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通过 LtnI 的生物工程深入了解类细菌素免疫。

Insights into Lantibiotic Immunity Provided by Bioengineering of LtnI.

机构信息

Department of Microbiology, University College Cork, Cork, Ireland.

出版信息

Antimicrob Agents Chemother. 2012 Oct;56(10):5122-33. doi: 10.1128/AAC.00979-12. Epub 2012 Jul 16.

Abstract

The lantibiotic lacticin 3147 has been the focus of much research due to its broad spectrum of activity against many microbial targets, including drug-resistant pathogens. In order to protect itself, a lacticin 3147 producer must possess a cognate immunity mechanism. Lacticin 3147 immunity is provided by an ABC transporter, LtnFE, and a dedicated immunity protein, LtnI, both of which are capable of independently providing a degree of protection. In the study described here, we carried out an in-depth investigation of LtnI structure-function relationships through the creation of a series of fusion proteins and LtnI determinants that have been the subject of random and site-directed mutagenesis. We establish that LtnI is a transmembrane protein that contains a number of individual residues and regions, such as those between amino acids 20 and 27 and amino acids 76 and 83, which are essential for LtnI function. Finally, as a consequence of the screening of a bank of 28,000 strains producing different LtnI derivatives, we identified one variant (LtnI I81V) that provides enhanced protection. To our knowledge, this is the first report of a lantibiotic immunity protein with enhanced functionality.

摘要

由于其对许多微生物靶标(包括耐药病原体)的广泛活性,乳链菌肽 3147 一直是许多研究的焦点。为了保护自身,乳链菌肽 3147 的生产者必须具有同源免疫机制。乳链菌肽 3147 的免疫由 ABC 转运蛋白 LtnFE 和专门的免疫蛋白 LtnI 提供,两者都能够独立提供一定程度的保护。在本研究中,我们通过创建一系列融合蛋白和随机和定点突变的 LtnI 决定簇,对 LtnI 的结构-功能关系进行了深入研究。我们确定 LtnI 是一种跨膜蛋白,包含许多单个残基和区域,例如氨基酸 20 到 27 之间以及氨基酸 76 和 83 之间的区域,这些区域对于 LtnI 功能至关重要。最后,作为对产生不同 LtnI 衍生物的 28000 株菌株库进行筛选的结果,我们鉴定出一种变体(LtnI I81V),它提供了增强的保护作用。据我们所知,这是首例具有增强功能的抗生素免疫蛋白的报告。

相似文献

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Insights into Lantibiotic Immunity Provided by Bioengineering of LtnI.通过 LtnI 的生物工程深入了解类细菌素免疫。
Antimicrob Agents Chemother. 2012 Oct;56(10):5122-33. doi: 10.1128/AAC.00979-12. Epub 2012 Jul 16.

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