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LsrB-based and temperature-dependent identification of bacterial AI-2 receptor
The luxS gene is required for autoinducer-2 (AI-2) synthesis in many bacterial species. AI-2 is taken up by a specific receptor to regulate multiple bacterial activities. However, the lack of methods to identify AI-2 receptors has impeded investigations into the roles of AI-2. Here, a luxS mutant of...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5634988/ https://www.ncbi.nlm.nih.gov/pubmed/29019162 http://dx.doi.org/10.1186/s13568-017-0486-y |
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author | Zhang, Yuxi Qi, Kezong Jing, Yawei Zuo, Jiakun Hu, Jiangang Lv, Xiaolong Chen, Zhaoguo Mi, Rongsheng Huang, Yan Yu, Shengqing Han, Xiangan |
author_facet | Zhang, Yuxi Qi, Kezong Jing, Yawei Zuo, Jiakun Hu, Jiangang Lv, Xiaolong Chen, Zhaoguo Mi, Rongsheng Huang, Yan Yu, Shengqing Han, Xiangan |
author_sort | Zhang, Yuxi |
collection | PubMed |
description | The luxS gene is required for autoinducer-2 (AI-2) synthesis in many bacterial species. AI-2 is taken up by a specific receptor to regulate multiple bacterial activities. However, the lack of methods to identify AI-2 receptors has impeded investigations into the roles of AI-2. Here, a luxS mutant of Escherichia coli strain BL21 (DE3) was constructed (named BL21∆luxS), and the recombinant LsrB protein of Salmonella enterica was expressed in BL21∆luxS and BL21 cells, which were named LsrB (BL21∆luxS) and LsrB (BL21), respectively. The results of the activity of recombinant LsrB binding showed that LsrB (BL21) bound to endogenous AI-2 (produced from BL21 strain), while LsrB (BL21∆luxS) did not (as BL21∆luxS cannot produce AI-2). However, the results of recombinant LsrB binding showed that LsrB (BL21∆luxS) can bind exogenous AI-2, which was released from LsrB (BL21∆luxS) at 55 °C for 10 min, while LsrB (BL21) could not bind exogenous AI-2 (due to binding of endogenous AI-2 before). Furthermore, analysis of the thermal stability of AI-2 showed that that AI-2 activity was relatively high at incubation temperatures below 65 °C. These findings will be beneficial for screening of new AI-2 receptors in different bacterial species. |
format | Online Article Text |
id | pubmed-5634988 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-56349882017-10-24 LsrB-based and temperature-dependent identification of bacterial AI-2 receptor Zhang, Yuxi Qi, Kezong Jing, Yawei Zuo, Jiakun Hu, Jiangang Lv, Xiaolong Chen, Zhaoguo Mi, Rongsheng Huang, Yan Yu, Shengqing Han, Xiangan AMB Express Original Article The luxS gene is required for autoinducer-2 (AI-2) synthesis in many bacterial species. AI-2 is taken up by a specific receptor to regulate multiple bacterial activities. However, the lack of methods to identify AI-2 receptors has impeded investigations into the roles of AI-2. Here, a luxS mutant of Escherichia coli strain BL21 (DE3) was constructed (named BL21∆luxS), and the recombinant LsrB protein of Salmonella enterica was expressed in BL21∆luxS and BL21 cells, which were named LsrB (BL21∆luxS) and LsrB (BL21), respectively. The results of the activity of recombinant LsrB binding showed that LsrB (BL21) bound to endogenous AI-2 (produced from BL21 strain), while LsrB (BL21∆luxS) did not (as BL21∆luxS cannot produce AI-2). However, the results of recombinant LsrB binding showed that LsrB (BL21∆luxS) can bind exogenous AI-2, which was released from LsrB (BL21∆luxS) at 55 °C for 10 min, while LsrB (BL21) could not bind exogenous AI-2 (due to binding of endogenous AI-2 before). Furthermore, analysis of the thermal stability of AI-2 showed that that AI-2 activity was relatively high at incubation temperatures below 65 °C. These findings will be beneficial for screening of new AI-2 receptors in different bacterial species. Springer Berlin Heidelberg 2017-10-10 /pmc/articles/PMC5634988/ /pubmed/29019162 http://dx.doi.org/10.1186/s13568-017-0486-y Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Zhang, Yuxi Qi, Kezong Jing, Yawei Zuo, Jiakun Hu, Jiangang Lv, Xiaolong Chen, Zhaoguo Mi, Rongsheng Huang, Yan Yu, Shengqing Han, Xiangan LsrB-based and temperature-dependent identification of bacterial AI-2 receptor |
title | LsrB-based and temperature-dependent identification of bacterial AI-2 receptor |
title_full | LsrB-based and temperature-dependent identification of bacterial AI-2 receptor |
title_fullStr | LsrB-based and temperature-dependent identification of bacterial AI-2 receptor |
title_full_unstemmed | LsrB-based and temperature-dependent identification of bacterial AI-2 receptor |
title_short | LsrB-based and temperature-dependent identification of bacterial AI-2 receptor |
title_sort | lsrb-based and temperature-dependent identification of bacterial ai-2 receptor |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5634988/ https://www.ncbi.nlm.nih.gov/pubmed/29019162 http://dx.doi.org/10.1186/s13568-017-0486-y |
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