Augmentation of dietary glucosylceramide hydrolysis by the novel bacterium Glucerabacter canisensis NATH-2371T

The purpose of this study was to evaluate the effects of intragastrical administration of Glucerabacter canisensis NATH-2371 T on glucosylceramide (GluCer) digestion in mice. Although G. canisensis was unable to utilize starch and cellulose, coculture of G. canisensis with mouse fecal bacteria great...

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Published inBioscience, biotechnology, and biochemistry Vol. 82; no. 12; pp. 2191 - 2197
Main Authors Kawata, Misho, Suzuki, Masato, Akutsu, Shoko, Kawahara, Natsuki, Tsukamoto, Ami, Nobukawa, Shohei, Isozaki, Ryohei, Yuyama, Seika, Asanuma, Narito
Format Journal Article
LanguageEnglish
Published Taylor & Francis 02.12.2018
Oxford University Press
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Summary:The purpose of this study was to evaluate the effects of intragastrical administration of Glucerabacter canisensis NATH-2371 T on glucosylceramide (GluCer) digestion in mice. Although G. canisensis was unable to utilize starch and cellulose, coculture of G. canisensis with mouse fecal bacteria greatly increased GluCer hydrolysis in polysaccharide medium, indicating that G. canisensis grew in competition with other intestinal bacteria. Although most of the administered G. canisensis cells were detected in feces, some cells were present in the colorectum contents, which had GluCer-hydrolyzing activity. These results indicate that G. canisensis can viably transit through the mouse gut. Administration of G. canisensis to mice fed diets supplemented with GluCer or GluCer-containing foods significantly enhanced GluCer hydrolysis. Since G. canisensis did not show acute toxicity, it may be useful as a probiotic to augment GluCer hydrolysis in the large intestine. Abbreviations: GluCer: glucosylceramide; KPi: potassium phosphate buffer; C-M: chloroform-methanol A novel bacterium Glucerabacter canisensis NATH-2371 T was administrated to mice fed diets supplemented with glucosylceramide (GluCer) or GluCer-containing foods significantly enhanced GluCer hydrolysis.
ISSN:0916-8451
1347-6947
DOI:10.1080/09168451.2018.1505484