Title of article
Synthesis of a trigalacturonic acid analogue mimicking the expected transition state in the glycosidases Original Research Article
Author/Authors
Kazunori Yamamoto، نويسنده , , Shogo Noguchi، نويسنده , , Noboru Takada، نويسنده , , Kazuo Miyairi، نويسنده , , Masaru Hashimoto، نويسنده ,
Issue Information
دوهفته نامه با شماره پیاپی سال 2010
Pages
14
From page
572
To page
585
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 , Cyclohexene ring , Transition state structure
Journal title
Carbohydrate Research
Serial Year
2010
Journal title
Carbohydrate Research
Record number
966714
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