Department of Ornamental Horticulture, Agriculture Research Organization, The Volcani Center, PO Box 6, Bet Dagan 50250, Israel.
J Exp Bot. 2010 Mar;61(5):1393-403. doi: 10.1093/jxb/erq008. Epub 2010 Mar 4.
Brunfelsia calycina flowers change colour from purple to white due to anthocyanin degradation, parallel to an increase in fragrance and petal size. Here it was tested whether the production of the fragrant benzenoids is dependent on induction of the shikimate pathway, or if they are formed from the anthocyanin degradation products. An extensive characterization of the events taking place in Brunfelsia flowers is presented. Anthocyanin characterization was performed using ultraperfomance liquid chromatography-quadrupole time of flight-tandem mass specrometry (UPLC-QTOF-MS/MS). Volatiles emitted were identified by headspace solid phase microextraction-gas chromatography-mass spectrometry (HS-SPME-GC-MS). Accumulated proteins were identified by 2D gel electrophoresis. Transcription profiles were characterized by cross-species hybridization of Brunfelsia cDNAs to potato cDNA microarrays. Identification of accumulated metabolites was performed by UPLC-QTOF-MS non-targeted metabolite analysis. The results include characterization of the nine main anthocyanins in Brunfelsia flowers. In addition, 146 up-regulated genes, 19 volatiles, seven proteins, and 17 metabolites that increased during anthocyanin degradation were identified. A multilevel analysis suggests induction of the shikimate pathway. This pathway is the most probable source of the phenolic acids, which in turn are precursors of both the benzenoid and lignin production pathways. The knowledge obtained is valuable for future studies on degradation of anthocyanins, formation of volatiles, and the network of secondary metabolism in Brunfelsia and related species.
双色金鸡菊花朵的颜色会由紫色变为白色,这是由于其中的花青素降解,同时伴随着花香和花瓣大小的增加。本研究旨在测试花香苯丙素的产生是否依赖于莽草酸途径的诱导,或者它们是否是由花青素降解产物形成的。文中详细介绍了发生在双色金鸡菊花朵中的一系列事件。通过超高效液相色谱-四极杆飞行时间串联质谱(UPLC-QTOF-MS/MS)对花青素进行了特征分析。采用顶空固相微萃取-气相色谱-质谱联用(HS-SPME-GC-MS)鉴定挥发物。通过 2D 凝胶电泳鉴定积累的蛋白质。通过将双色金鸡菊 cDNA 与马铃薯 cDNA 微阵列进行交叉物种杂交来分析转录谱。通过 UPLC-QTOF-MS 非靶向代谢物分析鉴定积累的代谢物。研究结果包括对双色金鸡菊花中 9 种主要花青素的特征分析。此外,还鉴定出 146 个上调基因、19 种挥发物、7 种蛋白质和 17 种在花青素降解过程中增加的代谢物。多层次分析表明,莽草酸途径被诱导。该途径是酚酸的最可能来源,而酚酸又是苯丙素和木质素生物合成途径的前体。这些知识对于未来研究双色金鸡菊和相关物种中花青素的降解、挥发物的形成以及次生代谢网络具有重要价值。