PT - JOURNAL ARTICLE AU - Gordon Rix AU - Ella J. Watkins-Dulaney AU - Patrick J. Almhjell AU - Christina E. Boville AU - Frances H. Arnold AU - Chang C. Liu TI - Scalable, continuous evolution for the generation of diverse enzyme variants encompassing promiscuous activities AID - 10.1101/2020.06.01.128165 DP - 2020 Jan 01 TA - bioRxiv PG - 2020.06.01.128165 4099 - http://biorxiv.org/content/early/2020/06/02/2020.06.01.128165.short 4100 - http://biorxiv.org/content/early/2020/06/02/2020.06.01.128165.full AB - Enzyme orthologs sharing identical primary functions can have different promiscuous activities. While it is possible to mine this natural diversity to obtain useful biocatalysts, generating comparably rich ortholog diversity is difficult, as it is the product of deep evolutionary processes occurring in a multitude of separate species and populations. Here, we take a first step in recapitulating the depth and scale of natural ortholog evolution on laboratory timescales. Using a continuous directed evolution platform called OrthoRep, we rapidly evolved the Thermotoga maritima tryptophan synthase β-subunit (TmTrpB) through multi-mutation pathways in many independent replicates, selecting only onTmTrpB’s primary activity (synthesizing L-tryptophan from indole and L-serine). We find that the resulting sequence-diverseTmTrpB variants span a range of substrate profiles useful in industrial biocatalysis and suggest that the depth and scale of evolution that OrthoRep affords will be generally valuable in enzyme engineering and the evolution of new biomolecular functions.Competing Interest StatementC.E.B and F.H.A. are co-founders of Aralez Bio, focusing on the enzymatic synthesis of unnatural amino acids.