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 410 g of maleic acid at 30° C., to precipitate crystals of L-aspartic acid. After the addition, a temperature of the solution was 34.5° C., and pH value thereof was 3.8. L-aspartic acid crystals were separated by filtration, so as to recover 1.6 L of mother liquors. The crude crystals was 502 g (Excluding water) (89.1 wt % aspartic acid, 10.2 wt % malic acid, 250 μm average crystal size). The crystals were washed with 300 ml of water and dried so as to obtain 447 g of L-aspartic acid crystals (99.0 wt % aspartic acid, 0.62 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-028b46b42fe94d90913a93411b486536 |
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| Source note | uspto-grants-1996_07 |
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