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Toward reproducible PETase research: A standardized workflow for reliable enzyme production and comparison
K. Jiraskova, J. Ptacek, K. Vydra Bousova, J. Vondrasek
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, srovnávací studie
- MeSH
- Escherichia coli genetika metabolismus MeSH
- polyethylentereftaláty * metabolismus chemie MeSH
- průběh práce MeSH
- rekombinantní proteiny genetika izolace a purifikace chemie biosyntéza metabolismus MeSH
- Publikační typ
- časopisecké články MeSH
- srovnávací studie MeSH
The enzymatic degradation of polyethylene terephthalate (PET) by PETases has gained significant attention as a potential solution for plastic waste management. However, the absence of a standardized protocol for PETase production across studies presents a challenge for consistent enzyme characterization and activity comparison. Variations in production methods, including expression systems and purification techniques, may contribute to discrepancies in reported PETase activities. Here, we present the development of a unified protocol for the production of wild-type and engineered IsPETase variants. This protocol comprises standardized expression, purification, and quality control steps to ensure reproducibility and reliability. By enabling more accurate comparisons of PETase variants and addressing inconsistencies in PETase production, this approach facilitates collaborative efforts to advance plastic degradation technologies and lays the groundwork for accelerating research in enzymatic PET degradation and its applications in plastic waste management.
Citace poskytuje Crossref.org
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- $a The enzymatic degradation of polyethylene terephthalate (PET) by PETases has gained significant attention as a potential solution for plastic waste management. However, the absence of a standardized protocol for PETase production across studies presents a challenge for consistent enzyme characterization and activity comparison. Variations in production methods, including expression systems and purification techniques, may contribute to discrepancies in reported PETase activities. Here, we present the development of a unified protocol for the production of wild-type and engineered IsPETase variants. This protocol comprises standardized expression, purification, and quality control steps to ensure reproducibility and reliability. By enabling more accurate comparisons of PETase variants and addressing inconsistencies in PETase production, this approach facilitates collaborative efforts to advance plastic degradation technologies and lays the groundwork for accelerating research in enzymatic PET degradation and its applications in plastic waste management.
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