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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1692533Generated: October 25, 2026

(R)-mevalonate → (+-)-Mevalonolactone

https://huagongshe.com/reaction/1692533

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-mevalonateHCID 5288798—
Reactantaldehydo-L-arabinoseHCID 5460291—
SolventEthyl AcetateHCID 8857—
Product(+-)-MevalonolactoneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158383B2
Source datasetuspto-grants-2012_04
ORD IDord-1d1267ad8b0e44aca62028255b3c1832
Source noteuspto-grants-2012_04