| Literature DB >> 27485385 |
Liuqing Wen1, Kenneth Huang1, Yuan Zheng1, Yunpeng Liu1, He Zhu1, Peng George Wang2.
Abstract
A two-step enzymatic strategy for the efficient and convenient synthesis of 6-deoxy-l-sorbose was reported herein. In the first reaction step, the isomerization of l-fucose (6-deoxy-l-galactose) to l-fuculose (6-deoxy-l-tagatose) catalyzed by l-fucose isomerase (FucI), and the epimerization of l-fuculose to 6-deoxy-l-sorbose catalyzed by d-tagatose 3-epimerase (DTE) were coupled with the targeted phosphorylation of 6-deoxy-l-sorbose by fructose kinase from human (HK) in a one-pot reaction. The resultant 6-deoxy-l-sorbose 1-phosphate was purified by silver nitrate precipitation method. In the second reaction step, the phosphate group of the 6-deoxy-l-sorbose 1-phosphate was hydrolyzed with acid phosphatase (AphA) to produce 6-deoxy-l-sorbose in 81% yield with regard to l-fucose.Entities:
Keywords: 6-Deoxy-l-sorbose; Dephosphorylation; Enzymatic synthesis; One-pot multienzyme; Phosphorylation
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Year: 2016 PMID: 27485385 PMCID: PMC5067164 DOI: 10.1016/j.bmcl.2016.03.083
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823