双歧杆菌生物荧光标记质粒载体的构建

Q2 Agricultural and Biological Sciences Korean Journal for Food Science of Animal Resources Pub Date : 2018-09-01 Epub Date: 2018-09-30 DOI:10.5851/kosfa.2018.e17
Gi-Seong Moon, Arjan Narbad
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引用次数: 8

摘要

双歧杆菌被认为是我们肠道中最有益的微生物之一。许多关于双歧杆菌的研究都是为了了解它们在肠道中的作用。本研究的目的是为双歧杆菌开发一种生物发光标记质粒载体,以方便其在体外、原位和体内的可视化。用PCR扩增了原从长叶螺旋藻FI10564中分离到的质粒pFI2576复制子(2.0 kb),并将其克隆到pUC19质粒载体(2.68 kb)中。将克隆的复制子亚克隆到pTG262 (luc+)重组质粒载体(7.4 kb)中,将大肠杆菌与乳酸菌穿梭载体pLuc2 (8.5 kb)中的荧光素酶基因(luc+)插入到pTG262质粒载体中。将最终的重组DNA pTG262::pFI2576 rep (luc+)转移到链纹杆菌菌株中。该重组菌株在OD600值为0.352时,相对发光单位为3024个。因此,该重组质粒结构可广泛用于双歧杆菌的标记。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Construction of a Bioluminescent Labelling Plasmid Vector for Bifidobacteria.

Bifidobacterium is recognized as one of the most beneficial microorganisms in our gut. Many researches on bifidobacteria have been done to understand their roles in the gut. The objective of the present study was to develop a bioluminescent labelling plasmid vector for bifidobacteria to facilitate their visualization in vitro, in situ, and in vivo. A plasmid replicon (2.0 kb) of plasmid pFI2576 previously identified from B. longum FI10564 was amplified by PCR and cloned into pUC19 plasmid vector (2.68 kb). The cloned replicon was subcloned into pTG262 (luc+ ) recombinant plasmid vector (7.4 kb) where a luciferase gene (luc+ ) from pLuc2 (8.5 kb), an Escherichia coli and lactobacilli shuttle vector, was inserted into pTG262 plasmid vector. The final recombinant DNA, pTG262::pFI2576 rep (luc+ ), was transferred into a B. catenulatum strain. This recombinant strain showed 3,024 relative luminescence units at OD600 value of 0.352. Thus, this recombinant plasmid construct can be broadly used for labelling bifidobacteria.

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CiteScore
1.22
自引率
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审稿时长
4-8 weeks
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