Efficient chemoenzymatic synthesis of uridine 5′-diphosphate N-acetylglucosamine and uridine 5′-diphosphate N-trifluoacetyl glucosamine with three recombinant enzymes
Author:
Affiliation:
1. Institute of Bioengineering, College of Chemical and Biological Engineering, Zhejiang University, Hangzhou, P. R. China
2. School of Biological and Chemical Engineering, Zhejiang University of Science & Technology, Hangzhou, P. R. China
Funder
National Natural Science Foundation of China
National High Technology Research and Development Program of China
Publisher
Informa UK Limited
Subject
General Medicine,Biochemistry,Biotechnology
Link
https://www.tandfonline.com/doi/pdf/10.1080/10826068.2016.1188315
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1. Design of biologically active heparan sulfate and heparin using an enzyme-based approach
2. A Synthetic Antithrombin III Binding Pentasaccharide Is Now a Drug! What Comes Next?
3. Using an Enzymatic Combinatorial Approach to Identify Anticoagulant Heparan Sulfate Structures
4. Enzymatic Redesigning of Biologically Active Heparan Sulfate
5. Solution Structures of Chemoenzymatically Synthesized Heparin and Its Precursors
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