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. 2020 Oct 22;15(3):746–761. doi: 10.1038/s41396-020-00810-z

Fig. 4. Amino acid substitutions from BUL1 (D334G), YFR018C (L7F), and TIF35 (V272L) were engineered into the ancestral genetic background of S. cerevisiae (“Methods”).

Fig. 4

Growth rates were measured for the S. cerevisiae ancestor, the co-culture evolved S. cerevisiae clone E10-1 and the engineered three mutants. Stars indicate a significant difference from the ancestor (Bonferroni-corrected post-hoc t-tests).