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Phytosterol biosynthesis pathway in Mortierella alpina
Authors:David Nes W  Nichols Shawn D
Institution:Department of Chemistry and Biochemistry, Texas Tech University, Lubbock, TX 79409-1061, USA. wdavid.nes@ttu.edu
Abstract:The Zygomycetes fungus Mortierella alpina was cultured to growth arrest to assess the phytosterol biosynthesis pathway in a less-advanced fungus. The mycelium was found to produce 13 sterols, but no ergosterol. The sterol fractions were purified to homogeneity by HPLC and their identifies determined by a combination of GC-MS and 1H NMR spectroscopy. The principal sterol of the mycelium was cholesta-5, 24-dienol (desmosterol) (83%), with lesser amounts of 24beta-methyl-cholesta-5,25(27)-dienol (codisterol) (2%), 24-methyldesmosterol (6%), 24(28)-methylene cholesterol (3%) and lanosterol (3%) and several other minor compounds (3%). The total sterol accounted for approximately 0.07% of the mycelial dry wt. Mycelium fed methionine-methyl-2H3 for 6 days, generated 3 2H-24-methyl(ene) sterols, C28-2H2]24(28)-methylenecholesterol, C28-2H3]24-methylcholesta-5,24-dienol and C28-2H3]24beta-methyl-cholesta-5,25(27)-dienol. The formation of the 24-methyl sterols seems to be catalyzed by the direct methylation of a common Delta24-acceptor sterol thereby bypassing the intermediacy of an isomerization step for rearrangement of the Delta24(28)-bond to Delta25(25)-position as operates in Ascomycetes fungi and all plants.
Keywords:Sterol methyltransferase  Cholesterol  Ergosterol biosynthesis  Isotope labeling  Mortierella alpina  Fungal evolution
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