Evidence map›Paper›PMID 39979817›Full record

ArticleBMC plant biology2025

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.

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

Abstract read
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Article in BMC plant biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Arman Kamali DehghanDivision of Biotechnology, Department of Agronomy and Plant Breeding, College of Agricultural and Natural Resources, University of Tehran, Karaj, Iran.
Meisam ZargarDepartment of Agrobiotechnology, Institute of Agriculture, RUDN University, Moscow, 117198, Russia.
Mahsa BamneshinDivision of Biotechnology, Department of Agronomy and Plant Breeding, College of Agricultural and Natural Resources, University of Tehran, Karaj, Iran. mahsabamneshin@yahoo.com.
Mohtaram MahmoudiehDivision of Biotechnology, Department of Agronomy and Plant Breeding, College of Agricultural and Natural Resources, University of Tehran, Karaj, Iran.
Naser SafaieDepartment of Plant Pathology, Faculty of Agriculture, Tarbiat Modares University, Tehran, Iran.
Jun-Li YangCAS Key Laboratory of Chemistry of Northwestern Plant Resources and Key Laboratory for Natural Medicine of Gansu Province, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences (CAS), Lanzhou, 730000, People's Republic of China.
Mohammad Reza NaghaviDivision of Biotechnology, Department of Agronomy and Plant Breeding, College of Agricultural and Natural Resources, University of Tehran, Karaj, Iran. mnaghavi@ut.ac.ir.

Funding

International Center for Genetic Engineering and Biotechnology CRP/IRN22-03
6 · The paper itself

Abstract

backgroundThe 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.

resultsWe 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.

conclusionsOur 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.

Indexed as

FusariumPaclitaxelTaxoidsTaxusCell Culture TechniquesCells, CulturedCell SurvivalPhenylalanine Ammonia-Lyase10-deacetylbaccatine IIIPaclitaxelPhenylalanine Ammonia-LyaseTaxoids10-DABIIICell extractsCulture filtratesFusarium graminearumPaclitaxelSuspension cell cultureTaxus baccata

Identifiers

PMID39979817
PMCPMC11841233

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.