Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Yuxi, Qi, Kezong, Jing, Yawei, Zuo, Jiakun, Hu, Jiangang, Lv, Xiaolong, Chen, Zhaoguo, Mi, Rongsheng, Huang, Yan, Yu, Shengqing, Han, Xiangan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
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
_version_ 1783270190236041216
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
work_keys_str_mv AT zhangyuxi lsrbbasedandtemperaturedependentidentificationofbacterialai2receptor
AT qikezong lsrbbasedandtemperaturedependentidentificationofbacterialai2receptor
AT jingyawei lsrbbasedandtemperaturedependentidentificationofbacterialai2receptor
AT zuojiakun lsrbbasedandtemperaturedependentidentificationofbacterialai2receptor
AT hujiangang lsrbbasedandtemperaturedependentidentificationofbacterialai2receptor
AT lvxiaolong lsrbbasedandtemperaturedependentidentificationofbacterialai2receptor
AT chenzhaoguo lsrbbasedandtemperaturedependentidentificationofbacterialai2receptor
AT mirongsheng lsrbbasedandtemperaturedependentidentificationofbacterialai2receptor
AT huangyan lsrbbasedandtemperaturedependentidentificationofbacterialai2receptor
AT yushengqing lsrbbasedandtemperaturedependentidentificationofbacterialai2receptor
AT hanxiangan lsrbbasedandtemperaturedependentidentificationofbacterialai2receptor