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禾谷镰刀菌细胞提取物和培养滤液对欧洲红豆杉悬浮细胞培养中紫杉醇和10 - 去乙酰巴卡亭III产量的影响

The effects of Fusarium graminearum cell extracts and culture filtrates on the production of paclitaxel and 10-deacetylbaccatin III in suspension cell cultures of Taxus baccata L.

作者信息

Dehghan Arman Kamali, Zargar Meisam, Bamneshin Mahsa, Mahmoudieh Mohtaram, Safaie Naser, Yang Jun-Li, Naghavi Mohammad Reza

机构信息

Division of Biotechnology, Department of Agronomy and Plant Breeding, College of Agricultural and Natural Resources, University of Tehran, Karaj, Iran.

Department of Agrobiotechnology, Institute of Agriculture, RUDN University, Moscow, 117198, Russia.

出版信息

BMC Plant Biol. 2025 Feb 20;25(1):229. doi: 10.1186/s12870-025-06230-5.

Abstract

BACKGROUND

The genus Taxus (yew) is the sole producer of the paclitaxel with anticancer properties. The rising demand for plant-derived medicines has led to the overexploitation of various species and ecosystem degradation, which is further worsened by climate change. Taxus baccata L. cell culture represents a promising commercial approach for the production of taxanes. A variety of elicitors and signaling molecules have been utilized to enhance production taxanes with results significantly affected by several factors, including the specificity of the stimulant, its concentration, the timing of inoculation, and the duration of treatment. To date, no studies have revealed that the elicitors derived from Fusarium graminearum enhance 10-deacetylbaccatin III (10-DABIII) and paclitaxel production in T. baccata suspension cell cultures. Added to that, we evaluated the impact of these fungal elicitors on cell viability, growth, phenylalanine ammonia-lyase (PAL) activity, and the production levels of paclitaxel and 10-DABIII.

RESULTS

We investigated the effects of autoclaved cell extracts (ACE) and autoclaved culture filtrates (ACF) derived from F. graminearum on the suspension cell cultures of T. baccata. Our results indicated that the highest paclitaxel production, 9.438 µg/g dry weight, was achieved with a 10% autoclaved culture filtrate treatment. Furthermore, the autoclaved cell extracts significantly enhanced the levels of 10-DABIII, resulting in a remarkable 7.38-fold increase at a 5% concentration compared to the control on day 21. Treatment of the cell cultures of T. baccata with ACE and ACF decreased cell viability by 31% and 23%, respectively, compared to an 18% reduction observed in the control group after 21 days. The fungal elicitors initially induced the activity of PAL in the cell cultures, followed by a subsequent decline in this enzymatic activity.

CONCLUSIONS

Our study offers valuable insights for biotechnological applications in pharmaceutical and agricultural industries. Moreover, this research contributes to a better understanding of elicitor-mediated improvements in paclitaxel biosynthesis, paving the way for sustainable and efficient production in T. baccata cell cultures.

摘要

背景

红豆杉属(紫杉)是具有抗癌特性的紫杉醇的唯一生产者。对植物源药物需求的不断增加导致了对各种物种的过度开发和生态系统退化,而气候变化使这一情况进一步恶化。欧洲红豆杉细胞培养是生产紫杉烷的一种有前景的商业途径。多种诱导子和信号分子已被用于提高紫杉烷的产量,但其结果受到多种因素的显著影响,包括刺激物的特异性、其浓度、接种时间和处理持续时间。迄今为止,尚无研究表明禾谷镰刀菌来源的诱导子能提高欧洲红豆杉悬浮细胞培养物中10 - 去乙酰巴卡亭III(10 - DABIII)和紫杉醇的产量。此外,我们评估了这些真菌诱导子对细胞活力、生长、苯丙氨酸解氨酶(PAL)活性以及紫杉醇和10 - DABIII产量水平的影响。

结果

我们研究了禾谷镰刀菌的高压灭菌细胞提取物(ACE)和高压灭菌培养滤液(ACF)对欧洲红豆杉悬浮细胞培养物的影响。我们的结果表明,用10%的高压灭菌培养滤液处理可实现最高的紫杉醇产量,为9.438微克/克干重。此外,高压灭菌细胞提取物显著提高了10 - DABIII的水平,在第21天,5%浓度时与对照组相比显著增加了7.38倍。与21天后对照组观察到的18%的降低相比,用ACE和ACF处理欧洲红豆杉细胞培养物分别使细胞活力降低了31%和23%。真菌诱导子最初诱导细胞培养物中PAL的活性,随后该酶活性下降。

结论

我们的研究为制药和农业行业的生物技术应用提供了有价值的见解。此外,这项研究有助于更好地理解诱导子介导的紫杉醇生物合成的改进,为欧洲红豆杉细胞培养物的可持续和高效生产铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbcd/11841233/2ae575aa8b9f/12870_2025_6230_Fig1_HTML.jpg

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