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致病细菌中毒素-抗毒素系统的功能表征

Functional Characterization of the Toxin-Antitoxin System in the Pathogenic Bacterium .

作者信息

Choi Wonho, Yamaguchi Yoshihiro, Park Ji-Young, Park Sang-Hyun, Lee Hyeok-Won, Lim Byung-Kwan, Otto Michael, Inouye Masayori, Yoon Min-Ho, Park Jung-Ho

机构信息

Bio-Evaluation Center, Korea Research Institute of Bioscience and Biotechnology, Cheongju, Chungbuk 28116, Korea.

Pathogen Molecular Genetics Section, Laboratory of Bacteriology, National Institute of Allergy and Infectious Diseases, U.S. National Institutes of Health, Bethesda, MD 20814, USA.

出版信息

Microorganisms. 2021 May 20;9(5):1107. doi: 10.3390/microorganisms9051107.

Abstract

is a pathogen of various plants which transfers its own DNA (T-DNA) to the host plants. It is used for producing genetically modified plants with this ability. To control T-DNA transfer to the right place, toxin-antitoxin (TA) systems of were used to control the target site of transfer without any unintentional targeting. Here, we describe a toxin-antitoxin system, and , in the chromosome of . The toxin in the TA system has 33.3% identity and 45.5% similarity with MazF in . The expression of MazF-at caused cell growth inhibition, while cells with MazF-at co-expressed with MazE-at grew normally. In vivo and in vitro assays revealed that MazF-at inhibited protein synthesis by decreasing the cellular mRNA stability. Moreover, the catalytic residue of MazF-at was determined to be the 24th glutamic acid using site-directed mutagenesis. From the results, we concluded that MazF-at is a type II toxin-antitoxin system and a ribosome-independent endoribonuclease. Here, we characterized a TA system in whose understanding might help to find its physiological function and to develop further applications.

摘要

是多种植物的病原体,它将自身的DNA(T-DNA)转移到宿主植物中。利用这种能力可用于生产转基因植物。为了控制T-DNA转移到正确的位置,利用其毒素-抗毒素(TA)系统来控制转移的靶位点,而不会出现任何意外的靶向作用。在此,我们描述了存在于染色体中的一种毒素-抗毒素系统,即和。该TA系统中的毒素与中的MazF具有33.3%的同一性和45.5%的相似性。MazF-at的表达导致细胞生长抑制,而与MazE-at共表达的细胞则正常生长。体内和体外试验表明,MazF-at通过降低细胞mRNA稳定性来抑制蛋白质合成。此外,利用定点诱变确定MazF-at的催化残基为第24位谷氨酸。根据这些结果,我们得出结论,MazF-at是一种II型毒素-抗毒素系统,也是一种不依赖核糖体的核糖核酸酶。在此,我们对中的一个TA系统进行了表征,对其的了解可能有助于找到其生理功能并开发进一步的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cd1/8160871/a884cbdf5623/microorganisms-09-01107-g001.jpg

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