| Literature DB >> 32857448 |
Andrea Marchesi1, Fabio Parmeggiani1,2, João Louçano3, Ashley P Mattey1, Kun Huang1, Tanistha Gupta3, Mario Salwiczek3, Sabine L Flitsch1.
Abstract
Automated chemical oligosaccharide synthesis is an attractive concept that has been successfully applied to a large number of target structures, but requires excess quantities of suitably protected and activated building blocks. Herein we demonstrate the use of biocatalysis to supply such reagents for automated synthesis. By using the promiscuous NmLgtB-B β1-4 galactosyltransferase from Neisseria meningitidis we demonstrate fast and robust access to the LacNAc motif, common to many cell-surface glycans, starting from either lactose or sucrose as glycosyl donors. The enzymatic product was shown to be successfully incorporated as a complete unit into a tetrasaccharide target by automated assembly.Entities:
Keywords: biocatalysis; chemoenzymatic synthesis; glycans; oligosaccharides; transgalactosylation
Year: 2020 PMID: 32857448 PMCID: PMC7756758 DOI: 10.1002/anie.202008067
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336