EC Number   |
Substrates |
Organism |
Products |
Reversibility |
|---|
    3.1.1.3 | triolein + 3 H2O |
- |
Saccharolobus solfataricus DSM 1616 |
glycerol + 3 oleate |
enzyme can hydrolyze all positions of the ester bonds in triolein |
? |
| 3.1.1.3 | triolein + H2O |
the enzyme shows a preference for the hydrolysis of the sn-3 ester bond of triolein compared to the sn-1 position |
Yarrowia lipolytica |
1,2-diolein + oleate |
higher amount of 1,2-diolein |
? |
| 3.1.1.3 | triolein + H2O |
cis C18:1 |
Streptomyces rimosus |
diolein + oleate |
main product is oleic acid, further products are 1,3-dioleylglycerol, 1,2-dioleylglycerol, 2,3-dioleylglycerol, and minor product is 1-monooleylglycerol |
? |
| 3.1.1.3 | 4 triolein + H2O |
about 115% activity compared to olive oil |
Amycolatopsis mediterranei |
6 oleic acid + 1,3-diolein + 1,2-diolein + 1-monoolein + 2-monoolein |
oleic acid is the major product |
? |
| 3.1.1.3 | 3 triolein + 3 H2O |
- |
Pseudomonas aeruginosa |
1,3-diolein + 1,2-diolein + 2,3-diolein + 3 oleate |
shows random positional specificity for triolein hydrolysis |
? |
| 3.1.1.3 | triacylglycerol + H2O |
- |
Mus musculus |
diacylglycerol + a carboxylate |
the enzyme specifically generates sn-1,3 and, in the presence of its co-activator CGI-58, sn-1,3 and sn-2,3 diacylglycerol |
? |
| 3.1.1.3 | triacylglycerol + H2O |
- |
Mus musculus C57BL/6 |
diacylglycerol + a carboxylate |
the enzyme specifically generates sn-1,3 and, in the presence of its co-activator CGI-58, sn-1,3 and sn-2,3 diacylglycerol |
? |
| 3.1.1.3 | glycerol + phenylpropionic acid ethyl ester + H2O |
the immobilized lipase exhibits the highest activity towards phenylpropionic acid ethyl ester. 90% of glycerol is the optimum amount to perform the transesterification reaction |
Rhizomucor miehei |
glyceryl phenylpropionic ester + ethanol |
the maximum product yield is achieved after 4 h (78%) |
? |
| 3.1.1.3 | isophthalate + n-butanol |
- |
Geobacillus thermocatenulatus |
isophthalic acid monobutyl ester + H2O |
the yield is 14% for the monoester, no formation of diester in 1-butyl-3-methyl imidazolium tetrafluoroborate buffer |
? |
| 3.1.1.3 | isophthalate + 2-butanol |
- |
Geobacillus thermocatenulatus |
isophthalic acid mono(1-methylpropyl)ester + isophthalic acid di(1-methylpropyl)ester + H2O |
the yield is 34% monoester and 46% diester in 1-butyl-3-methyl imidazolium tetrafluoroborate buffer |
? |
