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精氨酸脱羧酶作为烟草生物碱中腐胺的来源。

Arginine decarboxylase as the source of putrescine for tobacco alkaloids.

作者信息

Tiburcio A F, Galston A W

机构信息

Department of Biology, Yale University, New Haven, Connecticut 06511, USA.

出版信息

Phytochemistry. 1986;25(1):107-10. doi: 10.1016/s0031-9422(00)94511-4.

Abstract

The putrescine which forms a part of nicotine and other pyrrolidine alkaloids is generally assumed to arise through the action of ornithine decarboxylase (ODC). However, we have previously noted that changes in the activity of arginine decarboxylase (ADC), an alternate source of putrescine, parallel changes in tissue alkaloids, while changes in ODC activity do not. This led us to undertake experiments to permit discrimination between ADC and ODC as enzymatic sources of putrescine destined for alkaloids. Two kinds of evidence presented here support a major role for ADC in the generation of putrescine going into alkaloids: (a) A specific 'suicide inhibitor' of ADC effectively inhibits the biosynthesis of nicotine and nornicotine in tobacco callus, while the analogous inhibitor of ODC is less effective, and (b) the flow of 14C from uniformly labelled arginine into nicotine is much more efficient than that from ornithine.

摘要

腐胺是尼古丁和其他吡咯烷生物碱的组成部分,一般认为它是通过鸟氨酸脱羧酶(ODC)的作用产生的。然而,我们之前已经注意到,作为腐胺另一个来源的精氨酸脱羧酶(ADC)的活性变化与组织生物碱的变化平行,而ODC活性的变化则不然。这促使我们进行实验,以区分ADC和ODC作为生物碱中腐胺的酶源。这里提出的两类证据支持了ADC在进入生物碱的腐胺生成中起主要作用:(a)一种特定的ADC“自杀抑制剂”能有效抑制烟草愈伤组织中尼古丁和去甲烟碱的生物合成,而类似的ODC抑制剂效果较差;(b)从均匀标记的精氨酸流入尼古丁的14C流比从鸟氨酸流入的效率高得多。

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