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Modulating Activity Evaluation of Gut Microbiota with Versatile Toluquinol
Gut microbiota have important implications for health by affecting the metabolism of diet and drugs. However, the specific microbial mediators and their mechanisms in modulating specific key intermediate metabolites from fungal origins still remain largely unclear. Toluquinol, as a key versatile pre...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9505934/ https://www.ncbi.nlm.nih.gov/pubmed/36142608 http://dx.doi.org/10.3390/ijms231810700 |
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author | Zhang, Long-Long Liu, Ya-Jun Chen, Yong-Hong Wu, Zhuang Liu, Bo-Ran Cheng, Qian-Yi Zhang, Ke-Qin Niu, Xue-Mei |
author_facet | Zhang, Long-Long Liu, Ya-Jun Chen, Yong-Hong Wu, Zhuang Liu, Bo-Ran Cheng, Qian-Yi Zhang, Ke-Qin Niu, Xue-Mei |
author_sort | Zhang, Long-Long |
collection | PubMed |
description | Gut microbiota have important implications for health by affecting the metabolism of diet and drugs. However, the specific microbial mediators and their mechanisms in modulating specific key intermediate metabolites from fungal origins still remain largely unclear. Toluquinol, as a key versatile precursor metabolite, is commonly distributed in many fungi, including Penicillium species and their strains for food production. The common 17 gut microbes were cultivated and fed with and without toluquinol. Metabolic analysis revealed that four strains, including the predominant Enterococcus species, could metabolize toluquinol and produce different metabolites. Chemical investigation on large-scale cultures led to isolation of four targeted metabolites and their structures were characterized with NMR, MS, and X-ray diffraction analysis, as four toluquinol derivatives (1–4) through O1/O4-acetyl and C5/C6-methylsulfonyl substitutions, respectively. The four metabolites were first synthesized in living organisms. Further experiments suggested that the rare methylsulfonyl groups in 3–4 were donated from solvent DMSO through Fenton’s reaction. Metabolite 1 displayed the strongest inhibitory effect on cancer cells A549, A2780, and G401 with IC(50) values at 0.224, 0.204, and 0.597 μM, respectively, while metabolite 3 displayed no effect. Our results suggest that the dominant Enterococcus species could modulate potential precursors of fungal origin and change their biological activity. |
format | Online Article Text |
id | pubmed-9505934 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-95059342022-09-24 Modulating Activity Evaluation of Gut Microbiota with Versatile Toluquinol Zhang, Long-Long Liu, Ya-Jun Chen, Yong-Hong Wu, Zhuang Liu, Bo-Ran Cheng, Qian-Yi Zhang, Ke-Qin Niu, Xue-Mei Int J Mol Sci Article Gut microbiota have important implications for health by affecting the metabolism of diet and drugs. However, the specific microbial mediators and their mechanisms in modulating specific key intermediate metabolites from fungal origins still remain largely unclear. Toluquinol, as a key versatile precursor metabolite, is commonly distributed in many fungi, including Penicillium species and their strains for food production. The common 17 gut microbes were cultivated and fed with and without toluquinol. Metabolic analysis revealed that four strains, including the predominant Enterococcus species, could metabolize toluquinol and produce different metabolites. Chemical investigation on large-scale cultures led to isolation of four targeted metabolites and their structures were characterized with NMR, MS, and X-ray diffraction analysis, as four toluquinol derivatives (1–4) through O1/O4-acetyl and C5/C6-methylsulfonyl substitutions, respectively. The four metabolites were first synthesized in living organisms. Further experiments suggested that the rare methylsulfonyl groups in 3–4 were donated from solvent DMSO through Fenton’s reaction. Metabolite 1 displayed the strongest inhibitory effect on cancer cells A549, A2780, and G401 with IC(50) values at 0.224, 0.204, and 0.597 μM, respectively, while metabolite 3 displayed no effect. Our results suggest that the dominant Enterococcus species could modulate potential precursors of fungal origin and change their biological activity. MDPI 2022-09-14 /pmc/articles/PMC9505934/ /pubmed/36142608 http://dx.doi.org/10.3390/ijms231810700 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Zhang, Long-Long Liu, Ya-Jun Chen, Yong-Hong Wu, Zhuang Liu, Bo-Ran Cheng, Qian-Yi Zhang, Ke-Qin Niu, Xue-Mei Modulating Activity Evaluation of Gut Microbiota with Versatile Toluquinol |
title | Modulating Activity Evaluation of Gut Microbiota with Versatile Toluquinol |
title_full | Modulating Activity Evaluation of Gut Microbiota with Versatile Toluquinol |
title_fullStr | Modulating Activity Evaluation of Gut Microbiota with Versatile Toluquinol |
title_full_unstemmed | Modulating Activity Evaluation of Gut Microbiota with Versatile Toluquinol |
title_short | Modulating Activity Evaluation of Gut Microbiota with Versatile Toluquinol |
title_sort | modulating activity evaluation of gut microbiota with versatile toluquinol |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9505934/ https://www.ncbi.nlm.nih.gov/pubmed/36142608 http://dx.doi.org/10.3390/ijms231810700 |
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