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Synthesis of a trigalacturonic acid analogue mimicking the expected transition state in the glycosidases
Authors:Kazunori Yamamoto
Affiliation:Faculty of Agriculture and Life Science, Hirosaki University, 3-Bunkyo-cho, Hirosaki 036-8561, Japan
Abstract:A trigalacturonic acid analogue carrying a cyclohexene framework in place of the central pyranose ring was synthesized as a molecular probe for the mechanistic investigation of endo-polygalacturonase 1 (endo-PG 1). Preliminary enzymatic studies revealed that this analogue inhibited endo-PG 1 activity by about 30% at 0.3 mM concentration.
Keywords:endo-Polygalacturonase 1   Trigalacturonic acid analogue   Transition state structure   Cyclohexene ring
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