Recent Advances in Ergosterol Biosynthesis and Regulation Mechanisms in Saccharomyces cerevisiae

Regulation of Sterol Synthesis in Eukaryotes

Espenshade, P. J., & Hughes, A. L. (2007) · Annual Review of Genetics · doi:10.1146/annurev.genet.41.110306.130315 · Cited by 593

Enzymes of the mevalonate pathway of isoprenoid biosynthesis

Miziorko, H. M. (2010) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2010.09.028 · Cited by 529

Osh Proteins Regulate Phosphoinositide Metabolism at ER-Plasma Membrane Contact Sites

Stefan, C. J., Manford, A. G., Baird, D., Yamada-Hanff, J., Mao, Y., & Emr, S. D. (2011) · Cell · doi:10.1016/j.cell.2010.12.034 · Cited by 499

Coordinated Remodeling of Cellular Metabolism during Iron Deficiency through Targeted mRNA Degradation

Puig, S., Askeland, E., & Thiele, D. J. (2005) · Cell · doi:10.1016/j.cell.2004.11.032 · Cited by 382

Yeast lipid metabolism at a glance

Klug, L., & Daum, G. (2014) · FEMS Yeast Research · doi:10.1111/1567-1364.12141 · Cited by 349

Regulation of HMG-CoA reductase in mammals and yeast

Burg, J. S., & Espenshade, P. J. (2011) · Progress in Lipid Research · doi:10.1016/j.plipres.2011.07.002 · Cited by 303

The Red Seaweed Gracilaria gracilis as a Multi Products Source

Francavilla, M., Franchi, M., Monteleone, M., & Caroppo, C. (2013) · Marine Drugs · doi:10.3390/md11103754 · Cited by 264

Relationship between ethanol tolerance, H+-ATPase activity and the lipid composition of the plasma membrane in different wine yeast strains

Aguilera, F. S., Peinado, R. A., Millán, C., Ortega, J. M., & Mauricio, J. C. (2006) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2006.02.002 · Cited by 253

ERGOSTEROL BIOSYNTHESIS: A FUNGAL PATHWAY FOR LIFE ON LAND?

Dupont, S., Lemetais, G., Ferreira, T., Cayot, P., Gervais, P., & Beney, L. (2012) · Evolution · doi:10.1111/j.1558-5646.2012.01667.x · Cited by 246

Oxysterol-binding Protein and Vesicle-associated Membrane Protein–associated Protein Are Required for Sterol-dependent Activation of the Ceramide Transport Protein

Perry, R. J., & Ridgway, N. D. (2006) · Molecular Biology of the Cell · doi:10.1091/mbc.e06-01-0060 · Cited by 234

Gut–brain communication mediates the impact of dietary lipids on cognitive capacity

Fan, C., Xu, J., Tong, H., Fang, Y., Chen, Y., Lin, Y., Chen, R., Chen, F., & Wu, G. (2024) · Food & Function · doi:10.1039/d3fo05288e · Cited by 10

Phytolacca tetramera berries extracts and its main constituents as potentiators of antifungal drugs against Candida spp.

Butassi, E., Blanc, A. R., & Svetaz, L. A. (2024) · Phytomedicine · doi:10.1016/j.phymed.2024.155569 · Cited by 10

Design, Synthesis, and Evaluation of Novel 4-Chloropyrazole-Based Pyridines as Potent Fungicide Candidates

Wang, Y., Kou, S., Huo, J., Sun, S., Wang, Y., Yang, H.-W., Zhao, S., Tang, L., Han, L., Zhang, J., et al. (2022) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.2c02350 · Cited by 10

Heterologous Biosynthesis of the Fungal Sesquiterpene Trichodermol in Saccharomyces cerevisiae

Liu, J., Zhai, Y., Zhang, Y., Zhu, S., Liu, G., & Che, Y. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.01773 · Cited by 10

Niemann-Pick Type C Proteins Are Required for Sterol Transport and Appressorium-Mediated Plant Penetration of Colletotrichum orbiculare

Kodama, S., Kajikawa, N., Fukada, F., & Kubo, Y. (2022) · mBio · doi:10.1128/mbio.02236-22 · Cited by 9

Spatial sterol metabolism unveiled by stimulated Raman imaging

Zhang, Y., Zhou, Y., Fang, W., Zhu, H., Ye, C., Zhang, D., & Lee, H. J. (2023) · Frontiers in Chemistry · doi:10.3389/fchem.2023.1166313 · Cited by 9

