STEREOCHEMISTRY AND THE MECHANISM OF ENZYMATIC REACTIONS

By D. Koshland. 1953

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Structural basis of sialyltransferase activity in trypanosomal sialidases (2000, background): “This scenario is plausible since all retaining glycosidases can also function as transglycosidases (Koshland, 1953).”
The structure of E. coli β-galactosidase (2005, background): “D - galactopyranoside). β -Galactosidase is a retaining glycosidase, where the product retains the same stereochemistry as the by Koshland [6] and later demonstrated experimentally [7].”
Lignocellulases: a review of emerging and developing enzymes, systems, and practices (2017, background): “, retention or inversion) of the anomeric carbon configuration (Koshland 1953; Garvey et al. 2013).”
Properties and applications of starch-converting enzymes of the alpha-amylase family. (2002, background): “Recently, studies with cy-clodextrin glycosyltransferase from Bacillus circu - have shown that the intermediate indeed covalently linked bond with the enzyme above-mentioned double displacement as proposed by two directly the (1953), only the three conserved catalytic residues directly a role.”