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Characterization and Properties of Cholesterol Desaturases from the Ciliate Tetrahymena thermophila
Author(s) -
Nusblat Alejandro D.,
Muñoz Luciana,
Valcarce German A.,
Nudel Clara B.
Publication year - 2005
Publication title -
journal of eukaryotic microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.067
H-Index - 77
eISSN - 1550-7408
pISSN - 1066-5234
DOI - 10.1111/j.1550-7408.2005.3279rr.x
Subject(s) - tetrahymena , biology , biochemistry , microsome , tetrahymena pyriformis , ciliate , cofactor , cytochrome p450 , cytochrome , cytochrome b5 , enzyme , paleontology
. Live Tetrahymena thermophila transforms exogenous cholesterol into 7,22‐ bis , dehydrocholesterol (DHC) by desaturation at positions C7(8) and C22(23) of the cholesterol moiety. In this first report on expression, isolation, characterization, and reconstitution of Tetrahymena' s cholesterol desaturases in cell‐free extracts, we describe conditions for increasing the expression of both desaturases based on the addition of specific sterols to the culture medium. Reactions performed in vitro, with isolated microsomes, yield only the mono‐unsaturated derivatives, 7‐DHC and/or 22‐DHC. However, selectivity towards one product can be improved with the addition of specific compounds: β‐mercaptoethanol inhibited C22(23) desaturase activity completely, while ethanol selectively increased this activity. Detergent‐solubilized microsomes showed no desaturase activity, but partial restoration could be achieved with addition of dilauroyl‐phosphatidylcholine liposomes (25%). Both cholesterol desaturases require molecular oxygen and cytochrome b 5 . NADH or NADPH can serve as reduced cofactors, albeit with different efficiency, delivered by reductases present in the microsomal fraction. Azide and cyanide, but not azole compounds, inhibited these desaturases, suggesting a key role for cytochrome b 5 in these reactions.