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Isolation of a Kaurene Synthetase Inhibitor from Castor Bean Seedlings and Cell Suspension Cultures

机译:从蓖麻子幼苗和细胞悬浮培养物中分离出一种贝壳杉烯合成酶抑制剂

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摘要

Biosynthesis of ent-kaurene was investigated in extracts of cell suspension cultures and seedlings of castor bean. Both cell-free extracts contain an inhibitor of kaurene synthetase. The inhibition affects mainly the cyclization of geranylgeranyl pyrophosphate to copalyl pyrophosphate (activity A) and has little or no effect on the further cyclization of copalyl pyrophosphate to ent-kaurene (activity B) in both castor bean and Fusarium moniliforme cell-free enzyme preparations. In castor bean cell suspension cultures, the inhibitor diffuses out of the cells to the growth medium. The inhibitor is stable to 100 C heat treatment for 10 minutes and exposure to pH values of 2.0 or 13.0, and it diffuses through a dialysis bag (104-dalton cutoff). Gel filtration chromatography of the inhibitor on a calibrated Bio-Gel P-10 column indicated a molecular weight of 7,500. Kinetic studies indicate that the inhibition of activity of A of kaurene synthetase is noncompetitive and reversible.
机译:在蓖麻子的细胞悬浮培养物和幼苗中研究了丁香酚的生物合成。两种无细胞提取物均含有一种贝壳杉烯合成酶抑制剂。抑制作用主要影响蓖麻籽和无镰孢镰刀菌无细胞酶制剂中的香叶基香叶基焦磷酸焦磷酸环化为焦磷酸焦磷酸酯(活性A),而对焦磷酸焦磷酸基戊酯进一步环化为戊烯(活性B)几乎没有影响。在蓖麻子细胞悬浮培养物中,抑制剂从细胞中扩散到生长培养基中。该抑制剂在100℃的热处理条件下稳定10分钟,并在pH值为2.0或13.0的条件下稳定,并通过透析袋扩散(10 4 -道尔顿截止)。在校准的Bio-Gel P-10色谱柱上对抑制剂进行凝胶过滤层析,表明分子量为7,500。动力学研究表明,对月桂烯合成酶A活性的抑制是非竞争性和可逆的。

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