Department of Vegetable and Field Crops, Institute of Plant Sciences, Agricultural Research Organization (ARO), Volcani Institute, 68 HaMaccabim Road, P.O. Box 15159, Rishon LeZion, 7505101, Israel.
Plant Physiol Biochem. 2024 Oct;215:108991. doi: 10.1016/j.plaphy.2024.108991. Epub 2024 Jul 31.
The chemical and transcriptional changes in the cuticle of pomegranate (Punica granatum L.) fruit grown under different environmental conditions were studied. We collected fruit from three orchards located in different regions in Israel, each with a distinct microclimate. Fruit were collected at six phenological stages, and cutin monomers in the fruit cuticle were profiled by gas chromatography-mass spectrometry (GC-MS), along with qPCR transcript-expression analyses of selected cutin-related genes. While fruit phenotypes were comparable along development in all three orchards, principal component analyses of cutin monomer profiles suggested clear separation between cuticle samples of young green fruit to those of maturing fruit. Moreover, total cutin contents in green fruit were lower in the orchard characterized by a hot and dry climate compared to orchards with moderate temperatures. The variances detected in total cutin contents between orchards corresponded well with the expression patterns of BODYGUARD, a key biosynthetic gene operating in the cutin biosynthetic pathway. Based on our extraction protocols, we found that the cutin polyester that builds the pomegranate fruit cuticle accumulates some levels of gallic acid-the precursor of punicalagin, a well-known potent antioxidant metabolite in pomegranate fruit. The gallic acid was also one of the predominant metabolites contributing to the variability between developmental stages and orchards, and its accumulation levels were opposite to the expression patterns of the UGT73AL1 gene which glycosylates gallic acid to synthesize punicalagin. To the best of our knowledge, this is the first detailed composition of the cutin polyester that forms the pomegranate fruit cuticle.
本研究旨在探讨不同环境条件下生长的石榴(Punica granatum L.)果实的角质层在化学成分和转录水平上的变化。我们从以色列三个具有不同微气候的果园中采集果实,每个果园都有不同的地理位置。在六个物候期收集果实,并通过气相色谱-质谱联用技术(GC-MS)对果实角质层中的角质单体进行分析,同时对选定的角质相关基因进行 qPCR 转录表达分析。尽管三个果园中果实的表型在整个发育过程中都相似,但角质单体图谱的主成分分析表明,幼果的角质层样本与成熟果实的角质层样本之间存在明显的分离。此外,与温度适中的果园相比,气候炎热干燥的果园中绿色果实的总角质含量较低。果园间总角质含量的差异与 BODYGUARD 基因的表达模式密切相关,后者是角质生物合成途径中的关键生物合成基因。根据我们的提取方案,我们发现构建石榴果实角质层的聚酯角质积累了一定水平的没食子酸——这是石榴果实中一种已知的强效抗氧化代谢物 punicalagin 的前体。没食子酸也是导致不同发育阶段和果园间差异的主要代谢物之一,其积累水平与 UGT73AL1 基因的表达模式相反,后者将没食子酸糖基化合成 punicalagin。据我们所知,这是首次详细分析形成石榴果实角质层的聚酯角质的组成。