Chen H U I-Y I N G, Xiong B I-X I A, Huang R O N G-B I N G, Ni Y I N G, Li X I A
Guangxi Key Laboratory of Electrochemical and Magneto-chemical Functional Materials, College of Chemistry and Bioengineering, Guilin University of Technology, Guilin, China; Zhaoqing University, Zhaoqing, China.
Guangxi Key Laboratory of Electrochemical and Magneto-chemical Functional Materials, College of Chemistry and Bioengineering, Guilin University of Technology, Guilin, China.
Plant Physiol Biochem. 2025 Mar;220:109441. doi: 10.1016/j.plaphy.2024.109441. Epub 2024 Dec 27.
Anthocyanin is the primary color-developing component in the pericarp of the passion fruit. Although the pericarp of the passion fruit is anticipated to be a significant source of anthocyanin, however, information regarding anthocyanin biosynthesis in the passion fruit pericarp remains unexplored. Based on metabolomics analysis, a total of five anthocyanins were identified in the purple-skinned passion fruit pericarp, among which three anthocyanins, petunidin-3-O-arabinoside, geranylgeranyl-3,5-O-diglucoside, and petunidin-3-O-rutinoside, play key roles in the coloration of the passion fruit pericarp. Based on proteomics analysis, a total of nine differential proteins are involved in the flavonoid metabolic process, which involves the following chalcone isomerase, flavonol synthase and anthocyanin synthasein. These proteins play important regulatory roles in anthocyanin biosynthesis and are the key regulators in anthocyanin accumulation. qRT-PCR was used to identify nine structural genes (PePAL2, PePAL4, PeC4H1, Pe4CL5, Pe4CL6, Pe4CL7, PeCHS2, PeCHS3 and PeUFGT2) playing key regulatory roles in anthocyanin synthesis in purple passion fruit pericarp. This study is expected to lay a foundation for the subsequent exploration of the regulatory mechanism of anthocyanin biosynthesis and the functional identification of related genes in passion fruit pericarp, and also to provide data support for the in-depth utilization of passion fruit resources.
花青素是西番莲果皮中主要的呈色成分。尽管西番莲果皮有望成为花青素的重要来源,然而,关于西番莲果皮中花青素生物合成的信息仍未得到探索。基于代谢组学分析,在紫色西番莲果皮中总共鉴定出五种花青素,其中三种花青素,即矮牵牛素-3-O-阿拉伯糖苷、香叶基香叶基-3,5-O-二葡萄糖苷和矮牵牛素-3-O-芸香糖苷,在西番莲果皮的着色过程中起关键作用。基于蛋白质组学分析,共有九种差异蛋白参与类黄酮代谢过程,其中包括查尔酮异构酶(chalcone isomerase),黄酮醇合酶(flavonol synthase)和花青素合酶(anthocyanin synthasein)。这些蛋白质在花青素生物合成中起重要的调节作用,是花青素积累的关键调节因子。采用qRT-PCR鉴定了九个在紫色西番莲果皮花青素合成中起关键调节作用的结构基因(PePAL2、PePAL4、PeC4H1、Pe4CL5、Pe4CL6、Pe4CL7、PeCHS2、PeCHS3和PeUFGT2)。本研究有望为后续探索西番莲果皮花青素生物合成调控机制及相关基因功能鉴定奠定基础,也为西番莲资源的深度利用提供数据支持。