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豌豆(Pisum sativum L.)细胞悬浮培养物中的豌豆素代谢

Pisatin metabolism in pea (Pisum sativum L.) cell suspension cultures.

作者信息

Borejsza-Wysocki Wlodzimierz, Borejsza-Wysocka Ewa, Hrazdina Geza

机构信息

Institute of Food Science, Cornell University, 14456-0462, Geneva, NY, USA.

出版信息

Plant Cell Rep. 1997 Feb;16(5):304-309. doi: 10.1007/BF01088286.

DOI:10.1007/BF01088286
PMID:30727668
Abstract

Cell suspension cultures were established from germinating pea (Pisum sativum L.) seeds. This cell culture, which accumulated pisatin, consisted mostly of single cells containing a few cell aggregates. The cells responded to treatment with a yeast glucan preparation with transient accumulation of pisatin in both cells and culture media. Addition of pisatin to cell cultures resulted in increased synthesis of pisatin. Phenylalanine ammonia-lyase, chalcone synthase and isoflavone reductase activities were present in untreated cells. Upon treatment with an elicitor preparation the activities of the first two enzymes showed a rapid, transient increase up to 20 hours after treatment. Isoflavone reductase showed a major and minor peak at 16 and 36 h, respectively, after elicitor treatment. The time course of the enzyme activity and pisatin accumulation is consistent with an elicitor-mediated response.

摘要

从发芽的豌豆(Pisum sativum L.)种子建立了细胞悬浮培养物。这种积累豌豆素的细胞培养物主要由含有一些细胞聚集体的单个细胞组成。这些细胞对酵母葡聚糖制剂处理有反应,细胞和培养基中豌豆素都会短暂积累。向细胞培养物中添加豌豆素导致豌豆素合成增加。未处理的细胞中存在苯丙氨酸解氨酶、查尔酮合酶和异黄酮还原酶活性。用诱导子制剂处理后,前两种酶的活性在处理后20小时内迅速、短暂增加。诱导子处理后,异黄酮还原酶分别在16小时和36小时出现一个主峰和一个次峰。酶活性和豌豆素积累的时间进程与诱导子介导的反应一致。

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本文引用的文献

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Elicitation of benzophenanthridine alkaloid synthesis in Eschscholtzia cell cultures.诱导植物细胞培养物中苯并菲啶生物碱的合成。
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Biosynthesis of the Phytoalexin Pisatin : Isoflavone Reduction and Further Metabolism of the Product Sophorol by Extracts of Pisum sativum.豌豆异黄酮素 pisatin 的生物合成:豌豆提取物对异黄酮的还原作用及产物大豆苷元 sophorol 的进一步代谢。
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Plant Physiol. 1982 Aug;70(2):506-10. doi: 10.1104/pp.70.2.506.
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Isolation of a phytoalexin from Pisum sativum L.从豌豆(Pisum sativum L.)中分离出一种植物抗毒素
Nature. 1960 Aug 27;187:799-800. doi: 10.1038/187799b0.