GH3 Ξ²-xylosidase (gene AmΞ²Xyl) from Alicyclobacillus mali FL18

Enzyme Description

Extremophile
Yes "thermo-acidophilic" organism
EC Number

Sequence

Length: 779 amino acids
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
18 measurements
Database ID
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

🧬

No structure available for this protein.