1972Food Hygiene and Safety Science (Shokuhin Eiseigaku Zasshi)Open access

Mechanism of Inactivation of Trypsin by Photo-chemical Reaction of Xanthene Dyes

Hiroki Murakami, Ko-hei SAKATA, Shoji Hatano, Tadao Watanabe

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Abstract

Trypsin-inactivating xanthene dyes such as phloxine, erythrosine, rose bengale and eosine have a photo-labile α-substituted carbonyl group in each structure. The photo-effects of bromine and iodine to trypsin were investigated. Iodine partially inhibited (40%) the enzymatic activity in the dark. Under the light condition, the inactivation was occurred so rapidly and extremely. It was assumed that some photo-excited state of halogen atom would be necessary for the inactivation of trypsin.

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Trypsin-inactivating xanthene dyes such as phloxine, erythrosine, rose bengale and eosine have a photo-labile α-substituted carbonyl group in each structure. The photo-effects of bromine and iodine to trypsin were investigated. Iodine partially inhibited (40%) the enzymatic activity in the dark. Under the light condition, the inactivation was occurred so rapidly and extremely. It was assumed that some photo-excited state of halogen atom would be necessary for the inactivation of trypsin.

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Available abstract

Trypsin-inactivating xanthene dyes such as phloxine, erythrosine, rose bengale and eosine have a photo-labile α-substituted carbonyl group in each structure. The photo-effects of bromine and iodine to trypsin were investigated. Iodine partially inhibited (40%) the enzymatic activity in the dark. Under the light condition, the inactivation was occurred so rapidly and extremely. It was assumed that some photo-excited state of halogen atom would be necessary for the inactivation of trypsin.

Key concepts: Xanthene, Erythrosine, Chemistry, Trypsin, Photochemistry, Iodine, Halogen, Bromine

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