University of Pittsburgh

Easier, Faster Oligosaccharide Synthesis

Oligosaccharides are increasingly useful in the fields of food, pharmaceuticals, and biochemical research. For food manufacturers, oligosaccharides are not only valuable as sweeteners, but as prebiotics they are important for cultivating healthy gut flora, and the natural occurrence of oligosaccharides in breastmilk has sparked interest among infant formula manufacturers. On the basic science side, oligosaccharides play an important role at the level of cell surface interactions and contribute to diseases from cancer to muscular dystrophy. Regardless of the application, though, carbohydrate production is a non-trivial process. We present a fast and simple yet robust method for constructing oligosaccharides, which could form the basis for automated carbohydrate synthesis.

Description

This novel one-pot glycosylation system uses a designer thioglycoside and global deprotection to streamline the oligosaccharide assembly process. Traditionally, carbohydrate chain elongation involves oxophilic or thiophilic activators, which are incompatible with acid-sensitive protecting groups. Instead, our system uses a carbophilic activator, which both facilitates glycosidic linkage formation and supports protecting groups that a common acid can remove all at once from the completed carbohydrate. Not only is this system faster and more user-friendly than existing methods, but with a yield greater than 93 percent for most oligosaccharides, it’s also more efficient.

Applications

- Prebiotics
- Infant formula
- Fat or sugar substitute
- Food texture improvement
- Glycobiology research
- Drug discovery

Advantages

- Faster oligosaccharide synthesis
- Excellent yield at room temperature
- Easy to prepare and use
- Shelf-stable and tolerant to protecting group manipulation

Invention Readiness

Tested in the laboratory

IP Status

https://patents.google.com/patent/US9399655B2