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Growth phenotypes of RHA1 strains on media supplemented with methanol. WT RHA1, ΔmadA and the complement strains ΔmadA-C were grown in microtiter plates on minimal medium containing 5 mM acetate (A) and a further 300 mM methanol (B). Complementing genes were on plasmids (Table 1). Cultures were induced with 1 µg/mL of thiostrepton at t = 0 h. Values represent the mean of biological triplicates. Error is given as standard deviation and represented as bands around the curves.
