Serine protease 2 (gene baapr2) from Bacillus altitudinis W3
Enzyme Description
Species
Extremophile
No
but "alkaline-stable" enzyme
EC Number
Sequence
MKVKSFGAGLCMASMLLASMTFGASDVSAKDQAKKEYMIGFSSSVQDKTQKQLVEKAGGHVKESIEKIDMMKVSLNEASKEKLHQAKEVTFIEEDQKAKTSGQSVPYGIKSIKAQKVHKRGYAGQNVKVAVLDSGIDGKHEDLHVTGGVSFVPTESDPLVDPHEHGTHVAGTIAALDNKVGVVGVAPKASIYAVKVADENGDGYYSWIIKGIEWAIENEMDVINISMGGASESEALKEAVDRAYDNGILIVASAGNAGSYGSLNTIDYPAKYSSVMAVASVDQRKQRAFDSSVGEEVEVSAPGVSTLSTIPHNEYGYKSGTSMASPHVAGAAAVILSKHPNLTNDELRERLTKTATKLGEPFYYGAGLVNVQKAAR
Shaolan Yang et al. (2020)
β Mining of alkaline proteases from Bacillus altitudinis W3 for desensitization of milk proteins: Their heterologous expression, purification, and characterization
International Journal of Biological Macromolecules
Β· doi:10.1016/j.ijbiomac.2019.10.252 β
Β· Stability - Incubation
▼
Database ID
UniProt: A0A6G6A873 β
Sequence Annotation
Explicit - Provided
Protein Source
Recombinant, host bacterium Bacillus subtilis WB600
Experimental Data (9 measurements)
9 measurements
| Property | Assay | Solvent | Solvent Volume | Aqueous Reference | Measured Value | Units | Solution | pH | Temperature | Substrate(s) | Product(s) | Cofactor(s) | Shaking | Comments |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Stability - Incubation | Activity after incubation (1 hour at 25Β°C), measured by absorbance spectrophotometry (colorimetric assay, change in Azo-peptides absorbance measurement, 440 nm) in aqueous phase | Dimethyl Sulfoxide (DMSO) | 0.5% | 100 | 98 | % | Incubation: 50 mM glycine-NaOH buffer, Assay: 50 mM glycine-NaOH buffer, 2 mM CaCl2 | Incubation: 8.5, Assay: 10 | Incubation: 25Β°C, Assay: 50Β°C | 2 g/L Azocasein | Azo-peptides , Peptides | β | β | Non-incubated control (in %), assay in aqueous phase | Uncertainty about whether assay was really in aqueous conditions or in the presence of organic solvent |
| Stability - Incubation | Activity after incubation (1 hour at 25Β°C), measured by absorbance spectrophotometry (colorimetric assay, change in Azo-peptides absorbance measurement, 440 nm) in aqueous phase | Methanol | 5% | 100 | 98 | % | Incubation: 50 mM glycine-NaOH buffer, Assay: 50 mM glycine-NaOH buffer, 2 mM CaCl2 | Incubation: 8.5, Assay: 10 | Incubation: 25Β°C, Assay: 50Β°C | 2 g/L Azocasein | Azo-peptides , Peptides | β | β | Non-incubated control (in %), assay in aqueous phase | Uncertainty about whether assay was really in aqueous conditions or in the presence of organic solvent |
| Stability - Incubation | Activity after incubation (1 hour at 25Β°C), measured by absorbance spectrophotometry (colorimetric assay, change in Azo-peptides absorbance measurement, 440 nm) in aqueous phase | Ethanol | 5% | 100 | 81 | % | Incubation: 50 mM glycine-NaOH buffer, Assay: 50 mM glycine-NaOH buffer, 2 mM CaCl2 | Incubation: 8.5, Assay: 10 | Incubation: 25Β°C, Assay: 50Β°C | 2 g/L Azocasein | Azo-peptides , Peptides | β | β | Non-incubated control (in %), assay in aqueous phase | Uncertainty about whether assay was really in aqueous conditions or in the presence of organic solvent |
| Stability - Incubation | Activity after incubation (1 hour at 25Β°C), measured by absorbance spectrophotometry (colorimetric assay, change in Azo-peptides absorbance measurement, 440 nm) in aqueous phase | Isopropanol | 5% | 100 | 74 | % | Incubation: 50 mM glycine-NaOH buffer, Assay: 50 mM glycine-NaOH buffer, 2 mM CaCl2 | Incubation: 8.5, Assay: 10 | Incubation: 25Β°C, Assay: 50Β°C | 2 g/L Azocasein | Azo-peptides , Peptides | β | β | Non-incubated control (in %), assay in aqueous phase | Uncertainty about whether assay was really in aqueous conditions or in the presence of organic solvent |
