Any feedback?
Please rate this page
(literature.php)
(0/150)

BRENDA support

Literature summary for 3.1.1.101 extracted from

  • Seo, H.; Kim, S.; Son, H.F.; Sagong, H.Y.; Joo, S.; Kim, K.J.
    Production of extracellular PETase from Ideonella sakaiensis using sec-dependent signal peptides in E. coli (2018), Biochem. Biophys. Res. Commun., 508, 250-255 .
    View publication on PubMed

Application

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(Commentary)

Cloned (Comment) Organism
expression in Escherichia coli Ideonella sakaiensis

Localization

Localization Comment Organism GeneOntology No. Textmining
extracellular
-
Ideonella sakaiensis
-
-

Organism

Organism UniProt Comment Textmining
Ideonella sakaiensis A0A0K8P6T7
-
-
Ideonella sakaiensis 201-F6 A0A0K8P6T7
-
-

Synonyms

Synonyms Comment Organism
PETase
-
Ideonella sakaiensis