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印度梨形孢培养滤液和细胞提取物诱导紫锥菊毛状根中菊苣酸的产生。

Piriformospora indica culture filtrate and cell extract induce chicoric acid production in Echinacea purpurea hairy roots.

作者信息

Khalili Samane, Moieni Ahmad, Safaie Naser, Sabet Mohammad Sadegh

机构信息

Department of Plant Genetics and Breeding, Faculty of Agriculture, Tarbiat Modares University, Tehran, P.O. Box: 14115-336, Iran.

Department of Plant Pathology, Faculty of Agriculture, Tarbiat Modares University, Tehran, P.O. Box: 14115-336, Iran.

出版信息

PLoS One. 2025 Jun 17;20(6):e0323961. doi: 10.1371/journal.pone.0323961. eCollection 2025.

Abstract

Echinacea purpurea (L.) Moench, commonly known as purple coneflower, is a significant medicinal plant renowned for its therapeutic properties, which are attributed to various phytochemical compounds, including caffeic acid derivatives (CADs). Chicoric acid is one of the CADs that has important immunostimulatory properties. This study employed a hairy roots (HRs) culture and an elicitation system to enhance the production of chicoric acid in E. purpurea. HRs cultures were established, and different concentrations (0, 1.25, 2.5, 5, and 10% v/v) of elicitors derived from Piriformospora indica culture filtrate (CF) and cell extract (CE) were added at two time points during the HRs growth period (on days 24 and 26). The effects of these treatments on the growth of HRs, chicoric acid production, and the expression of genes involved in the chicoric acid biosynthesis pathway were investigated. The highest dry weight of HRs (2.19 g/L, 1.36% higher than that in the control) was achieved in the HRs culture treated with 5% CF on the 24th day. In contrast, 5 and 10% (v/v) of P. indica CE, regardless of addition time, significantly decreased HRs growth compared to the control. The maximum production of chicoric acid (15.52 mg/g DW) was recorded after 48 h in the HRs culture treated with 5% CE on day 24, representing a 2.6-fold increase compared to the control (5.95 mg/g DW). Additionally, adding 2.5% CF to the HRs culture on day 26 resulted in a 2.3-fold increase compared to the control (13.5 mg/g DW) in chicoric acid biosynthesis. Real-time PCR assays revealed that the expression levels of the genes PAL, C4H, 4CL, C3H, and HCT were significantly upregulated after 3 and 12 h of elicitation with CE and CF. The highest gene expression was recorded for the C4H and PAL genes, 3 h after elicitation by CE (29.64 and 26.2-fold increases compared to the control culture). In contrast, the expressions of the 4CL and C3H genes peaked 12 h after elicitation with CF. The expression of the HCT gene also reached its highest level after 12 h of CE elicitation. Consistent with the chicoric acid production results, CE was found to be a more effective elicitor for inducing gene expression in the chicoric acid biosynthesis pathway. Overall, these findings indicate that HRs cultures and elicitors derived from P. indica are promising strategies to enhance chicoric acid production in E. purpurea (L.).

摘要

紫锥菊(Echinacea purpurea (L.) Moench),通常被称为紫松果菊,是一种重要的药用植物,以其治疗特性而闻名,这些特性归因于各种植物化学化合物,包括咖啡酸衍生物(CADs)。菊苣酸是具有重要免疫刺激特性的CADs之一。本研究采用毛状根(HRs)培养和诱导系统来提高紫锥菊中菊苣酸的产量。建立了HRs培养体系,并在HRs生长期间的两个时间点(第24天和第26天)添加不同浓度(0、1.25、2.5、5和10% v/v)来自印度梨形孢培养滤液(CF)和细胞提取物(CE)的诱导剂。研究了这些处理对HRs生长、菊苣酸产量以及菊苣酸生物合成途径相关基因表达的影响。在第24天用5% CF处理的HRs培养物中,HRs的最高干重(2.19 g/L,比对照高1.36%)得以实现。相比之下,5%和10%(v/v)的印度梨形孢CE,无论添加时间如何,与对照相比均显著降低了HRs的生长。在第24天用5% CE处理的HRs培养物中,48小时后菊苣酸的最大产量(15.52 mg/g DW)被记录下来,与对照(5.95 mg/g DW)相比增加了2.6倍。此外,在第26天向HRs培养物中添加2.5% CF,菊苣酸生物合成与对照(13.5 mg/g DW)相比增加了2.3倍。实时PCR分析表明,用CE和CF诱导3小时和12小时后,PAL、C4H、4CL、C3H和HCT基因的表达水平显著上调。CE诱导3小时后,C4H和PAL基因的表达最高(与对照培养物相比分别增加29.64倍和26.2倍)。相比之下,4CL和C3H基因的表达在CF诱导12小时后达到峰值。HCT基因的表达在CE诱导12小时后也达到最高水平。与菊苣酸产量结果一致,发现CE是诱导菊苣酸生物合成途径中基因表达的更有效诱导剂。总体而言,这些发现表明HRs培养和来自印度梨形孢的诱导剂是提高紫锥菊中菊苣酸产量的有前景的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b97/12173382/63d358459b3e/pone.0323961.g001.jpg

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