Skip to main content
Fig. 1 | BMC Biotechnology

Fig. 1

From: High-specificity synthesis of novel monomers by remodeled alcohol hydroxylase

Fig. 1

Schematic representation of the substrate specificities and regioselectivities of the native P450BM3 and the remodeled P450BM3. The native P450BM3 has a substrate preference for C12-C18 fatty acids and evenly oxidizes the ω-1, ω-2 and ω-3 carbons of the fatty acid substrates (a), while the remodeled P450BM3 exhibits a greatly improved regiospecificity of decanol hydroxylation, with 1,7-decanediol as the dominant product (b)

Back to article page