Evidence map›Paper›PMID 41214791›Full record

ArticleBiotechnology for biofuels and bioproducts2025

Transcriptomics-based analysis of acetate and propionate transport and metabolism in Yarrowia lipolytica.

Mia Žganjar, David Sanz-Mata, Urška Hancman, Neža Čadež, Cene Gostinčar, Cristina González-Fernández, Elia Tomás-Pejó, Uroš Petrovič

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In one paragraph

Article in Biotechnology for biofuels and bioproducts, 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

8 authors.

Mia ŽganjarDepartment of Molecular and Biomedical Sciences, Jožef Stefan Institute, Ljubljana, Slovenia.
David Sanz-MataBiotechnological Processes Unit, IMDEA Energy, Madrid, Spain.
Urška HancmanBiotechnical Faculty, Department of Biology, University of Ljubljana, Ljubljana, Slovenia.
Neža ČadežBiotechnical Faculty, Department of Food Science and Technology, University of Ljubljana, Ljubljana, Slovenia.
Cene GostinčarBiotechnical Faculty, Department of Biology, University of Ljubljana, Ljubljana, Slovenia.
Cristina González-FernándezBiotechnological Processes Unit, IMDEA Energy, Madrid, Spain.
Elia Tomás-PejóBiotechnological Processes Unit, IMDEA Energy, Madrid, Spain.
Uroš PetrovičDepartment of Molecular and Biomedical Sciences, Jožef Stefan Institute, Ljubljana, Slovenia. uros.petrovic@bf.uni-lj.si.

Funding

MICIU/AEI and NextGenerationEU/PRTR PCI2021-121936The Slovenian Research and Innovation Agency J4-4560
6 · The paper itself

Abstract

backgroundYarrowia lipolytica is a promising host for sustainable microbial oil production from waste-derived carboxylic acids such as acetate and propionate. Nonetheless, the molecular mechanisms underlying the metabolism and assimilation of these substrates, particularly under nitrogen limitation, are still not fully understood.

resultsWe conducted a multi-condition transcriptomic analysis of Y. lipolytica strain EXF-17398 under nitrogen-limiting conditions to investigate its transcriptional adaptation to acetate and propionate utilisation. Our results revealed distinct transcriptional responses associated with metabolic adaptation, including the coordinated regulation of Jen and Gpr carboxylate transporter families, suggesting a dual system for carboxylate uptake. JEN5 and GPR1 appear central to propionate and acetate utilisation, respectively. Our data suggest that propionate toxicity is mitigated through its conversion via the methylcitrate cycle and potentially the malonate semialdehyde pathway, preventing accumulation of cytotoxic propionyl-CoA in the cytosol. The upregulation of carnitine acyltransferases suggests active mitochondrial transport of acyl-CoAs, linking detoxification with energy metabolism. Under tested conditions, the de novo lipid synthesis was consistent with carbon overflow from acetyl-CoA and propionyl-CoA, supported by intracellular nitrogen recycling and redox balancing, independent of classical nitrogen regulatory pathways.

conclusionsThese findings illustrate the capacity of Y. lipolytica to coordinate carbon and nitrogen metabolism during carboxylate utilisation, such as acetate and propionate, offering insights to guide the optimisation of microbial oil production from renewable feedstocks.

Indexed as

AcetateCarboxylate transportLipid accumulationNitrogen limitationPropionateRNA-SeqYarrowia lipolytica

Identifiers

PMID41214791
PMCPMC12599084

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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.