Directed reconstruction of a novel ancestral alcohol dehydrogenase featuring shifted pH-profile, enhanced thermostability and expanded substrate spectrum

Ancestral enzymes are promising for industrial biotechnology due to high stability and catalytic promiscuity. An effective protocol was developed for the directed resurrection of ancestral enzymes. Employing genome mining with diaryl alcohol dehydrogenase KpADH as the probe, descendant enzymes D10 and D11 were firstly identified. Then through ancestral sequence reconstruction, A64 was resurrected with a specific activity of 4.3 Umiddotmg(-1). The optimum pH of A64 was 7.5, distinct from 5.5 of D10. The T15 50 and T-m values of A64 were 57.5 degrees C and 61.7 degrees C, significantly higher than those of the descendant counterpart. Substrate spectrum of A64 was quantitively characterized with a Shannon-Wiener index of 2.38, more expanded than D10, especially, towards bulky ketones in Group A and B. A64 also exhibited higher enantioselectivity. This study provides an effective protocol for constructing of ancestral enzymes and an efficient ancestral enzyme of industrial relevance for asymmetric synthesis of chiral alcohols.

Automated summary

An effective protocol was developed for the directed resurrection of ancestral enzymes. A highly efficient ancestral enzyme A64 with high stability and catalytic promiscuity was successfully resurrected, which has potential applications in asymmetric synthesis of chiral alcohols.