Protein preparation from cotyledons of Raphanus sativus seedlings grown in the dark catalyzed the transfer of the sinapoyl moiety of 1-O-sinapoyl-ß-D-glucose to the C-2 hydroxyl group of the glucose moiety of another molecule of 1-O-sinapcyl-ß-D-glucose to form 1,2-di-O-sinapoyl-ß-D-glucopyranose. In this synthesis the 1-O-acyl glucoside was used both as acyl donor and acceptor molecule. Maximal rate of product formation was found to be at pH 7.5 in 0.1M Hepes buffer.

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http://dx.doi.org/10.1016/S0176-1617(84)80116-9DOI Listing

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