Levansucrase from Bacillus subtilis

Enzyme Description

Extremophile
No
EC Number

Sequence

Length: 473 amino acids
MNIKKFAKQATVLTFTTALLAGGATQAFAKETNQKPYKETYGISHITRHDMLQIPEQQKNEKYQVPEFDSSTIKNISSAKGLDVWDSWPLQNADGTVANYHGYHIVFALAGDPKNADDTSIYMFYQKVGETSIDSWKNAGRVFKDSDKFDANDSILKDQTQEWSGSATFTSDGKIRLFYTDFSGKHYGKQTLTTAQVNVSASDSSLNINGVEDYKSIFDGDGKTYQNVQQFIDEGNYSSGDNHTLRDPHYVEDKGHKYLVFEANTGTEDGYQGEESLFNKAYYGKSTSFFRQESQKLLQSDKKRTAELANGALGMIELNDDYTLKKVMKPLIASNTVTDEIERANVFKMNGKWYLFTDSRGSKMTIDGITSNDIYMLGYVSNSLTGPYKPLNKTGLVLKMDLDPNDVTFTYSHFAVPQAKGNNVVITSYMTNRGFYADKQSTFAPSFLLNIKGKKTSVVKDSILEQGQLTVNK
E. Castillo et al. (2004) β€” Synthesis of levan in water-miscible organic solvents
Journal of Biotechnology  Β· doi:10.1016/j.jbiotec.2004.06.003 β†—  Β· Activity - Classical Stability - Incubation Specificity - Reaction Specificity
38 measurements
Database ID
UniProt: P05655 β†—
Sequence Annotation
Inferred - from protein name
Protein Source
Purified, bacterium Bacillus subtilis

Experimental Data (38 measurements)

