Passa al contenuto
Merck
  • TCA cycle involved enzymes SucA and Kgd, as well as MenD: efficient biocatalysts for asymmetric C-C bond formation.

TCA cycle involved enzymes SucA and Kgd, as well as MenD: efficient biocatalysts for asymmetric C-C bond formation.

Organic letters (2013-01-16)
Maryam Beigi, Simon Waltzer, Alexander Fries, Lothar Eggeling, Georg A Sprenger, Michael Müller
ABSTRACT

Asymmetric mixed carboligation reactions of α-ketoglutarate with different aldehydes were explored with the thiamine diphosphate dependent enzymes SucA from E. coli, Kgd from Mycobacterium tuberculosis, and MenD from E. coli. All three enzymes proved to be efficient biocatalysts to selectively deliver chiral δ-hydroxy-γ-keto acids with moderate to excellent stereoselectivity. The high regioselectivity is due to the preserved role of α-ketoglutarate as acyl donor for these enzyme-catalyzed reactions.

MATERIALI
N° Catalogo
Marchio
Descrizione del prodotto

Sigma-Aldrich
α-Ketoglutaric acid, BioReagent, suitable for cell culture, suitable for insect cell culture
Sigma-Aldrich
αAcido -chetoglutarico, ≥98% (enzymatic)
Sigma-Aldrich
α-Ketoglutaric acid disodium salt dihydrate, ≥98.0% (dried material, NT)
Sigma-Aldrich
α-Ketoglutaric acid, 99.0-101.0% (T)
Sigma-Aldrich
α-Ketoglutaric acid, ≥98.5% (NaOH, titration)
Sigma-Aldrich
α-Ketoglutaric acid sodium salt, ≥98% (titration)
Sigma-Aldrich
Pyruvate Oxidase from microorganisms, lyophilized powder, ≥1.5 U/mg
Supelco
α-Ketoglutaric acid disodium salt hydrate, ≥95%
Sigma-Aldrich
Pyruvate Oxidase from Aerococcus sp., lyophilized powder, ≥35 units/mg protein (biuret)
Sigma-Aldrich
α-Ketoglutarate Dehydrogenase from porcine heart, buffered aqueous glycerol solution, 0.1-1.0 units/mg protein (Lowry)
Sigma-Aldrich
α-Ketoglutaric acid sodium salt, BioUltra