期刊
EUKARYOTIC CELL
卷 6, 期 11, 页码 2018-2028出版社
AMER SOC MICROBIOLOGY
DOI: 10.1128/EC.00210-07
关键词
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资金
- NIAID NIH HHS [R01 AI044594-08, R01 AI044594] Funding Source: Medline
- PHS HHS [R01 A144594] Funding Source: Medline
We report the presence of a new fatty acyl coenzyme A (acyl-CoA) elongation system in Cryptosporidium and the functional characterization of the key enzyme, a single long-chain fatty acid elongase (LCE), in this parasite. This enzyme contains conserved motifs and predicted transmembrane domains characteristic to the elongase family and is placed within the EL06 family specific for saturated substrates. CpLCE1 gene transcripts are present at all life cycle stages, but the levels are highest in free sporozoites and in stages at 36 h and 60 h postinfection that typically contain free merozoites. Immunostaining revealed localization to the outer surface of sporozoites and to the parasitophorous vacuolar membrane. Recombinant CpLCE1 displayed allosteric kinetics towards malonyl-CoA and palmitoyl-CoA and Michaelis-Menten kinetics towards NADPH. Myristoyl-CoA (C-14:0) and palmitoyl-CoA (C-16:0) display the highest activity when used as substrates, and only one round of elongation occurs. CpLCE1 is fairly resistant to cerulenin, an inhibitor for both type I and 11 fatty acid synthases (i.e., maximum inhibitions of 20.5% and 32.7% were observed when C-16:0 and C-14:0 were used as substrates, respectively). These observations ultimately validate the function of CpLCE1.
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