RT Journal Article
SR Electronic
T1 Genetic code expansion in the engineered organism Vmax X2: High yield and exceptional fidelity
JF bioRxiv
FD Cold Spring Harbor Laboratory
SP 2021.06.22.449487
DO 10.1101/2021.06.22.449487
A1 Sebasthian Santiago
A1 Omer Ad
A1 Bhavana Shah
A1 Zhongqi Zhang
A1 Xizi Zhang
A1 Abhishek Chatterjee
A1 Alanna Schepartz
YR 2021
UL http://biorxiv.org/content/early/2021/06/22/2021.06.22.449487.abstract
AB We report that the recently introduced commercial strain of V. natriegens (Vmax X2) supports robust unnatural amino acid mutagenesis, generating exceptional yields of soluble protein containing up to 5 non-canonical α-amino acids (ncAA). The isolated yields of ncAA-containing superfolder green fluorescent protein (sfGFP) expressed in Vmax X2 are up to 25-fold higher than those achieved using commercial expression strains (Top10 and BL21) and more than10-fold higher than those achieved using two different genomically recoded E. coli strains that lack endogenous UAG stop codons and release factor 1 and have been optimized for improved fitness and preferred growth temperature (C321.ΔA.opt and C321.ΔA.exp). In addition to higher yields of soluble protein, Vmax X2 cells also generate proteins with significantly lower levels of mis-incorporated natural α-amino acids at the UAG-programmed position, especially in cases where the ncAA is an imperfect substrate for the chosen orthogonal aminoacyl tRNA synthetase (aaRS). This increase in fidelity implies that use of Vmax X2 cells as the expression host can obviate the need for time-consuming directed evolution experiments to improve specific activity of highly desirable but imperfect ncAA substrates.Competing Interest StatementThe authors have declared no competing interest.