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https://hdl.handle.net/20.500.14094/0100488524
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2025-04-24
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0100488524 (fulltext)
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メタデータID
0100488524
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open access
出版タイプ
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タイトル
Limosilactobacillus (Lactobacillus) fermentum ALAL020, a Probiotic Candidate Bacterium, Produces a Cyclic Dipeptide That Suppresses the Periodontal Pathogens Porphyromonas gingivalis and Prevotella intermedia
著者
Kawai, Tomomi ; Ohshima, Tomoko ; Tanaka, Takeshi ; Ikawa, Satoshi ; Tani, Atsushi ; Inazumi, Naoya ; Shin, Ryoichi ; Itoh, Yukie ; Meyer, Karen ; Maeda, Nobuko
著者名
Kawai, Tomomi
著者名
Ohshima, Tomoko
著者名
Tanaka, Takeshi
著者名
Ikawa, Satoshi
著者ID
A2022
研究者ID
1000010335333
ORCID
0000-0001-5788-2137
KUID
https://kuid-rm-web.ofc.kobe-u.ac.jp/search/detail?systemId=e6395afb727712fd520e17560c007669
著者名
Tani, Atsushi
谷, 篤史
タニ, アツシ
所属機関名
人間発達環境学研究科
著者名
Inazumi, Naoya
著者名
Shin, Ryoichi
著者名
Itoh, Yukie
著者名
Meyer, Karen
著者名
Maeda, Nobuko
言語
English (英語)
収録物名
Frontiers in Cellular and Infection Microbiology
巻(号)
12
ページ
804334
出版者
Frontiers
刊行日
2022-03-07
公開日
2024-04-04
抄録
Periodontal disease develops as a result of oral microbiota in dysbiosis, followed by the growth of periodontal pathogens such as Porphyromonas gingivalis and Prevotella intermedia. In case of acute symptoms, antibacterial agents and disinfectants are administered, however the appearance of drug-resistant bacteria and allergies cause problems. In recent years, studies on the effects of probiotics have been conducted as an alternative therapy for periodontitis. However, the basic mechanism of the inhibitory effect of probiotic bacteria on periodontal disease has not been clearly elucidated. To clarify the antibacterial mechanism of probiotics against periodontal pathogens, we used Limosilactobacillus (Lactobacillus) fermentum ALAL020, which showed the strongest antibacterial activity against P. gingivalis and P. intermedia among 50 screened lactic acid bacteria strains. The antibacterial substances produced were identified and structurally analyzed. After neutralizing the MRS liquid culture supernatant of ALAL020 strain, the molecular weight (m/z) of the main antibacterial substance separated by gel filtration column chromatography and reverse phase HPLC was 226.131. This low molecular weight compound was analyzed by LC-MS and disclosed the composition formula C₁₁H₁₈O₃N₂, however the molecular structure remained unknown. Then, structural analysis by NMR revealed C₁₁H₁₈O₃N₂ as the cyclic dipeptide, “hexahydro-7-hydroxy-3- (2-methylpropyl) pyrrolo [1,2-a] pyrazine-1,4-dion cyclo (Hyp-Leu) “. Based on the results of this analysis, cyclo (Hyp-Leu) was chemically synthesized and the antibacterial activity against P. gingivalis and P. intermedia was measured. The minimum inhibitory concentration (MIC) was 2.5 g/L and the minimum bactericidal concentration (MBC) was shown to be less than 5 g/L. In addition, an in vitro epithelial tissue irritation test at 10 g/L showed no tissue toxicity. So far there are no reports of this peptide being produced by probiotic bacteria. Furthermore, antibacterial activity of this cyclic dipeptide against periodontal disease bacteria has not been confirmed. The results of this study might lead to a comprehensive understanding of the antibacterial mechanism against periodontal disease bacteria in future, and are considered applicable for the prevention of periodontal disease.
キーワード
antibacterial peptide
periodontal
pathogen
cyclic dipeptide
probiotics
nuclear magnetic resonance analysis
chemical synthesis
カテゴリ
人間発達環境学研究科
学術雑誌論文
権利
© 2022 Kawai, Ohshima, Tanaka, Ikawa, Tani, Inazumi, Shin, Itoh, Meyer and Maeda.
Creative Commons Attribution License
関連情報
DOI
https://doi.org/10.3389/fcimb.2022.804334
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資源タイプ
journal article
eISSN
2235-2988
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