Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Hydroxyacetonitrile | HCID 7857 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Product | Glycolic Acid | HCID 757 | — |
| Product | Hydroxyacetonitrile | HCID 7857 | — |
| Product | 2-Hydroxyacetamide | HCID 69021 | — |
Reaction Steps
The reaction described in Example 1 is repeated except that the mutant strains A. facilis 72-PF-15 or 72-PF-17 are used instead of A. facilis 72W. A suspension of 0.50 g (wet cell paste) A. facilis 72-PF-15 or 72-PF-17 in 8.44 mL of 0 020 M potassium phosphate buffer (pH 6.0) is placed into a 15-mL polypropylene centrifuge tube. To the tube is then added 1.06 mL of a 55 wt % solution of glycolonitrile in water (1.0 M final concentration of glycolonitrile in the suspension), and the resulting suspension mixed on a rotating platform at 25° C. Samples of the suspension for analysis (0.200 mL) are first adjusted to pH 2.5 with 6 N HCl to stop the reaction, centrifuged, and the supernatant filtered using a 0.2 micron filter. After sufficient time, complete conversion of glycolonitrile to glycolic acid is obtained with no production of byproduct glycolamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06383786B1 |
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| Source dataset | uspto-grants-2002_05 |
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| ORD ID | ord-d34f6d0544494e0491cc6e75e55af3b7 |
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| Source note | uspto-grants-2002_05 |
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