Abscinazole-E1, a novel chemical tool for exploring the role of ABA 8′-hydroxylase CYP707A

Abscinazole-E1, a novel chemical tool for exploring the role of ABA 8′-hydroxylase CYP707A
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DOI:
10.1016/j.bmc.2010.11.011
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发表时间:
2011-01-01
影响因子:
3.5
通讯作者:
Todoroki, Yasushi
Todoroki, Yasushi
中科院分区:
医学3区
文献类型:
--
作者:
Okazaki, Mariko;Nimitkeatkai, Hataitip;Todoroki, Yasushi

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我们开发了脱落酸(阿坝)8 ′-羟化酶(CYP 707 A)特异性抑制剂阿贝唑-E1(Abz-E1)。该抑制剂被设计和合成为烯效唑(UNI)的放大类似物,烯效唑(UNI)是一种众所周知的植物生长阻滞剂,其抑制赤霉素生物合成酶(对映贝壳杉烯氧化酶,CYP 701 A)以及CYP 707 A。我们的研究结果表明,Abz-E1作为一个有效的抑制剂的CYP 707 A和CYP 701 A的不良抑制剂在体外和体内。施用Abz-E1可提高植物的脱水耐性,并增加内源阿坝。(C)2010爱思唯尔有限公司版权所有。
We developed abscinazole-E1 (Abz-E1), a specific inhibitor of abscisic acid (ABA) 8'-hydroxylase (CYP707A). This inhibitor was designed and synthesized as an enlarged analogue of uniconazole (UNI), a well-known plant growth retardant, which inhibits a gibberellin biosynthetic enzyme (ent-kaurene oxidase, CYP701A) as well as CYP707A. Our results showed that Abz-E1 functions as a potent inhibitor of CYP707A and a poor inhibitor of CYP701A both in vitro and in vivo. Abz-E1 application to plants resulted in improved desiccation tolerance and an increase in endogenous ABA. (C) 2010 Elsevier Ltd. All rights reserved.