Bidirectional Regulation of AdpAch in Controlling the Expression of scnRI and scnRII in the Natamycin Biosynthesis of Streptomyces chattanoogensis L10

AdpA, an AraC/XylS family protein, had been proved as a key regulator for secondary metabolism and morphological differentiation in Streptomyces griseus. Here, we identify AdpAch, an ortholog of AdpA, as a “higher level” pleiotropic regulator of natamycin biosynthesis with bidirectional regulatory a...

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Main Authors: Pin Yu, Qing-Ting Bu, Yi-Li Tang, Xu-Ming Mao, Yong-Quan Li
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-03-01
Series:Frontiers in Microbiology
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fmicb.2018.00316/full
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spelling doaj-f84c7a5a10504623a232dc07442b44122020-11-24T22:26:04ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2018-03-01910.3389/fmicb.2018.00316342689Bidirectional Regulation of AdpAch in Controlling the Expression of scnRI and scnRII in the Natamycin Biosynthesis of Streptomyces chattanoogensis L10Pin Yu0Pin Yu1Pin Yu2Qing-Ting Bu3Qing-Ting Bu4Yi-Li Tang5Yi-Li Tang6Xu-Ming Mao7Xu-Ming Mao8Yong-Quan Li9Yong-Quan Li10Institute of Pharmaceutical Biotechnology, Zhejiang University, Hangzhou, ChinaZhejiang Provincial Key Laboratory for Microbial Biochemistry and Metabolic Engineering, Hangzhou, ChinaCollege of Life Sciences, Zhejiang University, Hangzhou, ChinaInstitute of Pharmaceutical Biotechnology, Zhejiang University, Hangzhou, ChinaZhejiang Provincial Key Laboratory for Microbial Biochemistry and Metabolic Engineering, Hangzhou, ChinaInstitute of Pharmaceutical Biotechnology, Zhejiang University, Hangzhou, ChinaZhejiang Provincial Key Laboratory for Microbial Biochemistry and Metabolic Engineering, Hangzhou, ChinaInstitute of Pharmaceutical Biotechnology, Zhejiang University, Hangzhou, ChinaZhejiang Provincial Key Laboratory for Microbial Biochemistry and Metabolic Engineering, Hangzhou, ChinaInstitute of Pharmaceutical Biotechnology, Zhejiang University, Hangzhou, ChinaZhejiang Provincial Key Laboratory for Microbial Biochemistry and Metabolic Engineering, Hangzhou, ChinaAdpA, an AraC/XylS family protein, had been proved as a key regulator for secondary metabolism and morphological differentiation in Streptomyces griseus. Here, we identify AdpAch, an ortholog of AdpA, as a “higher level” pleiotropic regulator of natamycin biosynthesis with bidirectional regulatory ability in Streptomyces chattanoogensis L10. DNase I footprinting revealed six AdpAch-binding sites in the scnRI–scnRII intergenic region. Further analysis using the xylE reporter gene fused to the scnRI–scnRII intergenic region of mutated binding sites demonstrated that the expression of scnRI and scnRII was under the control of AdpAch. AdpAch showed a bi-stable regulatory ability where it firstly binds to the Site C and Site D to activate the transcription of the two pathway-specific genes, scnRI and scnRII, and then binds to other sites where it acts as an inhibitor. When Site A and Site F were mutated in vivo, the production of natamycin was increased by 21% and 25%, respectively. These findings indicated an autoregulatory mechanism where AdpAch serves as a master switch with bidirectional regulation for natamycin biosynthesis.http://journal.frontiersin.org/article/10.3389/fmicb.2018.00316/fullbidirectional regulationAdpAnatamycin biosynthesisStreptomyces chattanoogensis L10pathway-specific gene
collection DOAJ
language English
format Article
sources DOAJ
author Pin Yu
Pin Yu
Pin Yu
Qing-Ting Bu
Qing-Ting Bu
Yi-Li Tang
Yi-Li Tang
Xu-Ming Mao
Xu-Ming Mao
Yong-Quan Li
Yong-Quan Li
spellingShingle Pin Yu
Pin Yu
Pin Yu
Qing-Ting Bu
Qing-Ting Bu
Yi-Li Tang
Yi-Li Tang
Xu-Ming Mao
Xu-Ming Mao
Yong-Quan Li
Yong-Quan Li
Bidirectional Regulation of AdpAch in Controlling the Expression of scnRI and scnRII in the Natamycin Biosynthesis of Streptomyces chattanoogensis L10
Frontiers in Microbiology
bidirectional regulation
AdpA
natamycin biosynthesis
Streptomyces chattanoogensis L10
pathway-specific gene
author_facet Pin Yu
Pin Yu
Pin Yu
Qing-Ting Bu
Qing-Ting Bu
Yi-Li Tang
Yi-Li Tang
Xu-Ming Mao
Xu-Ming Mao
Yong-Quan Li
Yong-Quan Li
author_sort Pin Yu
title Bidirectional Regulation of AdpAch in Controlling the Expression of scnRI and scnRII in the Natamycin Biosynthesis of Streptomyces chattanoogensis L10
title_short Bidirectional Regulation of AdpAch in Controlling the Expression of scnRI and scnRII in the Natamycin Biosynthesis of Streptomyces chattanoogensis L10
title_full Bidirectional Regulation of AdpAch in Controlling the Expression of scnRI and scnRII in the Natamycin Biosynthesis of Streptomyces chattanoogensis L10
title_fullStr Bidirectional Regulation of AdpAch in Controlling the Expression of scnRI and scnRII in the Natamycin Biosynthesis of Streptomyces chattanoogensis L10
title_full_unstemmed Bidirectional Regulation of AdpAch in Controlling the Expression of scnRI and scnRII in the Natamycin Biosynthesis of Streptomyces chattanoogensis L10
title_sort bidirectional regulation of adpach in controlling the expression of scnri and scnrii in the natamycin biosynthesis of streptomyces chattanoogensis l10
publisher Frontiers Media S.A.
series Frontiers in Microbiology
issn 1664-302X
publishDate 2018-03-01
description AdpA, an AraC/XylS family protein, had been proved as a key regulator for secondary metabolism and morphological differentiation in Streptomyces griseus. Here, we identify AdpAch, an ortholog of AdpA, as a “higher level” pleiotropic regulator of natamycin biosynthesis with bidirectional regulatory ability in Streptomyces chattanoogensis L10. DNase I footprinting revealed six AdpAch-binding sites in the scnRI–scnRII intergenic region. Further analysis using the xylE reporter gene fused to the scnRI–scnRII intergenic region of mutated binding sites demonstrated that the expression of scnRI and scnRII was under the control of AdpAch. AdpAch showed a bi-stable regulatory ability where it firstly binds to the Site C and Site D to activate the transcription of the two pathway-specific genes, scnRI and scnRII, and then binds to other sites where it acts as an inhibitor. When Site A and Site F were mutated in vivo, the production of natamycin was increased by 21% and 25%, respectively. These findings indicated an autoregulatory mechanism where AdpAch serves as a master switch with bidirectional regulation for natamycin biosynthesis.
topic bidirectional regulation
AdpA
natamycin biosynthesis
Streptomyces chattanoogensis L10
pathway-specific gene
url http://journal.frontiersin.org/article/10.3389/fmicb.2018.00316/full
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