液泡定位的小檗碱桥酶样蛋白是烟草中尼古丁生物合成晚期步骤所必需的。
Vacuole-localized berberine bridge enzyme-like proteins are required for a late step of nicotine biosynthesis in tobacco.
机构信息
Graduate School of Biological Sciences, Nara Institute of Science and Technology, Ikoma, Nara 630-0192, Japan.
出版信息
Plant Physiol. 2011 Apr;155(4):2010-22. doi: 10.1104/pp.110.170878. Epub 2011 Feb 22.
Tobacco (Nicotiana tabacum) plants synthesize nicotine and related pyridine-type alkaloids, such as anatabine, in their roots and accumulate them in their aerial parts as chemical defenses against herbivores. Herbivory-induced jasmonate signaling activates structural genes for nicotine biosynthesis and transport by way of the NICOTINE (NIC) regulatory loci. The biosynthesis of tobacco alkaloids involves the condensation of an unidentified nicotinic acid-derived metabolite with the N-methylpyrrolinium cation or with itself, but the exact enzymatic reactions and enzymes involved remain unclear. Here, we report that jasmonate-inducible tobacco genes encoding flavin-containing oxidases of the berberine bridge enzyme family (BBLs) are expressed in the roots and regulated by the NIC loci. When expression of the BBL genes was suppressed in tobacco hairy roots or in tobacco plants, nicotine production was highly reduced, with a gradual accumulation of a novel nicotine metabolite, dihydromethanicotine. In the jasmonate-elicited cultured tobacco cells, suppression of BBL expression efficiently inhibited the formation of anatabine and other pyridine alkaloids. Subcellular fractionation and localization of green fluorescent protein-tagged BBLs showed that BBLs are localized in the vacuoles. These results indicate that BBLs are involved in a late oxidation step subsequent to the pyridine ring condensation reaction in the biosynthesis of tobacco alkaloids.
烟草(Nicotiana tabacum)植物在其根部合成尼古丁和相关的吡啶型生物碱,如去甲烟碱,并将其积累在其地上部分,作为对草食动物的化学防御。草食性诱导的茉莉酸信号通过尼古丁(NIC)调节基因座激活尼古丁生物合成和运输的结构基因。烟草生物碱的生物合成涉及到未鉴定的烟酸衍生代谢物与 N-甲基吡咯啉阳离子或自身的缩合,但确切的酶促反应和涉及的酶仍然不清楚。在这里,我们报告说,茉莉酸诱导的烟草基因编码属于小檗碱桥酶家族(BBLs)的黄素氧化酶在根部表达,并受 NIC 基因座调控。当烟草发根或烟草植物中 BBL 基因的表达受到抑制时,尼古丁的产生显著降低,同时逐渐积累一种新的尼古丁代谢物,二氢甲尼古丁。在茉莉酸诱导的培养烟草细胞中,抑制 BBL 表达有效地抑制了去甲烟碱和其他吡啶生物碱的形成。绿色荧光蛋白标记的 BBL 的亚细胞分离和定位显示,BBLs 定位于液泡中。这些结果表明,BBLs 参与了烟草生物碱生物合成中吡啶环缩合反应后的后期氧化步骤。
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