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首页> 外文期刊>Angewandte Chemie >Self-Resistance to an Antitumor Antibiotic: A DNA Glycosylase Triggers the Base-Excision Repair System in Yatakemycin Biosynthesis
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Self-Resistance to an Antitumor Antibiotic: A DNA Glycosylase Triggers the Base-Excision Repair System in Yatakemycin Biosynthesis

机译:抗肿瘤抗生素的自我抗性:DNA糖基化酶触发Yatakemycin生物合成中的碱基切除修复系统

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摘要

Most of the antibiotics in clinical use to treat human disease are natural products produced by microorganisms. A general hypothesis is that antibiotic-resistance genes and mechanisms have co-evolved with antibiotic biosynthesis as a self-protection scheme.Nature has evolved three major ways for avoidance of suicide in antibiotic-producing microbes: antibiotic modification, target-protecting enzymes, and export pumps. However, other resistance mechanisms have yet to be discovered, especially for the highly toxic molecules that interrupt basic biological processes (for example DNA, protein, cell-wall biosynthesis).
机译:临床上用于治疗人类疾病的大多数抗生素是微生物产生的天然产物。一个普遍的假设是,抗生素抗性基因和机制与抗生素生物合成共同发展为一种自我保护方案。自然界已经进化出三种主要的方法来避免在生产抗生素的微生物中自杀:抗生素修饰,靶标保护酶和出口泵。然而,还没有发现其他抗性机制,特别是对于中断基本生物学过程(例如DNA,蛋白质,细胞壁生物合成)的高毒性分子。

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