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Cloning of phytoene desaturase and expression analysis of carotenogenic genes in persimmon (Diospyros kaki L.) fruits

机译:柿果实中八氢番茄红素去饱和酶的克隆及其致龋基因的表达分析

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Persimmon is a commercially important fruit crop, and the fruit is rich in different kinds of bioactive compounds, among which carotenoids contribute significantly to its color and nutritional value. In this study, the cDNA of phytoene desaturase gene (PDS) was isolated by rapid amplification of cDNA ends (RACE) technique. Sequence analysis indicated that the full-length cDNA of PDS was 2064 bp, encoding 586 amino acids and containing one open reading frame (ORF) of 1761 bp. Homology analysis showed that DkPDS, which had been submitted in GenBank with accession number GU112527, shared high similarities of 80–86% with PDS cloned from other plants. Prediction of deduced proteins showed that there was no signal peptide and transmembrane topological structure in DkPDS. It was a hydrophilic and stable protein, and located in chloroplast. To examine the specific expression patterns of carotenogenic genes we had cloned from persimmon, including phytoene synthase (DkPSY), DkPDS, ζ-carotene desaturase (DkZDS), lycopene β-cyclase (DkLCYB) and β-carotene hydroxylase (DkBCH), real-time quantitative PCR (Q-PCR) was performed in flesh at five different developmental stages. The results revealed that the expression levels of DkPSY, DkPDS and DkZDS gradually increased. Nevertheless, the expression level of DkLCYB was very low and maintained relatively stable. The expression level of DkBCH was also at a low level from stage 1 to 4, and then reached the maximum at stage 5. In addition, the expression level of DkZDS was higher than that of other genes. Carotenoid detection demonstrated that both β-cryptoxanthin and total carotenoids increased with fruit development, and zeaxanthin had little change, but with a sudden increase in final stage.
机译:柿子是一种重要的商业水果,其果实中含有多种生物活性化合物,其中的类胡萝卜素对其颜色和营养价值具有重要作用。在这项研究中,通过快速扩增cDNA末端(RACE)技术分离出八氢番茄红素去饱和酶基因(PDS)的cDNA。序列分析表明,PDS的全长cDNA为2064 bp,编码586个氨基酸,含有一个1761 bp的开放阅读框(ORF)。同源性分析表明,已在GenBank中提交,登录号为GU112527的DkPDS与从其他植物克隆的PDS具有80-86%的高度相似性。推导的蛋白质的预测表明,DkPDS中没有信号肽和跨膜拓扑结构。它是一种亲水且稳定的蛋白质,位于叶绿体中。为了检查我们从柿子中克隆的致龋基因的特定表达模式,包括八氢番茄红素合酶(DkPSY),DkPDS,ζ-胡萝卜素去饱和酶(DkZDS),番茄红素β-环化酶(DkLCYB)和β-胡萝卜素羟化酶(DkBCH),在五个不同的发育阶段在果肉中进行时间定量PCR(Q-PCR)。结果表明,DkPSY,DkPDS和DkZDS的表达水平逐渐升高。但是,DkLCYB的表达水平非常低,并且保持相对稳定。从第1阶段到第4阶段,DkBCH的表达水平也处于较低水平,然后在第5阶段达到最高水平。此外,DkZDS的表达水平高于其他基因。类胡萝卜素检测表明,β-隐黄质和总类胡萝卜素均随果实发育而增加,玉米黄质变化不大,但最终阶段却突然增加。

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