Abstract
Ethanolamine kinase (ATP:ethanolamineO-phosphotransferase, EC 2.7.1.82) catalyzes the committed step of phosphatidylethanolamine synthesis via the CDP-ethanolamine pathway. The gene encoding ethanolamine kinase (EKI1) was identified from the SaccharomycesGenome Data Base (locus YDR147W) based on its homology to theSaccharomyces cerevisiae CKI1-encoded choline kinase, which also exhibits ethanolamine kinase activity. The EKI1 gene was isolated and used to construct eki1Δ andeki1Δ cki1Δ mutants. A multicopy plasmid containing the EKI1 gene directed the overexpression of ethanolamine kinase activity in wild-type, eki1Δ mutant,cki1Δ mutant, and eki1Δ cki1Δ double mutant cells. The heterologous expression of the S. cerevisiae EKI1 gene in Sf-9 insect cells resulted in a 165,500-fold overexpression of ethanolamine kinase activity relative to control insect cells. The EKI1 gene product also exhibited choline kinase activity. Biochemical analyses of the enzyme expressed in insect cells, in eki1Δ mutants, and incki1Δ mutants indicated that ethanolamine was the preferred substrate. The eki1Δ mutant did not exhibit a growth phenotype. Biochemical analyses of eki1Δ,cki1Δ, and eki1Δ cki1Δ mutants showed that the EKI1 and CKI1 gene products encoded all of the ethanolamine kinase and choline kinase activities in S. cerevisiae. In vivo labeling experiments showed that the EKI1 and CKI1 gene products had overlapping functions with respect to phospholipid synthesis. Whereas theEKI1 gene product was primarily responsible for phosphatidylethanolamine synthesis via the CDP-ethanolamine pathway, the CKI1 gene product was primarily responsible for phosphatidylcholine synthesis via the CDP-choline pathway. Unlikecki1Δ mutants, eki1Δ mutants did not suppress the essential function of Sec14p.