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Carbon catabolite regulation of secondary metabolite formation, an old but not well‐established regulatory system

Secondary microbial metabolites have various functions for the producer microorganisms, which allow them to interact and survive in adverse environments. In addition to these functions, other biological activities may have clinical relevance, as diverse as antimicrobial, anticancer and hypocholester...

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Autores principales: Ruiz‐Villafán, Beatriz, Cruz‐Bautista, Rodrigo, Manzo‐Ruiz, Monserrat, Passari, Ajit Kumar, Villarreal‐Gómez, Karen, Rodríguez‐Sanoja, Romina, Sánchez, Sergio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8966007/
https://www.ncbi.nlm.nih.gov/pubmed/33675560
http://dx.doi.org/10.1111/1751-7915.13791
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author Ruiz‐Villafán, Beatriz
Cruz‐Bautista, Rodrigo
Manzo‐Ruiz, Monserrat
Passari, Ajit Kumar
Villarreal‐Gómez, Karen
Rodríguez‐Sanoja, Romina
Sánchez, Sergio
author_facet Ruiz‐Villafán, Beatriz
Cruz‐Bautista, Rodrigo
Manzo‐Ruiz, Monserrat
Passari, Ajit Kumar
Villarreal‐Gómez, Karen
Rodríguez‐Sanoja, Romina
Sánchez, Sergio
author_sort Ruiz‐Villafán, Beatriz
collection PubMed
description Secondary microbial metabolites have various functions for the producer microorganisms, which allow them to interact and survive in adverse environments. In addition to these functions, other biological activities may have clinical relevance, as diverse as antimicrobial, anticancer and hypocholesterolaemic effects. These metabolites are usually formed during the idiophase of growth and have a wide diversity in their chemical structures. Their synthesis is under the impact of the type and concentration of the culture media nutrients. Some of the molecular mechanisms that affect the synthesis of secondary metabolites in bacteria (Gram‐positive and negative) and fungi are partially known. Moreover, all microorganisms have their peculiarities in the control mechanisms of carbon sources, even those belonging to the same genus. This regulatory knowledge is necessary to establish culture conditions and manipulation methods for genetic improvement and product fermentation. As the carbon source is one of the essential nutritional factors for antibiotic production, its study has been imperative both at the industrial and research levels. This review aims to draw the utmost recent advances performed to clarify the molecular mechanisms of the negative effect exerted by the carbon source on the secondary metabolite formation, emphasizing those found in Streptomyces, one of the genera most profitable antibiotic producers.
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spelling pubmed-89660072022-04-05 Carbon catabolite regulation of secondary metabolite formation, an old but not well‐established regulatory system Ruiz‐Villafán, Beatriz Cruz‐Bautista, Rodrigo Manzo‐Ruiz, Monserrat Passari, Ajit Kumar Villarreal‐Gómez, Karen Rodríguez‐Sanoja, Romina Sánchez, Sergio Microb Biotechnol Minireviews Secondary microbial metabolites have various functions for the producer microorganisms, which allow them to interact and survive in adverse environments. In addition to these functions, other biological activities may have clinical relevance, as diverse as antimicrobial, anticancer and hypocholesterolaemic effects. These metabolites are usually formed during the idiophase of growth and have a wide diversity in their chemical structures. Their synthesis is under the impact of the type and concentration of the culture media nutrients. Some of the molecular mechanisms that affect the synthesis of secondary metabolites in bacteria (Gram‐positive and negative) and fungi are partially known. Moreover, all microorganisms have their peculiarities in the control mechanisms of carbon sources, even those belonging to the same genus. This regulatory knowledge is necessary to establish culture conditions and manipulation methods for genetic improvement and product fermentation. As the carbon source is one of the essential nutritional factors for antibiotic production, its study has been imperative both at the industrial and research levels. This review aims to draw the utmost recent advances performed to clarify the molecular mechanisms of the negative effect exerted by the carbon source on the secondary metabolite formation, emphasizing those found in Streptomyces, one of the genera most profitable antibiotic producers. John Wiley and Sons Inc. 2021-03-06 /pmc/articles/PMC8966007/ /pubmed/33675560 http://dx.doi.org/10.1111/1751-7915.13791 Text en © 2021 The Authors. Microbial Biotechnology published by John Wiley & Sons Ltd and Society for Applied Microbiology. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Minireviews
Ruiz‐Villafán, Beatriz
Cruz‐Bautista, Rodrigo
Manzo‐Ruiz, Monserrat
Passari, Ajit Kumar
Villarreal‐Gómez, Karen
Rodríguez‐Sanoja, Romina
Sánchez, Sergio
Carbon catabolite regulation of secondary metabolite formation, an old but not well‐established regulatory system
title Carbon catabolite regulation of secondary metabolite formation, an old but not well‐established regulatory system
title_full Carbon catabolite regulation of secondary metabolite formation, an old but not well‐established regulatory system
title_fullStr Carbon catabolite regulation of secondary metabolite formation, an old but not well‐established regulatory system
title_full_unstemmed Carbon catabolite regulation of secondary metabolite formation, an old but not well‐established regulatory system
title_short Carbon catabolite regulation of secondary metabolite formation, an old but not well‐established regulatory system
title_sort carbon catabolite regulation of secondary metabolite formation, an old but not well‐established regulatory system
topic Minireviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8966007/
https://www.ncbi.nlm.nih.gov/pubmed/33675560
http://dx.doi.org/10.1111/1751-7915.13791
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