| Stability - Incubation | Activity after incubation (1 hour at 25Β°C), measured by absorbance spectrophotometry (colorimetric assay, change in Azo-peptides absorbance measurement, 440 nm) in aqueous phase | Acetone | 5% | 100 | 93 | % | Incubation: 50 mM glycine-NaOH buffer, Assay: 50 mM glycine-NaOH buffer, 2 mM CaCl2 | Incubation: 8.5, Assay: 10 | Incubation: 25Β°C, Assay: 50Β°C | 2 g/L Azocasein | Azo-peptides , Peptides | β | β | Non-incubated control (in %), assay in aqueous phase | Uncertainty about whether assay was really in aqueous conditions or in the presence of organic solvent |
| Stability - Incubation | Activity after incubation (1 hour at 25Β°C), measured by absorbance spectrophotometry (colorimetric assay, change in Azo-peptides absorbance measurement, 440 nm) in aqueous phase | Acetonitrile | 5% | 100 | 73 | % | Incubation: 50 mM glycine-NaOH buffer, Assay: 50 mM glycine-NaOH buffer, 2 mM CaCl2 | Incubation: 8.5, Assay: 10 | Incubation: 25Β°C, Assay: 50Β°C | 2 g/L Azocasein | Azo-peptides , Peptides | β | β | Non-incubated control (in %), assay in aqueous phase | Uncertainty about whether assay was really in aqueous conditions or in the presence of organic solvent |
| Stability - Incubation | Activity after incubation (1 hour at 25Β°C), measured by absorbance spectrophotometry (colorimetric assay, change in Azo-peptides absorbance measurement, 440 nm) in aqueous phase | Dichloromethane | 5% | 100 | 35 | % | Incubation: 50 mM glycine-NaOH buffer, Assay: 50 mM glycine-NaOH buffer, 2 mM CaCl2 | Incubation: 8.5, Assay: 10 | Incubation: 25Β°C, Assay: 50Β°C | 2 g/L Azocasein | Azo-peptides , Peptides | β | β | Non-incubated control (in %), assay in aqueous phase | Uncertainty about whether assay was really in aqueous conditions or in the presence of organic solvent |
| Stability - Incubation | Activity after incubation (1 hour at 25Β°C), measured by absorbance spectrophotometry (colorimetric assay, change in Azo-peptides absorbance measurement, 440 nm) in aqueous phase | n-Hexane | 5% | 100 | 103 | % | Incubation: 50 mM glycine-NaOH buffer, Assay: 50 mM glycine-NaOH buffer, 2 mM CaCl2 | Incubation: 8.5, Assay: 10 | Incubation: 25Β°C, Assay: 50Β°C | 2 g/L Azocasein | Azo-peptides , Peptides | β | β | Non-incubated control (in %), assay in aqueous phase | Uncertainty about whether assay was really in aqueous conditions or in the presence of organic solvent |
| Stability - Incubation | Activity after incubation (1 hour at 25Β°C), measured by absorbance spectrophotometry (colorimetric assay, change in Azo-peptides absorbance measurement, 440 nm) in aqueous phase | Ethyl Acetate | 5% | 100 | 66 | % | Incubation: 50 mM glycine-NaOH buffer, Assay: 50 mM glycine-NaOH buffer, 2 mM CaCl2 | Incubation: 8.5, Assay: 10 | Incubation: 25Β°C, Assay: 50Β°C | 2 g/L Azocasein | Azo-peptides , Peptides | β | β | Non-incubated control (in %), assay in aqueous phase | Uncertainty about whether assay was really in aqueous conditions or in the presence of organic solvent |
Visualization : Stability β Incubation
One bar per measurement. Colour = solvent, shade = solvent volume.