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Production of a selective antibacterial fatty acid against Staphylococcus aureus by Bifidobacterium strains
Aims: C16 monounsaturated fatty acid (C16:1) show antibacterial activity against Staphylococcus aureus, a pathogen associated with various diseases such as atopic dermatitis and bacteremia, while the compound does not exhibit antibacterial activity against Staphylococcus epidermidis, an epidermal co...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
OAE Publishing Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10688799/ https://www.ncbi.nlm.nih.gov/pubmed/38045611 http://dx.doi.org/10.20517/mrr.2022.24 |
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author | Kikukawa, Hiroshi Nagao, Toshihiro Ota, Mitsuki Takashima, Shigeo Kitaguchi, Kohji Yanase, Emiko Maeda, Sadatoshi Hara, Kiyotaka Y. |
author_facet | Kikukawa, Hiroshi Nagao, Toshihiro Ota, Mitsuki Takashima, Shigeo Kitaguchi, Kohji Yanase, Emiko Maeda, Sadatoshi Hara, Kiyotaka Y. |
author_sort | Kikukawa, Hiroshi |
collection | PubMed |
description | Aims: C16 monounsaturated fatty acid (C16:1) show antibacterial activity against Staphylococcus aureus, a pathogen associated with various diseases such as atopic dermatitis and bacteremia, while the compound does not exhibit antibacterial activity against Staphylococcus epidermidis, an epidermal commensal that inhibits the growth of S. aureus. In this study, we aimed to find bifidobacterial strains with the ability to produce C16:1 and to find a practical manner to utilize C16:1-producing strains in industry. Methods: Various Bifidobacterium strains were screened for their content of C16:1. The chemical identity of C16:1 produced by a selected strain was analyzed by gas chromatography-mass spectrometry (GC-MS) and liquid chromatography-mass spectrometry (LC-MS). Medium components that affect the C16:1 content of the selected strain were investigated. Antibacterial activity against staphylococci was compared between the authentic C16:1 isomers and total fatty acids (TFA) extracted from the selected strain. Results: B. adolescentis 12451, B. adolescentis 12-111, B. boum JCM 1211, and Bifidobacterium sp. JCM 7042 showed high C16:1 content among the tested strains. TFA extracted from Bifidobacterium sp. JCM 7042 contained C16:1 at 2.3% as the fatty acid constituent (2.4 mg/L of broth). Through GC-MS and LC-MS analyses, the C16:1 synthesized by Bifidobacterium sp. JCM 7042 was identified as 7-cis-hexadecenoic acid (7-cis-C16:1). The authentic 7-cis-C16:1 showed strong and selective antibacterial activity against S. aureus, similar to 6-cis-C16:1, with a minimum inhibitory concentration (MIC) of < 10 µg/mL. Components that increase C16:1 productivity were not found in the MRS and TOS media; however, Tween 80 was shown to considerably reduce the C16:1 ratio in TFA. Antibacterial activity against S. aureus was observed when the TFA extracted from Bifidobacterium sp. JCM 7042 contained high level of 7-cis-C16:1 (6.1% in TFA) but not when it contained low level of 7-cis-C16:1 (0.1% in TFA). Conclusion: The fatty acid, 7-cis-C16:1, which can selectively inhibit the S. aureus growth, is accumulated in TFA of several bifidobacteria. The TFA extracted from cultured cells of Bifidobacterium sp. JCM 7042 demonstrated antibacterial activity. From a practical viewpoint, our findings are important for developing an efficient method to produce novel skin care cosmetics, functional dairy foods, and other commodities. |
format | Online Article Text |
