Transcriptome Analysis Revealed the Molecular Mechanism of Acetic Acid Increasing Monascus Pigment Production in Monascus ruber CICC41233

The addition of acetic acid to <i>Monascus ruber</i> cultures is usually used to inhibit the growth of heterotrophic bacteria; however, we found that acetic acid also promotes the growth of <i>M. ruber</i> CICC41233, as well as the synthesis of <i>Monascus</i> pigments (MPs). Compared with no acetic acid or HCl addition, the diameter of <i>M. ruber</i> CICC41233 colonies increased significantly under acetic acid conditions. On the sixth day of fermentation, the yield of total pigments in <i>M. ruber</i> increased significantly by 9.97 times (compared with no acetic acid) and 13.9 times (compared with hydrochloric acid). The transcriptomics data showed that the differentially expressed genes between <i>M. ruber</i> with acetic acid and without acetic acid were mainly involved in starch and sucrose metabolism, glycolysis/gluconeogenesis, pyruvate metabolism, TCA cycle, and oxidative phosphorylation, and that these differentially expressed genes were not involved in amino acid metabolism. Gene expression analysis showed that the relative expression levels of MP synthesis genes (<i>MpPKS5</i>, <i>MppA</i>, <i>MpFasB</i>, <i>MppB</i>, <i>MppD</i>, and <i>MppR2</i>) were significantly up-regulated under acetic acid conditions. This study clarified the metabolic mechanism of acetic acid promoting the growth of <i>M. ruber</i> and the synthesis of MPs, which provided some theoretical guidance for the large-scale production of MPs in the industry in future.

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Publication Details

Journal
Journal of Fungi
Published
2025-01-09
DOI
https://doi.org/10.3390/jof11010049
Citations
1
Primary Topic
Microbial Metabolism and Applications
Type
article
Field-Weighted Citation Impact
1.23

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article

Transcriptome Analysis Revealed the Molecular Mechanism of Acetic Acid Increasing Monascus Pigment Production in Monascus ruber CICC41233

Xiaosheng Wu, Chuannan Long, Weiwei Wu, Shilong Wang et al.
1 citations
Journal of Fungi
Microbial Metabolism and Applications
1.23
article

Transcriptome Analysis Revealed the Molecular Mechanism of Acetic Acid Increasing Monascus Pigment Production in Monascus ruber CICC41233

Xiaosheng Wu, Chuannan Long, Weiwei Wu, Shilong Wang, Jingjing Cui, Weiyu Li
article en
1 citations

Abstract

The addition of acetic acid to <i>Monascus ruber</i> cultures is usually used to inhibit the growth of heterotrophic bacteria; however, we found that acetic acid also promotes the growth of <i>M. ruber</i> CICC41233, as well as the synthesis of <i>Monascus</i> pigments (MPs). Compared with no acetic acid or HCl addition, the diameter of <i>M. ruber</i> CICC41233 colonies increased significantly under acetic acid conditions. On the sixth day of fermentation, the yield of total pigments in <i>M. ruber</i> increased significantly by 9.97 times (compared with no acetic acid) and 13.9 times (compared with hydrochloric acid). The transcriptomics data showed that the differentially expressed genes between <i>M. ruber</i> with acetic acid and without acetic acid were mainly involved in starch and sucrose metabolism, glycolysis/gluconeogenesis, pyruvate metabolism, TCA cycle, and oxidative phosphorylation, and that these differentially expressed genes were not involved in amino acid metabolism. Gene expression analysis showed that the relative expression levels of MP synthesis genes (<i>MpPKS5</i>, <i>MppA</i>, <i>MpFasB</i>, <i>MppB</i>, <i>MppD</i>, and <i>MppR2</i>) were significantly up-regulated under acetic acid conditions. This study clarified the metabolic mechanism of acetic acid promoting the growth of <i>M. ruber</i> and the synthesis of MPs, which provided some theoretical guidance for the large-scale production of MPs in the industry in future.

Journal of FungiVol. 11(1)
Jiangxi Science and Technology Normal University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Jiangxi Province
Industry, innovation and infrastructure
Openalex Percentile: Top 26%
Microbial Metabolism and Applications
1.23
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