Literature DB >> 14510400

Chemo-enzymatic syntheses of natural and unnatural 2'-deoxynucleosides.

Hironori Komatsu1, Hirokazu Awano, Hiroki Ishibashi, Toshihiro Oikawa, Ichirou Ikeda, Tadashi Araki.   

Abstract

A chemo-enzymatic method for preparations of natural and unnatural deoxynucleosides was developed. The method consists of chemical synthesis of natural and unnatural deoxyribose 1-phosphates and their enzymatic conversion to deoxynucleosides. A highly stereoselective synthesis of 2-deoxyribose 1-phosphate was first achieved by an unprecedented application of crystallization-induced asymmetric transformation. Additionally, we first discovered a 2'-deoxycytidine producing enzyme. The discovery and the development of a scalable synthetic process of 2-deoxyribose 1-phosphate enabled us to manufacture all four natural 2'-deoxynucleosides practically. The methodology was applied to the synthesis of 2',3'-dideoxy-3'-fluoroguanosine via synthetic 2,3-dideoxy-3-fluororibose 1-phosphate.

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Year:  2003        PMID: 14510400     DOI: 10.1093/nass/3.1.101

Source DB:  PubMed          Journal:  Nucleic Acids Res Suppl


  2 in total

1.  Design and directed evolution of a dideoxy purine nucleoside phosphorylase.

Authors:  David P Nannemann; Kristian W Kaufmann; Jens Meiler; Brian O Bachmann
Journal:  Protein Eng Des Sel       Date:  2010-06-04       Impact factor: 1.650

2.  New trends in nucleoside biotechnology.

Authors:  I A Mikhailopulo; A I Miroshnikov
Journal:  Acta Naturae       Date:  2010-07       Impact factor: 1.845

  2 in total

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