[Protein degradation in bacteria: focus on the ClpP protease].

Fumihiro Ishikawa, Michio Homma, Genzoh Tanabe, Takayuki Uchihashi
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Abstract

Proteins in the cells are born (synthesized), work, and die (decomposed). In the life of a protein, its birth is obviously important, but how it dies is equally important in living organisms. Proteases secreted into the outside of cells are used to decompose the external proteins and the degradation products are taken as the nutrients. On the other hand, there are also proteases that decompose unnecessary or harmful proteins which are generated in the cells. In eukaryotes, a large enzyme complex called the proteasome is primarily responsible for degradation of such proteins. Bacteria, which are prokaryotes, have a similar system as the proteasome. We would like to explain the bacterial degradation system of proteins or the death of proteins, which is performed by ATP-dependent protease Clp, with a particular focus on the ClpXP complex, and with an aspect as a target for antibiotics against bacteria.

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[细菌中的蛋白质降解:聚焦 ClpP 蛋白酶】。]
蛋白质在细胞中诞生(合成)、工作和死亡(分解)。在蛋白质的一生中,它的诞生显然很重要,但在生物体内,它如何死亡同样重要。分泌到细胞外的蛋白酶用于分解外部的蛋白质,而降解产物则被当作营养物质。另一方面,也有一些蛋白酶用于分解细胞内产生的不必要或有害的蛋白质。在真核生物中,一种叫做蛋白酶体的大型酶复合物主要负责降解这类蛋白质。属于原核生物的细菌也有一个与蛋白酶体类似的系统。我们想解释一下细菌的蛋白质降解系统或蛋白质死亡系统,它是由依赖 ATP 的蛋白酶 Clp 执行的,尤其侧重于 ClpXP 复合物,并将其作为抗生素对付细菌的一个目标。
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[Protein degradation in bacteria: focus on the ClpP protease]. [Rhodococcus equi infections in humans: an emerging zoonotic pathogen]. [Development of next-generation antimicrobials with unique mechanisms of action]. [Population genetics of enterohemorrhagic Escherichia coli using whole-genome sequencing analyses]. [Research on mechanisms of drug resistance and virulence expression in pathogenic Escherichia coli].
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