The thrB gene of E. coli coding for homoserine kinase [EC 2.7.1.39] wa
s introduced into the pRc/RSV mammalian expression vector. Transfectio
n of the CHO cell line with the resulting pRSV-Bneo plasmid by electro
poration yielded a stably transformed clone accumulating o-homoserine
phosphate. Assay for homoserine kinase in cell extracts revealed enzym
e activity of 6.0 . 10(-3) units per mg protein, which was 75% that in
E. coli cells cultured in the minimal medium and about 20 times that
in the 3T3 clones obtained before.