Protein kinases Elm1 and Sak1 of Saccharomyces cerevisiae exerted different functions under high-glucose and heat shock stresses

Wang, L., Xu, Y., Jiang, H.-Y., Song, Z., Lin, X., Hu, X.-P., & Li, C. (2022) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-022-11840-2 · Cited by 9

Ergosterol supplementation improves furfural tolerance of Saccharomyces cerevisiae to produce ethanol and its underlying mechanism

Jia, Y., Zhang, Q., Dai, J., Zheng, X., Meng, X., Zhou, R., Yang, H., Yao, L., & Chen, X. (2022) · BioResources · doi:10.15376/biores.18.1.228-246 · Cited by 8

Proteomic analysis reveals the mechanisms of improved biocontrol efficacy of Sporidiobolus pararoseus Y16 induced by γ-aminobutyric acid

Zhao, L., Zhou, Y., Liang, L., Dhanasekaran, S., Zhang, X., Yang, X., Wu, M., Song, Y., & Zhang, H. (2023) · Biological Control · doi:10.1016/j.biocontrol.2023.105313 · Cited by 8

An Integrated Transcriptomics and Lipidomics Analysis Reveals That Ergosterol Is Required for Host Defense Against Bacterial Infection in Drosophila

Deng, Z., Yang, Y., Luo, J., Zhang, B., Liu, J., Shui, G., Jiao, R., & Wei, C. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.933137 · Cited by 8

1,2, 4‐Triazole benzamide derivative TPB against Gaeumannomyces graminis var. tritici as a novel dual‐target fungicide inhibiting ergosterol synthesis and adenine nucleotide transferase function

Wang, L., Song, X., Cheng, Y., Cheng, S., Chen, T., Li, H., Yan, J., Wang, X., & Zhou, H. (2023) · Pest Management Science · doi:10.1002/ps.7900 · Cited by 8

Rap1 overexpression boosts triterpenoid saponin production in yeast by enhancing precursor supply and heterologous gene expression

Byun, J., Nguyen, T. T., Cho, B., Park, S.-H., & Kim, S. (2025) · Microbial Cell Factories · doi:10.1186/s12934-025-02667-3 · Cited by 7

Himalayan Mushrooms as a Natural Source of Ergosterol and Vitamin D2: A Review of Nutraceutical and Functional Food Perspectives

Panthari, P., Khantwal, G., Kumar, M., Shang, X., Lee, J., Haniyyah, S., Sharma, K., & Saini, R. K. (2025) · Foods · doi:10.3390/foods14203516 · Cited by 7

Development of a High-Titer Culture Medium for the Production of Cholesterol by Engineered Saccharomyces cerevisiae and Its Fed-Batch Cultivation Strategy

Wang, L.-X., Zheng, G.-F., Xin, X., & An, F. (2021) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.2106.06026 · Cited by 7

Rewiring metabolism and restoring sterol homeostasis for overproduction of campesterol in Saccharomyces cerevisiae

Liu, W., Dong, X., Li, H., Gong, J., Zhang, X., Shi, J., Xu, Z., Koffas, M. A. G., & Li, H. (2025) · Chemical Engineering Journal · doi:10.1016/j.cej.2025.163686 · Cited by 7

Interplay between acetylation and ubiquitination of imitation switch chromatin remodeler Isw1 confers multidrug resistance in Cryptococcus neoformans

Meng, Y., Ni, Y., Li, Z., Jiang, T., Sun, T., Li, Y., Gao, X., Li, H., Suo, C., Li, C., et al. (2024) · eLife · doi:10.7554/elife.85728 · Cited by 7

Effects on Gene Transcription Profile and Fatty Acid Composition by Genetic Modification of Mevalonate Diphosphate Decarboxylase MVD/Erg19 in Aspergillus Oryzae

Hu, Z., Huang, H., Sun, Y., Niu, Y., Xu, W., Liu, Q., Zhang, Z., Jiang, C., Li, Y., & Zeng, B. (2019) · Microorganisms · doi:10.3390/microorganisms7090342 · Cited by 7

Comparative study on the role of various sterols in enhancing ovarian development and metabolic functions in Pacific white shrimp (Litopenaeus vannamei) broodstock

