Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiamine Hydrochloride | HCID 6202 | — |
| Reactant | Calcium Carbonate | HCID 10112 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal | HCID 107526 | — |
| Reactant | Biotin | HCID 171548 | — |
| Reactant | Monobasic potassium phosphate | HCID 516951 | — |
| Reactant | Ammonium Sulfate | HCID 6097028 | — |
| Catalyst | Manganese Sulfate | HCID 24580 | — |
| Product | L-Glutamic Acid | HCID 33032 | — |
Reaction Steps
The thus obtained odhA gene-disrupted strain is isolated in a medium containing sugar. In the process of isolation, a spontaneous mutation is introduced into the chromosomal yggB gene at a high frequency. Then, the ability of the isolated strain to produce L-glutamic acid is evaluated by culturing the strain in a medium containing excess biotin. For example, a candidate strain is inoculated in 20 ml of culture medium (30 g/l glucose, 15 g/l ammonium sulfate, 1 g/l KH2PO4, 0.4 g/l MgSO4.7H2O, 0.01 g/l FeSO4.7H2O, 0.01 g/l MnSO4.4-5H2O, 200 μg/l vitamin B1, 300 μg/l biotin, 0.48 g/l soybean hydrolysates (total nitrogen), adjusted to pH 8.0 with KOH: autoclaved at 115° C. for 10 minutes), followed by addition of 1 g of heat-sterilized calcium carbonate, and the strain is cultured with shaking. After the sugar is completely consumed, the amount of accumulated L-glutamic acid is measured. Strains which produce L-glutamic acid, for example, those which produce not less than 50% (yield per sugar) of L-glutamic acid are selected, and the nucleotide sequence of the yggB gene of the selected strains are determined to obtain a strain in which a mutation is introduced into the yggB gene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07927844B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-8478266df02142f09e688f1d70b86d21 |
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| Source note | uspto-grants-2011_04 |
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