120095-01-4Relevant academic research and scientific papers
Porcine liver (2 → 3)-α-sialyltransferase: Substrate specificity studies and application of the immobilized enzyme to the synthesis of various sialylated oligosaccharide sequences
Lubineau, Andre,Basset-Carpentier, Karine,Auge, Claudine
, p. 161 - 167 (2007/10/03)
In search of substrate analogues for the porcine liver β-D-Galp-(1 → 3)-D-Galp-NAc: CMP-Neu5Ac-(2 → 3')-α-sialyltransferase, three disaccharides β-D-Galp-(1→3)-β-D-Gal p-O-CH3 (5), β-D-Galp-(1→3)-β-D-(2-OAc)-Gal p-O-CH3 (7) and β-D-G
A SIMPLE STRATEGY FOR CHANGING THE REGIOSELECTIVITY OF GLYCOSIDASE-CATALYSED FORMATION OF DISACCHARIDES: PART II, ENZYMIC SYNTHESIS in situ OF VARIOUS ACCEPTOR GLYCOSIDES
Nilsson, Kurt G. I.
, p. 53 - 60 (2007/10/02)
β-D-Galactosidase induced the formation of allyl, benzyl, and trimethylsilylethyl β-D-galactopyranosides on a 1-20-g scale from lactose and allyl alcohol, benzyl alcohol, and trimethylsilylethanol, respectively.Similarly, α-D-galactosidase catalysed the formation of allyl α-D-galactopyranoside from raffinose and allyl alcohol.The galactosides were used as acceptors for the preparation of the following disaccharide glycosides: β-D-Gal-(1->3)-β-D-Gal-OCH2CH=CH2, β-D-Gal-(1->6)-β-D-Gal-OCH2CH=CH2, β-D-Gal-(1->3)-β-D-Gal-OBn, β-D-Gal-(1->6)-β-D-Gal-OBn, β-D-Gal-(1->3)-β-D-Gal-OCH2CH2SiMe3, and α-D-Gal-(1->3)-α-D-Gal-OCH2CH=CH2.The β-D-galactosidase-catalysed reactions were efficient enough to allow the one pot preparation of the various β-linked mono- and digalactosides from lactose and alcohol.
