Incremental truncation of PHA synthases results in altered product specificity

PHA synthase is the key enzyme involved in the biosynthesis of microbial polymers, polyhydroxyalkanoates (PHA). In this study, we created a hybrid library of PHA synthase gene with different crossover points by an incremental truncation method between the C-terminal fragments of the phaCCn (phaC from Cupriavidus necator) and the N-terminal fragments of the phaC1Pa (phaC from Pseudomonas aeruginosa). As the truncation of the hybrid enzyme increased, the in vivo PHB synthesis ability of the hybrids declined gradually. PHA synthase PhaCCn with a deletion on N-terminal up to 83 amino acid residues showed no synthase activity. While with the removal of up to 270 amino acids from the N-terminus, the activity of the truncated PhaCCn could be complemented by the N-terminus of PhaC1Pa. Three of the hybrid enzymes W188, W235 and W272 (named by the deleted nucleic acid number) were found to have altered product specificities.

► A hybrid library of PHA synthases (PhbCCn and PhaC1Pa) was constructed by incremental truncation method.
► The activity of the truncated PhaCCn could be complemented by the N-terminus of PhaC1Pa.
► Three of the hybrid enzymes were found to have altered product specificity.