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四环素破坏酶:一类新型的四环素失活酶

The Tetracycline Destructases: A Novel Family of Tetracycline-Inactivating Enzymes.

作者信息

Forsberg Kevin J, Patel Sanket, Wencewicz Timothy A, Dantas Gautam

机构信息

Center for Genome Sciences & Systems Biology, Washington University School of Medicine, St. Louis, MO 63108, USA.

Center for Genome Sciences & Systems Biology, Washington University School of Medicine, St. Louis, MO 63108, USA; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63108, USA.

出版信息

Chem Biol. 2015 Jul 23;22(7):888-97. doi: 10.1016/j.chembiol.2015.05.017. Epub 2015 Jun 18.

DOI:10.1016/j.chembiol.2015.05.017
PMID:26097034
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4515146/
Abstract

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.

摘要

与使其他天然产物抗生素失活的酶相比,能够使四环素失活的酶出奇地罕见。我们描述了一类黄素酶,以前未被识别为抗性基因,它们能够降解四环素类抗生素。通过土壤功能宏基因组筛选,我们发现了9个通过酶促失活赋予高水平四环素抗性的基因。我们还证明,第十种酶,即人类病原体长滩军团菌中一个未表征的同源物,同样能使四环素失活。这些酶在体外通过已知机制和以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,并且与涉及水平基因转移的基因相邻。由于在医院中很少观察到四环素失活,这些酶可能在致病生物中填补了一个空白生态位,因此应该监测它们传播到临床的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9bf/4515146/9533c95cdf65/nihms-697506-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9bf/4515146/1ef6d1f0fa91/nihms-697506-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9bf/4515146/95b8c7af2ba4/nihms-697506-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9bf/4515146/d330cc82b2ec/nihms-697506-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9bf/4515146/39c8f7983f2c/nihms-697506-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9bf/4515146/d3ed1bc93b22/nihms-697506-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9bf/4515146/9533c95cdf65/nihms-697506-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9bf/4515146/1ef6d1f0fa91/nihms-697506-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9bf/4515146/95b8c7af2ba4/nihms-697506-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9bf/4515146/d330cc82b2ec/nihms-697506-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9bf/4515146/39c8f7983f2c/nihms-697506-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9bf/4515146/d3ed1bc93b22/nihms-697506-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9bf/4515146/9533c95cdf65/nihms-697506-f0006.jpg

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本文引用的文献

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Binding assays enable discovery of Tet(X) inhibitors that combat tetracycline destructase resistance.结合试验有助于发现对抗四环素破坏酶耐药性的Tet(X)抑制剂。
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The tetracycline resistome is shaped by selection for specific resistance mechanisms by each antibiotic generation.四环素抗性组是由每一代抗生素对特定抗性机制的选择所塑造的。
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