利用计算机建模和点突变破译谷氨酸棒杆菌应激反应sigma因子σD和σH的启动子识别特异性。

IF 3 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
J. Blumenstein, H. Dostálová, L. Rucká, V. Štěpánek, T. Busche, J. Kalinowski, M. Pátek, I. Barvík
{"title":"利用计算机建模和点突变破译谷氨酸棒杆菌应激反应sigma因子σD和σH的启动子识别特异性。","authors":"J. Blumenstein,&nbsp;H. Dostálová,&nbsp;L. Rucká,&nbsp;V. Štěpánek,&nbsp;T. Busche,&nbsp;J. Kalinowski,&nbsp;M. Pátek,&nbsp;I. Barvík","doi":"10.1007/s10822-024-00577-x","DOIUrl":null,"url":null,"abstract":"<div><p>This study aimed to reveal interactions of the stress response sigma subunits (factors) σ<sup>D</sup> and σ<sup>H</sup> of RNA polymerase and promoters in Gram-positive bacterium <i>Corynebacterium glutamicum</i> by combining wet-lab obtained data and in silico modeling. Computer modeling-guided point mutagenesis of <i>C. glutamicum</i> σ<sup>H</sup> subunit led to the creation of a panel of σ<sup>H</sup> variants. Their ability to initiate transcription from naturally occurring hybrid σ<sup>D</sup>/σ<sup>H</sup>-dependent promoter P<i>cg0441</i> and two control canonical promoters (σ<sup>D</sup>-dependent P<i>rsdA</i> and σ<sup>H</sup>-dependent P<i>uvrD3</i>) was measured and interpreted using molecular dynamics simulations of homology models of all complexes. The results led us to design the artificial hybrid promoter P<i>D</i><sub><i>35</i></sub><i>H</i><sub><i>10</i></sub> combining the −10 element of the P<i>uvrD3</i> promoter and the −35 element of the P<i>rsdA</i> promoter. This artificial hybrid promoter P<i>D</i><sub><i>35-rsdA</i></sub><i>H</i><sub><i>10-uvrD3</i></sub> showed almost optimal properties needed for the bio-orthogonal transcription (not interfering with the native biological processes).</p></div>","PeriodicalId":621,"journal":{"name":"Journal of Computer-Aided Molecular Design","volume":"39 1","pages":""},"PeriodicalIF":3.0000,"publicationDate":"2024-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s10822-024-00577-x.pdf","citationCount":"0","resultStr":"{\"title\":\"Promoter recognition specificity of Corynebacterium glutamicum stress response sigma factors σD and σH deciphered using computer modeling and point mutagenesis\",\"authors\":\"J. Blumenstein,&nbsp;H. Dostálová,&nbsp;L. Rucká,&nbsp;V. Štěpánek,&nbsp;T. Busche,&nbsp;J. Kalinowski,&nbsp;M. Pátek,&nbsp;I. Barvík\",\"doi\":\"10.1007/s10822-024-00577-x\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>This study aimed to reveal interactions of the stress response sigma subunits (factors) σ<sup>D</sup> and σ<sup>H</sup> of RNA polymerase and promoters in Gram-positive bacterium <i>Corynebacterium glutamicum</i> by combining wet-lab obtained data and in silico modeling. Computer modeling-guided point mutagenesis of <i>C. glutamicum</i> σ<sup>H</sup> subunit led to the creation of a panel of σ<sup>H</sup> variants. Their ability to initiate transcription from naturally occurring hybrid σ<sup>D</sup>/σ<sup>H</sup>-dependent promoter P<i>cg0441</i> and two control canonical promoters (σ<sup>D</sup>-dependent P<i>rsdA</i> and σ<sup>H</sup>-dependent P<i>uvrD3</i>) was measured and interpreted using molecular dynamics simulations of homology models of all complexes. The results led us to design the artificial hybrid promoter P<i>D</i><sub><i>35</i></sub><i>H</i><sub><i>10</i></sub> combining the −10 element of the P<i>uvrD3</i> promoter and the −35 element of the P<i>rsdA</i> promoter. This artificial hybrid promoter P<i>D</i><sub><i>35-rsdA</i></sub><i>H</i><sub><i>10-uvrD3</i></sub> showed almost optimal properties needed for the bio-orthogonal transcription (not interfering with the native biological processes).</p></div>\",\"PeriodicalId\":621,\"journal\":{\"name\":\"Journal of Computer-Aided Molecular Design\",\"volume\":\"39 1\",\"pages\":\"\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2024-11-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://link.springer.com/content/pdf/10.1007/s10822-024-00577-x.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Computer-Aided Molecular Design\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s10822-024-00577-x\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Computer-Aided Molecular Design","FirstCategoryId":"99","ListUrlMain":"https://link.springer.com/article/10.1007/s10822-024-00577-x","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

本研究旨在通过将湿实验室获得的数据与硅学建模相结合,揭示革兰氏阳性菌谷氨酸棒杆菌(Corynebacterium glutamicum)RNA聚合酶的应激反应sigma亚基(因子)σD和σH与启动子之间的相互作用。计算机建模指导下的谷氨酸棒杆菌σH亚基点突变产生了一系列σH变体。通过对所有复合体的同源模型进行分子动力学模拟,我们测量并解释了它们从天然存在的σD/σH依赖性混合启动子Pcg0441和两个对照规范启动子(σD依赖性PrsdA和σH依赖性PuvrD3)启动转录的能力。这些结果促使我们设计了人工混合启动子 PD35H10,它结合了 PuvrD3 启动子的 -10 元件和 PrsdA 启动子的 -35 元件。这种人工混合启动子 PD35-rsdAH10-uvrD3 几乎表现出了生物正交转录(不干扰原生生物过程)所需的最佳特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Promoter recognition specificity of Corynebacterium glutamicum stress response sigma factors σD and σH deciphered using computer modeling and point mutagenesis

This study aimed to reveal interactions of the stress response sigma subunits (factors) σD and σH of RNA polymerase and promoters in Gram-positive bacterium Corynebacterium glutamicum by combining wet-lab obtained data and in silico modeling. Computer modeling-guided point mutagenesis of C. glutamicum σH subunit led to the creation of a panel of σH variants. Their ability to initiate transcription from naturally occurring hybrid σDH-dependent promoter Pcg0441 and two control canonical promoters (σD-dependent PrsdA and σH-dependent PuvrD3) was measured and interpreted using molecular dynamics simulations of homology models of all complexes. The results led us to design the artificial hybrid promoter PD35H10 combining the −10 element of the PuvrD3 promoter and the −35 element of the PrsdA promoter. This artificial hybrid promoter PD35-rsdAH10-uvrD3 showed almost optimal properties needed for the bio-orthogonal transcription (not interfering with the native biological processes).

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of Computer-Aided Molecular Design
Journal of Computer-Aided Molecular Design 生物-计算机:跨学科应用
CiteScore
8.00
自引率
8.60%
发文量
56
审稿时长
3 months
期刊介绍: The Journal of Computer-Aided Molecular Design provides a form for disseminating information on both the theory and the application of computer-based methods in the analysis and design of molecules. The scope of the journal encompasses papers which report new and original research and applications in the following areas: - theoretical chemistry; - computational chemistry; - computer and molecular graphics; - molecular modeling; - protein engineering; - drug design; - expert systems; - general structure-property relationships; - molecular dynamics; - chemical database development and usage.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信