Choline oxidase from Arthrobacter globiformis

Enzyme Description

Extremophile
No
EC Number

Sequence

Length: 546 amino acids
MHIDNIENLSDREFDYIVVGGGSAGAAVAARLSEDPAVSVALVEAGPDDRGVPEVLQLDRWMELLESGYDWDYPIEPQENGNSFMRHARAKVMGGCSSHNSCIAFWAPREDLDEWEAKYGATGWNAEAAWPLYKRLETNEDAGPDAPHHGDSGPVHLMNVPPKDPTGVALLDACEQAGIPRAKFNTGTTVVNGANFFQINRRADGTRSSSSVSYIHPIVEQENFTLLTGLRARQLVFDADRRCTGVDIVDSAFGHTHRLTARNEVVLSTGAIDTPKLLMLSGIGPAAHLAEHGIEVLVDSPGVGEHLQDHPEGVVQFEAKQPMVAESTQWWEIGIFTPTEDGLDRPDLMMHYGSVPFDMNTLRHGYPTTENGFSLTPNVTHARSRGTVRLRSRDFRDKPMVDPRYFTDPEGHDMRVMVAGIRKAREIAAQPAMAEWTGRELSPGVEAQTDEELQDYIRKTHNTVYHPVGTVRMGAVEDEMSPLDPELRVKGVTGLRVADASVMPEHVTVNPNITVMMIGERCADLIRSARAGETTTADAELSAALA
Rachel S. Heath et al. (2018) β€” An Engineered Alcohol Oxidase for the Oxidation of Primary Alcohols
ChemBioChem  Β· doi:10.1002/cbic.201800556 β†—  Β· Activity + Stability - Conversion
12 measurements
Database ID
UniProt: Q7X2H8 β†—
Sequence Annotation
Explicit - Provided PDB Accession Number
Protein Source
Recombinant, host bacterium Escherichia coli BL21 (DE3)

Experimental Data (12 measurements)

