained without antibiotics, bacteriocins or genomic manipulations. These include (i) a promoter, P , from a phylogenetically distant bacterium, Salmonella typhimurium, which drives up to 5-fold higher level of gene expression compared to previously reported promoters and (ii) multiple toxin-antitoxin systems as a self-contained and easy-to-implement plasmid retention strategy that facilitates the engineering of tuneable transient genetically modified organisms. These modules and the fundamental factors underlying their functionality that are described in this work will greatly contribute to expanding the genetic programmability of lactobacilli for healthcare applications.

摘要

乳杆菌在自然界中无处不在,通常作为共生菌和益生菌与动物有益地相关联,并广泛用于食品发酵。由于这种紧密的联系,人们对将其用于人类和动物的医疗保健应用非常感兴趣,因为人们非常希望获得高性能和多功能的遗传元件。我们首次在植物乳杆菌中描述了两个遗传模块,它们使用可以在没有抗生素、细菌素或基因组操作的情况下保留的质粒来实现高水平的基因表达。这些包括 (i) 来自亲缘关系较远的细菌鼠伤寒沙门氏菌的启动子 P ,与以前报道的启动子相比,其基因表达水平提高了 5 倍以上,以及 (ii) 多种毒素-抗毒素系统作为一种自成一体且易于实施的质粒保留策略,可促进可调节的瞬时基因修饰生物体的工程设计。这些模块及其功能的基本因素在这项工作中进行了描述,将极大地有助于扩展乳杆菌在医疗保健应用中的遗传可编程性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8da/10221531/356a3c602c7f/MBT2-16-1264-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8da/10221531/8961d2c961a4/MBT2-16-1264-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8da/10221531/bae66d273e92/MBT2-16-1264-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8da/10221531/d96834dcf8ea/MBT2-16-1264-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8da/10221531/356a3c602c7f/MBT2-16-1264-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8da/10221531/8961d2c961a4/MBT2-16-1264-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8da/10221531/bae66d273e92/MBT2-16-1264-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8da/10221531/d96834dcf8ea/MBT2-16-1264-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8da/10221531/356a3c602c7f/MBT2-16-1264-g005.jpg

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