Immobilization of the metagenomic lipase, LipG9, on porous pellets of poly‐hydroxybutyrate produced by the double emulsion solvent evaporation technique.

This work aimed to produce porous poly‐hydroxybutyrate (PHB) pellets in order to evaluate the pellets as a support for immobilization of the metagenomic lipase, LipG9. Four types of pelletized PHB particles with different morphological characteristics were obtained using the double emulsion and solvent evaporation technique (DESE). The micropores of these PHB pellets had similar average diameters (about 3 nm), but the pellets had different specific surface areas: 11.7 m2 g−1 for the PHB powder, 8.4 m2 g−1 for the control pellets (Ø < 0.5 mm, produced without the pore forming agent), 10.0 m2 g−1 for the small pellets (Ø < 0.5 mm), 9.5 m2 g−1 for the medium pellets (0.5 < Ø < 0.8 mm) and 8.4 m2 g−1 for the large pellets (Ø > 1.4 mm). Purified LipG9 was immobilized by adsorption on these pellets, and the results were compared with those obtained with PHB powder. The highest immobilization yield (83%) was obtained for the medium PHB pellets, followed by large (76%) and small (55%) PHB pellets. The activity of LipG9 immobilized on the pellets, for the synthesis of ethyl oleate in n‐hexane, was highest for the medium pellets (22 U g−1). The immobilization yield was high for PHB powder (99%) but the esterification activity was slightly lower (20 U g−1). These results show that pelletized PHB beads can be used for the immobilization of lipases, with the advantage that pelletized PHB will perform better than PHB powder in large‐scale enzyme bioreactors. [ABSTRACT FROM AUTHOR]