Alleviating the trade-off by site-guided function switch of nitrilase to nitrile hydratase

Catalytic promiscuity makes nitrilase-mediated unnatural reactivity a promising pathway in the production of primary amides. However, during the functional switch of nitrilase, a trade-off between the newly developed hydration activity and relative activity hinders the application of nitrilase in the production of amides. Our previous study showed that the mutant F193N (Mut0) of nitrilase NIT6803 from Synechocystis sp. PCC6803 improved the hydration activity as the amide ratio increased to 73.4%, whereas the relative activity was only 50.1% of that of the wild-type (WT). In this study, we succeeded in alleviating the trade-off of Mut0 through an evolutionary combination of the key identified sites 101, 192, and 201. Inside the active pocket, the co-evolution of residue Q192 was identified by hotspot prediction to correlate with N193, and Q192H exhibited an improved amide ratio of 76.9% with a relative activity of up to 72%. Outside the active pocket, the flexible loop surface residue G101 and homodimer A interface residue I201 were identified using sequence alignment-based mutations. Further evolutionary combination of the three key sites yielded the best triple mutant G101K/Q192H/ I201M, which had the highest amide ratio of 98.5% and considerably recovered relative activity of 82.6% while retaining only 1.5% of the carboxylic acid ratio. The transition-state analogue sheds light on the basis of the almost identical switch of the reaction pathways, and our results expand the toolbox of nitrilase-catalysed promiscuity for amide formation.

Automated summary

Catalytic promiscuity enables nitrilase-mediated unnatural reactivity as a promising pathway for primary amide production. However, the trade-off between hydration activity and relative activity during the functional switch of nitrilase hinders its application. This study successfully alleviated the trade-off through an evolutionary combination of key sites, expanding the toolbox for nitrilase-catalysed promiscuity in amide formation.