New features of intramolecular copigmentation by acylated anthocyanins

被引:64
作者
Figueiredo, P [1 ]
George, F
Tatsuzawa, F
Toki, K
Saito, N
Brouillard, R
机构
[1] Univ Lusofono Humanidades & Tecnol, Lisbon, Portugal
[2] Univ Strasbourg 1, Inst Chim, CNRS, Lab Chim Polyphenols, F-67008 Strasbourg, France
[3] Chiba Univ, Fac Hort, Matsudo, Chiba 271, Japan
[4] Minami Kyushu Univ, Lab Floriculture, Miyazaki 884, Japan
[5] Meiji Gakuin Univ, Chem Lab, Totsuka Ku, Yokohama, Kanagawa, Japan
关键词
Dendrobium cv. Pramot; xLaeliocattleya cv. Mini Purple; Bletilla striata; Phalaenopsis; Senecio cruentus; intramolecular copigmentation; acylated anthocyanins; Malonyl effect;
D O I
10.1016/S0031-9422(98)00685-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Three series of structurally related anthocyanins, extracted from the red-purple flowers of Dendrobium 'Pramot', xLaeliocattleya cv. Mini Purple, Bletilla striata and Phalaenopsis all belonging to the Orchidaceae family and another series extracted from the pink flowers of Senecio cruentus (Compositae) allowed the confirmation of the existence of strong intramolecular copigmentation effects. These interactions confer stability to the coloured forms of the molecules, in a wide range of slightly acidic to neutral aqueous media. Moreover, the existence of structural relationships among the four series stressed the different influences exerted by the diverse substituent groups. The existence of a malonylglucoside attached to position 3 of all but three of the molecules put forward a new role for the malonyl residue, in this particular position. (C) 1999 Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:125 / 132
页数:8
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