Khanom Sanjida, Jang Jinhoon, Lee Ok Ran
Department of Applied Plant Science, College of Agriculture and Life Science, Chonnam National University, Gwangju, Republic of Korea.
J Ginseng Res. 2019 Oct;43(4):645-653. doi: 10.1016/j.jgr.2019.04.005. Epub 2019 Apr 20.
Cytochrome P450 enzymes catalyze a wide range of reactions in plant metabolism. Besides their physiological functions on primary and secondary metabolites, P450s are also involved in herbicide detoxification via hydroxylation or dealkylation. Ginseng as a perennial plant offers more sustainable solutions to herbicide resistance.
Tissue-specific gene expression and differentially modulated transcripts were monitored by quantitative real-time polymerase chain reaction. As a tool to evaluate the function of , the 35S promoter was used to overexpress the gene in Arabidopsis. Protein localization was visualized using confocal microscopy by tagging the fluorescent protein. Tolerance to herbicides was analyzed by growing seeds and seedlings on Murashige and Skoog medium containing chlorotoluron.
The expression of was three-fold more in leaves compared with other tissues from two-year-old ginseng plants. Transcript levels were similarly upregulated by treatment with abscisic acid, hydrogen peroxide, and NaCl, the highest being with salicylic acid. Jasmonic acid treatment did not alter the mRNA levels of Transgenic lines displayed slightly reduced plant height and were able to tolerate the herbicide chlorotoluron. Reduced stem elongation might be correlated with increased expression of genes involved in bioconversion of gibberellin to inactive forms. PgCYP736A12 protein localized to the cytoplasm and nucleus.
does not respond to the well-known secondary metabolite elicitor jasmonic acid, which suggests that it may not function in ginsenoside biosynthesis. Heterologous overexpression of reveals that this gene is actually involved in herbicide metabolism.
细胞色素P450酶催化植物新陈代谢中的多种反应。除了在初级和次级代谢产物中的生理功能外,P450酶还通过羟基化或脱烷基作用参与除草剂解毒。人参作为一种多年生植物,为除草剂抗性提供了更可持续的解决方案。
通过定量实时聚合酶链反应监测组织特异性基因表达和差异调节转录本。作为评估该基因功能的工具,使用35S启动子在拟南芥中过表达该基因。通过标记荧光蛋白,利用共聚焦显微镜观察蛋白质定位。通过在含有绿麦隆的Murashige和Skoog培养基上种植种子和幼苗来分析对除草剂的耐受性。
与两年生人参植株的其他组织相比,该基因在叶片中的表达量高出三倍。脱落酸、过氧化氢和氯化钠处理同样上调了转录水平,其中水杨酸处理后的转录水平最高。茉莉酸处理未改变该基因的mRNA水平。转基因株系的株高略有降低,并且能够耐受除草剂绿麦隆。茎伸长减少可能与参与赤霉素生物转化为无活性形式的基因表达增加有关。PgCYP736A12蛋白定位于细胞质和细胞核。
该基因对著名的次级代谢产物诱导剂茉莉酸无反应,这表明它可能在人参皂苷生物合成中不起作用。该基因的异源过表达表明该基因实际上参与除草剂代谢。