Biotechnology Bulletin ›› 2026, Vol. 42 ›› Issue (2): 293-305.doi: 10.13560/j.cnki.biotech.bull.1985.2025-0417

Previous Articles     Next Articles

Identification and Functional Characterization of the 4-Coumarate∶coenzyme A Ligase Gene Family in Angelica sinensis (Oliv.) Diels

LI Le-song1,2,3(), ZHANG Jin-jin1,2,3, HE Jia-die1,2,3, LIANG Yan-li1,2, YANG Sheng-chao1,3, LI Meng-fei4, ZHAO Yan1,2,3()   

  1. 1.National-Local Joint Engineering Research Center on Germplasm Innovation & Utilization of Chinese Medicinal Materials in Southwest China, Key Laboratory of Medicinal Plant Biology, Yunnan Agricultural University, Kunming 650201
    2.College of Agronomy and Biotechnology, Yunnan Agricultural University, Kunming 650201
    3.Yunnan Characteristic Plant Extraction Laboratory, Kunming 650106
    4.Agronomy College, Gansu Agricultural University, Lanzhou 730070
  • Received:2025-04-20 Online:2026-02-26 Published:2026-03-17
  • Contact: ZHAO Yan E-mail:lls15126334094@163.com;zhaoyankm@126.com

Abstract:

Objective Exploring the role of 4-coumarate: coenzyme A ligase (4CL) in lignin biosynthesis in the roots of Angelica sinensis (Oliv.) Diels, laying the foundation for targeted regulation of A. sinensis medicinal quality through genetic improvement or cultivation methods. Method The 4CL gene family of A. sinensis was identified using bioinformatics methods. The analysis on protein physicochemical properties, secondary structure prediction, gene structure, promoter cis-acting elements, and systematic evolution were conducted. The gene function was verified through heterologous expression in Escherichia coli and enzymatic assay in vitro, and its expression characteristics were analyzed by real-time quantitative PCR. Result A total of 12 As4CLs were identified in the genome of A. sinensis, encoding 415‒572 amino acids, relative molecular weights ranging from 45 to 62 kD, and isoelectric points ranging from 5.47 to 9.06. The secondary structure is mainly composed of irregular coils and α-helices. System evolution analysis categorizes As4CL6 and As4CL7 as Group I, while the remaining As4CLs belong to Group Ⅲ. The amino acid sequence alignment results showed that As4CLs contain two functionally conserved domains, Box I and Box Ⅱ. Promoter analysis showed that the As4CLs contain abundant light responsive elements, hormone responsive elements, and abiotic stress responsive elements. In vitro enzymatic assay showed that both As4CL6 and As4CL7 catalyzed 4-coumaric acid, caffeic acid, and ferulic acid to form corresponding coenzyme A thioesters, and both enzymes have the strongest affinity for ferulic acid. The RT-qPCR results showed that the expressions of As4CL6 and As4CL7 were higher in the roots of A. sinensis with bolting than in the roots unbolting. Conclusion The genes of As4CL6 and As4CL7 are successfully cloned, and enzymatic assay in vitro confirm that the two recombinant proteins demonstrate catalytic activity towards three substrates.

Key words: 4-coumarate: coenzyme A ligase, Angelica sinensis, bolting, RT-qPCR