12 measurements
Mutation Property Assay Solvent Solvent Volume Aqueous ReferenceWT Reference Measured Value Units Solution pH Temperature Substrate(s) Product(s) Cofactor(s) Shaking Comments
WT Activity + Stability - Conversion Conversion after incubation (24 hours at 30Β°C) in the presence of organic solvent, measured by gas chromatography Ethyl Acetate 50% 22 β€” 2 % 100 mm potassium phosphate buffer 8 30Β°C 1-Hexanol, Molecular oxygen Hβ‚‚Oβ‚‚ (Hydrogen Peroxide) , Hexanal FAD 200 rpm Classical aqueous control (in %)
WT Activity + Stability - Conversion Conversion after incubation (24 hours at 30Β°C) in the presence of organic solvent, measured by gas chromatography n-Heptane 50% 22 β€” 19 % 100 mm potassium phosphate buffer 8 30Β°C 1-Hexanol, Molecular oxygen Hβ‚‚Oβ‚‚ (Hydrogen Peroxide) , Hexanal FAD 200 rpm Classical aqueous control (in %)
WT Activity + Stability - Conversion Conversion after incubation (24 hours at 30Β°C) in the presence of organic solvent, measured by gas chromatography Cyclohexane 50% 22 β€” 4 % 100 mm potassium phosphate buffer 8 30Β°C 1-Hexanol, Molecular oxygen Hβ‚‚Oβ‚‚ (Hydrogen Peroxide) , Hexanal FAD 200 rpm Classical aqueous control (in %)
WT Activity + Stability - Conversion Conversion after incubation (24 hours at 30Β°C) in the presence of organic solvent, measured by gas chromatography tert-Butyl Methyl Ether (MTBE) 50% 22 β€” 2 % 100 mm potassium phosphate buffer 8 30Β°C 1-Hexanol, Molecular oxygen Hβ‚‚Oβ‚‚ (Hydrogen Peroxide) , Hexanal FAD 200 rpm Classical aqueous control (in %)
WT Activity + Stability - Conversion Conversion after incubation (24 hours at 30Β°C) in the presence of organic solvent, measured by gas chromatography Toluene 50% 22 β€” 0 % 100 mm potassium phosphate buffer 8 30Β°C 1-Hexanol, Molecular oxygen Hβ‚‚Oβ‚‚ (Hydrogen Peroxide) , Hexanal FAD 200 rpm Classical aqueous control (in %)
WT Activity + Stability - Conversion Conversion after incubation (24 hours at 30Β°C) in the presence of organic solvent, measured by gas chromatography Dichloromethane 50% 22 β€” 0 % 100 mm potassium phosphate buffer 8 30Β°C 1-Hexanol, Molecular oxygen Hβ‚‚Oβ‚‚ (Hydrogen Peroxide) , Hexanal FAD 200 rpm Classical aqueous control (in %)
F357R/M359R Activity + Stability - Conversion Conversion after incubation (24 hours at 30Β°C) in the presence of organic solvent, measured by gas chromatography Ethyl Acetate 50% 54 2 70 % 100 mm potassium phosphate buffer 8 30Β°C 1-Hexanol, Molecular oxygen Hβ‚‚Oβ‚‚ (Hydrogen Peroxide) , Hexanal FAD 200 rpm Classical aqueous control (in %)
F357R/M359R Activity + Stability - Conversion Conversion after incubation (24 hours at 30Β°C) in the presence of organic solvent, measured by gas chromatography n-Heptane 50% 54 19 87 % 100 mm potassium phosphate buffer 8 30Β°C 1-Hexanol, Molecular oxygen Hβ‚‚Oβ‚‚ (Hydrogen Peroxide) , Hexanal FAD 200 rpm Classical aqueous control (in %)
F357R/M359R Activity + Stability - Conversion Conversion after incubation (24 hours at 30Β°C) in the presence of organic solvent, measured by gas chromatography Cyclohexane 50% 54 4 83 % 100 mm potassium phosphate buffer 8 30Β°C 1-Hexanol, Molecular oxygen Hβ‚‚Oβ‚‚ (Hydrogen Peroxide) , Hexanal FAD 200 rpm Classical aqueous control (in %)
F357R/M359R Activity + Stability - Conversion Conversion after incubation (24 hours at 30Β°C) in the presence of organic solvent, measured by gas chromatography tert-Butyl Methyl Ether (MTBE) 50% 54 2 34 % 100 mm potassium phosphate buffer 8 30Β°C 1-Hexanol, Molecular oxygen Hβ‚‚Oβ‚‚ (Hydrogen Peroxide) , Hexanal FAD 200 rpm Classical aqueous control (in %)
F357R/M359R Activity + Stability - Conversion Conversion after incubation (24 hours at 30Β°C) in the presence of organic solvent, measured by gas chromatography Toluene 50% 54 0 32 % 100 mm potassium phosphate buffer 8 30Β°C 1-Hexanol, Molecular oxygen Hβ‚‚Oβ‚‚ (Hydrogen Peroxide) , Hexanal FAD 200 rpm Classical aqueous control (in %)
F357R/M359R Activity + Stability - Conversion Conversion after incubation (24 hours at 30Β°C) in the presence of organic solvent, measured by gas chromatography Dichloromethane 50% 54 0 14 % 100 mm potassium phosphate buffer 8 30Β°C 1-Hexanol, Molecular oxygen Hβ‚‚Oβ‚‚ (Hydrogen Peroxide) , Hexanal FAD 200 rpm Classical aqueous control (in %)

Mutations in this dataset (2)

WT F357R/M359R

Visualization : Activity + Stability β€” Conversion

One bar per measurement. Colour = solvent, shade = solvent volume. β€” β€” β€” Reference value. Hover for details.

Mutation Effect

Mutation impact on enzyme stability and function in the presence of organic solvent: comparison of wild-type and mutant values in identical conditions.

Structure

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