GH3 Ξ²-xylosidase (gene AmΞ²Xyl) from Alicyclobacillus mali FL18
Enzyme Description
Species
Extremophile
Yes
"thermo-acidophilic" organism
EC Number
Sequence
MYLDPAQSVDARVDALLADMTLEEKVAQLTSIWAFEILDDLRFSAEKAAAVLGQGIGQVTRIGGATNLDPPDVARLANQIQRYLRDHTRLGIPALIHEESCSGYMAKGATCFPQTIGIASTWDVDLAQRIGAIIRDQMRAVGARQALAPLLDVARDPRWGRVEETFGEDPYLVAQMGIAYVRGLQGEDLSQGVMATGKHFVGYGASEGGMNWAPAHIPERELREVYLFPFEAAVREAGLGAIMPGYHELDGVPCHDNPGLLRETLRGRWGFQGLVVSDYFAVNQLFEYHQVARDKAEAAALAVRAGVDVELPTRDVYGKPLIEAVARGLVSVAEIDELVRRVLTWKFRLGLFDHPFVDEGAAIAVFDNAEQRKVAREAAEKSLVLLKNDGLLPLAPRGTIAVIGPNAHTTRNLVGDYAYPCHIESLLEQSEDNVFQTPLPSGVKHVDEFIPMRTILEAIGHRVGSEAQVVYAKGCDVLEGEDADLDEAVALAAQSDVAVVVVGDRAGLTDACTTGESRDRATLSLIGRQEELVRRVLATGTKTVVVLVSGRPLAIPDIAERANAVLEAWLPGEEGAEAVAAVLFGDVNPSGKLPVTIPRSVGQVPIYYGHKPSGGRSHWKGAYVDESNLPLYPFGHGLSYTAFEYRDLTLSASELGVHGEIEVACVIENVGARAGEEVVQLYARDVAADVTRPVKVLCGFARVPLAPGEKARVRFRVSAHQFGFYNREMRYVVEPGEIEIMVGASSEDIRLRGMVRIHGAMTEIEHEKVYQSAVNVERM
Flora Salzano et al. (2022)
β Alicyclobacillus mali FL18 as a Novel Source of Glycosyl Hydrolases: Characterization of a New Thermophilic Ξ²-Xylosidase Tolerant to Monosaccharides
International Journal of Molecular Sciences
Β· doi:10.3390/ijms232214310 β
Β· Activity - Classical
▼
Database ID
UniProt: A0ABS0F573 β
Sequence Annotation
Explicit - Provided GenBank Accession Number
Protein Source
Recombinant, host bacterium Escherichia coli BL21 (DE3)
Experimental Data (18 measurements)
18 measurements
| 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 (p-nitrophenol absorbance measurement, 405 nm) in the presence of organic solvent | Ethanol | 40% | 100 | 562 | % | 50 mM sodium citrate, 1 mM DTT | 5.6 | 60Β°C | 4 mM p-nitrophenyl Ξ²-D-xylopyranoside | D-Xylose , p-Nitrophenol | β | β | Classical aqueous control (in %) |
| Activity - Classical | Activity measured by absorbance spectrophotometry (p-nitrophenol absorbance measurement, 405 nm) in the presence of organic solvent | Methanol | 60% | 100 | 221 | % | 50 mM sodium citrate, 1 mM DTT | 5.6 | 60Β°C | 4 mM p-nitrophenyl Ξ²-D-xylopyranoside | D-Xylose , p-Nitrophenol | β | β | Classical aqueous control (in %) |
| Activity - Classical | Activity measured by absorbance spectrophotometry (p-nitrophenol absorbance measurement, 405 nm) in the presence of organic solvent | Methanol | 50% | 100 | 490 | % | 50 mM sodium citrate, 1 mM DTT | 5.6 | 60Β°C | 4 mM p-nitrophenyl Ξ²-D-xylopyranoside | D-Xylose , p-Nitrophenol | β | β | Classical aqueous control (in %) |
| Activity - Classical | Activity measured by absorbance spectrophotometry (p-nitrophenol absorbance measurement, 405 nm) in the presence of organic solvent | Methanol | 40% | 100 | 778 | % | 50 mM sodium citrate, 1 mM DTT | 5.6 | 60Β°C | 4 mM p-nitrophenyl Ξ²-D-xylopyranoside | D-Xylose , p-Nitrophenol | β | β | Classical aqueous control (in %) |
| Activity - Classical | Activity measured by absorbance spectrophotometry (p-nitrophenol absorbance measurement, 405 nm) in the presence of organic solvent | Methanol | 30% | 100 | 1246 | % | 50 mM sodium citrate, 1 mM DTT | 5.6 | 60Β°C | 4 mM p-nitrophenyl Ξ²-D-xylopyranoside | D-Xylose , p-Nitrophenol | β | β | Classical aqueous control (in %) |
| Activity - Classical | Activity measured by absorbance spectrophotometry (p-nitrophenol absorbance measurement, 405 nm) in the presence of organic solvent | Methanol | 20% | 100 | 1065 | % | 50 mM sodium citrate, 1 mM DTT | 5.6 | 60Β°C | 4 mM p-nitrophenyl Ξ²-D-xylopyranoside | D-Xylose , p-Nitrophenol | β | β | Classical aqueous control (in %) |
| Activity - Classical | Activity measured by absorbance spectrophotometry (p-nitrophenol absorbance measurement, 405 nm) in the presence of organic solvent | Methanol | 10% | 100 | 482 | % | 50 mM sodium citrate, 1 mM DTT | 5.6 | 60Β°C | 4 mM p-nitrophenyl Ξ²-D-xylopyranoside | D-Xylose , p-Nitrophenol | β | β | Classical aqueous control (in %) |