Liang, X., Xiao, X., Gao, X., Wen, M., Song, Y., Xu, C., Han, F., & Li, E. (2024) · Aquaculture · doi:10.1016/j.aquaculture.2024.741934 · Cited by 6

Reengineering of ergosterol biosynthesis in Saccharomyces cerevisiae and its sustainable application in citrus peel processing industry

Chen, H., Wang, Y., Zhang, Y., Peng, N., Zhang, S., She, Y., Yang, Y., Liu, X., Deng, Z., & Gu, X. (2025) · New Biotechnology · doi:10.1016/j.nbt.2025.10.002 · Cited by 6

Harnessing a Nonconventional Yeast for 7-Dehydrocholesterol Overproduction

Shi, Y., Zhang, L., Zhang, H., Fan, C., Zhu, M., Yang, H., Xia, Y., Zhou, L., Shen, W., & Chen, X. (2025) · ACS Sustainable Chemistry & Engineering · doi:10.1021/acssuschemeng.5c08538 · Cited by 6

Lipid-Centric Approaches in Combating Infectious Diseases: Antibacterials, Antifungals and Antivirals with Lipid-Associated Mechanisms of Action

Ostroumova, O. S., & Efimova, S. S. (2023) · Antibiotics · doi:10.3390/antibiotics12121716 · Cited by 7

Gene Editing of Candida glycerinogenes by Designed Toxin–Antitoxin Cassette

Lv, W., Lu, X., Zhuge, B., & Zong, H. (2024) · ACS Synthetic Biology · doi:10.1021/acssynbio.3c00640 · Cited by 6

Functional study of two ER localized sterol C-14 reductases in Aspergillus oryzae

Shang, Y., Jin, Q., Li, G., Yan, H., Yu, M., & Hu, Z. (2024) · 3 Biotech · doi:10.1007/s13205-024-03988-7 · Cited by 6

Lipid-Like Biofilm from a Clinical Brain Isolate of Aspergillus terreus: Quantification, Structural Characterization and Stages of the Formation Cycle

Rayón-López, G., Carapia-Minero, N., Medina‐Canales, M. G., García‐Pérez, B. E., Reséndiz-Sánchez, J., Pérez, N. O., Rodríguez-Tovar, A. V., & Ramírez‐Granillo, A. (2022) · Mycopathologia · doi:10.1007/s11046-022-00692-z · Cited by 7

Undesired effect of vancomycin prolonged treatment: enhanced biofilm production of the nosocomial pathogen Candida auris

Maione, A., Pietra, A. L., Salvatore, M. M., Guida, M., Galdiero, E., & de Alteriis, E. (2022) · Antibiotics · doi:10.3390/antibiotics11121771 · Cited by 6

Zinc Starvation Induces Cell Wall Remodeling and Activates the Antioxidant Defense System in Fonsecaea pedrosoi

Santos, T. A. D. O., Soares, L. W., Oliveira, L. N., Moraes, D., Mendes, M. S., Soares, C. M. D. A., Bailão, A. M., & Bailão, M. G. S. (2024) · Journal of Fungi · doi:10.3390/jof10020118 · Cited by 7

Phytosterols: Structural variations, biosynthetic pathways, and their biological roles

Tan, C., & Men, S. (2026) · Journal of Integrative Plant Biology · doi:10.1111/jipb.70135 · Cited by 5

Interactions of the emerging fungus Candida auris with Acanthamoeba castellanii reveal phenotypic changes with direct implications on the response to stress and virulence

Valente, M. R., Alcântara, L. M., Cintra, D. S., Mendoza, S. R., Medeiros, E. G., Gomes, K. X., Honorato, L., Almeida, M. D. A., Vieira, C. B., Nosanchuk, J. D., et al. (2024) · Microbiology Spectrum · doi:10.1128/spectrum.01746-24 · Cited by 5

Expression pattern, subcellular localization of Aspergillus oryzae ergosterol synthases, and their effects on ergosterol and fatty acid metabolism

Tian, X., Qin, K., Deng, Y., Xue, P., Huang, C., Liu, S., & Hu, Z. (2025) · Applied and Environmental Microbiology · doi:10.1128/aem.02273-24 · Cited by 5

Ergosterol and Lanosterol Derivatives: Synthesis and Possible Biomedical Applications

Stefaniak‐Skorupa, J., & Milewska, M. J. (2025) · ChemMedChem · doi:10.1002/cmdc.202400948 · Cited by 6

