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This study focuses on the molecular cloning and functional expression of rice bran lipase (RBL) from Oryza sativa, highlighting its industrial significance as a biocatalyst. The research demonstrates that E. coli is not an optimal host for RBL expression, with successful results achieved using Pichia pastoris, leading to a maximum recombinant lipase activity of 152.6 U/mL. Additionally, the study explores the substrate specificity of RBL through molecular docking, revealing a correlation between catalytic e

Author

khiem-tt

Language

EN