Literature DB >> 33153306

Synthesis of selected unnatural sugar nucleotides for biotechnological applications.

Meng Qiao1, Bingzhi Li1, Yuan Ji1, Lei Lin2, Robert Linhardt3,4, Xing Zhang1.   

Abstract

Sugar nucleotides are the principal building blocks for the synthesis of most complex carbohydrates and are crucial intermediates in carbohydrate metabolism. Uridine diphosphate (UDP) monosaccharides are among the most common sugar nucleotide donors and are transferred to glycosyl acceptors by glycosyltransferases or synthases in glycan biosynthetic pathways. These natural nucleotide donors have great biological importance, however, the synthesis and application of unnatural sugar nucleotides that are not available from in vivo biosynthesis are not well explored. In this review, we summarize the progress in the preparation of unnatural sugar nucleotides, in particular, the widely studied UDP-GlcNAc/GalNAc analogs. We focus on the "two-block" synthetic pathway that is initiated from monosaccharides, in which the first block is the synthesis of sugar-1-phosphate and the second block is the diphosphate bond formation. The biotechnological applications of these unnatural sugar nucleotides showing their physiological and pharmacological potential are discussed.

Entities:  

Keywords:  Sugar nucleotides; biotechnology applications; chemical synthesis; enzymatic synthesis; glycans

Mesh:

Substances:

Year:  2020        PMID: 33153306      PMCID: PMC7891891          DOI: 10.1080/07388551.2020.1844623

Source DB:  PubMed          Journal:  Crit Rev Biotechnol        ISSN: 0738-8551            Impact factor:   8.429


  74 in total

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8.  Clickable Galactose Analogues for Imaging Glycans in Developing Zebrafish.

Authors:  Jessica L Daughtry; Wendy Cao; Johnny Ye; Jeremy M Baskin
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9.  Tailored design and synthesis of heparan sulfate oligosaccharide analogues using sequential one-pot multienzyme systems.

Authors:  Yi Chen; Yanhong Li; Hai Yu; Go Sugiarto; Vireak Thon; Joel Hwang; Li Ding; Liana Hie; Xi Chen
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10.  Bioorthogonal chemistry: fishing for selectivity in a sea of functionality.

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Journal:  Angew Chem Int Ed Engl       Date:  2009       Impact factor: 15.336

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