𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Use of L- [14C]glycerotetrulose for the enzymatic preparation of 14C- labelled intermediates of the pentose phosphate pathway

✍ Scribed by M. G. Clark; P. F. Blackmore; J. F. Williams


Publisher
John Wiley and Sons
Year
1972
Tongue
French
Weight
529 KB
Volume
8
Category
Article
ISSN
0022-2135

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


An enzymatic method for the synthesis of
✍ Toshiharu Yagi; Masashi Takasugi; Shinpei Yamamoto; Mitsuhiro Nozaki πŸ“‚ Article πŸ“… 1986 πŸ› Elsevier Science 🌐 English βš– 461 KB

A new enzymatic method for the synthesis of ['4C]pyridoxal 5'-phosphate is presented. [ r4C]Pyridoxal 5'-phosphate was synthesized from [ "C]pyridoxine through the successive actions of pyridoxal kinase and pyridoxamine 5'-phosphate oxidase in a reaction mixture containing ATP, ['4C]pyridoxine. and

An enzymatic method for the preparation
✍ P. F. Blackmore; M. G. Clark; J. F. Williams πŸ“‚ Article πŸ“… 1972 πŸ› John Wiley and Sons 🌐 French βš– 211 KB

## B i o l o g i c a l l y l a b e l l e d [l-14C) g l y c e r o l ( L -[ l -' " C ) g l y c e r o l ) 048 prepared by a two s t e p p r o c e s s . S t e p one i n v o 1 v e d t h e p r e p a r a t i o n of [I -C ] g 2 y ce r o 1 3 -p ho sp ha t e from l4C02 and D-ribuloee 1,5 -diphoephate u s i

The enzymatic preparation of L(+)-3-hydr
✍ George Dombrowski Jr.; Kuen-Lan Chao; Kenneth R. Swiatek πŸ“‚ Article πŸ“… 1980 πŸ› John Wiley and Sons 🌐 French βš– 162 KB

## Abstract L(+)‐3‐hydroxy(3‐^14^C)butyrate was prepared by treating the D, L‐racemic mixture with the stereospecific D‐(βˆ’)‐3‐hydroxybutyrate dehydrogenase enzyme. The unfavorable equilibrium position of the dehydrogenase was overcome by the addition of acetaldehyde and alcohol dehydrogenase. The D

A new synthesis for the preparation of 1
✍ D. BΓ‘nfi; S. MlinkΓ³; T. PalΓ‘gyi πŸ“‚ Article πŸ“… 1971 πŸ› John Wiley and Sons 🌐 French βš– 135 KB

## Abstract A convenient gas catalytic process has been developed for the synthesis of radioactive alkali cyanides on micro or semimicro scale. The carbon content of barium carbonate used as starting material can be quantitatively transformed into potassium cyanide in a simple process.