id | pubmed-10688799 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | OAE Publishing Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106887992023-12-02 Production of a selective antibacterial fatty acid against Staphylococcus aureus by Bifidobacterium strains Kikukawa, Hiroshi Nagao, Toshihiro Ota, Mitsuki Takashima, Shigeo Kitaguchi, Kohji Yanase, Emiko Maeda, Sadatoshi Hara, Kiyotaka Y. Microbiome Res Rep Original Article Aims: C16 monounsaturated fatty acid (C16:1) show antibacterial activity against Staphylococcus aureus, a pathogen associated with various diseases such as atopic dermatitis and bacteremia, while the compound does not exhibit antibacterial activity against Staphylococcus epidermidis, an epidermal commensal that inhibits the growth of S. aureus. In this study, we aimed to find bifidobacterial strains with the ability to produce C16:1 and to find a practical manner to utilize C16:1-producing strains in industry. Methods: Various Bifidobacterium strains were screened for their content of C16:1. The chemical identity of C16:1 produced by a selected strain was analyzed by gas chromatography-mass spectrometry (GC-MS) and liquid chromatography-mass spectrometry (LC-MS). Medium components that affect the C16:1 content of the selected strain were investigated. Antibacterial activity against staphylococci was compared between the authentic C16:1 isomers and total fatty acids (TFA) extracted from the selected strain. Results: B. adolescentis 12451, B. adolescentis 12-111, B. boum JCM 1211, and Bifidobacterium sp. JCM 7042 showed high C16:1 content among the tested strains. TFA extracted from Bifidobacterium sp. JCM 7042 contained C16:1 at 2.3% as the fatty acid constituent (2.4 mg/L of broth). Through GC-MS and LC-MS analyses, the C16:1 synthesized by Bifidobacterium sp. JCM 7042 was identified as 7-cis-hexadecenoic acid (7-cis-C16:1). The authentic 7-cis-C16:1 showed strong and selective antibacterial activity against S. aureus, similar to 6-cis-C16:1, with a minimum inhibitory concentration (MIC) of < 10 µg/mL. Components that increase C16:1 productivity were not found in the MRS and TOS media; however, Tween 80 was shown to considerably reduce the C16:1 ratio in TFA. Antibacterial activity against S. aureus was observed when the TFA extracted from Bifidobacterium sp. JCM 7042 contained high level of 7-cis-C16:1 (6.1% in TFA) but not when it contained low level of 7-cis-C16:1 (0.1% in TFA). Conclusion: The fatty acid, 7-cis-C16:1, which can selectively inhibit the S. aureus growth, is accumulated in TFA of several bifidobacteria. The TFA extracted from cultured cells of Bifidobacterium sp. JCM 7042 demonstrated antibacterial activity. From a practical viewpoint, our findings are important for developing an efficient method to produce novel skin care cosmetics, functional dairy foods, and other commodities. OAE Publishing Inc. 2023-02-22 /pmc/articles/PMC10688799/ /pubmed/38045611 http://dx.doi.org/10.20517/mrr.2022.24 Text en © The Author(s) 2023. https://creativecommons.org/licenses/by/4.0/© The Author(s) 2023. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, sharing, adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as long as 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 Kikukawa, Hiroshi Nagao, Toshihiro Ota, Mitsuki Takashima, Shigeo Kitaguchi, Kohji Yanase, Emiko Maeda, Sadatoshi Hara, Kiyotaka Y. Production of a selective antibacterial fatty acid against Staphylococcus aureus by Bifidobacterium strains |
title | Production of a selective antibacterial fatty acid against Staphylococcus aureus by Bifidobacterium strains |
title_full | Production of a selective antibacterial fatty acid against Staphylococcus aureus by Bifidobacterium strains |
title_fullStr | Production of a selective antibacterial fatty acid against Staphylococcus aureus by Bifidobacterium strains |
title_full_unstemmed | Production of a selective antibacterial fatty acid against Staphylococcus aureus by Bifidobacterium strains |
title_short | Production of a selective antibacterial fatty acid against Staphylococcus aureus by Bifidobacterium strains |
title_sort | production of a selective antibacterial fatty acid against staphylococcus aureus by bifidobacterium strains |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10688799/ https://www.ncbi.nlm.nih.gov/pubmed/38045611 http://dx.doi.org/10.20517/mrr.2022.24 |
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