Roche Diagnostics Operations, Inc.

Technische Universitat Graz

Roche Diagnostics Gmbh

F. Hoffmann-La Roche Ag

Christiane Luley

Bernd Nidetzky

Harald Sobek

Rainer Mueller

Helmut Schwab

Alfred Engel

Michael Greif

Marco Thomann

Bernhard Suppmann

Sebastian Malik

Christine Jung

Thornthan Sawangwan

Mario Müller

Tibor Czabany

Doris Ribitsch

Katharina Schmoelzer

Sabine Zitzenbacher

The present invention relates to a method for producing 2-O-glyceryl-&#x3b1;-D-glucopyranoside (&#x3b1;GG; FIG.) from a glucosyl donor and a glucosyl acceptor comprising the steps: providing a sucrose phosphorylase (EC 2.4.1.7), incubating said sucrose phosphorylase with a mixture comprising a glucosyl donor and glycerol as glucosyl acceptor and isolating and/or purifying 2-O-glyceryl-&#x3b1;-D-glucopyranoside.

Method for producing 2-O-glyceryl-alpha-D-glucopyranoside

The present disclosure is directed to the use of certain glycosyltransferase variants having N-terminal truncation deletions. It was found that the combination of two different truncation variants of human &#x3b2;-galactoside-&#x3b1;-2,6-sialyltransferase I (hST6Gal-I) exhibited different specific sialyltransferase enzymatic activities. In one example, under conditions wherein the first variant &#x394;89 hST6Gal-I catalyzed formation of bi-sialylated target molecules the second variant &#x394;108 hST6Gal-I catalyzed formation of mono-sialylated target molecules. Thus, disclosed are variants of mammalian glycosyltransferase, nucleic acids encoding the same, methods and means for recombinantly producing the variants of mammalian glycosyltransferase and use thereof, particularly for sialylating in a quantitatively controlled manner terminal acceptor groups of glycan moieties being part of glycoproteins such as immunoglobulins.

Quantitative control of sialylation and specific mono-sialylation

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Graz, Austria

Christiane Luley