# Native oleaginous yeasts Rhodotorula mucilaginosa and Solicoccozyma gelidoterrea: a sustainable biotechnological alternative for lipid production with potential application in diets for farmed fish

**Authors:** Paola Díaz-Navarrete, Luis Marileo, Hugo Madrid, Wladimir Mardones, David Correa Galeote, Nicolle Parra, Sebastián Dehnhardt-Amengual, Patricio Dantagnan

PMC · DOI: 10.3389/ffunb.2026.1664434 · Frontiers in Fungal Biology · 2026-02-10

## TL;DR

This study explores two native yeast strains from Chile that can produce lipids efficiently, offering a sustainable alternative for fish feed in aquaculture.

## Contribution

The study provides the first evidence of lipid accumulation in Solicoccozyma gelidoterrea and reveals contrasting lipid metabolic strategies in native oleaginous yeasts.

## Key findings

- Rhodotorula mucilaginosa achieved 30% lipid content under optimal conditions (25°C and C/N 20).
- Solicoccozyma gelidoterrea accumulated 26.6% lipid at 7°C and C/N 20, showing cold adaptation.
- Both yeasts displayed distinct fatty acid profiles, with R. mucilaginosa enriched in unsaturated fatty acids.

## Abstract

The rapid global expansion of aquaculture has intensified the demand for sustainable and alternative lipid sources for fish feed formulations, driving interest in microbial platforms with specialized metabolic capabilities. Among these, oleaginous yeasts have emerged as promising candidates due to their ability to accumulate substantial intracellular lipid reserves and to modulate fatty acid composition in response to environmental and nutritional cues.

In this study, the lipid production potential and physiological responses of two native yeast strains isolated from volcanic soils of southern Chile were investigated. The strains were identified by ITS sequencing as Solicoccozyma gelidoterrea (7C) and Rhodotorula mucilaginosa (Rho 6S). Growth kinetics, substrate utilization, and lipid accumulation were systematically evaluated under different carbon sources, carbon-to-nitrogen (C/N) ratios, and temperature regimes (7–25 °C). Response surface methodology was applied to determine the combined effects of nutritional and thermal factors on biomass production and lipid yield, while fatty acid composition was analyzed to elucidate lipid remodeling strategies.

R. mucilaginosa exhibited pronounced metabolic versatility, characterized by higher maximum specific growth rates on alternative carbon sources such as xylose, sucrose, and raffinose. Under optimal conditions (25 °C and C/N 20), this strain achieved a lipid content of 30% and a biomass concentration of 2.54 g/L. In contrast, S. gelidoterrea displayed a distinct physiological profile associated with cold adaptation, reaching optimal lipid accumulation at 7 °C and C/N 20, with 26.6% lipid content and 2.11 g/L biomass. Increasing the C/N ratio to 90 significantly constrained lipid accumulation in both strains, highlighting the central role of nitrogen availability in regulating yeast lipid metabolism. Fatty acid profiling revealed clear species-specific lipid remodeling patterns: R. mucilaginosa produced a nutritionally favorable lipid profile enriched in mono and polyunsaturated fatty acids, reflected by high MUFA/SAFA and PUFA/SAFA ratios. In contrast, S. gelidoterrea exhibited a distinctive lipid profile dominated by monounsaturated fatty acids, particularly oleic acid, under nitrogen limited and low temperature conditions, and demonstrated the capacity to synthesize long chain polyunsaturated fatty acids under stress conditions, suggesting the activation of adaptive and stress responsive lipid metabolic pathways.

This study provides the first evidence of lipid accumulation and fatty acid composition in S. gelidoterrea and puts into evidence contrasting lipid metabolic strategies among native oleaginous yeasts. Collectively, these findings contribute to a deeper understanding of fungal lipid physiology and environmental adaptation and support the potential of native yeast strains as sustainable lipid sources for functional foods and aquaculture nutrition.