Divergent patterns of selection on metabolite levels and gene expression

Kern, A., Yang, G. X., Khosla, N. M., Ang, R. M. L., Snyder, M. P., & Fraser, H. B. (2021) · BMC Ecology and Evolution · doi:10.1186/s12862-021-01915-5 · Cited by 5

Chemical compounds from the Kenyan polypore Trametes elegans (Spreng:Fr.) Fr (Polyporaceae) and their antimicrobial activity

Mayaka, R. K., Langat, M. K., Njue, A. W., Cheplogoi, P. K., & Omolo, J. O. (2019) · International Journal of Biological and Chemical Sciences · doi:10.4314/ijbcs.v13i4.37 · Cited by 5

Toxicity mechanisms of metal ions in sugarcane molasses to Saccharomyces cerevisiae: Integrated physiological and transcriptomic insights

Tang, M., Yuan, R., Huang, G., Long, Z., Liang, X., Meng, H., & Long, X. (2025) · Food Bioscience · doi:10.1016/j.fbio.2025.107770 · Cited by 4

Dynamics of the lipid body lipidome in the oleaginous yeast Yarrowia sp

Joshi, A. R., Barvkar, V. T., Kashikar, A. S., Gaikwad, P., & RaviKumar, A. (2024) · FEMS Yeast Research · doi:10.1093/femsyr/foae021 · Cited by 4

Mechanism and Engineering Strategies of Sterol Homeostasis in Yeast

Li, M., Yu, H., & Ye, L. (2025) · ACS Synthetic Biology · doi:10.1021/acssynbio.5c00508 · Cited by 4

A TECHNOLOGY FOR OBTAINING A PROTEIN CONCENTRATE FROM YEAST BIOMASS OF Kluyveromyces marxianus Van der Walt (1965)

Фоменко, И. А. (2021) · Sel skokhozyaistvennaya Biologiya · doi:10.15389/agrobiology.2021.6.1172eng · Cited by 4

Long non-coding RNAs and their potential function in response to postharvest senescence of Sparassis latifolia during cold storage

Weng, M., Zhang, D., Wang, H., Yang, C., Lin, H., Pan, Y., & Lin, Y. (2024) · Scientific Reports · doi:10.1038/s41598-023-46744-2 · Cited by 4

Oleogels Produced by Direct Methods Using as Gelator: Fatty Acids (Including 12-HSA), Fatty Alcohols, Ceramides, Lecithins, Sterols, Cellulose Fibers, and Fumed Silica

Li, L., Liu, G., & Guo, Z. (2024) · Springer eBooks · doi:10.1007/978-3-031-46831-5_8 · Cited by 4

D-Limonene Inhibits Pichia kluyveri Y-11519 in Sichuan Pickles by Disrupting Metabolism

Zeng, C., Sun, Y., Lin, H., Li, Z., Zhang, Q., Cai, T., Xiang, W., Tang, J., & Yasurin, P. (2024) · Molecules · doi:10.3390/molecules29153561 · Cited by 4

Sterols in fresh and preserved button mushroom (Agaricus bisporus) products

Sommer, K., & Vetter, W. (2025) · European Food Research and Technology · doi:10.1007/s00217-025-04659-4 · Cited by 4

The analysis of transcriptomics reveals the function of TrPLD3 in the pathogenicity of Trichothecium roseum infecting apples

Li, X., Zhang, Q., Liu, Q., Xu, X., Li, J., Zhu, D., Zong, Y., Xue, H., & Bi, Y. (2025) · Postharvest Biology and Technology · doi:10.1016/j.postharvbio.2025.113628 · Cited by 4

Multi-omics analysis of Taiwanofungus gaoligongensis: effects of different cultivation methods on secondary metabolites

He, T., Yuan, X., Xiao, L., Hu, T., Wang, Y., Zhao, X., Li, L., Peng, C., Zhang, H., & Zheng, Y. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1620693 · Cited by 3

Complex Kinetic Models Predict β-Carotene Production and Reveal Flux Limitations in Recombinant Saccharomyces cerevisiae Strains

Elizondo, B. R., & Saa, P. A. (2025) · ACS Synthetic Biology · doi:10.1021/acssynbio.5c00256 · Cited by 3

