Distribution of enzymes involved in the lipid metabolism of Mucoromycota shows repeated loss of ergosterol synthesis genes in plant-associated fungi
Author:
Sokołowska Blanka1, Orłowska Małgorzata2, Okrasińska Alicja2, Piłsyk Sebastian1, Pawłowska Julia2, Muszewska Anna3ORCID
Affiliation:
1. Instytut Biochemii i Biofizyki Polskiej Akademii Nauk 2. Uniwersytet Warszawski Wydzial Biologii 3. Polish Academy of Sciences Institute of Biochemistry and Biophysics: Polska Akademia Nauk Instytut Biochemii i Biofizyki
Abstract
Abstract
Mucoromycota is a phylum of early diverging fungal (EDF) lineages, of mostly plant-associated terrestrial fungi. Some strains have been selected as promising biotechnological organisms due to their ability to produce polyunsaturated fatty acids (PUFAs) and efficient conversion of nutrients into lipids. Others get their lipids from the host plant and are unable to produce even the essential ones on their own. Following the advancement in EDF genome sequencing, we carried out a systematic survey of lipid metabolism protein families across different EDF lineages. This enabled us to explore the genomic basis of the previously documented ability to produce several types of lipids within the fungal tree of life. For the first time we demonstrate that ergosterol is not being produced by several independent groups of plant-associated fungi due to the losses of different ERG genes. Instead, they possess an ancestral pathway leading to the synthesis of cholesterol, which is absent in other fungal lineages. The lack of diacylglycerol kinase in both Mortierellomycotina and Blastocladiomycota opens the question on sterol equilibrium regulation in these organisms. Early diverging fungi retained most of beta oxidation components common with animals including Nudt7, Nudt12 and Nudt19 pointing at peroxisome divergence in Dikarya. Finally, Glomeromycotina and Mortierellomycotina representatives have a similar set of desaturases and elongases related to the synthesis of complex, polyunsaturated fatty acids pointing at an ancient expansion of fatty acid metabolism currently being explored by biotechnological studies.
Publisher
Research Square Platform LLC
Reference171 articles.
1. Akoh, C. C., & Min, D. B. (2002). Food Lipids: Chemistry, Nutrition, and Biotechnology, Second Edition. CRC Press. 2. Alcazar-Fuoli, L., & Mellado, E. (2012). Ergosterol biosynthesis in Aspergillus fumigatus: its relevance as an antifungal target and role in antifungal drug resistance. Frontiers in Microbiology, 3, 439. 3. Alvarez, F. J., Douglas, L. M., & Konopka, J. B. (2007). Sterol-rich plasma membrane domains in fungi. Eukaryotic Cell, 6(5), 755–763. 4. Amses, K. R., Simmons, D. R., Longcore, J. E., Mondo, S. J., Seto, K., Jerônimo, G. H., Bonds, A. E., Quandt, C. A., Davis, W. J., Chang, Y., Federici, B. A., Kuo, A., LaButti, K., Pangilinan, J., Andreopoulos, W., Tritt, A., Riley, R., Hundley, H., Johnson, J., … James, T. Y. (2022). Diploid-dominant life cycles characterize the early evolution of Fungi. Proceedings of the National Academy of Sciences of the United States of America, 119(36), e2116841119. 5. Arora, P., Goyal, A., Natarajan, V. T., Rajakumara, E., Verma, P., Gupta, R., Yousuf, M., Trivedi, O. A., Mohanty, D., Tyagi, A., Sankaranarayanan, R., & Gokhale, R. S. (2009). Mechanistic and functional insights into fatty acid activation in Mycobacterium tuberculosis. Nature Chemical Biology, 5(3), 166–173.
|
|