Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | L-Glutamine | HCID 5961 | — |
| Reactant | Ethylenediaminetetraacetic Acid | HCID 6049 | — |
| Reactant | (-)-Asparagine | HCID 6267 | — |
| Reactant | Borate | HCID 26574 | — |
| Reactant | Alanine methyl ester hydrochloride | HCID 2733257 | — |
| Product | L-Glutamine | HCID 5961 | — |
| Product | L-Alanine methyl ester | HCID 82335 | — |
| Product | L-Alanyl-L-Glutamine | HCID 123935 | — |
| Product | L-Alaninamide | HCID 444939 | — |
Reaction Steps
This purified enzyme was then added to borate buffer (pH 9.0) containing EDTA, L-alanine methyl ester hydrochloride and L-glutamine (or L-asparagine), mixed to the total volume of 1 mL (for the final concentrations, the amount of enzyme added was 2 units as alanine amide decomposition activity, EDTA was at 10 mM, L-alanine methyl ester hydrochloride was at 100 mM and L-glutamine (or L-asparagine) was at 200 mM borate buffer at 100 mM), and allowed to react for 4 hours at 30° C. (Note that the number of units of enzyme does not indicate the production activity with respect to producing L-alanyl-L-glutamine from L-alanine methyl ester and L-glutamine, but rather simply indicates L-alanine amide decomposition activity.) The amount of L-alanyl-L-glutamine produced at this time was 50.2 mM, while the amount of L-alanyl-L-asparagine produced was 49.8 mM.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07618796B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-0f83f64a25ef4536b61a8d8d1500cdaf |
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| Source note | uspto-grants-2009_11 |
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