Compartment engineering in yeast: a path to increased biochemical production

Wang, Y., Cao, L., Rong, L., Ding, C., Liu, C., Ye, Q., Huang, Q., Zhang, C., Xu, N., Mao, J., et al. (2025) · Chemical Engineering Journal · doi:10.1016/j.cej.2025.169279 · Cited by 3

Enhanced ergosterol biosynthesis in Saccharomyces cerevisiae via rational multigenetic modification and two-stage fermentation

Xie, Y., Fan, C., Piao, M., & Jia, L. (2025) · Process Biochemistry · doi:10.1016/j.procbio.2025.11.011 · Cited by 3

An Insight into the Repurposing of Phytoconstituents obtained from Delhi’s Aravalli Biodiversity Park as Antifungal Agents

Kaur, A., Sharma, K., Sharma, N., & Aggarwal, G. (2024) · Infectious Disorders - Drug Targets · doi:10.2174/0118715265282411240119061441 · Cited by 3

Resistance mechanisms of Saccharomyces cerevisiae against silver nanoparticles with different sizes and coatings

Yang, Y., Hou, J., & Luan, J. (2024) · Food and Chemical Toxicology · doi:10.1016/j.fct.2024.114581 · Cited by 3

Changes in Ergosterol Biosynthesis Alter the Response to Cycloheximide, 4-Nitroquinoline-N-Oxide, Weak Organic Acids, and Virulence in Candida glabrata

Eliaš, D., Hervay, N. T., Černáková, L., & Gbelská, Y. (2024) · Journal of Fungi · doi:10.3390/jof10100669 · Cited by 3

Deciphering the antiochratoxigenic activity of plant extracts and Debaryomyces hansenii against Penicillium nordicum in a “chorizo”-based medium by proteomic analysis

Roncero, E., Andrade, M. J., Álvarez, M., Cebrián, E., & Delgado, J. (2024) · Meat Science · doi:10.1016/j.meatsci.2024.109591 · Cited by 3

Novel cell factory for the production of 24-epi-ergosterol, an un-natural semi-synthetic precursor for the production of brassinolide in Yarrowia lipolytica

Wang, Y., Liu, S.-W., Sheng, Z., Feng, Y., Wang, Y., Jiang, Y., Zhu, L., Wu, M., Yang, L., & Lin, J. (2025) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-025-04314-w · Cited by 3

ПОЛУЧЕНИЕ БЕЛКОВОГО КОНЦЕНТРА ИЗ ДРОЖЖЕВОЙ БИОМАССЫ Kluyveromyces marxianus Van der Walt (1965)

производств, Ф. В. М. Г. У. П., & ФОМЕНКО, И. А. (2021) · Sel skokhozyaistvennaya Biologiya · doi:10.15389/agrobiology.2021.6.1172rus · Cited by 3

The Miraculous of Rhizopus arrhizus in the Structural Modifications of Steroidal Skeleton

Azizuddin, & Iqbal, M. (2024) · Letters in Organic Chemistry · doi:10.2174/0115701786302791240506114902 · Cited by 2

Inhibitory effect and mechanism of action of Carvacrol as a promising natural food preservative against Fusarium acuminatum causing postharvest rot of garlic scapes (Allium sativum L)

Li, P., Liu, J., Zhang, L., Wu, W., He, C., Tan, B., Tang, S., & Yu, L. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1637313 · Cited by 2

The structure-dependent effects of newly synthesised cationic gemini surfactants against yeast cells

Mazurkiewicz, E., Obłąk, E., Paściak, M., Gamian, A., Ciesielska, M., Lamch, Ł., & Wilk, K. A. (2025) · Scientific Reports · doi:10.1038/s41598-025-30210-2 · Cited by 2

Engineering Yarrowia lipolytica for high-level ergosterol production

Liu, X., Chen, Q., Zhao, W., Li, Q., Xiao, L., He, Q., Zeng, W., & Zhou, J. (2026) · Synthetic and Systems Biotechnology · doi:10.1016/j.synbio.2026.01.001 · Cited by 2

Fermentation techniques for protein enrichment of cassava peel

Júnior, A. R. B. D. O., de Oliveira, C. E. D. A. S. R., Matos, I. G. D. S., Ribeiro, L. F. S., Estumano, J. A. D. S., Lima, J. G. S., Faturi, C., & da Silva, T. C. (2026) · Journal of the Science of Food and Agriculture · doi:10.1002/jsfa.70525 · Cited by 2

