Biotechnology Research Center and Department of Biotechnology, Toyama Prefectural University, 5180 Kurokawa, Imizu, Toyama, 939-0398, Japan.
Asano Active Enzyme Molecule Project, ERATO, JST, 5180 Kurokawa, Imizu, Toyama, 939-0398, Japan.
Plant Mol Biol. 2016 Jun;91(3):229-39. doi: 10.1007/s11103-016-0459-6. Epub 2016 Feb 29.
The giant knotweed Fallopia sachalinensis (Polygonaceae) synthesizes phenylacetonitrile (PAN) from L-phenylalanine when infested by the Japanese beetle Popillia japonica or treated with methyl jasmonate (MeJA). Here we identified (E/Z)-phenylacetaldoxime (PAOx) as the biosynthetic precursor of PAN and identified a cytochrome P450 that catalysed the conversion of (E/Z)-PAOx to PAN. Incorporation of deuterium-labelled (E/Z)-PAOx into PAN emitted from the leaves of F. sachalinensis was detected using gas chromatography-mass spectrometry. Further, using liquid chromatography-tandem mass spectrometry, we detected the accumulation of (E/Z)-PAOx in MeJA-treated leaves. These results showed that (E/Z)-PAOx is the biosynthetic precursor of PAN. MeJA-induced mRNAs were analysed by differential expression analysis using a next-generation sequencer. Of the 74,329 contigs obtained from RNA-seq and de novo assembly, 252 contigs were induced by MeJA treatment. Full-length cDNAs encoding MeJA-induced cytochrome P450s CYP71AT96, CYP82AN1, CYP82D125 and CYP715A35 were cloned using 5'- and 3'-RACE and were expressed using a baculovirus expression system. Among these cytochrome P450s, CYP71AT96 catalysed the conversion of (E/Z)-PAOx to PAN in the presence of NADPH and a cytochrome P450 reductase. It also acted on (E/Z)-4-hydroxyphenylacetaldoxime and (E/Z)-indole-3-acetaldoxime. The broad substrate specificity of CYP71AT96 was similar to that of aldoxime metabolizing cytochrome P450s. Quantitative RT-PCR analysis showed that CYP71AT96 expression was highly induced because of treatment with MeJA as well as feeding by the Japanese beetle. These results indicate that CYP71AT96 likely contributes the herbivore-induced PAN biosynthesis in F. sachalinensis.
大型葛藤(Polygonaceae)在受到日本甲虫 Popillia japonica 侵害或用茉莉酸甲酯(MeJA)处理时,会从 L-苯丙氨酸合成苯乙腈(PAN)。在这里,我们确定(E/Z)-苯乙酮肟(PAOx)是 PAN 的生物合成前体,并鉴定出一种细胞色素 P450,它催化(E/Z)-PAOx 转化为 PAN。使用气相色谱-质谱法检测从 F. sachalinensis 叶片中释放的氘标记的(E/Z)-PAOx 掺入 PAN 中。此外,使用液相色谱-串联质谱法,我们检测到 MeJA 处理叶片中(E/Z)-PAOx 的积累。这些结果表明(E/Z)-PAOx 是 PAN 的生物合成前体。使用下一代测序仪通过差异表达分析分析 MeJA 诱导的 mRNA。从 RNA-seq 和从头组装中获得的 74329 个连续体中,有 252 个连续体被 MeJA 处理诱导。使用 5'-和 3'-RACE 克隆全长 cDNA 编码 MeJA 诱导的细胞色素 P450 CYP71AT96、CYP82AN1、CYP82D125 和 CYP715A35,并使用杆状病毒表达系统进行表达。在这些细胞色素 P450 中,CYP71AT96 在 NADPH 和细胞色素 P450 还原酶存在下催化(E/Z)-PAOx 转化为 PAN。它还作用于(E/Z)-4-羟基苯乙酮肟和(E/Z)-吲哚-3-乙酮肟。CYP71AT96 的广泛底物特异性与醛肟代谢细胞色素 P450 相似。定量 RT-PCR 分析表明,由于 MeJA 处理以及日本甲虫的取食,CYP71AT96 的表达高度诱导。这些结果表明 CYP71AT96 可能有助于 F. sachalinensis 中食草动物诱导的 PAN 生物合成。