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Literature summary for 2.4.1.9 extracted from

  • Antosova, M.; Illeova, V.; Vandakova, M.; Druzkovska, A.; Polakovic, M.
    Chromatographic separation and kinetic properties of fructosyltransferase from Aureobasidium pullulans (2008), J. Biotechnol., 135, 58-63.
    View publication on PubMed

Molecular Weight [Da]

Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
570000
-
gel filtration Aureobasidium pullulans

Organism

Organism UniProt Comment Textmining
Aureobasidium pullulans
-
-
-

Purification (Commentary)

Purification (Comment) Organism
partial Aureobasidium pullulans

Specific Activity [micromol/min/mg]

Specific Activity Minimum [µmol/min/mg] Specific Activity Maximum [µmol/min/mg] Comment Organism
459
-
pH 5.5, 55°C Aureobasidium pullulans

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
additional information the production of fructooligosaccharide by this enzyme is possible only in the presence of sucrose which is an exclusive donor of fructosyl residue in the transferase reaction. The acceptor can be another molecule of sucrose or frucotoligosaccharide Aureobasidium pullulans ?
-
?
sucrose + H2O hydrolytic activity. Transglycosylation activity is higher in the whole concentration range tested and completely dominating at higher sucrose concentrations Aureobasidium pullulans alpha-D-glucose + beta-D-fructose
-
?
sucrose + sucrose transgylcosylation activity. Transglycosylation activity is higher in the whole concentration range tested and completely dominating at higher sucrose concentrations Aureobasidium pullulans [(beta-D-fructose-(2-1))n]-alpha-D-glucose + alpha-D-glucose
-
?