## An enzymatic synthesis of ["Cl acetyl coenzyme A from [l-l'c] acetate is described. "COZ was reacted with methylmagnesium bromide in diethyl ether at 0 'C. The excess of Grignard reagent was hydrolyzed by adding methanol. After evaporation of the solvents, the residue was redissolved in hydroch
Enzymatic synthesis of carbon-11 N-acetyl-D-glucosamine
✍ Scribed by Geert Mannens; Guido Slegers; Patrick Goethals; Albert Claeys
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- French
- Weight
- 371 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
An enzymatic synthesis of [^11^C]N‐acetyl‐D‐glucosamine is described. ^11^CO~2~ is reacted with methylmagnesium bromide to form [1‐^11^C]acetate. The latter is converted to [^11^C]acetylcoenzyme A by passage over an enzyme reactor containing immobilized acetylcoenzyme A synthetase (Acetate: CoA ligase (AMP forming); EC 6.2.1.1).
[^11^C]Acetylcoenzyme A is purified on‐line and concentrated on an anionexchange column. Elution is achieved with 1.5 M glucosamine HCl pH 8.0 and the [^11^C]acetylcoenzyme A fraction is collected in an ultrafiltration cell containing the enzyme glucosamine N‐acetyltransferase (acetylcoenzyme A: 2‐amino‐2‐deoxy‐D‐glucose N‐acetyltransferase EC 2.3.1.3).
📜 SIMILAR VOLUMES
## Abstract A rapid chemical synthesis of 2‐[__carbonyl‐^11^C__]acetamido‐2‐deoxy‐D‐glucopyranose (__N__‐[__carbonyl__‐^11^C]acetyl‐D‐glucosamine) starting from [^11^C]carbon dioxide is described. The total time required for the synthesis, the radiochemical yield, and purity of the titled sugar are