Plants in the Nicotiana genus produce nicotine and related pyridine alkaloids as a part of their chemical defense against insect herbivores. These alkaloids are formed by condensation of a derivative of nicotinic acid, but the enzyme(s) involved in the final condensation step remains elusive. In Nicotiana tabacum, an orphan reductase A622 and its close homolog A622L are coordinately expressed in the root, upregulated by methyl jasmonate treatment, and controlled by the NIC regulatory loci specific to the biosynthesis of tobacco alkaloids. Conditional suppression of A622 and A622L by RNA interference inhibited cell growth, severely decreased the formation of all tobacco alkaloids, and concomitantly induced an accumulation of nicotinic acid beta-N-glucoside, a probable detoxification metabolite of nicotinic acid, in both hairy roots and methyl jasmonate-elicited cultured cells of tobacco. N-methylpyrrolinium cation, a precursor of the pyrrolidine moiety of nicotine, also accumulated in the A622(L)-knockdown hairy roots. We propose that the tobacco A622-like reductases of the PIP family are involved in either the formation of a nicotinic acid-derived precursor or the final condensation reaction of tobacco alkaloids.

译文

烟草属植物产生尼古丁和相关的吡啶生物碱,作为其对昆虫食草动物的化学防御的一部分。这些生物碱是由烟酸衍生物的缩合形成的,但是最终缩合步骤中涉及的酶仍然难以捉摸。在烟草中,孤儿还原酶A622及其紧密同源物A622L在根部协同表达,通过茉莉酸甲酯处理上调,并受烟草生物碱生物合成特异性的NIC调节基因座控制。RNA干扰对A622和A622L的条件抑制抑制了细胞的生长,严重减少了所有烟草生物碱的形成,并同时诱导了烟酸 β-N-葡萄糖苷的积累,烟酸 β-N-葡萄糖苷是烟酸的可能解毒代谢产物,在毛状根和茉莉酸甲酯诱导的烟草培养细胞中。N-甲基吡咯烷阳离子,尼古丁的吡咯烷部分的前体,也积累在A622(L)-敲低的毛状根中。我们建议PIP家族的烟草A622-like还原酶参与烟酸衍生前体的形成或烟草生物碱的最终缩合反应。

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