HuagongsheHuagongshe Chemistry Print Report · For research reference only
sodium (4R)-4-[(3R,5S,7R,8R,9R,10S,12S,13R,14R,17R)-3,7,12-trihydroxy-8,10,13-trimethyl-1,2,3,4,5,6,7,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]pentanoate → Palmitic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | sodium (4R)-4-[(3R,5S,7R,8R,9R,10S,12S,13R,14R,17R)-3,7,12-trihydroxy-8,10,13-trimethyl-1,2,3,4,5,6,7,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]pentanoate | HCID 44582063 | — |
| Solvent | Calcium Chloride | HCID 5284359 | — |
| Product | Palmitic Acid | HCID 985 | 47% |
| Product | Stearic Acid | HCID 5281 | — |
| Product | Oleic Acid | HCID 445639 | — |
Reaction Steps
To 0.5 mL of a cultured cell fraction of Pyrococcus horikoshii JCM 9974 were added 2 mg of each of these substrates, 40 μl of 100 mM sodium cholate and 100 μL of 20 mM calcium chloride. The resultant reaction solution was reacted at 75° C. overnight. From the reaction solution, a fraction containing the fatty acid produced was extracted with isooctane and then subjected to gas chromatography. As a result, a decomposition product including 47-48% of oleic acid, oleic acid, palmitic acid or linolenic acid resulted from the decomposition by phospholipase A2 and 47-48% of palmitic acid, stearic acid, oleic acid or stearic acid resulted from the decomposition by phospholipase A1 was obtained from each of the substrates.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06001626 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-c8c00cdd1b30490b9b3d5e825036be32 |
| Source note | uspto-grants-1999_12 |