## Linked entities

- **Species:** Solicoccozyma gelidoterrea (taxon 2877759), Rhodotorula mucilaginosa (taxon 5537), Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** ACC1 (acetyl-CoA carboxylase ACC1) [NCBI Gene 855750] {aka ABP2, FAS3, MTR7}, OLE1 (stearoyl-CoA 9-desaturase) [NCBI Gene 852825] {aka MDM2}
- **Diseases:** PD (MESH:D010300), inflammation (MESH:D007249)
- **Chemicals:** disaccharide (MESH:D004187), Lipid (MESH:D008055), ARA (MESH:D016718), G418 (MESH:C010680), soybean oil (MESH:D013024), phosphate (MESH:D010710), PI (MESH:D010716), Sucrose (MESH:D013395), phosphorus (MESH:D010758), beta-carotene (MESH:D019207), Maltodextrin (MESH:C008315), chloroform (MESH:D002725), hexane (MESH:D006586), sugars (MESH:D000073893), PUFAs (MESH:D005231), DHA (MESH:D004281), (NH4)2SO4 (MESH:D000645), heptadecanoic acid (MESH:C013102), sterol (MESH:D013261), p-coumaric acid (MESH:C495469), agarose (MESH:D012685), oxygen (MESH:D010100), CuSO4 (MESH:D019327), Caffeine (MESH:D002110), Xylose (MESH:D014994), Glycerol (MESH:D005990), phospholipid (MESH:D010743), LA (MESH:D007811), olive oil (MESH:D000069463), EPA (MESH:D015118), AL (MESH:D000535), MgCl2 (MESH:D015636), C18:2 omega6c (-), metal (MESH:D008670), Fructose (MESH:D005632), Raffinose (MESH:D011887), H2O2 (MESH:D006861), Sorbitol (MESH:D013012), NaCl (MESH:D012965), PE (MESH:C483858), helium (MESH:D006371), carotenoids (MESH:D002338), Linoleic Acid (MESH:D019787), Methanol (MESH:D000432), sulfur (MESH:D013455), n-6 fatty acids (MESH:D043371), 18:3n-3 (MESH:D017962), Maltose (MESH:D008320), 3,5-dinitrosalicylic acid (MESH:C027011), magnesium (MESH:D008274), PA (MESH:D010712), TG (MESH:D014280), Glucose (MESH:D005947), linoleic acids (MESH:D008041), Ethanol (MESH:D000431), ALA (MESH:D000409), PC (MESH:D010713), Galactose (MESH:D005690), vegetable oils (MESH:D010938), saccharide (MESH:D002241)
- **Species:** Candida tropicalis (species) [taxon 5482], Piskurozyma cylindrica (species) [taxon 104406], Rhodotorula mucilaginosa (species) [taxon 5537], Trichosporon asahii (species) [taxon 82508], Papiliotrema laurentii (species) [taxon 5418], Debaryomyces hansenii (species) [taxon 4959], Rhodotorula toruloides (species) [taxon 5286], Rhodotorula glutinis (species) [taxon 5535], Solicoccozyma (genus) [taxon 1851575], Tausonia pullulans (species) [taxon 82525], Naganishia albida (species) [taxon 100951], Rhodotorula graminis (species) [taxon 29898], Salmo salar (Atlantic salmon, species) [taxon 8030], Apiotrichum domesticum (species) [taxon 82514], Solicoccozyma gelidoterrea (species) [taxon 2877759], Brassica napus var. napus (annual rape, varietas) [taxon 138011], Solicoccozyma terricola (species) [taxon 104414], Homo sapiens (human, species) [taxon 9606], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Oncorhynchus mykiss (rainbow trout, species) [taxon 8022], [Candida] diddensiae (species) [taxon 45543], Lipomyces starkeyi (species) [taxon 29829], Sparus aurata (gilthead bream, species) [taxon 8175], Salvelinus alpinus (Arctic char, species) [taxon 8036], Proterorhinus sp. DN (species) [taxon 1211348], Actinopterygii (fishes, superclass) [taxon 7898], Yarrowia lipolytica (species) [taxon 4952], Solicoccozyma aeria (species) [taxon 89915], Lipomyces tetrasporus (species) [taxon 54092], Metschnikowia reukaufii (species) [taxon 27327]
- **Mutations:** 16 C-C, 7 C-C, 20 C-C, 25 C-C, C with a C

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12929513/full.md

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12929513/full.md

## References

83 references — full list in the complete paper: https://tomesphere.com/paper/PMC12929513/full.md

---
Source: https://tomesphere.com/paper/PMC12929513