首页> 美国卫生研究院文献>Plant Physiology >Regulation of the Cinnamate 4-Hydroxylase (CYP73A1) in Jerusalem Artichoke Tubers in Response to Wounding and Chemical Treatments.
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Regulation of the Cinnamate 4-Hydroxylase (CYP73A1) in Jerusalem Artichoke Tubers in Response to Wounding and Chemical Treatments.

机译:洋蓟块茎中肉桂酸4-羟化酶(CYP73A1)的调节以应对创伤和化学治疗。

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摘要

trans-Cinnamate 4-hydroxylase (C4H) is a plant-specific cytochrome (P450) that is encoded by the gene CYP73A and catalyzes the second step of the multibranched phenylpropanoid pathway. Increases in C4H activity in response to physical and chemical stresses have been well documented, but the mechanism of these increases has never been studied in detail. This paper reports on the regulatory mechanism controlling C4H activity in Jerusalem artichoke (Helianthus tuberosus) tubers in response to wounding and chemical treatments. We compared induction of C4H and other P450-catalyzed activities. C4H was moderately induced by chemicals relative to other P450s. Increases in enzyme activity, C4H protein, and transcripts were quantified and compared in tuber tissue 48 h after wounding and chemical treatments. Our data suggest that induction of the enzyme activity results primarily from gene activation. Time-course experiments were performed after wounding and aminopyrine treatment. Compared with wounded tissues, aminopyrine triggered an additional and delayed peak of transcript accumulation. The timing of the induced changes in activity, protein, and transcripts confirms that C4H induction results primarily from an increase in CYP73A1 mRNA, in both wounded and aminopyrine-treated tissues. However, posttranscriptional mechanisms might also contribute to the regulation of C4H activity.
机译:反肉桂酸4-羟化酶(C4H)是一种植物特异的细胞色素(P450),由基因CYP73A编码,并催化多分支苯基丙烷途径的第二步。 C4H活性响应物理和化学应力的增加已经有充分的文献记载,但是这些增加的机制尚未得到详细研究。本文报道了针对伤害和化学疗法控制洋蓟块茎中C4H活性的调控机制。我们比较了C4H和其他P450催化活性的诱导。相对于其他P450,化学物质可适度诱导C4H。伤口和化学处理后48小时,在块茎组织中定量和比较了酶活性,C4H蛋白和转录本的增加。我们的数据表明,酶活性的诱导主要来自基因激活。伤口和氨基比林治疗后进行时程实验。与受伤的组织相比,氨基比林触发了转录物积累的额外且延迟的峰值。活性,蛋白质和转录本诱导变化的时机证实,C4H诱导主要是由CYP73A1 mRNA在伤口组织和氨基比林处理的组织中的增加所致。但是,转录后机制也可能有助于C4H活性的调节。

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