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罗汉果果实高效瞬时表达系统的建立及两种 NADPH-细胞色素 P450 还原酶的功能表征。

Development of an efficient transient expression system for Siraitia grosvenorii fruit and functional characterization of two NADPH-cytochrome P450 reductases.

机构信息

Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100193, China.

Guilin GFS Monk Fruit Corp, Guilin, 541006, China.

出版信息

Phytochemistry. 2021 Sep;189:112824. doi: 10.1016/j.phytochem.2021.112824. Epub 2021 Jun 6.

Abstract

Siraitia grosvenorii (Luo hanguo or monk fruit) is a valuable medicinal herb for which the market demand has increased dramatically worldwide. As promising natural sweeteners, mogrosides have received much attention from researchers because of their extremely high sweetness and lack of calories. Nevertheless, owing to the absence of genetic transformation methods, the molecular mechanisms underlying the regulation of mogroside biosynthesis have not yet been fully elucidated. Therefore, an effective method for gene function analysis needs to be developed for S. grosvenorii fruit. As a powerful approach, transient expression has become a versatile method to elucidate the biological functions of genes and proteins in various plant species. In this study, PBI121 with a β-glucuronidase (GUS) marker and tobacco rattle virus (TRV) were used as vectors for overexpression and silencing, respectively, of the SgCPR1 and SgCPR2 genes in S. grosvenorii fruit. The effectiveness of transient expression was validated by GUS staining in S. grosvenorii fruit, and the expression levels of SgCPR1 and SgCPR2 increased significantly after infiltration for 36 h. In addition, TRV-induced gene silencing suppressed the expression of SgCPR1 and SgCPR2 in S. grosvenorii fruit. More importantly, the production of the major secondary metabolites mogrol, mogroside IIE (MIIE) and mogroside III (MIII) was activated by the overexpression of SgCPR1 and SgCPR2 in S. grosvenorii fruit, with levels 1-2 times those in the control group. Moreover, the accumulation of mogrol, MIIE and MIII was decreased in the SgCPR1 and SgCPR2 gene silencing assays. Therefore, this transient expression approach was available for S. grosvenorii fruit, providing insight into the expression of the SgCPR1 and SgCPR2 genes involved in the mogroside biosynthesis pathway. Our study also suggests that this method has potential applications in the exploration of the molecular mechanisms, biochemical hypotheses and functional characteristics of S. grosvenorii genes.

摘要

罗汉果(Luo hanguo 或 monk fruit)是一种有价值的药用植物,其全球市场需求急剧增加。作为有前途的天然甜味剂,罗汉果苷因其极高的甜度和缺乏卡路里而受到研究人员的广泛关注。然而,由于缺乏遗传转化方法,罗汉果苷生物合成调控的分子机制尚未完全阐明。因此,需要为罗汉果果实开发一种有效的基因功能分析方法。作为一种强大的方法,瞬时表达已成为阐明各种植物物种中基因和蛋白质生物学功能的通用方法。在这项研究中,使用 PBI121 作为带有β-葡萄糖醛酸酶(GUS)标记的载体,以及烟草脆裂病毒(TRV)作为过表达和沉默载体,分别在罗汉果果实中过表达和沉默 SgCPR1 和 SgCPR2 基因。通过 GUS 染色在罗汉果果实中验证了瞬时表达的有效性,并且在渗透 36 小时后,SgCPR1 和 SgCPR2 的表达水平显著增加。此外,TRV 诱导的基因沉默抑制了罗汉果果实中 SgCPR1 和 SgCPR2 的表达。更重要的是,SgCPR1 和 SgCPR2 的过表达激活了罗汉果果实中主要次生代谢物 mogrol、mogroside IIE(MIIE)和 mogroside III(MIII)的产生,其水平是对照组的 1-2 倍。此外,在 SgCPR1 和 SgCPR2 基因沉默试验中,mogrol、MIIE 和 MIII 的积累减少。因此,这种瞬时表达方法可用于罗汉果果实,为研究参与罗汉果苷生物合成途径的 SgCPR1 和 SgCPR2 基因的表达提供了依据。我们的研究还表明,该方法在探索罗汉果基因的分子机制、生化假设和功能特征方面具有潜在应用。

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