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Immunochemical identification of the pssA gene product as phosphatidylserine synthase I of Chinese hamster ovary cells
Author(s) -
Saito Kyoko,
Kuge Osamu,
Akamatsu Yuzuru,
Nishijima Masahiro
Publication year - 1996
Publication title -
febs letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.593
H-Index - 257
eISSN - 1873-3468
pISSN - 0014-5793
DOI - 10.1016/0014-5793(96)01049-6
Subject(s) - chinese hamster ovary cell , microbiology and biotechnology , phosphatidylserine , biochemistry , biology , complementary dna , immunoprecipitation , cytosol , gene product , atp synthase , microsome , enzyme , gene , gene expression , membrane , phospholipid , receptor
We have previously shown that a Chinese hamster ovary (CHO) cell mutant defective in phosphatidylserine synthase I recovers the enzyme activity on transfection with a pssA cDNA clone isolated from the parental CHO‐K1. The resultant transfectant, CDT‐1, exhibited about 20‐fold higher specific activity of the enzyme in the membrane fraction than CHO‐K1 cells. Polyclonal antibodies against two peptides of the predicted pssA product cross‐reacted with a membrane protein having an apparent molecular mass of 42 kDa, which was overproduced in CDT‐1 cells. By immunoprecipitation with the antibody, phosphatidylserine synthase I activity as well as the 42‐kDa protein was eliminated from solubilized membrane proteins of CDT‐1 cells. Both the enzyme activity and the 42‐kDa protein of CHO‐K1 cells were enriched in the mitochondria‐associated membrane fraction and the microsome fraction, but neither was enriched in the mitochondria fraction or the cytosol fraction. These results suggest that the pssA gene encodes phosphatidylserine synthase I.