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首页> 外文期刊>日本作物學會紀事 >Studies on the Breaking of Dormancy in Barnyardgrass Seed : III. Change of the dormancy-breaking effect of various compounds concerning with oxidation-reduction system by dormancy stage
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Studies on the Breaking of Dormancy in Barnyardgrass Seed : III. Change of the dormancy-breaking effect of various compounds concerning with oxidation-reduction system by dormancy stage

机译:Barnyardgrass种子中休眠突破的研究:III。各种化合物与休眠阶段氧化还原系统的休眠效果的变化

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This paper forms the third part of a series of investigations on the control of the breaking of dormancy in barnyardgrass (Echinochloa Crusgalli var. oryzicola Ohwi) seed. This investigation evaluated the dormancy-breaking effect of various compounds concerning with endogenous oxidation-reduction system and the change of its effect through the dormancy-breaking process. 1) In deep dormancy stage, hydroquinone and benzoquinone showed a stimulative effect on the breaking of dormancy in considerable degree. Moreover, as the dormancy became shallow, the effect of these compounds was higher than in deep stage. 2) In shallower dormancy stage, guaiacol, resorcinol and L-ascorbic acid had effect as remarkable as hydroquinone. However, no effect was shown by pyrogallol and catechol in any dormancy stage. 3) In shallow stage, o-cresol showed a marked effect on the breaking of dormancy, but m- and p-cresol had no effect. 4) There is no relationship between the dormancy-breaking effect and the inhibition of oxygen up-take, comparing with guaiacol, resorcinol, catechol and pyrogallol treatments. The results obtained suggest that the inhibition of tyrosinase (polyphenol oxidase) is the critical factor in the dormancy-breaking action of hydroquinone, resorcinol, quaiacol and L-ascorbic acid, which are known not to be substrates of tyrosinase and to be inhibitors of the enzyme.
机译:本文形成了对禁止休眠中休眠(Echinochloa Crusgalli var的休眠突破的一系列调查的第三部分。奥西辛洛拉ohwi)种子。该研究评估了各种化合物关于内源性氧化还原系统的休眠性破裂效果,以及通过休眠破裂过程的效果的变化。 1)在深层休眠阶段,氢醌和苯醌在相当程度下对休眠突破的刺激作用。而且,随着休眠变浅,这些化合物的效果高于深阶段。 2)在较浅的休眠阶段,GuaiaCol,间苯二酚和L-抗坏血酸具有显着作为氢醌的效果。然而,在任何休眠阶段的吡羟镓和儿茶酚中没有显示任何效果。 3)在浅阶段,O-甲酚对休眠的破裂显示出明显的影响,但M-和P-甲酚无效。 4)休眠破裂效应与氧气抑制之间没有关系,与愈牙醇,间苯二酚,儿茶酚和吡尔治疗相比。得到的结果表明,酪氨酸酶(多酚氧化酶)的抑制是氢醌,间苯二酚,Quaiacol和L-抗坏血酸的休眠作用的关键因素,这已知不作为酪氨酸酶的基材并是抑制剂酶。

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