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Kojibiose (2-O-α-D-Glucopyranosyl-D-Glucose): Isolation and Structure: Chemical Synthesis
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  • Published: 09 November 1957

Kojibiose (2-O-α-D-Glucopyranosyl-D-Glucose): Isolation and Structure: Chemical Synthesis

  • K. MATSUDA1 

Nature volume 180, page 985 (1957)Cite this article

  • 495 Accesses

  • 23 Citations

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Abstract

I HAVE previously pointed out that kojibiose (one of the unfermentable gluco-bioses in koji extract) is believed to have most probably 1,2-α-glucosidic linkage from the following facts: (a) acid hydrolysis gave glucose as the only product detectable by paper chromatography1; (b) resistance to almond β-glucosidase eliminates the β-linkage1; (c) the low M G value2 (0.31) in borate buffer (pH 9.8) suggests that the linkage cannot be 1, 3- or 1, 6-, and the R F value in butanol/pyridine/water (3 : 2 : 1.5) is different from that of maltose as well as from sakébiose (nigerose) and isomaltose3; (d) the stain of this sugar on the paper chromatogram sprayed by aniline hydrogen phthalate has a colour similar to that of sophorose3; (e) this sugar gives no phenylosazone by the usual method, though it showed reducing power against Fehling's solution4.

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Author information

Authors and Affiliations

  1. Department of Agricultural Chemistry, Faculty of Agriculture, Tôhoku University, Sendai, Japan

    K. MATSUDA

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  1. K. MATSUDA
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MATSUDA, K. Kojibiose (2-O-α-D-Glucopyranosyl-D-Glucose): Isolation and Structure: Chemical Synthesis. Nature 180, 985 (1957). https://doi.org/10.1038/180985a0

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  • Issue Date: 09 November 1957

  • DOI: https://doi.org/10.1038/180985a0

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