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诱导子介导的长春花细胞悬浮培养物中色氨酸脱羧酶和异胡豆苷合成酶活性的诱导

Elicitor-mediated induction of tryptophan decarboxylase and strictosidine synthase activities in cell suspension cultures of Catharanthus roseus.

作者信息

Eilert U, De Luca V, Constabel F, Kurz W G

出版信息

Arch Biochem Biophys. 1987 May 1;254(2):491-7. doi: 10.1016/0003-9861(87)90128-7.

Abstract

Treatment of one cell line (No. 615) of Catharanthus roseus c.v. Little Delicata with an elicitor preparation of autoclaved and homogenized Pythium aphanidermatum culture resulted in rapid accumulation of indole alkaloids. Alkaloid formation was preceded by rapid transient increases in the extractable activities of the enzymes tryptophan decarboxylase and strictosidine synthase. The induction of these two enzyme activities occurred when cells were transferred to alkaloid production medium or treatment with fungal elicitors. Treatment of this cell line with translational or transcriptional inhibitors prevented the Pythium-induced increases of enzyme activity as well as alkaloid accumulation. When cells were transferred to alkaloid production medium the induction of strictosidine synthase activity preceded that of tryptophan decarboxylase by many hours even when cells were also treated with Pythium elicitor. Results suggested that tryptophan decarboxylase induction proceeds only when endogenous tryptamine levels were decreased by two-third. The internal cellular level of tryptamine, therefore, could regulate expression of tryptophan decarboxylase, whereas induction of strictosidine synthase or of another enzyme in the biosynthetic pathway could control channeling of tryptamine into alkaloids. The results demonstrate that fungal elicitors can be used to facilitate studies of the factors which regulate expression of indole alkaloid pathway enzymes and their ultimate pathway products.

摘要

用灭菌并匀浆的瓜果腐霉菌培养物制备的激发子处理长春花小粉蝶品种的一个细胞系(615号),导致吲哚生物碱迅速积累。生物碱形成之前,色氨酸脱羧酶和裂环马钱子苷合酶的可提取活性迅速短暂增加。当细胞转移到生物碱生产培养基或用真菌激发子处理时,这两种酶活性被诱导。用翻译或转录抑制剂处理该细胞系可阻止瓜果腐霉菌诱导的酶活性增加以及生物碱积累。当细胞转移到生物碱生产培养基时,即使细胞也用瓜果腐霉菌激发子处理,裂环马钱子苷合酶活性的诱导也比色氨酸脱羧酶早许多小时。结果表明,只有当内源性色胺水平降低三分之二时,色氨酸脱羧酶诱导才会进行。因此,细胞内色胺水平可以调节色氨酸脱羧酶的表达,而裂环马钱子苷合酶或生物合成途径中另一种酶的诱导可以控制色胺向生物碱的转化。结果表明,真菌激发子可用于促进对调节吲哚生物碱途径酶表达及其最终途径产物的因素的研究。

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