四环素破坏酶:一个新的四环素失活酶家族。

Chemistry & biology Pub Date : 2015-07-23 Epub Date: 2015-06-18 DOI:10.1016/j.chembiol.2015.05.017
Kevin J Forsberg, Sanket Patel, Timothy A Wencewicz, Gautam Dantas
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引用次数: 130

摘要

与使其他天然抗生素失活的酶相比,能够使四环素失活的酶是罕见的。我们描述了一个黄酶家族,以前无法识别为抗性基因,能够降解四环素抗生素。从土壤功能宏基因组选择中,我们发现了9个通过酶失活赋予高水平四环素抗性的基因。我们还证明,第十个酶,人类病原体长滩军团菌的一个未表征的同源物,类似地灭活四环素。这些酶在体外通过已知机制和先前未描述的活性催化四环素的氧化。四环素失活基因在不同的土壤类型中被鉴定出来,包含大量的序列多样性,并且与水平基因转移相关的基因相邻。由于在医院很少观察到四环素失活,这些酶可能填补了病原生物的空白生态位,因此应监测其传播到临床的潜力。
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The Tetracycline Destructases: A Novel Family of Tetracycline-Inactivating Enzymes.

Enzymes capable of inactivating tetracycline are paradoxically rare compared with enzymes that inactivate other natural-product antibiotics. We describe a family of flavoenzymes, previously unrecognizable as resistance genes, which are capable of degrading tetracycline antibiotics. From soil functional metagenomic selections, we discovered nine genes that confer high-level tetracycline resistance by enzymatic inactivation. We also demonstrate that a tenth enzyme, an uncharacterized homolog in the human pathogen Legionella longbeachae, similarly inactivates tetracycline. These enzymes catalyze the oxidation of tetracyclines in vitro both by known mechanisms and via previously undescribed activity. Tetracycline-inactivation genes were identified in diverse soil types, encompass substantial sequence diversity, and are adjacent to genes implicated in horizontal gene transfer. Because tetracycline inactivation is scarcely observed in hospitals, these enzymes may fill an empty niche in pathogenic organisms, and should therefore be monitored for their dissemination potential into the clinic.

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来源期刊
Chemistry & biology
Chemistry & biology 生物-生化与分子生物学
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审稿时长
4-8 weeks
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