| Activity - Classical | Activity measured by absorbance spectrophotometry (p-nitrophenol absorbance measurement, 405 nm) in the presence of organic solvent | Ethanol | 60% | 100 | 126 | % | 50 mM sodium citrate, 1 mM DTT | 5.6 | 60Β°C | 4 mM p-nitrophenyl Ξ²-D-xylopyranoside | D-Xylose , p-Nitrophenol | β | β | Classical aqueous control (in %) |
| Activity - Classical | Activity measured by absorbance spectrophotometry (p-nitrophenol absorbance measurement, 405 nm) in the presence of organic solvent | Ethanol | 50% | 100 | 357 | % | 50 mM sodium citrate, 1 mM DTT | 5.6 | 60Β°C | 4 mM p-nitrophenyl Ξ²-D-xylopyranoside | D-Xylose , p-Nitrophenol | β | β | Classical aqueous control (in %) |
| Activity - Classical | Activity measured by absorbance spectrophotometry (p-nitrophenol absorbance measurement, 405 nm) in the presence of organic solvent | Dimethyl Sulfoxide (DMSO) | 10% | 100 | 222 | % | 50 mM sodium citrate, 1 mM DTT | 5.6 | 60Β°C | 4 mM p-nitrophenyl Ξ²-D-xylopyranoside | D-Xylose , p-Nitrophenol | β | β | Classical aqueous control (in %) |
| Activity - Classical | Activity measured by absorbance spectrophotometry (p-nitrophenol absorbance measurement, 405 nm) in the presence of organic solvent | Ethanol | 30% | 100 | 600 | % | 50 mM sodium citrate, 1 mM DTT | 5.6 | 60Β°C | 4 mM p-nitrophenyl Ξ²-D-xylopyranoside | D-Xylose , p-Nitrophenol | β | β | Classical aqueous control (in %) |
| Activity - Classical | Activity measured by absorbance spectrophotometry (p-nitrophenol absorbance measurement, 405 nm) in the presence of organic solvent | Ethanol | 20% | 100 | 847 | % | 50 mM sodium citrate, 1 mM DTT | 5.6 | 60Β°C | 4 mM p-nitrophenyl Ξ²-D-xylopyranoside | D-Xylose , p-Nitrophenol | β | β | Classical aqueous control (in %) |
| Activity - Classical | Activity measured by absorbance spectrophotometry (p-nitrophenol absorbance measurement, 405 nm) in the presence of organic solvent | Ethanol | 10% | 100 | 612 | % | 50 mM sodium citrate, 1 mM DTT | 5.6 | 60Β°C | 4 mM p-nitrophenyl Ξ²-D-xylopyranoside | D-Xylose , p-Nitrophenol | β | β | Classical aqueous control (in %) |
| Activity - Classical | Activity measured by absorbance spectrophotometry (p-nitrophenol absorbance measurement, 405 nm) in the presence of organic solvent | Dimethyl Sulfoxide (DMSO) | 60% | 100 | 15 | % | 50 mM sodium citrate, 1 mM DTT | 5.6 | 60Β°C | 4 mM p-nitrophenyl Ξ²-D-xylopyranoside | D-Xylose , p-Nitrophenol | β | β | Classical aqueous control (in %) |
| Activity - Classical | Activity measured by absorbance spectrophotometry (p-nitrophenol absorbance measurement, 405 nm) in the presence of organic solvent | Dimethyl Sulfoxide (DMSO) | 50% | 100 | 110 | % | 50 mM sodium citrate, 1 mM DTT | 5.6 | 60Β°C | 4 mM p-nitrophenyl Ξ²-D-xylopyranoside | D-Xylose , p-Nitrophenol | β | β | Classical aqueous control (in %) |
| Activity - Classical | Activity measured by absorbance spectrophotometry (p-nitrophenol absorbance measurement, 405 nm) in the presence of organic solvent | Dimethyl Sulfoxide (DMSO) | 40% | 100 | 280 | % | 50 mM sodium citrate, 1 mM DTT | 5.6 | 60Β°C | 4 mM p-nitrophenyl Ξ²-D-xylopyranoside | D-Xylose , p-Nitrophenol | β | β | Classical aqueous control (in %) |
| Activity - Classical | Activity measured by absorbance spectrophotometry (p-nitrophenol absorbance measurement, 405 nm) in the presence of organic solvent | Dimethyl Sulfoxide (DMSO) | 30% | 100 | 461 | % | 50 mM sodium citrate, 1 mM DTT | 5.6 | 60Β°C | 4 mM p-nitrophenyl Ξ²-D-xylopyranoside | D-Xylose , p-Nitrophenol | β | β | Classical aqueous control (in %) |
| Activity - Classical | Activity measured by absorbance spectrophotometry (p-nitrophenol absorbance measurement, 405 nm) in the presence of organic solvent | Dimethyl Sulfoxide (DMSO) | 20% | 100 | 387 | % | 50 mM sodium citrate, 1 mM DTT | 5.6 | 60Β°C | 4 mM p-nitrophenyl Ξ²-D-xylopyranoside | D-Xylose , p-Nitrophenol | β | β | Classical aqueous control (in %) |
Visualization : Activity β Classical
One bar per measurement. Colour = solvent, shade = solvent volume.
Structure
π§¬
No structure available for this protein.