首页> 外文OA文献 >Studies on the Production of Digitalis Cardenolides by Plant Tissue Culture: II. EFFECT OF LIGHT AND PLANT GROWTH SUBSTANCES ON DIGITOXIN FORMATION BY UNDIFFERENTIATED CELLS AND SHOOT-FORMING CULTURES OF DIGITALIS PURPUREA L. GROWN IN LIQUID MEDIA
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Studies on the Production of Digitalis Cardenolides by Plant Tissue Culture: II. EFFECT OF LIGHT AND PLANT GROWTH SUBSTANCES ON DIGITOXIN FORMATION BY UNDIFFERENTIATED CELLS AND SHOOT-FORMING CULTURES OF DIGITALIS PURPUREA L. GROWN IN LIQUID MEDIA

机译:通过植物组织培养生产洋地黄香芹素的研究:II。液体培养基中光和植物生长物质对洋地黄生长的未分化细胞和芽生培养物对地高辛形成的影响

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摘要

Undifferentiated, highly chlorophyllous cell cultures; undifferentiated white cell cultures; green, shoot-forming cultures; and white, shoot-forming cultures of Digitalis purpurea L. were established and subcultured every 3 weeks in liquid media in the light or in the dark. The digitoxin content, the chlorophyll content, and the ribulose bisphosphate carboxylase activity of these cultures were assayed. The light-grown, green, shoot-forming cultures accumulated considerable amounts of digitoxin (about 20 to 40 micrograms per gram dry weight), and the white, shoot-forming cultures without chloroplasts accumulated about one-third that amount of digitoxin. The chlorophyll content and the ribulose bisphosphate carboxylase activity of the undifferentiated green cells were about the same as they were in the green, shoot-forming cultures, but the digitoxin content of the former was extremely low (about 0.05 to 0.2 microgram per gram dry weight), which is about the same as that in undifferentiated white cells without chloroplasts. Thus, it was concluded that the chloroplasts are not essential for the synthesis of digitoxin in Digitalis cells. The optimum concentrations of the tested compounds for accumulation of digitoxin were: benzyladenine, 0.01 to 1 milligram per liter; indoleacetic acid, 0.1 to 1 milligram per liter; α-naphthaleneacetic acid; 0.1 milligram per liter; and 2,4-dichlorophenoxyacetic acid, 0.01 milligram per liter.
机译:未分化的高度叶绿素的细胞培养物;未分化的白细胞培养;绿色,形成芽的文化;建立了洋地黄的白色和白色芽形成培养物,每3周在明亮或黑暗的液体培养基中传代培养。测定了这些培养物中的洋地黄毒素含量,叶绿素含量和核糖二磷酸羧化酶活性。浅色,绿色,形成芽的培养物积累了大量的洋地黄毒素(每克干重约20至40微克),而没有叶绿体的白色,形成芽的培养物积累了约三倍洋地黄毒素的三分之一。未分化的绿色细胞的叶绿素含量和核糖二磷酸核糖羧化酶活性与绿色,新芽形成的培养物中的叶绿素含量和核糖二磷酸羧化酶活性大致相同,但前者的洋地黄毒素含量极低(每克干重约0.05至0.2微克) ),与不含叶绿体的未分化白细胞中的相同。因此,可以得出结论,叶绿体对于洋地黄细胞中洋地黄毒苷的合成不是必需的。用于积累洋地黄毒素的测试化合物的最佳浓度为:苄基腺嘌呤,每升0.01至1毫克;吲哚乙酸,每升0.1至1毫克; α-萘乙酸;每升0.1毫克;和2,4-二氯苯氧基乙酸,每升0.01毫克。

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