The full-length coding sequences were cloned into the pGADT7 vector or the pGBKT7 vector. The primers of related genes were listed in Table S1 (see online supplementary material). Target combinations were transformed into AH109 yeast and incubated on selective SD/−Leu/−Trp/-His/−Ade medium with Aureobasidin A (AbA) and X-α-gal.
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