- 4,6-dimethoxy-1,3,5-triazine oligoxyloglucans: novel one-step preparable substrates for studying action of endo-beta-1,4-glucanase III from Trichoderma reesei.
4,6-dimethoxy-1,3,5-triazine oligoxyloglucans: novel one-step preparable substrates for studying action of endo-beta-1,4-glucanase III from Trichoderma reesei.
Bioorganic & medicinal chemistry letters (2010-06-10)
Atsushi Kobayashi, Tomonari Tanaka, Kazuhito Watanabe, Masaki Ishihara, Masato Noguchi, Hirofumi Okada, Yasushi Morikawa, Shin-ichiro Shoda
PMID20529686
ABSTRACT
Two kinds of 4,6-dimethoxy-1,3,5-triazine (DMT) oligoxyloglucans, DMT-beta-XXXG and DMT-beta-XLLG, have been synthesized via one-step procedure starting from the corresponding unprotected oligoxyloglucans in water. The resulting DMT derivatives were found to be hydrolyzed by endo-beta-1,4-D-glucanase III from Trichoderma reesei (EGIII) and utilized as substrates for determination of the kinetic parameters of EGIII. The present DMT-method would be a convenient analytical tool for studying the action of glycosyl hydrolases due to the extremely simple synthetic process of DMT-glycosides without using protecting groups.
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