EC Number | KM Value [mM] | KM Value Maximum [mM] | Substrate | Comment | Organism | Structure |
---|---|---|---|---|---|---|
1.11.2.1 | 480 | - |
propylbenzene | pH not specified in the publication, temperature not specified in the publication | Cyclocybe aegerita | |
1.11.2.1 | 694 | - |
ethylbenzene | pH not specified in the publication, temperature not specified in the publication | Cyclocybe aegerita |
EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
1.11.2.1 | Cyclocybe aegerita | - |
- |
- |
EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
1.11.2.1 | (1E)-prop-1-en-1-ylbenzene + H2O2 | - |
Cyclocybe aegerita | 2-methyl-3-phenyloxirane + H2O | 71% conversion, 7% enantiomeric excess | ? | |
1.11.2.1 | (1Z)-prop-1-en-1-ylbenzene + H2O2 | - |
Cyclocybe aegerita | 2-methyl-3-phenyloxirane + H2O | 96% conversion, 29% enantiomeric excess | ? | |
1.11.2.1 | 1,2,3,4-tetrahydronaphthalene + H2O2 | - |
Cyclocybe aegerita | (1R)-1,2,3,4-tetrahydronaphthalen-1-ol | 85% conversion, 99% enantiomeric excess | ? | |
1.11.2.1 | 1-methyl-1H-indene + H2O2 | - |
Cyclocybe aegerita | (1aS,6aR)-6-methyl-6,6a-dihydro-1aH-indeno[1,2-b]oxirene + H2O | 96% conversion, 2.3% enantiomeric excess | ? | |
1.11.2.1 | 2,3-dihydro-1H-indene + H2O2 | - |
Cyclocybe aegerita | (1R)-2,3-dihydro-1H-inden-1-ol + H2O | 77% conversion, 87% enantiomeric excess | ? | |
1.11.2.1 | ethylbenzene + H2O2 | - |
Cyclocybe aegerita | (R)-1-phenylethanol | 95% conversion, 99% enantiomeric excess | ? | |
1.11.2.1 | additional information | the transferred oxygen exclusively originates from the peroxide. Benzylic hydroxylation leads exclusively to the (R)-1-phenylalkanols. For (R)-1-phenylethanol, (R)-1-phenylpropanol and (R)-1-tetralol, the enantiomeric excess reaches >99%. For longer chain lengths, the enantiomeric excesses and total turnover numbers decrease while the number of by-products, e.g. 1-phenylketones, increase | Cyclocybe aegerita | ? | - |
? | |
1.11.2.1 | n-butylbenzene + H2O2 | - |
Cyclocybe aegerita | (R)-1-phenylbutanol | 52% conversion, 40% enantiomeric excess | ? | |
1.11.2.1 | n-pentylbenzene + H2O2 | - |
Cyclocybe aegerita | 1-phenylpentanol | 8.4% conversion, 99% enantiomeric excess | ? | |
1.11.2.1 | propylbenzene + H2O2 | - |
Cyclocybe aegerita | (R)-1-phenylpropanol | 64% conversion, 99% enantiomeric excess | ? |
EC Number | Turnover Number Minimum [1/s] | Turnover Number Maximum [1/s] | Substrate | Comment | Organism | Structure |
---|---|---|---|---|---|---|
1.11.2.1 | 194 | - |
propylbenzene | pH not specified in the publication, temperature not specified in the publication | Cyclocybe aegerita | |
1.11.2.1 | 410 | - |
ethylbenzene | pH not specified in the publication, temperature not specified in the publication | Cyclocybe aegerita |
EC Number | kcat/KM Value [1/mMs-1] | kcat/KM Value Maximum [1/mMs-1] | Substrate | Comment | Organism | Structure |
---|---|---|---|---|---|---|
1.11.2.1 | 405 | - |
propylbenzene | pH not specified in the publication, temperature not specified in the publication | Cyclocybe aegerita | |
1.11.2.1 | 590 | - |
ethylbenzene | pH not specified in the publication, temperature not specified in the publication | Cyclocybe aegerita |