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A TonB-dependent receptor regulates antifungal HSAF biosynthesis in Lysobacter

Lysobacter species are Gram-negative bacteria that are emerging as new sources of antibiotics, including HSAF (Heat Stable Antifungal Factor), which was identified from L. enzymogenes with a new mode of action. LesR, a LuxR solo, was recently shown to regulate the HSAF biosynthesis via an unidentifi...

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Autores principales: Wang, Ruping, Xu, Huiyong, Du, Liangcheng, Chou, Shan-Ho, Liu, Hongxia, Liu, Youzhou, Liu, Fengquan, Qian, Guoliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4886534/
https://www.ncbi.nlm.nih.gov/pubmed/27241275
http://dx.doi.org/10.1038/srep26881
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author Wang, Ruping
Xu, Huiyong
Du, Liangcheng
Chou, Shan-Ho
Liu, Hongxia
Liu, Youzhou
Liu, Fengquan
Qian, Guoliang
author_facet Wang, Ruping
Xu, Huiyong
Du, Liangcheng
Chou, Shan-Ho
Liu, Hongxia
Liu, Youzhou
Liu, Fengquan
Qian, Guoliang
author_sort Wang, Ruping
collection PubMed
description Lysobacter species are Gram-negative bacteria that are emerging as new sources of antibiotics, including HSAF (Heat Stable Antifungal Factor), which was identified from L. enzymogenes with a new mode of action. LesR, a LuxR solo, was recently shown to regulate the HSAF biosynthesis via an unidentified mechanism in L. enzymogenes OH11. Here, we used a comparative proteomic approach to identify the LesR targets and found that LesR influenced the expression of 33 proteins belonging to 10 functional groups, with 9 proteins belonging to the TBDR (TonB-Dependent Receptor) family. The fundamental role of bacterial TBDR in nutrient uptake motivates us to explore their potential regulation on HSAF biosynthesis which is also modulated by nutrient condition. Six out of 9 TBDR coding genes were individually in-frame deleted. Phenotypic and gene-expression assays showed that TBDR7, whose level was lower in a strain overexpressing lesR, was involved in regulating HSAF yield. TBDR7 was not involved in the growth, but played a vital role in transcribing the key HSAF biosynthetic gene. Taken together, the current lesR-based proteomic study provides the first report that TBDR7 plays a key role in regulating antibiotic (HSAF) biosynthesis, a function which has never been found for TBDRs in bacteria.
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spelling pubmed-48865342016-06-08 A TonB-dependent receptor regulates antifungal HSAF biosynthesis in Lysobacter Wang, Ruping Xu, Huiyong Du, Liangcheng Chou, Shan-Ho Liu, Hongxia Liu, Youzhou Liu, Fengquan Qian, Guoliang Sci Rep Article Lysobacter species are Gram-negative bacteria that are emerging as new sources of antibiotics, including HSAF (Heat Stable Antifungal Factor), which was identified from L. enzymogenes with a new mode of action. LesR, a LuxR solo, was recently shown to regulate the HSAF biosynthesis via an unidentified mechanism in L. enzymogenes OH11. Here, we used a comparative proteomic approach to identify the LesR targets and found that LesR influenced the expression of 33 proteins belonging to 10 functional groups, with 9 proteins belonging to the TBDR (TonB-Dependent Receptor) family. The fundamental role of bacterial TBDR in nutrient uptake motivates us to explore their potential regulation on HSAF biosynthesis which is also modulated by nutrient condition. Six out of 9 TBDR coding genes were individually in-frame deleted. Phenotypic and gene-expression assays showed that TBDR7, whose level was lower in a strain overexpressing lesR, was involved in regulating HSAF yield. TBDR7 was not involved in the growth, but played a vital role in transcribing the key HSAF biosynthetic gene. Taken together, the current lesR-based proteomic study provides the first report that TBDR7 plays a key role in regulating antibiotic (HSAF) biosynthesis, a function which has never been found for TBDRs in bacteria. Nature Publishing Group 2016-05-31 /pmc/articles/PMC4886534/ /pubmed/27241275 http://dx.doi.org/10.1038/srep26881 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Wang, Ruping
Xu, Huiyong
Du, Liangcheng
Chou, Shan-Ho
Liu, Hongxia
Liu, Youzhou
Liu, Fengquan
Qian, Guoliang
A TonB-dependent receptor regulates antifungal HSAF biosynthesis in Lysobacter
title A TonB-dependent receptor regulates antifungal HSAF biosynthesis in Lysobacter
title_full A TonB-dependent receptor regulates antifungal HSAF biosynthesis in Lysobacter
title_fullStr A TonB-dependent receptor regulates antifungal HSAF biosynthesis in Lysobacter
title_full_unstemmed A TonB-dependent receptor regulates antifungal HSAF biosynthesis in Lysobacter
title_short A TonB-dependent receptor regulates antifungal HSAF biosynthesis in Lysobacter
title_sort tonb-dependent receptor regulates antifungal hsaf biosynthesis in lysobacter
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4886534/
https://www.ncbi.nlm.nih.gov/pubmed/27241275
http://dx.doi.org/10.1038/srep26881
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