38 measurements β€” page 2 of 2
Property Assay Solvent Solvent Volume Aqueous Reference Measured Value Units Solution pH Temperature Substrate(s) Product(s) Cofactor(s) Shaking Comments
Activity - Classical Activity measured by absorbance spectrophotometry (DNS assay) in the presence of organic solvent Acetone 20% 100.0 86.0 % 50 mM phosphate buffer 6 30Β°C 100 g/L Sucrose Reducing sugars β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (DNS assay) in the presence of organic solvent tert-Butanol 30% 100.0 130.0 % 50 mM phosphate buffer 6 30Β°C 100 g/L Sucrose Reducing sugars β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (DNS assay) in the presence of organic solvent Acetonitrile 30% 100.0 86.0 % 50 mM phosphate buffer 6 30Β°C 100 g/L Sucrose Reducing sugars β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (DNS assay) in the presence of organic solvent Acetone 30% 100.0 84.0 % 50 mM phosphate buffer 6 30Β°C 100 g/L Sucrose Reducing sugars β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (DNS assay) in the presence of organic solvent Acetonitrile 40% 100.0 83.0 % 50 mM phosphate buffer 6 30Β°C 100 g/L Sucrose Reducing sugars β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (DNS assay) in the presence of organic solvent Acetonitrile 20% 100.0 97.0 % 50 mM phosphate buffer 6 30Β°C 100 g/L Sucrose Reducing sugars β€” β€” Classical aqueous control (in %)
Specificity - Reaction Specificity Transferase (rather than hydrolysis) activity percentage, measured by HPLC after 20 hour incubation at 30Β°C in the presence of organic solvent tert-Butanol 83% 44.9 83.2 transferase activity % 50 mM phosphate buffer 6 37Β°C 100 g/L Sucrose Reducing sugars β€” β€” Classical aqueous control (in transferase activity %)
Specificity - Reaction Specificity Transferase (rather than hydrolysis) activity percentage, measured by HPLC after 20 hour incubation at 30Β°C in the presence of organic solvent tert-Butanol 75% 44.9 82.4 transferase activity % 50 mM phosphate buffer 6 37Β°C 100 g/L Sucrose Reducing sugars β€” β€” Classical aqueous control (in transferase activity %)
Specificity - Reaction Specificity Transferase (rather than hydrolysis) activity percentage, measured by HPLC after 20 hour incubation at 30Β°C in the presence of organic solvent tert-Butanol 63% 44.9 83.5 transferase activity % 50 mM phosphate buffer 6 37Β°C 100 g/L Sucrose Reducing sugars β€” β€” Classical aqueous control (in transferase activity %)
Specificity - Reaction Specificity Transferase (rather than hydrolysis) activity percentage, measured by HPLC after 20 hour incubation at 30Β°C in the presence of organic solvent tert-Butanol 50% 44.9 83.2 transferase activity % 50 mM phosphate buffer 6 37Β°C 100 g/L Sucrose Reducing sugars β€” β€” Classical aqueous control (in transferase activity %)
Specificity - Reaction Specificity Transferase (rather than hydrolysis) activity percentage, measured by HPLC after 20 hour incubation at 30Β°C in the presence of organic solvent tert-Butanol 30% 44.9 74.1 transferase activity % 50 mM phosphate buffer 6 37Β°C 100 g/L Sucrose Reducing sugars β€” β€” Classical aqueous control (in transferase activity %)
Specificity - Reaction Specificity Transferase (rather than hydrolysis) activity percentage, measured by HPLC after 20 hour incubation at 30Β°C in the presence of organic solvent tert-Butanol 15% 44.9 54.6 transferase activity % 50 mM phosphate buffer 6 37Β°C 100 g/L Sucrose Reducing sugars β€” β€” Classical aqueous control (in transferase activity %)
Stability - Incubation Activity after incubation (1 day at 30Β°C) measured by absorbance spectrophotometry (DNS assay) in aqueous phase tert-Butanol 83% 100.0 75.0 % Incubation: 50 mM phosphate buffer, Assay: 50 mM phosphate buffer Incubation: 6, Assay: 6 30Β°C 100 g/L Sucrose Reducing sugars β€” β€” Non-incubated control (in %), assay in aqueous phase | Clear about assay in aqueous phase ("diluting the sample enough to measure the residual activity in water.")
Stability - Incubation Activity after incubation (1 day at 30Β°C) measured by absorbance spectrophotometry (DNS assay) in aqueous phase tert-Butanol 75% 100.0 54.0 % Incubation: 50 mM phosphate buffer, Assay: 50 mM phosphate buffer Incubation: 6, Assay: 6 30Β°C 100 g/L Sucrose Reducing sugars β€” β€” Non-incubated control (in %), assay in aqueous phase | Clear about assay in aqueous phase ("diluting the sample enough to measure the residual activity in water.")
Stability - Incubation Activity after incubation (1 day at 30Β°C) measured by absorbance spectrophotometry (DNS assay) in aqueous phase tert-Butanol 63% 100.0 51.0 % Incubation: 50 mM phosphate buffer, Assay: 50 mM phosphate buffer Incubation: 6, Assay: 6 30Β°C 100 g/L Sucrose Reducing sugars β€” β€” Non-incubated control (in %), assay in aqueous phase | Clear about assay in aqueous phase ("diluting the sample enough to measure the residual activity in water.")
Stability - Incubation Activity after incubation (1 day at 30Β°C) measured by absorbance spectrophotometry (DNS assay) in aqueous phase tert-Butanol 50% 100.0 63.0 % Incubation: 50 mM phosphate buffer, Assay: 50 mM phosphate buffer Incubation: 6, Assay: 6 30Β°C 100 g/L Sucrose Reducing sugars β€” β€” Non-incubated control (in %), assay in aqueous phase | Clear about assay in aqueous phase ("diluting the sample enough to measure the residual activity in water.")
Stability - Incubation Activity after incubation (1 day at 30Β°C) measured by absorbance spectrophotometry (DNS assay) in aqueous phase tert-Butanol 30% 100.0 68.0 % Incubation: 50 mM phosphate buffer, Assay: 50 mM phosphate buffer Incubation: 6, Assay: 6 30Β°C 100 g/L Sucrose Reducing sugars β€” β€” Non-incubated control (in %), assay in aqueous phase | Clear about assay in aqueous phase ("diluting the sample enough to measure the residual activity in water.")
Stability - Incubation Activity after incubation (1 day at 30Β°C) measured by absorbance spectrophotometry (DNS assay) in aqueous phase tert-Butanol 15% 100.0 99.0 % Incubation: 50 mM phosphate buffer, Assay: 50 mM phosphate buffer Incubation: 6, Assay: 6 30Β°C 100 g/L Sucrose Reducing sugars β€” β€” Non-incubated control (in %), assay in aqueous phase | Clear about assay in aqueous phase ("diluting the sample enough to measure the residual activity in water.")
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Visualization : Activity β€” Classical

One bar per measurement. Colour = solvent, shade = solvent volume.

Visualization : Stability β€” Incubation

One bar per measurement. Colour = solvent, shade = solvent volume.

Visualization : Specificity β€” Reaction Specificity

One bar per measurement. Colour = solvent, shade = solvent volume.

Structure

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