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NAD(+)-dependent HDAC inhibitor stimulates Monascus pigment production but inhibit citrinin
Monascus species are edible fungi due to the production of food colorant and other beneficial compounds. Hence, it has been an attractive thesis to improve their productivities. Increasing numbers of investigations revealed that regulating the activities of histone deacetylases can significantly per...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5568183/ https://www.ncbi.nlm.nih.gov/pubmed/28836182 http://dx.doi.org/10.1186/s13568-017-0467-1 |
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author | Hu, Yan Zhou, Youxiang Mao, Zejing Li, Huihui Chen, Fusheng Shao, Yanchun |
author_facet | Hu, Yan Zhou, Youxiang Mao, Zejing Li, Huihui Chen, Fusheng Shao, Yanchun |
author_sort | Hu, Yan |
collection | PubMed |
description | Monascus species are edible fungi due to the production of food colorant and other beneficial compounds. Hence, it has been an attractive thesis to improve their productivities. Increasing numbers of investigations revealed that regulating the activities of histone deacetylases can significantly perturb secondary metabolites (SM) production at a global level. In this study, dihydrocoumarin (DHC, an inhibitor of the Sirtuin family of NAD(+)-dependent deacetylases) was used to treat Monascus ruber for evaluating its effects on organism growth and SM production. The results revealed that the variation trends of colonial sizes, biomass and mycotoxin were in a dose-dependent manner. Generally, they decreased with the increased DHC concentrations in the designed range. But the variation trend of pigment was different. Comparison of SM profile, three new peaks occurred to the mycelia extractions from DHC-treated strain corresponding to molecular weights 402, 416 and 444, respectively. These three compounds were identified as Monasfluol B, Monascus azaphilone C and acetyl-monasfluol B (a new Monascus chemical pigment structure). In short, DHC can stimulate M. ruber strain to produce more pigment-like polyketides but inhibition of mycotoxin (citrinin). ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13568-017-0467-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5568183 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-55681832017-09-11 NAD(+)-dependent HDAC inhibitor stimulates Monascus pigment production but inhibit citrinin Hu, Yan Zhou, Youxiang Mao, Zejing Li, Huihui Chen, Fusheng Shao, Yanchun AMB Express Original Article Monascus species are edible fungi due to the production of food colorant and other beneficial compounds. Hence, it has been an attractive thesis to improve their productivities. Increasing numbers of investigations revealed that regulating the activities of histone deacetylases can significantly perturb secondary metabolites (SM) production at a global level. In this study, dihydrocoumarin (DHC, an inhibitor of the Sirtuin family of NAD(+)-dependent deacetylases) was used to treat Monascus ruber for evaluating its effects on organism growth and SM production. The results revealed that the variation trends of colonial sizes, biomass and mycotoxin were in a dose-dependent manner. Generally, they decreased with the increased DHC concentrations in the designed range. But the variation trend of pigment was different. Comparison of SM profile, three new peaks occurred to the mycelia extractions from DHC-treated strain corresponding to molecular weights 402, 416 and 444, respectively. These three compounds were identified as Monasfluol B, Monascus azaphilone C and acetyl-monasfluol B (a new Monascus chemical pigment structure). In short, DHC can stimulate M. ruber strain to produce more pigment-like polyketides but inhibition of mycotoxin (citrinin). ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13568-017-0467-1) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2017-08-23 /pmc/articles/PMC5568183/ /pubmed/28836182 http://dx.doi.org/10.1186/s13568-017-0467-1 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 Hu, Yan Zhou, Youxiang Mao, Zejing Li, Huihui Chen, Fusheng Shao, Yanchun NAD(+)-dependent HDAC inhibitor stimulates Monascus pigment production but inhibit citrinin |
title | NAD(+)-dependent HDAC inhibitor stimulates Monascus pigment production but inhibit citrinin |
title_full | NAD(+)-dependent HDAC inhibitor stimulates Monascus pigment production but inhibit citrinin |
title_fullStr | NAD(+)-dependent HDAC inhibitor stimulates Monascus pigment production but inhibit citrinin |
title_full_unstemmed | NAD(+)-dependent HDAC inhibitor stimulates Monascus pigment production but inhibit citrinin |
title_short | NAD(+)-dependent HDAC inhibitor stimulates Monascus pigment production but inhibit citrinin |
title_sort | nad(+)-dependent hdac inhibitor stimulates monascus pigment production but inhibit citrinin |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5568183/ https://www.ncbi.nlm.nih.gov/pubmed/28836182 http://dx.doi.org/10.1186/s13568-017-0467-1 |
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