Graf_2021_Methods.Enzymol_648_337

Reference

Title : Structural analysis of PET-degrading enzymes PETase and MHETase from Ideonella sakaiensis - Graf_2021_Methods.Enzymol_648_337
Author(s) : Graf LG , Michels EAP , Yew Y , Liu W , Palm GJ , Weber G
Ref : Methods Enzymol , 648 :337 , 2021
Abstract :

The concept of biocatalytic PET degradation for industrial recycling processes had made a big step when the bacterium Ideonella sakaiensis was discovered to break PET down to its building blocks at ambient temperature. This process involves two enzymes: cleavage of ester bonds in PET by PETase and in MHET, the resulting intermediate, by MHETase. To understand and further improve this unique capability, structural analysis of the involved enzymes was aimed at from early on. We describe a repertoire of methods to this end, including protein expression and purification, crystallization of apo and substrate-bound enzymes, and modeling of PETase complexed with a ligand.

PubMedSearch : Graf_2021_Methods.Enzymol_648_337
PubMedID: 33579411
Gene_locus related to this paper: idesa-mheth , idesa-peth

Related information

Citations formats

Graf LG, Michels EAP, Yew Y, Liu W, Palm GJ, Weber G (2021)
Structural analysis of PET-degrading enzymes PETase and MHETase from Ideonella sakaiensis
Methods Enzymol 648 :337

Graf LG, Michels EAP, Yew Y, Liu W, Palm GJ, Weber G (2021)
Methods Enzymol 648 :337