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Crotonylation of key metabolic enzymes regulates carbon catabolite repression in Streptomyces roseosporus
Due to the plethora natural products made by Streptomyces, the regulation of its metabolism are of great interest, whereas there is a lack of detailed understanding of the role of posttranslational modifications (PTM) beyond traditional transcriptional regulation. Herein with Streptomyces roseosporu...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7181814/ https://www.ncbi.nlm.nih.gov/pubmed/32332843 http://dx.doi.org/10.1038/s42003-020-0924-2 |
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author | Sun, Chen-Fan Xu, Wei-Feng Zhao, Qing-Wei Luo, Shuai Chen, Xin-Ai Li, Yong-Quan Mao, Xu-Ming |
author_facet | Sun, Chen-Fan Xu, Wei-Feng Zhao, Qing-Wei Luo, Shuai Chen, Xin-Ai Li, Yong-Quan Mao, Xu-Ming |
author_sort | Sun, Chen-Fan |
collection | PubMed |
description | Due to the plethora natural products made by Streptomyces, the regulation of its metabolism are of great interest, whereas there is a lack of detailed understanding of the role of posttranslational modifications (PTM) beyond traditional transcriptional regulation. Herein with Streptomyces roseosporus as a model, we showed that crotonylation is widespread on key enzymes for various metabolic pathways, and sufficient crotonylation in primary metabolism and timely elimination in secondary metabolism are required for proper Streptomyces metabolism. Particularly, the glucose kinase Glk, a keyplayer of carbon catabolite repression (CCR) regulating bacterial metabolism, is identified reversibly crotonylated by the decrotonylase CobB and the crotonyl-transferase Kct1 to negatively control its activity. Furthermore, crotonylation positively regulates CCR for Streptomyces metabolism through modulation of the ratio of glucose uptake/Glk activity and utilization of carbon sources. Thus, our results revealed a regulatory mechanism that crotonylation globally regulates Streptomyces metabolism at least through positive modulation of CCR. |
format | Online Article Text |
id | pubmed-7181814 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-71818142020-04-29 Crotonylation of key metabolic enzymes regulates carbon catabolite repression in Streptomyces roseosporus Sun, Chen-Fan Xu, Wei-Feng Zhao, Qing-Wei Luo, Shuai Chen, Xin-Ai Li, Yong-Quan Mao, Xu-Ming Commun Biol Article Due to the plethora natural products made by Streptomyces, the regulation of its metabolism are of great interest, whereas there is a lack of detailed understanding of the role of posttranslational modifications (PTM) beyond traditional transcriptional regulation. Herein with Streptomyces roseosporus as a model, we showed that crotonylation is widespread on key enzymes for various metabolic pathways, and sufficient crotonylation in primary metabolism and timely elimination in secondary metabolism are required for proper Streptomyces metabolism. Particularly, the glucose kinase Glk, a keyplayer of carbon catabolite repression (CCR) regulating bacterial metabolism, is identified reversibly crotonylated by the decrotonylase CobB and the crotonyl-transferase Kct1 to negatively control its activity. Furthermore, crotonylation positively regulates CCR for Streptomyces metabolism through modulation of the ratio of glucose uptake/Glk activity and utilization of carbon sources. Thus, our results revealed a regulatory mechanism that crotonylation globally regulates Streptomyces metabolism at least through positive modulation of CCR. Nature Publishing Group UK 2020-04-24 /pmc/articles/PMC7181814/ /pubmed/32332843 http://dx.doi.org/10.1038/s42003-020-0924-2 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Sun, Chen-Fan Xu, Wei-Feng Zhao, Qing-Wei Luo, Shuai Chen, Xin-Ai Li, Yong-Quan Mao, Xu-Ming Crotonylation of key metabolic enzymes regulates carbon catabolite repression in Streptomyces roseosporus |
title | Crotonylation of key metabolic enzymes regulates carbon catabolite repression in Streptomyces roseosporus |
title_full | Crotonylation of key metabolic enzymes regulates carbon catabolite repression in Streptomyces roseosporus |
title_fullStr | Crotonylation of key metabolic enzymes regulates carbon catabolite repression in Streptomyces roseosporus |
title_full_unstemmed | Crotonylation of key metabolic enzymes regulates carbon catabolite repression in Streptomyces roseosporus |
title_short | Crotonylation of key metabolic enzymes regulates carbon catabolite repression in Streptomyces roseosporus |
title_sort | crotonylation of key metabolic enzymes regulates carbon catabolite repression in streptomyces roseosporus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7181814/ https://www.ncbi.nlm.nih.gov/pubmed/32332843 http://dx.doi.org/10.1038/s42003-020-0924-2 |
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