Literature DB >> 9720215

Anomer-selective glucosylation of l-menthol by yeast alpha-glucosidase.

H Nakagawa1, M Yoshiyama, S Shimura, K Kirimura, S Usami.   

Abstract

l-Menthol was glucosylated by the alpha-glucosidase (EC 3.2.1.20) of Saccharomyces cerevisiae using maltose as the glucosyl donor. When 50 mg of l-menthol and 1.6 M maltose in 10 mM citrate-phosphate buffer (pH 5.5) were incubated at 45 degrees C, l-menthyl alpha-D-glucopyranoside (alpha-MenG) was alpha-anomer-selectively formed as a product. The specificity of the alpha-linkage was confirmed by 13C-NMR analysis. In the reaction mixture after 2 h, alpha-MenG was mainly accumulated in a crystalline form and the concentration of dissolved alpha-MenG was constant at 1.4 mM. The molar conversion yield of alpha-MenG produced based on the supplied l-menthol was maximally 30.7% at 48 h of reaction.

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Year:  1998        PMID: 9720215     DOI: 10.1271/bbb.62.1332

Source DB:  PubMed          Journal:  Biosci Biotechnol Biochem        ISSN: 0916-8451            Impact factor:   2.043


  2 in total

1.  Engineering a Carbohydrate-processing Transglycosidase into Glycosyltransferase for Natural Product Glycodiversification.

Authors:  Chaoning Liang; Yi Zhang; Yan Jia; Youhai Li; Shikun Lu; Jian-Ming Jin; Shuang-Yan Tang
Journal:  Sci Rep       Date:  2016-02-12       Impact factor: 4.379

2.  Improvement of the pharmacological activity of menthol via enzymatic β-anomer-selective glycosylation.

Authors:  Ha-Young Choi; Bo-Min Kim; Abubaker M A Morgan; Joong Su Kim; Won-Gon Kim
Journal:  AMB Express       Date:  2017-08-29       Impact factor: 3.298

  2 in total

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