Contemporary approaches in anti-aging therapy

Fertu, I. D., Ștefan, C. S., Iacob, A. D., & Tudor, S. S. (2026) · Electronic Journal of General Medicine · doi:10.29333/ejgm/18092 · Cited by 2

Unraveling the antagonistic mechanisms of Hanseniaspora volatile organic compounds against Botrytis cinerea, a causal agent of postharvest decay

Tejero, P., Olmo, S., Hernández, A. H., Rodríguez, A., Aranda, E., & Martín, A. (2026) · Biological Control · doi:10.1016/j.biocontrol.2026.106005 · Cited by 2

Dual defense mechanisms from a novel marine fungus Nigrograna chlamydospora sp. nov. B143: antifungal and anti-aflatoxigenic properties against Aspergillus flavus

Ou, X., Wang, Q., Huang, S., Li, Y., Yang, L., Luo, Y., Wang, S., Liang, M., Pan, L., Liu, B., et al. (2026) · Frontiers in Microbiology · doi:10.3389/fmicb.2026.1801199 · Cited by 2

One-step gram-scale synthesis of striasteroid B inspired by its nonenzymatic formation

Cheng, S., Chen, C., Chen, Y., Cai, J., Tang, L., Zhou, X., & Fu, P. (2026) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2026.110320 · Cited by 2

Los isoprenoides como fuente de biocombustibles

Luqueño-Bocardo, O. I., Pardo, J. P., Guerra‐Sánchez, G., González, J., Matus‐Ortega, G., & Romero‐Aguilar, L. (2021) · TIP Revista Especializada en Ciencias Químico-Biológicas · doi:10.22201/fesz.23958723e.2021.0.291 · Cited by 2

BIOSYNTHESIS OF COPPER OXIDE NANOPARTICLES AND EVALUATION OF THEIR ANTIMICROBIAL PROPERTIES

Okoye, U. C., Okhamafe, A. O., & Arhewoh, M. I. (2023) · International Journal of Pharmacy and Pharmaceutical Sciences · doi:10.22159/ijpps.2023v15i5.46635 · Cited by 2

Targeting lipid metabolism in plants for non-animal sources of nutraceuticals towards sustainable food production and scale up

Puri, S., Mandal, S. K., Srivastava, A., Agrawal, I., & Deepa, P. R. (2023) · Food Bioscience · doi:10.1016/j.fbio.2023.102904 · Cited by 2

Stress modulation strategies in Kluyveromyces marxianus: Unravelling the effects of shear force and aeration for enhanced specific ergosterol production

Vidra, A., & Németh, Á. (2024) · Acta Alimentaria · doi:10.1556/066.2024.00034 · Cited by 2

Specificity of Membrane‐Associated J‐Domain Protein, Caj1, in Amphotericin B Tolerance in Budding Yeast

Sagarika, P., Dobriyal, N., Deepsika, P., Vairagkar, A., Das, A., & Sahi, C. (2024) · Molecular Microbiology · doi:10.1111/mmi.15318 · Cited by 2

Biosynthesis of lanosterol in Escherichia coli

Sun, W., Chen, Y., Shah, S. B., Bai, Y., & Tan, Z. (2025) · Synthetic and Systems Biotechnology · doi:10.1016/j.synbio.2025.05.006 · Cited by 2

Unlocking the biological potential of methyl antcinate A: a new frontier in cancer and inflammation application

Sharif, M., Irfan, M., Kousar, K., Mamurova, A., Duarte‐Peña, L., Hernández‐Parra, H., Cortés, H., Peña‐Corona, S. I., Khan, K., Habtemariam, S., et al. (2024) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-024-03544-3 · Cited by 2

Enhancement and Mechanism of Ergosterol Biosynthesis in Termite Ball Fungus Athelia termitophila by Methyl Jasmonate

Fang, Y.-G., Khan, Z., Hu, F., Su, X.-H., & Xing, L. (2025) · Current Issues in Molecular Biology · doi:10.3390/cimb47030149 · Cited by 2

Ketoconazole-loaded nanoemulsion in situ gel system for ocular delivery: development and evaluation

Makhijani, S., Nerkar, P. P., & Mahajan, H. S. (2025) · Journal of Dispersion Science and Technology · doi:10.1080/01932691.2025.2564320 · Cited by 1

