Related Experiment Video
Updated: Jan 9, 2026

Defining Substrate Specificities for Lipase and Phospholipase Candidates
Published on: November 23, 2016
Computational Study of a Versatile Lipase for the Degradation of Polylactic Acid
Carlos Murguiondo1, Mario García de Lacoba1, Valentina Acosta-Borreros1
1Centro de Investigaciones Biológicas Margarita Salas (CIB-CSIC), Ramiro de Maeztu 9, Madrid, Community of Madrid ES 28040, Spain.
Abstract:
Biocatalysis is an emerging and sustainable approach to depolymerize highly hydrophobic plastic polyesters such as poly-(lactic acid) (PLA), a bioplastic widely used in packaging and disposable items. Some enzymes, including lipases, cutinases, and proteases, have been described to hydrolyze PLA, but the activity strongly depends on stereochemistry and crystallinity. In this study, we explored the activity of the versatile lipase fromOphiostoma piceae (OPE) and three engineered variants (N81A, N94A, and N81/94A) on polylactic acid (PLA), comparing the experimental data with predictions from two computational methodologies, Thermal Titration Molecular Dynamics (a classical method) and the machine learning-guided XLPFE scoring function. Experimentally, mutant N81A showed the highest PLA hydrolytic activity, followed by WT OPE, with N94A and N81/94A being substantially less effective. This combined approach served to validate the reliability of these computational strategies for predicting enzyme interactions and highlights the importance of using long enough model substrates to guide future enzyme optimization.
Related Concept Videos
Lipid Catabolism
Lipid Digestion
Formation of Lipopolysaccharides

