Application | Comment | Organism |
---|---|---|
degradation | due to its low structural stability and solubility, it is difficult to apply standard laboratory-level Ideonella sakaiensis PETase expression and purification procedures in industry. To overcome this difficulty, the expression of IsPETase can be improved by using a secretion system. The extracellular enzyme is successfully produced using pET22b-SPMalE:IsPETase and pET22b-SPLamB:IsPETase expression systems. The secreted IsPETase has PET-degradation activity. The work will be used for development of a new Escherichia coli strain capable of degrading and assimilating PET in its culture medium | Ideonella sakaiensis |
Cloned (Comment) | Organism |
---|---|
expression in Escherichia coli | Ideonella sakaiensis |
Localization | Comment | Organism | GeneOntology No. | Textmining |
---|---|---|---|---|
extracellular | - |
Ideonella sakaiensis | - |
- |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Ideonella sakaiensis | A0A0K8P6T7 | - |
- |
Ideonella sakaiensis 201-F6 | A0A0K8P6T7 | - |
- |
Synonyms | Comment | Organism |
---|---|---|
PETase | - |
Ideonella sakaiensis |