Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | Diammonium maleate | HCID 10997209 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ammonium Aspartate | HCID 86590683 | 98.8% |
Reaction Steps
According to the same procedure of Example 1, 600 g maleic acid was dissolved in deionized water, and 705 g of 25 wt % aqueous ammonia solution (molar ratio to maleic acid was about 2.0) was added thereon. The cells of Alcaligenes faecalis ATCC 8750 were added to 2 L of an ammonium maleate substrate solution (pH 8.4) containing 600 g maleic acid, and the substrate solution were gently stirred at 30° C. for 72 hours. After the reaction, ammonium L-aspartate was formed with a molar yield of 98.8% based on maleic acid. To the reaction solution from which the cells had been removed by centrifugation, was added 610 g maleic acid at 30° C. After the addition, a temperature of the solution was 37.0° C., and pH value thereof was 3.8. L-aspartic acid crystals were separated by filtration, so as to recover 1.5 L of mother liquors. The crude crystals was 769 g (excluding water) (88.0 wt % aspartic acid, 11.4 wt % maleic acid, 250 μm average crystal size). The crystals were washed with about 600 ml of water and dried so as to obtain 675 g of L-aspartic acid crystals (98.8 wt % aspartic acid, 0.77 wt % maleic acid, 100 μm average crystal size).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05541090 |
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| Source dataset | uspto-grants-1996_07 |
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| ORD ID | ord-3ae3bf38ed6642a7987f13ef3f67673a |
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| Source note | uspto-grants-1996_07 |
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