Guangdong Provincial Key Laboratory of Applied Botany, Key Laboratory of Post-Harvest Handling of Fruits, Ministry of Agriculture, South China Botanical Garden, Chinese Academy of Sciences, Guangzhou 510650, China; University of Chinese Academy of Sciences, Beijing 100049, China.
Guangdong Provincial Key Laboratory of Applied Botany, Key Laboratory of Post-Harvest Handling of Fruits, Ministry of Agriculture, South China Botanical Garden, Chinese Academy of Sciences, Guangzhou 510650, China.
J Proteomics. 2019 Oct 30;209:103506. doi: 10.1016/j.jprot.2019.103506. Epub 2019 Aug 24.
Softening is important for quality formation in some climacteric fruits. The molecular mechanism underlying fruit softening is, however, not well understood. In this study, we performed a comparative cell wall proteomics analysis on pre-climacteric (P1) and post-climacteric (P2) banana fruit, corresponding to fruit at the mature green stage and softening ripening stage, respectively, using isobaric tags for relative and absolute quantitation (iTRAQ) technology. A total of 5230 proteins were identified in both sample groups, of which 928 were predicted to be secreted proteins. Of the secreted proteins, 162 were differentially expressed in P2 versus P1. The majority of these proteins had catalytic activity, binding activity, electron carrier activity and antioxidant activity. Compared with P1, P2 had 105 and 57 up- and down-regulated proteins, respectively. GO and KEGG-pathway analysis of these differentially expressed secreted proteins revealed that most were implicated in cell wall metabolism, stress and defense response, signaling, and protein metabolism and modification. Quantitative RT-PCR further validated some key differentially expressed secreted proteins associated with cell wall metabolism, stress and defense response, signaling and protein destination. Our results represent the first cell wall proteome of banana fruit and comprehensive proteomic study of banana fruit softening. SIGNIFICANCE: Softening, which is the consequence of cell wall and turgor modification, is one of the most important factors determining banana fruit quality. The molecular mechanism regulating fruit softening in harvested banana is not currently well understood. In this study, we performed a comparative cell wall proteome analysis for pre-climacteric (P1) and post-climacteric (P2) banana fruit, corresponding to the mature green stage and softening ripening stage, respectively, using iTRAQ technology. We found 162 differentially expressed secreted proteins that were mainly implicated in cell wall metabolism, stress response and defense, signaling, and protein metabolism and modification. We have presented the first cell wall proteome of banana fruit and conducted a comprehensive proteomic study of banana fruit softening that will help to develop strategies to improve the sensorial quality and reduce post-harvest fruit losses.
软化对于某些呼吸跃变型果实的品质形成很重要。然而,果实软化的分子机制尚不清楚。在这项研究中,我们使用 iTRAQ 技术对采前(P1)和采后(P2)香蕉果实进行了比较细胞壁蛋白质组学分析,分别对应于成熟绿熟期和软化成熟期。在这两个样品组中,共鉴定出 5230 种蛋白质,其中 928 种被预测为分泌蛋白。在 P2 与 P1 的比较中,有 162 种分泌蛋白表达差异。这些蛋白质大多数具有催化活性、结合活性、电子载体活性和抗氧化活性。与 P1 相比,P2 分别有 105 个和 57 个上调和下调的蛋白。这些差异表达的分泌蛋白的 GO 和 KEGG 通路分析表明,它们大多数与细胞壁代谢、应激和防御反应、信号转导以及蛋白质代谢和修饰有关。定量 RT-PCR 进一步验证了一些与细胞壁代谢、应激和防御反应、信号转导以及蛋白质定位相关的关键差异表达的分泌蛋白。我们的研究结果代表了香蕉果实细胞壁蛋白质组的首次研究,也是对香蕉果实软化的综合蛋白质组学研究。意义:软化是决定香蕉果实品质的最重要因素之一,它是细胞壁和膨压改变的结果。目前对收获后香蕉果实软化的分子调控机制尚不清楚。在这项研究中,我们使用 iTRAQ 技术对采前(P1)和采后(P2)香蕉果实进行了比较细胞壁蛋白质组学分析,分别对应于成熟绿熟期和软化成熟期。我们发现了 162 种差异表达的分泌蛋白,它们主要参与细胞壁代谢、应激反应和防御、信号转导以及蛋白质代谢和修饰。我们展示了香蕉果实的第一个细胞壁蛋白质组,并对香蕉果实软化进行了全面的蛋白质组学研究,这将有助于制定提高感官品质和减少采后果实损失的策略。