Application of Azotometry. XIX. Determination of Proline in Proteins
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Utilizing the reaction of its secondary amino group, proline in proteins was determined in the presence of other amino acids. The material proteins were first hydrolyzed and then allowed to react with nitrous acid to convert the proline therein into N-nitrosoproline, when all the other amino acids were changed into the corresponding hydroxy acids. N-Nitrosoproline was then reduced to N-aminoproline with zinc dust and hydrochloric acid, and finally the N-amino compound was determined by azotometry by oxidation with potassium ferricyanide. Incidentally, the secondary amino group in the ring of tryptophan, histidine, and prolidine, and the guanidine group of arginine do not interfere with the present method.
- 公益社団法人日本薬学会の論文
- 1960-07-25
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関連論文
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- Application of Azotometry. XIX. Determination of Proline in Proteins
- Application of Azotometry. XVIII. Determination of Pyridine and its Derivatives
- Application of Azotometry. XVII. Determination of Glycosamine.
- Application of Azotometry. XVI. Quantitative Determination of Secondary Amines.