Carrier-Free Immobilization of Multi-Enzyme Complex Facilitates In Vitro Synthetic Enzymatic Biosystem for Biomanufacturing

A method is developed for carrier-free immobilization of multi-enzyme complexes with more than four enzymes by utilization of polypeptide interactions (SpyCatcher-SpyTag and dockerin-cohesin) and enzyme component self-oligomerization. Two pairs of scaffoldins with different arrangements of SpyCatcher-SpyTag and cohesins are prepared to recruit the four dockerin-containing cascade enzymes (i. e., alpha-glucan phosphorylase, phosphoglucomutase, inositol 1-phosphate synthase, and inositol 1-phosphatase) that can convert starch into inositol, forming multi-enzyme complexes. These self-assembled enzyme complexes show higher initial reaction rates than the four-enzyme cocktail. Moreover, water-insoluble self-assembled multi-enzyme complexes are observed, being the carrier-free immobilized multi-enzyme complex aggregates. These immobilized enzyme complexes can be recycled easily by simple centrifuging followed by resuspension for another round of reaction. Not only can these immobilized enzyme complexes be obtained by mixing the purified enzyme components, but also by the mixing of crude cell extracts. Therefore, the strategy for the carrier-free immobilization of enzyme complex sheds light on improving the catalytic capability of in vitro synthetic enzymatic biosystems.

Automated summary

A method for carrier-free immobilization of multi-enzyme complexes with more than four enzymes is developed using polypeptide interactions and enzyme component self-oligomerization. The self-assembled enzyme complexes show higher initial reaction rates than the four-enzyme cocktail. Water-insoluble self-assembled multi-enzyme complexes are observed, serving as carrier-free immobilized multi-enzyme complex aggregates. These immobilized enzyme complexes can be easily recycled and obtained from either purified enzyme components or crude cell extracts. This strategy sheds light on improving the catalytic capability of in vitro synthetic enzymatic biosystems.