posted on 2023-09-26, 10:06authored byWan-Wen Ting, I-Son Ng
The deaminase-fused
T7 RNA polymerase (T7RNAP) presents a promising
toolkit for in vivo target-specific enzyme evolution,
offering the unique advantage of simultaneous DNA modification and
screening. Previous studies have reported the mutation efficiency
of base editors relying on different resources. In contrast, the mechanism
underlying the T7RNAP/T7 system is well-understood. Therefore, this
study aimed to establish a new platform, termed dT7-Muta, by tuning
the binding efficiency between T7RNAP and the T7 promoter for gene
mutagenesis. The strategy for proof-of-concept involves alterations
in the fluorescence distribution through dT7-Muta and screening of
the mutants via flow cytometry. The cis-aconitate
decarboxylase from Aspergillus terreus (AtCadA) was evolved and screened via an itaconate-induced biosensor
as proof-of-function of enzyme evolution. First, the degenerated codons
were designed within the binding and initial region of T7 promoters
(dT7s), including upstream (U), central (C), and downstream (D) regions.
Three strength variants of dT7 promoter from each design, i.e., strong
(S), medium (M), and weak (W), were used for evaluation. Mutation
using dT7s of varying strength resulted in a broader fluorescence
distribution in sfGFP mutants from the promoters CW and DS. On the
other hand, broader fluorescence distribution was observed in the
AtCadA mutants from the original promoter T7, UW, and DS, with the
highest fluorescence and itaconic acid titer at 860 a.u. and 0.51
g/L, respectively. The present platform introduces a novel aspect
of the deaminase-based mutagenesis, emphasizing the potential of altering
the binding efficiency between T7RNAP and the T7 promoter for further
efforts in enzyme evolution.