Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | Diammonium maleate | HCID 10997209 | — |
| Product | Ammonium Aspartate | HCID 86590683 | 99% |
Reaction Steps
According to the same procedure of Example 1, cells of Alcaligenes faecalis ATCC 8750 was added to 2 L of an ammonium maleate substrate solution containing 400 g of maleic acid, and the substrate solution was gently stirred at 30° C. for 24 hours. After the reaction, ammonium L-aspartate was formed with a molar yield of 99.0% based on maleic acid. To the reaction solution from which the cells had been removed by centrifugation, was added 1.23 kg of 33.3 wt % maleic acid aqueous solution at 30° C. After the addition, a temperature of the solution was 38.5° C., and pH value of thereof was 3.7. L-aspartic acid crystals were separated by filtration, so as to recover 2.37 L of mother liquors. The crude crystals were 481 g (excluding water) (93.6 wt % aspartic acid, 6.0 wt % maleic acid, 250 μm average crystal size). The crystals were washed with about 300 ml of water and dried so as to obtain 448 g (excluding water) of L-aspartic acid crystals (99.1 wt % aspartic acid weight, 0.50 wt % maleic acid, 200 μm average crystal size).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05541090 |
|---|
| Source dataset | uspto-grants-1996_07 |
|---|
| ORD ID | ord-0b3154c644174968a509e8847b67b9f7 |
|---|
| Source note | uspto-grants-1996_07 |
|---|