s p e c i f i c a c t i v i t y . I o d i n a t i o n of o c h r a t o x i n B by c a r r i e r -f r e e N a ' 251 u s i n g t h e c h l o r a m i n e method y i e l d e d ' 251-ochratoxin w i t h a h i g h s p e c i f i c a c t i v i t y . Another 1 2 5 1 -d e r i v a t i v e of o c h r a t o x i n
Preparation of 3H-labeled ochratoxins
β Scribed by Fred C. Chang; F. S. Chu
- Publisher
- John Wiley and Sons
- Year
- 1976
- Tongue
- French
- Weight
- 284 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0022-2135
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β¦ Synopsis
Abstract
^3^HβOchratoxins A, B, and C were obtained by tritiation of the toxins with tritiated water in acetic acid and platinum at 80Β° C overnight. The toxins were purified by solvent partition and thin layer chromatography with the recovery yield being 80% and the specific activity being 2.6 β 3.0 Ci/mmol. Hydrolysis of ^3^Hβochratoxin A with carboxypeptidase A revealed that 80.9% of the tritium in ochratoxin A molecule distributed on the phenylalanine residue with only 19.1% in ochratoxin a moiety.
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