Univ Lyon, Université Claude Bernard Lyon 1, CNRS, INRAE, VetAgro Sup, UMR Ecologie Microbienne, F-69622 Villeurbanne, France.
Univ Lyon, Université Claude Bernard Lyon 1, CNRS, INRAE, VetAgro Sup, UMR Ecologie Microbienne, F-69622 Villeurbanne, France; Université d'Orléans, CNRS, Institut de Chimie Organique et Analytique, F-45067 Orléans, France.
J Chromatogr B Analyt Technol Biomed Life Sci. 2021 Jan 1;1162:122458. doi: 10.1016/j.jchromb.2020.122458. Epub 2020 Nov 26.
Opines are low-molecular-weight metabolites specifically biosynthesized by agrobacteria-transformed plant cells when plants are struck by crown gall and hairy root diseases, which cause uncontrolled tissue overgrowth. Transferred DNA is sustainably incorporated into the genomes of the transformed plant cells, so that opines constitute a persistent biomarker of plant infection by pathogenic agrobacteria and can be targeted for crown gall/hairy root disease diagnosis. We developed a general, rapid, specific and sensitive analytical method for overall opine detection using ultra-high-performance liquid chromatography-electrospray ionization quadrupole time-of-flight mass spectrometry (UHPLC-ESI-MS-QTOF), with easy preparation of samples. Based on MS, MS/MS and chromatography data, the detection selectivity of a wide range of standard opines was validated in pure solution and in different plant extracts. The method was successfully used to detect different structural types of opines, including opines for which standard compounds are unavailable, in tumors or hairy roots induced by pathogenic strains. As the method can detect a wide range of opines in a single run, it represents a powerful tool for plant gall analysis and crown gall/hairy root disease diagnosis. Using an appropriate dilution of plant extract and a matrix-based calibration curve, the quantification ability of the method was validated for three opines belonging to different families (nopaline, octopine, mannopine), which were accurately quantified in plant tissue extracts.
农杆菌转化的植物细胞在受到根癌病和发根病侵袭时会特异性地生物合成低分子量代谢物——植物冠瘿碱和发状根碱,这两种物质会导致组织不受控制地过度生长。转移 DNA 可持续地整合到转化植物细胞的基因组中,因此植物冠瘿病/发根病诊断可以针对植物感染致病农杆菌的持久性生物标志物——植物冠瘿碱进行。我们开发了一种通用、快速、特异、灵敏的基于超高效液相色谱-电喷雾电离四极杆飞行时间质谱(UHPLC-ESI-MS-QTOF)的整体植物冠瘿碱检测分析方法,该方法样品制备简单。基于 MS、MS/MS 和色谱数据,在纯溶液和不同植物提取物中验证了标准植物冠瘿碱的检测选择性。该方法成功地用于检测由致病菌株诱导的肿瘤或发根中的不同结构类型的植物冠瘿碱,包括标准化合物不可用的植物冠瘿碱。由于该方法可以在单次运行中检测到广泛的植物冠瘿碱,因此它是植物瘿瘤分析和植物冠瘿病/发根病诊断的有力工具。通过适当稀释植物提取物并采用基质校准曲线,对该方法对属于不同家族的三种植物冠瘿碱(胭脂碱、瓜氨酸、甘露碱)的定量能力进行了验证,这些植物冠瘿碱在植物组织提取物中得到了准确的定量。