252 PHYSIOLOGICAL CHEMISTRY 



Hammarsten's Method. Grind a piece of fresh beef pancreas 

 in the meat grinder, throw the pulp into 200-300 c.c. of hot 

 water, and boil for about ten minutes. Filter hot. The filtrate 

 will be pale yellow and fairly clear. Cool under the tap, and 

 acidify with sufficient acetic acid to make the concentration of 

 acid 0.5-1.0%. The nueleoprotein is precipitated and quickly 

 settles to the bottom. What other groups of proteins are pre- 

 cipitated in this way? Filter off the precipitate, suspend it in 

 200 c.c. distilled water, and add ammonia cautiously until the 

 precipitate has just dissolved. Reprecipitate the nueleoprotein 

 with acetic acid as above. If a pure product is desired, the proc- 

 ess of dissolving in alkali and reprecipitation with acid should be 

 repeated several times. The precipitate is filtered off, washed 

 with water containing a few drops of acetic acid, and then with 

 about 50 c.c. of hot alcohol in small portions (be careful of fire). 

 Spread the washed nueleoprotein upon a carefully cleaned spot 

 on a tile, and manipulate it to remove" the alcohol. 



ii. With small portions of the nueleoprotein prepared in (i) 

 perform the Millon, biuret, and xanthoproteic tests. All are 

 positive. 



iii. Note that nueleoprotein was not coagulated by boiling. 



iv. Fuse a small portion of nueleoprotein with fusion mixture, 

 dissolve the residue in dilute nitric acid and test for phosphorus 

 and iron. Both tests should be positive. 



v. Cover a small portion of nueleoprotein with pepsin solu- 

 tion, and incubate at least 24 hours. Note the undigested 

 residue of nuclein. 



vi. Hydrolysis of nueleoprotein. Mix up the remainder of the 

 nueleoprotein with 10 times its volume of 5% hydrochloric acid, 

 and boil in the hood for about half an hour. To identify the de- 

 composition products of nueleoprotein divide the liquid into four 

 parts and make the following tests: For sugar with Fehling's 

 test; for phosphate; for purine bases. To detect purine bases, 

 add an excess of ammonia, and then a small amount of silver 

 nitrate. Under these conditions purine bases are precipitated as 

 their silver salts. 



