Plant growth-promoting endophytic consortium improved artemisinin biosynthesis via modulating antioxidants, gene expression, and transcriptional profile in Artemisia annua (L.) under stressed environments

IF 6.8 Q1 PLANT SCIENCES Plant Stress Pub Date : 2025-03-01 Epub Date: 2025-01-26 DOI:10.1016/j.stress.2025.100757
Arpita Tripathi , Praveen Pandey , Shakti Nath Tripathi , Alok Kalra
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Abstract

Artemisia annua L., an important medicinal plant in traditional Chinese medicine, produces an array of secondary metabolites, most notably artemisinin, a potent anti-malarial phytomolecule. However, its low concentration restricts its supply, necessitating a sustainable approach for increasing in planta artemisinin biosynthesis. The biosynthesis of secondary metabolites in plants relies on a multi-step cellular cascade known to be triggered by linked endophytes. Since no single endophyte can up-regulate every step in the biosynthesis process, we tried a consortium of four endophytes: ART1 (Bacillus subtilis), ART2 (Bacillus licheniformis), ART7 (Burkholderia sp.) and ART9 (Acinetobacter pittii) regulating key artemisinin biosynthesis pathway genes and transcriptional factors (TFs) for attaining maximum artemisinin yield. Intriguingly, all the endophytes inoculated plants showed enhanced growth, greater adaptability, and ability to mitigate environmental stresses, which might be attributed to the improved accumulation of chlorophyll, carotenoid, protein, catalase (CAT), superoxide dismutase (SOD), ascorbate peroxidase (APX) and glutathione reductase (GR) while reduction in proline and 1-Aminocyclopropane-1-carboxylic acid (ACC) level. Moreover, consortia and ART7 enhanced remarkable biomass in all four environments viz., normal (41.78 %, 29.05 %), drought (62.91 %, 29.37 %), salinity (35.15 %, 23.71 %), and waterlogging (48.37 %, 39.52 %); as well as artemisinin content in normal (51.61 %, 41.16 %), drought (32.87 %, 28.76 %), salinity (25.64 %, 19.23 %), and waterlogging (31.57 %, 28.07 %) compared to control. This stimulation of artemisinin by consortia and ART7 emerged from the up-regulation of major structural genes like CYP7AV1, DXS1, HMGR, DXR1, FPS, ADS, ADH2, SQC, ALDH, HMGS, ADH1, and ISPH while down-regulation of SQS, that enabled the metabolic flux flowed toward artemisinin biosynthesis and were able to disrupt the restricted enzymatic stages in the artemisinin biosynthesis pathway; besides, TFs such as bZIP, AP2, C3H, ARF, E2F, MYB, WRKY, MYC, and ERF modulate gene expression, and these proved as possible candidates for studying adaptation to multiple stress and their mechanisms. In summary, our study reflects the potential of the endophytic consortium for strengthening one endophyte's functional vulnerability with another to gain maximum artemisinin yield and plant tolerance against various stresses via regulating essential metabolic pathway genes.

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植物促生长内生菌联合体通过调节逆境环境下黄花蒿(Artemisia annua, L.)的抗氧化剂、基因表达和转录谱来促进青蒿素的生物合成
黄花蒿(Artemisia annua L.)是一种重要的中药药用植物,可产生一系列次生代谢物,其中最著名的是青蒿素(artemisinin),一种有效的抗疟疾植物分子。然而,其低浓度限制了其供应,需要一种可持续的方法来增加植物青蒿素的生物合成。植物次生代谢物的生物合成依赖于一个多步骤的细胞级联,已知由相关内生菌触发。由于没有单一的内生菌可以上调生物合成过程的每一步,我们尝试了四个内生菌的联合:ART1(枯草芽孢杆菌),ART2(地衣芽孢杆菌),ART7(伯氏杆菌)和ART9(皮蒂不动杆菌)调节关键的青蒿素生物合成途径基因和转录因子(tf),以获得最大的青蒿素产量。有趣的是,所有内生菌接种的植株均表现出生长增强、适应性增强和环境胁迫缓解能力增强,这可能是由于叶绿素、类胡萝卜素、蛋白质、过氧化氢酶(CAT)、超氧化物歧化酶(SOD)、抗坏血酸过氧化物酶(APX)和谷胱甘肽还原酶(GR)积累增加,脯氨酸和1-氨基环丙烷-1-羧酸(ACC)水平降低所致。此外,在正常(41.78%、29.05%)、干旱(62.91%、29.37%)、盐度(35.15%、23.71%)和涝渍(48.37%、39.52%)4种环境下,群落和ART7均显著提高了生物量;正常(51.61%,41.16%)、干旱(32.87%,28.76%)、盐渍化(25.64%,19.23%)、涝渍(31.57%,28.07%)对照中青蒿素含量较高。通过上调CYP7AV1、DXS1、HMGR、DXR1、FPS、ADS、ADH2、SQC、ALDH、HMGS、ADH1和ISPH等主要结构基因,而下调SQS对青蒿素的刺激,使代谢通量流向青蒿素的生物合成,并能够破坏青蒿素生物合成途径中的限制性酶促阶段;此外,bZIP、AP2、C3H、ARF、E2F、MYB、WRKY、MYC和ERF等tf可调节基因表达,是研究多种应激适应及其机制的可能候选者。总之,我们的研究反映了内生菌联盟通过调节必需代谢途径基因来增强内生菌之间的功能脆弱性,从而获得最大的青蒿素产量和植物对各种胁迫的耐受性的潜力。
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来源期刊
Plant Stress
Plant Stress PLANT SCIENCES-
CiteScore
5.20
自引率
8.00%
发文量
76
审稿时长
63 days
期刊介绍: The journal Plant Stress deals with plant (or other photoautotrophs, such as algae, cyanobacteria and lichens) responses to abiotic and biotic stress factors that can result in limited growth and productivity. Such responses can be analyzed and described at a physiological, biochemical and molecular level. Experimental approaches/technologies aiming to improve growth and productivity with a potential for downstream validation under stress conditions will also be considered. Both fundamental and applied research manuscripts are welcome, provided that clear mechanistic hypotheses are made and descriptive approaches are avoided. In addition, high-quality review articles will also be considered, provided they follow a critical approach and stimulate thought for future research avenues. Plant Stress welcomes high-quality manuscripts related (but not limited) to interactions between plants and: Lack of water (drought) and excess (flooding), Salinity stress, Elevated temperature and/or low temperature (chilling and freezing), Hypoxia and/or anoxia, Mineral nutrient excess and/or deficiency, Heavy metals and/or metalloids, Plant priming (chemical, biological, physiological, nanomaterial, biostimulant) approaches for improved stress protection, Viral, phytoplasma, bacterial and fungal plant-pathogen interactions. The journal welcomes basic and applied research articles, as well as review articles and short communications. All submitted manuscripts will be subject to a thorough peer-reviewing process.
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