## Abstract The modified method for biosynthesis of L‐methionine‐^35^S and L‐cystine‐^35^S from baker's yeast (__Saccharomyces cerevisiae__) is described. The yeast was cultivated in a sulphur‐deplated medium containing carrier‐free Na~2~^35^SO~4~, under air bubbling during 24 hours. Yeast proteins
Preparation of L-cysteine-35S hydrochloride by reduction of L-cystine-35s
✍ Scribed by M. B. Skakun-Todorovi; S. R. Albahari
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- French
- Weight
- 201 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
The method for the synthesis of L-cysteine hydrochloride labelled with 35S is described. L -C ~s t i n e -~~S obtained from baker's yeast was reduced with tin in hydrochloric acid and radiochemically pure L-cysteine-35S hydrochloride was isolated by ion-exchange chromatography on a column.
The obtained L -~y s t e i n e -~~S hydrochloride was stable in aqueous solution, pH 2, for six months and had specific activity of 20-125 mCi/mmol and radiochemical purity better than 9 5 % .
📜 SIMILAR VOLUMES
L-[ 35S]Homocysteine thiolactone has been synthesized by demethylation of L-{ 35S]Methionine with sodium in liquid ammonia and subsequent lactonisation in acid solution. The radiochemical yield of the carrier added synthesis was in the range of 45 to 50 % with a radiochemical purity higher than 96 %
## Abstract The synthesis of L‐[^35^S]cysteine sulfinic acid (L‐2‐amino‐3‐[^35^S] sulfino‐propanoic acid) in 65% yield from S‐[^35^S]cystine is described. The procedure was designed for use with milligram quantities of starting material and requires no purification of intermediates. L‐[^35^S]Cystin
## Abstract High specific activity L‐^35^ S‐cysteine and L‐^35^ S‐methionine were synthesised by using a wild type diploid strain of baker's __yeast—Saccharomyces cerevisiae__. Yeast cells were grown in a sulphur depleted synthetic medium in which Na~2~ ^35^ SO~4~ (50 mCi/ml) was supplemented as th
## Abstract The title compound was synthesized at the gram level in 66% yield by addition of [^34^S]thioacetic acid to α‐acetamidoacrylic acid, followed by acid hydrolysis.
The order of the exchange reaction between potassium ethyl xanthate and elemental sulphur was determined. A mixture of ethanol and toluene was used as the solvent for the routine preparation of 35S-labelled ethyl, n-butyl, n-hexyl and n-octyl xanthates at a temperature of 200 C. The dependence of th