Literature DB >> 21555267

Enzymatic synthesis of capsaicin 4-O-β-xylooligosaccharides by β-xylosidase from Aspergillus sp.

Hisashi Katsuragi1, Kei Shimoda, Ryohei Yamamoto, Takahiro Ohara, Hiroki Hamada.   

Abstract

Capsaicin 4-O-β-xylooligosaccharides were synthesized by a biocatalytic xylosylation using Aspergillus sp. β-xylosidase. Capsaicin was converted into three new capsaicin glycosides, i.e. capsaicin 4-O-β-xyloside, capsaicin 4-O-β-xylobioside, and capsaicin 4-O-β-xylotrioside in 15, 12 and 10% yield, respectively. All products were isolated from the reaction mixtures by preparative HPLC. The structures of the products were determined by NMR spectroscopic method.

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Year:  2011        PMID: 21555267     DOI: 10.1556/ABiol.62.2011.2.5

Source DB:  PubMed          Journal:  Acta Biol Hung        ISSN: 0236-5383


  2 in total

1.  Chemo-enzymatic synthesis of glycolyl-ester-linked taxol-monosaccharide conjugate and its drug delivery system using hepatitis B virus envelope L bio-nanocapsules.

Authors:  Kei Shimoda; Manabu Hamada; Masaharu Seno; Tadakatsu Mandai; Hiroki Hamada
Journal:  Biochem Insights       Date:  2012-07-09

2.  Chemo-enzymatic synthesis of ester-linked docetaxel-monosaccharide conjugates as water-soluble prodrugs.

Authors:  Kei Shimoda; Naoji Kubota
Journal:  Molecules       Date:  2011-08-09       Impact factor: 4.411

  2 in total

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