Fig. 2From: Promoter engineering enables overproduction of foreign proteins from a single copy expression cassette in Bacillus subtilisOptimization of the core region of the Pylb promoter. a the core regions of the Pylb promoter were changed to corresponding consensus sequence. The nucleotides in bold italic indicate mutated sequences. b The BgaB expression level under the control of Pylb derivatives. c SDS-PAGE analysis of the BgaB expression. Equal amounts (30 μg) of total protein were loaded into each lane. The band corresponding to BgaB was marked. All cultures were grown in triplicate, and each experiment was performed at least twice. Error bars indicate standard deviations. CK represents the intracellular protein of strain WB800Back to article page