反应 #1779715

ord-1d1267ad8b0e44aca62028255b3c1832

反应方程式

C[C@@](O)(CCO)CC(=O)[O-]
mevalonate
O=C[C@H](O)[C@@H](O)[C@@H](O)CO
(+)-L-arabinose
C[C@@](O)(CCO)CC(=O)[O-]
mevalonate
CC1(O)CCOC(=O)C1
mevalonolactone

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONcontaining Cm50
  2. 2
    workup.WAITgrown for 24 hours at 37° C
  3. 3
    workup.ADDITIONAn aliquot of culture (560 μl) was mixed with 140 μl of 0.5 M

实验过程

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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08158383B2uspto-grants-2012_04