Makoto Yamashita
Research Subjects
Makoto Yamashita has a total of 5 co-authors. Here are the top co-authors by number of shared publications:
- Haruka Onodera
Institute of Health Science, Kirin Holdings Co., Ltd., 2-26-1-12-12 Muraoka-Higashi, Fujisawa 255-8555, Japan
1 shared publication - Takeshi Kokubo
Institute of Health Sciences, Kirin Holdings Co., Ltd., 2-26-1-12-12 Muraoka-Higashi, Fujisawa 251-8555, Japan
1 shared publication - Yohei Sato
Institute of Health Sciences, Kirin Holdings Co., Ltd., 2-26-1-12-12 Muraoka-Higashi, Fujisawa 251-8555, Japan
1 shared publication - Yosuke Komatsu
Graduate School of Life Science, Hokkaido University, Sapporo, Japan
1 shared publication - Yuta Watanabe
Institute of Health Sciences, Kirin Holdings Co., Ltd., 2-26-1-12-12 Muraoka-Higashi, Fujisawa 251-8555, Japan
1 shared publication
Latest Publications
- Open Access
- 21 July 2025
- Published by MDPI AG in Microorganisms
- Vol. 13 (7) , 1705
HMOs Induce Butyrate Production of Faecalibacterium prausnitzii via Cross-Feeding by Bifidobacterium bifidum with Different Mechanisms for HMO Types
Human milk oligosaccharides (HMOs) have garnered significant attention as one of the bioactive components in human milk, with growing applications in infant formula and food products. HMOs enhance butyrate production, which is produced by butyrate-producing bacteria such as Faecalibacterium prausnitzii and contributes to gut health through its diverse biological functions. However, the specific mechanisms by which individual HMOs promote butyrate production remain unclear. In this study, we conducted in vitro co-culture experiments of F. prausnitzii and Bifidobacterium bifidum, examining their relative abundance, fatty acid production, residual sugar levels, and gene expression. Our results revealed that B. bifidum utilizes HMOs and provides the constituent sugars to F. prausnitzii, thereby promoting butyrate production by F. prausnitzii. Furthermore, we found that the underlying mechanisms vary depending on the structure of the HMOs. Specifically, 2′-fucosyllactose and 3′-sialyllactose enhance the butyrate production efficiency of F. prausnitzii, while 6′-sialyllactose primarily promotes the growth of F. prausnitzii. These findings not only deepen our understanding of how HMOs influence infant gut health but also suggest new directions for developing nutritional products that leverage the distinct functional properties of each HMO.
- 21 July 2025
- Published by MDPI AG in Microorganisms
- Vol. 13 (7) , 1705
Open AccessHMOs Induce Butyrate Production of Faecalibacterium prausnitzii via Cross-Feeding by Bifidobacterium bifidum with Different Mechanisms for HMO Types
Human milk oligosaccharides (HMOs) have garnered significant attention as one of the bioactive components in human milk, with growing applications in infant formula and food products. HMOs enhance butyrate production, which is produced by butyrate-producing bacteria such as Faecalibacterium prausnitzii and contributes to gut health through its diverse biological functions. However, the specific mechanisms by which individual HMOs promote butyrate production remain unclear. In this study, we conducted in vitro co-culture experiments of F. prausnitzii and Bifidobacterium bifidum, examining their relative abundance, fatty acid production, residual sugar levels, and gene expression. Our results revealed that B. bifidum utilizes HMOs and provides the constituent sugars to F. prausnitzii, thereby promoting butyrate production by F. prausnitzii. Furthermore, we found that the underlying mechanisms vary depending on the structure of the HMOs. Specifically, 2′-fucosyllactose and 3′-sialyllactose enhance the butyrate production efficiency of F. prausnitzii, while 6′-sialyllactose primarily promotes the growth of F. prausnitzii. These findings not only deepen our understanding of how HMOs influence infant gut health but also suggest new directions for developing nutritional products that leverage the distinct functional properties of each HMO.