Phosphatidylserine synthase I and II of mammalian cells

Biochim Biophys Acta. 1997 Sep 4;1348(1-2):151-6. doi: 10.1016/s0005-2760(97)00137-9.

Abstract

Phosphatidylserine (PtdSer) in mammalian cells is synthesized through an exchange of free L-serine for the base moiety of pre-existing phospholipids. Studies on PtdSer biosynthesis in Chinese hamster ovary (CHO) cells have suggested that the serine base-exchange is catalyzed by at least two different enzymes; one, named PtdSer synthase I (PSS I), uses phosphatidylcholine (PtdCho) and possibly phosphatidylethanolamine (PtdEtn) as phosphatidyl donors for the serine base-exchange, and the other, named PtdSer synthase II (PSS II), uses PtdEtn but not PtdCho as a phosphatidyl donor. Recently, cDNAs of the PSS I and II have been isolated from CHO-K1 cells. This review will briefly describe the current understanding of PtdSer synthases of mammalian cells, mainly CHO cells.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Amino Acid Sequence
  • Animals
  • CHO Cells
  • Cloning, Molecular
  • Cricetinae
  • Isoenzymes / chemistry
  • Isoenzymes / genetics
  • Isoenzymes / metabolism*
  • Molecular Sequence Data
  • Nitrogenous Group Transferases / chemistry
  • Nitrogenous Group Transferases / genetics
  • Nitrogenous Group Transferases / metabolism*
  • Protein Conformation
  • Sequence Homology, Amino Acid
  • Substrate Specificity

Substances

  • Isoenzymes
  • Nitrogenous Group Transferases
  • Ptdss2 protein, mouse
  • phospholipid serine base exchange enzyme