Ergosterol Regulation of Plant Physiology; An Underlooked Perspective

Tyagi, M., Paul, P. K., & Rameshwari, R. (2025) · The Botanical Review · doi:10.1007/s12229-025-09321-y · Cited by 1

Characterization and Expression Analysis of the Sterol C-5 Desaturase Gene PcERG3 in the Mycobiont of the Lichen Peltigera canina Under Abiotic Stresses

Swid, M. A., Koulintchenko, M. V., Onele, A. O., Leksin, I. Y., Rakhmatullina, D. F., Galeeva, E. I., Valitova, Y. N., Minibayeva, F. V., & BECKETT, R. P. (2025) · Microbiology Research · doi:10.3390/microbiolres16070139 · Cited by 1

Molecular Responses of Saccharomyces cerevisiae to Growth Under Conditions of Increasing Corn Syrup and Decreasing Molasses

Chen, B., Heng, Y. C., Almunawar, S. N. A., Wanjaya, E. R., Elejalde, U., & Kittelmann, S. (2025) · Fermentation · doi:10.3390/fermentation11080432 · Cited by 1

Molecular targets of ergosterol and its derivatives in cancer therapy: Recent trends and strategies to improve its bioavailability

Shivali, Kumar, H., & Agnihotri, N. (2025) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2025.106928 · Cited by 1

Lipids in Beer: The Good, The Bad, and The Ugly

Britton, S. J., & Bamforth, C. W. (2026) · Journal of the American Society of Brewing Chemists · doi:10.1080/03610470.2025.2591551 · Cited by 1

Metabolite Profiling and Cytotoxic Investigation of Senecio biafrae Oliv. and Hiern (Compositae) on Nauplii Brine Shrimps and Cancer Cell Lines

Akinola, F. T., Oriyomi, O. V., Ogundele, S. B., Adekola, M. B., Agbedahunsi, J. M., & Babalola, O. O. (2024) · Asian Journal of Biological Sciences · doi:10.3923/ajbs.2024.291.306 · Cited by 1

Systematic Investigation of Ergosterol Fermentation by Kluyveromyces marxianus Y.00243 via Statistical Design

Vidra, A., Kaleta, Z., & Németh, Á. (2021) · Periodica Polytechnica Chemical Engineering · doi:10.3311/ppch.18202 · Cited by 1

Current Status of Practical Applications: Probiotics in Dairy Cattle

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Additional file 1 of Methanol bioconversion into C3, C4, and C5 platform chemicals by the yeast Ogataea polymorpha

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Additional file 1 of Divergent patterns of selection on metabolite levels and gene expression

Kern, A., Yang, G. X., Khosla, N. M., Ang, R. M. L., Snyder, M. P., & Fraser, H. B. (2021) · Figshare · doi:10.6084/m9.figshare.16702978

Additional file 5 of Divergent patterns of selection on metabolite levels and gene expression

Kern, A., Yang, G. X., Khosla, N. M., Ang, R. M. L., Snyder, M. P., & Fraser, H. B. (2021) · Figshare · doi:10.6084/m9.figshare.16702996

Additional file 4 of Divergent patterns of selection on metabolite levels and gene expression

Kern, A., Yang, G. X., Khosla, N. M., Ang, R. M. L., Snyder, M. P., & Fraser, H. B. (2021) · Figshare · doi:10.6084/m9.figshare.16702993

Additional file 1 of Boosting the epoxidation of squalene to produce triterpenoids in Saccharomyces cerevisiae

Du, M.-M., Zhang, G.-G., Zhu, Z.-T., Zhao, Y.-Q., Gao, B., Tao, X.-Y., Wang, F.-Q., & Wei, D.-Z. (2023) · Figshare · doi:10.6084/m9.figshare.22767335

Additional file 2 of Methanol bioconversion into C3, C4, and C5 platform chemicals by the yeast Ogataea polymorpha

Wefelmeier, K., Schmitz, S., Kösters, B. J., Liebal, U. W., & Blank, L. M. (2024) · Figshare · doi:10.6084/m9.figshare.24940898

Additional file 3 of Divergent patterns of selection on metabolite levels and gene expression

Kern, A., Yang, G. X., Khosla, N. M., Ang, R. M. L., Snyder, M. P., & Fraser, H. B. (2021) · Figshare · doi:10.6084/m9.figshare.16702987

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