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霍乱弧菌外膜蛋白W在毕赤酵母中的克隆

Cloning of Vibrio cholerae outer membrane protein W in Pichia pastoris.

作者信息

Alizadeh Javad, Ranjbar Reza, Kamali Mehdi, Farhadi Nima, Davari Amin, Sadeghifard Nourkhoda

机构信息

Molecular Biology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran.

Nanobiotechnology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran.

出版信息

Iran J Microbiol. 2013 Sep;5(3):252-8.

Abstract

BACKGROUND AND OBJECTIVE

The outer membrane protein W (ompW) of Vibrio cholerae is involved in stimulating the immune response via induction of protective immunity. It also plays an important role in bacterial pathogenesis by increasing the adaptability of pathogenic strains. In this study we aimed to clone V. cholerae ompW gene in the strain X-33 of Pichia pastoris.

MATERIALS AND METHODS

A gene encoding ompW was cloned into the Ppicza vector downstream of alcohol oxidase promoter. Then recombinant vector was transformed into the genome of the strain X-33 of P. pastoris. After growth of zeocin-resistant transformants, clones were selected and subsequently confirmed for cloning by PCR enzymatic digestion and sequencing.

RESULTS

PCR, enzymatic digestion and sequencing showed that the ompW gene was correctly cloned into P. pastoris genome.

CONCLUSION

Results of our study showed that the methylotrophic yeast P. pastoris can be considered as an appropriate host instead of mammalian and prokaryotic systems for cloning of ompW. As far as data show, this is the first time that ompW of V. cholera is cloned into the methylotrophic P. pastoris.

摘要

背景与目的

霍乱弧菌外膜蛋白W(ompW)通过诱导保护性免疫参与刺激免疫反应。它还通过提高致病菌株的适应性在细菌致病过程中发挥重要作用。在本研究中,我们旨在将霍乱弧菌ompW基因克隆到毕赤酵母X-33菌株中。

材料与方法

将编码ompW的基因克隆到醇氧化酶启动子下游的Ppicza载体中。然后将重组载体转化到毕赤酵母X-33菌株的基因组中。在筛选出对博来霉素有抗性的转化子后,挑选克隆并随后通过PCR、酶切和测序确认克隆情况。

结果

PCR、酶切和测序表明ompW基因已正确克隆到毕赤酵母基因组中。

结论

我们的研究结果表明,甲基营养型酵母毕赤酵母可被视为用于克隆ompW的合适宿主,而非哺乳动物和原核系统。据现有数据显示,这是首次将霍乱弧菌的ompW克隆到甲基营养型毕赤酵母中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4851/3895563/38b3e1908b0d/IJM-5-252-g001.jpg

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