Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (R)-mevalonate | HCID 5288798 | — |
| Reactant | aldehydo-L-arabinose | HCID 5460291 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (+-)-Mevalonolactone | HCID 10428 | — |
Reaction Steps
GC-MS analysis for in vivo mevalonate production. As for screening the single mutation library, a single colony harboring pBADMevT (wild type tHMGR or its mutant variants) was inoculated into LB medium containing Cm50 and grown overnight at 37° C. An aliquot (50 μl) of this seed culture was inoculated into fresh LB medium (5 ml) containing Cm50 and 13.3 mM (+)-L-arabinose, and grown for 24 hours at 37° C. An aliquot of culture (560 μl) was mixed with 140 μl of 0.5 M HC1 to dehydrate the mevalonate to form mevalonolactone, and 700 μl of ethyl acetate was then added to the sample. The mixture was vortexed for 5 minutes, and the ethyl acetate was analyzed by GC-MS using a GC oven temperature program of 90° C. for 1 min, then ramping 30° C./min to 250° C. for CyclosilB capillary column analysis. Mevalonolactone was identified from its mass spectra and retention time by comparison to an authentic standard.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08158383B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-1d1267ad8b0e44aca62028255b3c1832 |
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| Source note | uspto-grants-2012_04 |
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