synthesis of phospholipids with yeast phospholipase B, a phospholipid deacylating enzyme.

The gene encoding the phospholipid deacylation enzyme, phospholipase B (Sc), was successfully expressed in . The enzyme (Scplb1p) was engineered to have a histidine-tag at the C-terminal end and was purified by metal (Ni) affinity chromatography. Enzymatic properties, optimal pH, and substrate specificity were similar to those reported previously. For example, deacylation activity was observed in acidic pH in the absence of Ca and was additive in neutral pH in the presence of Ca, and the enzyme had the same substrate priority as reported previously, with the exception of PE, suggesting that yeast phospholipase B could be produced in its native structure in bacterial cells. Scplb1p retained transacylation activity in aqueous medium, and esterified lysophosphatidylcholine with free fatty acid to form phosphatidylcholine in a non-aqueous, glycerin medium. We propose that phospholipase B could serve as an additional tool for enzyme-mediated phospholipid synthesis.