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Investigation of phenyllactic acid as a potent tyrosinase inhibitor produced by probiotics
Melanogenesis is responsible for skin pigmentation and the enzymatic browning of foods. Tyrosinases play a major role in melanin synthesis, and many attempts have been made to identify new natural tyrosinase inhibitors, but few have sought to do in microbes. Postbiotics are bioactive compounds produ...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9772785/ https://www.ncbi.nlm.nih.gov/pubmed/36569188 http://dx.doi.org/10.1016/j.crfs.2022.100413 |
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author | Shin, Minhye Truong, Van-Long Lee, Minjee Kim, Donggyu Kim, Myun Soo Cho, Hana Jung, Young Hoon Yang, Jungwoo Jeong, Woo Sik Kim, Younghoon |
author_facet | Shin, Minhye Truong, Van-Long Lee, Minjee Kim, Donggyu Kim, Myun Soo Cho, Hana Jung, Young Hoon Yang, Jungwoo Jeong, Woo Sik Kim, Younghoon |
author_sort | Shin, Minhye |
collection | PubMed |
description | Melanogenesis is responsible for skin pigmentation and the enzymatic browning of foods. Tyrosinases play a major role in melanin synthesis, and many attempts have been made to identify new natural tyrosinase inhibitors, but few have sought to do in microbes. Postbiotics are bioactive compounds produced by the metabolism of probiotics and have been reported to be safe and effective. In this study, we evaluated the tyrosinase inhibitory effects of culture supernatants of probiotics and discovered novel bacterial metabolites that can be used as a potent tyrosinase inhibitor based on metabolomics. Cultures of Bifidobacterium bifidum IDCC 4201 and Lactiplantibacillus plantarum IDCC 3501 showed effective anti-tyrosinase, reduced melanin synthesis, and altered protein expression associated with the melanogenesis pathway. Comparative metabolomics analyses conducted by GC-MS identified metabolites commonly produced by B. bifidum and L. plantarum. Of eight selected metabolites, phenyllactic acid exhibited significant tyrosinase-inhibitory activity. Our findings suggest that applications of probiotic culture supernatants containing high amounts of phenyllactic acid have potential use as anti-melanogenesis agents in food and medicines. |
format | Online Article Text |
id | pubmed-9772785 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-97727852022-12-23 Investigation of phenyllactic acid as a potent tyrosinase inhibitor produced by probiotics Shin, Minhye Truong, Van-Long Lee, Minjee Kim, Donggyu Kim, Myun Soo Cho, Hana Jung, Young Hoon Yang, Jungwoo Jeong, Woo Sik Kim, Younghoon Curr Res Food Sci Research Article Melanogenesis is responsible for skin pigmentation and the enzymatic browning of foods. Tyrosinases play a major role in melanin synthesis, and many attempts have been made to identify new natural tyrosinase inhibitors, but few have sought to do in microbes. Postbiotics are bioactive compounds produced by the metabolism of probiotics and have been reported to be safe and effective. In this study, we evaluated the tyrosinase inhibitory effects of culture supernatants of probiotics and discovered novel bacterial metabolites that can be used as a potent tyrosinase inhibitor based on metabolomics. Cultures of Bifidobacterium bifidum IDCC 4201 and Lactiplantibacillus plantarum IDCC 3501 showed effective anti-tyrosinase, reduced melanin synthesis, and altered protein expression associated with the melanogenesis pathway. Comparative metabolomics analyses conducted by GC-MS identified metabolites commonly produced by B. bifidum and L. plantarum. Of eight selected metabolites, phenyllactic acid exhibited significant tyrosinase-inhibitory activity. Our findings suggest that applications of probiotic culture supernatants containing high amounts of phenyllactic acid have potential use as anti-melanogenesis agents in food and medicines. Elsevier 2022-12-09 /pmc/articles/PMC9772785/ /pubmed/36569188 http://dx.doi.org/10.1016/j.crfs.2022.100413 Text en © 2022 Published by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Shin, Minhye Truong, Van-Long Lee, Minjee Kim, Donggyu Kim, Myun Soo Cho, Hana Jung, Young Hoon Yang, Jungwoo Jeong, Woo Sik Kim, Younghoon Investigation of phenyllactic acid as a potent tyrosinase inhibitor produced by probiotics |
title | Investigation of phenyllactic acid as a potent tyrosinase inhibitor produced by probiotics |
title_full | Investigation of phenyllactic acid as a potent tyrosinase inhibitor produced by probiotics |
title_fullStr | Investigation of phenyllactic acid as a potent tyrosinase inhibitor produced by probiotics |
title_full_unstemmed | Investigation of phenyllactic acid as a potent tyrosinase inhibitor produced by probiotics |
title_short | Investigation of phenyllactic acid as a potent tyrosinase inhibitor produced by probiotics |
title_sort | investigation of phenyllactic acid as a potent tyrosinase inhibitor produced by probiotics |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9772785/ https://www.ncbi.nlm.nih.gov/pubmed/36569188 http://dx.doi.org/10.1016/j.crfs.2022.100413 |
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