首页> 外文OA文献 >Stable Isotope Labeling, in Vivo, of d- and l-Tryptophan Pools in Lemna gibba and the Low Incorporation of Label into Indole-3-Acetic Acid 1
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Stable Isotope Labeling, in Vivo, of d- and l-Tryptophan Pools in Lemna gibba and the Low Incorporation of Label into Indole-3-Acetic Acid 1

机译:Lemna gibba中d和l色氨酸池的体内稳定同位素标记以及标记物在吲哚-3-乙酸中的低掺入1

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摘要

We present evidence that the role of tryptophan and other potential intermediates in the pathways that could lead to indole derivatives needs to be reexamined. Two lines of Lemna gibba were tested for uptake of [15N-indole]-labeled tryptophan isomers and incorporation of that label into free indole-3-acetic acid (IAA). Both lines required levels of l-[15N]tryptophan 2 to 3 orders of magnitude over endogenous levels in order to obtain measurable incorporation of label into IAA. Labeled l-tryptophan was extractable from plant tissue after feeding and showed no measurable isomerization into d-tryptophan. d-[15N]tryptophan supplied to Lemna at rates of approximately 400 times excess of endogenous d-tryptophan levels (to yield an isotopic enrichment equal to that which allowed detection of the incorporation of l-tryptophan into IAA), did not result in measurable incorporation of label into free IAA. These results demonstrate that l-tryptophan is a more direct precursor to IAA than the d isomer and suggest (a) that the availability of tryptophan in vivo is not a limiting factor in the biosynthesis of IAA, thus implying that other regulatory mechanisms are in operation and (b) that l-tryptophan also may not be a primary precursor to IAA in plants.
机译:我们提供的证据表明,色氨酸和其他可能的中间体在可能导致吲哚衍生物的途径中的作用需要重新研究。测试了两个Lemna gibba品系对[15N-吲哚]标记的色氨酸异构体的吸收,并将该标记掺入游离的吲哚-3-乙酸(IAA)中。两条线都要求1- [15N]色氨酸的水平比内源水平高2至3个数量级,以便获得可测量的标记掺入IAA的水平。饲喂后可从植物组织中提取标记的l-色氨酸,并且没有可测量的异构化成d-色氨酸。提供给Lemna的d- [15N]色氨酸的速率约为内源性d-色氨酸水平的400倍以上(产生的同位素富集程度等于检测到I-色氨酸掺入IAA的同位素富集程度),无法测量将标签并入免费的IAA中。这些结果表明,l-色氨酸比d-异构体是IAA的更直接前体,并表明(a)体内色氨酸的可用性不是IAA生物合成的限制因素,因此暗示其他调节机制正在发挥作用。 (b)l-色氨酸也可能不是植物中IAA的主要前体。

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