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Título

Ergosterol biosynthesis in novel melanized fungi from hypersaline environments

AutorMéjanelle, Laurence; López, Jordi F.; Gunde-Cimerman, Nina; Grimalt, Joan O.
Palabras claveHortaea werneckii
Alternaria alternata
Cladosporium sphaerospermum
Cladosporium sp
Fecha de publicaciónmar-2001
EditorAmerican Society for Biochemistry and Molecular Biology
CitaciónJournal of Lipid Research 42(3): 352-358 (2001)
ResumenHalotolerant and halophilic melanized fungi were recently described in hypersaline waters. A close study of the sterol composition of such fungi, namely Hortaea werneckii, Alternaria alternata, Cladosporium sphaerospermum, Cladosporium sp., and Aureobasidium pullulans revealed the dominance of ergosterol and the presence of 29 intermediates of its biosynthesis pathway. The presence or absence of intermediates from distinct synthesis routes gave insight into the operative synthetic pathways from 4,4,14-trimethylcholesta-8,24-dien-3 beta-ol (lanosterol) to ergosterol in melanized fungi and in Saccharomyces cerevisiae, a reference yeast cultured in parallel. In all studied melanized fungi, initial methylation at C-24 took place before C-14 and C-4 demethylation, involving a different reaction sequence from that observed in S. cerevisiae. Further transformation was observed to occur through various routes. In A. alternata, isomerization at C-7 takes place prior to desaturation at C-5 and C-22, and methylene reduction at C-24. In addition to these pathways in Cladosporium spp., H. werneckii, and A. pullulans, ergosterol may also be synthesized through reduction of the C-24 methylene group before desaturation at C-5 and C-22 or vice versa. Moreover, in all studied melanized fungi except A. alternata, ergosterol biosynthesis may also proceed through C-24 methylene reduction prior to C-4 demethylation.
Descripción8 pages, 3 figures, 1 table.-- PMID: 11254746 [PubMed].
Versión del editorhttp://www.jlr.org/cgi/pmidlookup?view=long&pmid=11254746
URIhttp://hdl.handle.net/10261/26771
ISSN0022-2275 (Print)
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