Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Urea | HCID 1176 | — |
| Reactant | Sucrose | HCID 5988 | — |
| Reactant | Thiamine Hydrochloride | HCID 6202 | — |
| Reactant | Biotin | HCID 171548 | — |
| Reactant | Monobasic potassium phosphate | HCID 516951 | — |
| Catalyst | Iron | HCID 23925 | — |
| Product | L-Aspartic Acid | HCID 5960 | — |
Reaction Steps
An aqueous solution medium containing 13 g/dl of sucrose, 0.5 g/dl of urea, 0.1 g/dl of KH2PO4, 0.04 g/dl of MgSO4.7H2O, ppm each of Fe and Mn ions, 5 μg/l of biotin, 200 μg/l of thiamine hydrochloride and 0.3 ml/dl of soybean protein hydrochloric acid hydrolysate "AJI-EKI" (total nitrogen of 7%), adjusted to pH 7.2 was prepared and 20 ml of the medium was separately charged into a shake flask of 500 ml volume. After sterilization, Asp-producing bacteria, Brevibacterium flavum (FERM BP-2178) and His-producing bacteria, Brevibacterium flavum (ATCC 21406), which had been previously grown on bouillon slants, were inoculated in the same flask followed by spinner culture at 31° C. for 72 hours. During the incubation, an aqueous urea solution having a concentration of 40 g/dl was supplemented by small portions to keep the pH between 6.5 to 8.0. In the fermentation broth, 0.95 g/dl of L-aspartic acid and 0.85 g/dl of L-histidine were accumulated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05196326 |
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| Source dataset | uspto-grants-1993_03 |
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| ORD ID | ord-db47c05bf73746e3a8a9cb155122eda2 |
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| Source note | uspto-grants-1993_03 |
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