Evidence map›Paper›PMID 41266566›Full record

ArticleScientific reports2025

A comprehensive evaluation of metabolically engineered Cynara cardunculus calli as platform for valuable fatty acid derivatives production.

Raul Pirona, Elisa Cappetta, Monica De Palma, Rosa D'Alessandro, Antonio Luca Langellotti, Alfredo Ambrosone, Teresa Docimo

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Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Raul PironaInstitute of Agricultural Biology and Biotechnology, National Research Council, 20133, Milan, Italy.
Elisa CappettaInstitute of Biosciences and Bioresources, National Research Council, 80055, Portici, Italy.
Monica De PalmaInstitute of Biosciences and Bioresources, National Research Council, 80055, Portici, Italy.
Rosa D'AlessandroInstitute of Biosciences and Bioresources, National Research Council, 80055, Portici, Italy.
Antonio Luca LangellottiCAISIAL Centre, University of Naples Federico II, 80055, Portici, NA, Italy.
Alfredo AmbrosoneDepartment of Pharmacy, University of Salerno, 84084, Fisciano, Italy.
Teresa DocimoInstitute of Biosciences and Bioresources, National Research Council, 80055, Portici, Italy. teresa.docimo@cnr.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increasing global demand for energy along with climate change claims for sustainable and renewable energy sources. In this study, we investigated transcriptomic changes in two cardoon (Cynara cardunculus L. var. altilis) calli cell culture lines engineered for production of valuable fatty acids, therefore suitable for large-scale production of biofuel precursors, as alternative to triacylglycerols (TAGs) engineered plants. Namely, to gain insight in the molecular effects of genetic transformation, we analyzed the transcriptome of SAD-OE line (overexpressing stearic acid desaturase), and FAD-KD line (a fatty acid desaturase RNA interference line, FAD2.2-RNAi) accumulating oleic and linoleic acids, respectively. Differentially expressed genes (DEGs) involved in fatty acid metabolism and streamed pathways such as glycolysis, pyruvate, glycerolipid, and glycerophospholipid metabolism, were enriched in the KEGG analysis in both lines. In addition to analyzing DEGs, we used qRT-PCR to monitor key regulatory and biosynthetic genes involved in TAGs formation and assembly, aiming to understand their transcriptional dynamics over ten days of cell growth in liquid culture. In transgenic scaled up lines, upon observing increased lipid accumulation, we investigated how genetic transformation influenced sugar metabolism. Fructan depletion analysis further supported their role as carbon sources for TAG biosynthesis. Confocal microscopy confirmed a significantly higher accumulation of oil bodies in transgenic lines compared to wild-type (WT) calli. Overall, this study presents a comprehensive characterization of a cardoon cell-based platform for large-scale vegetable oil production. Unlike whole plants, these engineered cell cultures do not suffer from severe oxidative stress or growth and metabolic impairments, making them a promising alternative for sustainable fatty acid biosynthesis.

Indexed as

CynaraFatty AcidsMetabolic EngineeringGene Expression ProfilingGene Expression Regulation, PlantPlants, Genetically ModifiedTranscriptomeTriglyceridesFatty AcidsTriglyceridesConfocal microscopyFatty acidsOil bodiesPlant cell culturesRNA-seqTAGs

Identifiers

PMID41266566
PMCPMC12635154

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LicenceCC BY-NC-ND
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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.