QUERCETIN-INDUCED BENZOPHENANTHRIDINE ALKALOID PRODUCTION IN SUSPENSION CELL-CULTURES OF SANGUINARIA-CANADENSIS

被引:41
作者
MAHADY, GB
BEECHER, CWW
机构
[1] UNIV ILLINOIS,DEPT MED CHEM & PHARMACOGNOSY,CHICAGO,IL 60612
[2] UNIV ILLINOIS,PROGRAM COLLABORAT RES PHARMACEUT SCI,CHICAGO,IL 60612
关键词
SANGUINARIA CANADENSIS; PAPAVERACEAE; SANGUINARINE; CHELERYTHRINE; QUERCETIN; ELICITOR; CALCIUM;
D O I
10.1055/s-2006-959570
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Addition of micromolar concentrations of quercetin or rutin to suspension cell cultures of Sanguinaria canadensis L. (bloodroot) induced the biosynthesis of sanguinarine and chelerythrine in a dose-dependent manner. In contrast, related compounds: baicalein, naringin, naringenin, catechin, caffeic acid and benzoic acid displayed very weak inductive activity. Of the two active flavonoids, quercetin was the most effective for inducing benzophenanthridine alkaloid biosynthesis, with doses of 100 mu M increasing alkaloid production over 375 % as compared to negative controls. Quercetin's inductive effects were similar to that of an elicitor derived from fungus Penicillium expansum (PE-elicitor). Suppression of quercetin and PE-induced alkaloid biosynthesis by low doses of actinomycin D (5 mu g/ml), alpha-amanitin (20 mu g/ml), or cycloheximide (1 mu g/ml) demonstrate a requirement for both RNA and de novo cytoplasmic protein synthesis and suggest that alterations in gene expression are involved in the inductive mechanism. Furthermore, quercetin-induced alkaloid biosynthesis was significantly reduced by pretreatment of the cells with the calcium chelator, EGTA (3 mM), or the calcium channel inhibitor, verapamil (100 mu M), suggesting that this process was calcium dependent.
引用
收藏
页码:553 / 557
页数:5
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