EC Number   |
Substrates |
Organism |
Products |
Reversibility |
|---|
   3.1.1.42 | 1-phenylethyl alcohol + 5-chlorogenic acid |
- |
Aspergillus japonicus |
(S)-1-phenylethyl caffeate + quinate |
transesterification reaction, about 50% molar conversion yield |
? |
| 3.1.1.42 | 2-phenylethyl alcohol + 5-chlorogenic acid |
- |
Aspergillus japonicus |
2-phenylethyl caffeate + quinate |
transesterification reaction, about 50% molar conversion yield |
? |
| 3.1.1.42 | 2-phenylethyl bromide + 5-chlorogenic acid |
- |
Aspergillus japonicus |
2-phenylethyl caffeate + 5-bromo-quinate |
substitution reaction, about 2.3% molar conversion yield, no substrate: phenylethyl chloride, phenylethyl iodide |
? |
| 3.1.1.42 | 3,5-di-O-caffeylquinic acid + H2O |
- |
Aspergillus niger |
? |
- |
? |
| 3.1.1.42 | 3-(3,4-dihydroxyphenyl)-propionic acid + 1-phenylethyl alcohol |
- |
Aspergillus japonicus |
? |
- |
? |
| 3.1.1.42 | 3-caffeoylquinic acid + H2O |
- |
bacterium |
caffeate + quinate |
- |
? |
| 3.1.1.42 | 4-caffeoylquinic acid + H2O |
- |
bacterium |
caffeate + quinate |
- |
? |
| 3.1.1.42 | 5-caffeoylquinic acid + H2O |
- |
Aspergillus japonicus |
methyl caffeate + quinate |
different structures of substrates for synthesis of methyl caffeate with chlorogenate hydrolase, overview |
? |
| 3.1.1.42 | alpha-L-galactopyranosyl-(1,2)-beta-D-xylopyranosyl-(1,2)-5-O-trans-feruloyl-L-arabinofuranose + H2O |
27% of the activity with chlorogenate |
Ustilago maydis |
? |
- |
? |
| 3.1.1.42 | beta-D-xylopyranosyl-(1,2)-5-O-trans-feruloyl-L-arabinofuranose + H2O |
54% of the activity with chlorogenate |
Ustilago maydis |
? |
- |
? |
