The Delta12 acyl-lipid desaturase of Synechocystis sp. PCC 6803 was overexpressed in Escherichia coli as an active enzyme. The overexpressed protein was associated with cell membranes; it represented about 10% of the total cellular protein and 25% of the total membrane protein. The enzyme in the membrane fraction exhibited strong fatty-acid desaturase activity. The desaturase in salt-washed membranes was stabilized by the presence of sorbitol. Storage of salt-washed membranes in 2 M sorbitol at 4 degrees C and at pH 7-8 for six days resulted in the loss of less than 10% of the desaturase activity. The desaturase activity had a positive temperature coefficient, a result that suggests that the increase in the desaturation of fatty acids at low temperature might not be caused by the activation of desaturases at low temperature but, rather, by the increased synthesis of desaturases de novo.
Copyright 1998 Elsevier Science B.V.