albicans strain (Asai et al., 1999). Several enzymes of the postsqualene ergosterol biosynthetic pathway require molecular oxygen, making ergosterol biosynthesis an oxygen-dependent process. When grown under aerobic conditions, S. cerevisiae is FDA approved Drug Library able to synthesize sterols, and is unable to acquire exogenous sterols, a phenomenon known as aerobic sterol exclusion (Andreasen & Stier, 1953). Under anaerobic conditions, the activity of the postsqualene sterol pathway is decreased, and as a consequence, sterol

scavenging becomes the major mechanism for obtaining sterols (Andreasen & Stier, 1953). While S. cerevisiae is only able to take up exogenous sterols during anaerobic growth, some filamentous fungi such as Aspergillus fumigatus are able to take up sterols under aerobic conditions (Xiong et al., 2005). The molecular mechanisms behind aerobic sterol exclusion have not been elucidated, but heme has been implicated in the process. Cells are able to sense oxygen availability through Buparlisib nmr the levels

of heme, which is produced in an oxygen-dependent mechanism. Heme stimulates transcription through the Hap1 transcriptional activator, and both heme and Hap1 are involved in aerobic ergosterol biosynthesis. Hap1 is responsible for aerobic induction and anaerobic repression of ROX1 (Ushinsky & Keng, 1994), a well-known repressor of hypoxic genes, which is activated upon expression of Hap1 in a heme-dependent mechanism (Keng, 1992). Many genes involved in the later steps of ergosterol biosynthesis require molecular oxygen for catalysis, and as a result, these enzymes are downregulated as the supply of oxygen declines. Likewise, because heme production is dependent on the supply of oxygen, heme-mediated Rox1 repression of hypoxic genes declines as oxygen levels decrease, resulting in an increased expression of nearly all cAMP Rox1 repressed genes (Kwast et al., 1997). The upregulation of hypoxic genes and decreased activity of

ergosterol biosynthetic genes results in exogenous sterol uptake. Many genes involved in cholesterol biosynthesis have homologs in ergosterol biosynthesis, and while many of these have been identified within the P. carinii genome, P. carinii does not appear to encode all of the genes necessary to synthesize cholesterol through a de novo pathway (e.g. C-5 desaturase). Thus, it is unlikely that P. carinii is able to synthesize cholesterol, and most, if not all, of the cholesterol found within the membranes of P. carinii was scavenged from host cells by P. carinii. The ability of P. carinii to scavenge lipids was confirmed after incubation of P. carinii with the fluorescent fatty acid analog Bodipy-C12. Fluorescent microscopy and fluorimetry indicated that P. carinii readily scavenged Bodipy-C12 from the medium and incorporated the fatty acid uniformly in all morphological forms of P. carinii (Furlong et al., 1997). Uptake of Bodipy-C12 by P.