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 |
Gene_locus | idesa-mheth idesa-peth |
Family | Polyesterase-lipase-cutinase |
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