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

BRENDA support

Literature summary for 3.1.6.1 extracted from

  • Kim, M.; Kim, J.; Nam, S.
    Constitutive overexpression of Pseudoalteromonas carrageenovora arylsulfatase in E. coli fed-batch culture (2011), Korean J. Chem. Engin., 28, 1101-1104.
No PubMed abstract available

Cloned(Commentary)

Cloned (Comment) Organism
astA gene from Pseudoalteromonas carrageenovora genome is subcloned into pHCEIA vector employing the hyper constitutive expression promoter from the D-amino acid aminotransferase gene of Geobacillus toebii. When the cell is cultured on fermentor containing MaxyBroth-HD medium with 1% glycerol, the enzyme activity reaches 12.8 micromol/min/mL. On MaxyBroth-HD medium with 2% glycerol, the cell shows 2.7fold higher arylsulfatase expression than that with 1% glycerol. The fed-batch cultivation employing MaxyBroth-HD medium and additional feeding of glycerol gave about 143 micromol/min/mL of arylsulfatase at 20 h, which corresponds to 4fold higher enzyme activity than that of 2% glycerol batch culture Pseudoalteromonas carrageenovora

Organism

Organism UniProt Comment Textmining
Pseudoalteromonas carrageenovora
-
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
4-nitrophenyl sulfate + H2O
-
Pseudoalteromonas carrageenovora 4-nitrophenol + sulfate
-
?

Synonyms

Synonyms Comment Organism
arylsulfatase gene
-
Pseudoalteromonas carrageenovora
AstA
-
Pseudoalteromonas carrageenovora