Literature DB >> 19872018

STUDIES IN THE PHYSICAL CHEMISTRY OF THE PROTEINS : II. THE RELATION BETWEEN THE SOLUBILITY OF CASEIN AND ITS CAPACITY TO COMBINE WITH BASE. THE SOLUBILITY OF CASEIN IN SYSTEMS CONTAINING THE PROTEIN AND SODIUM HYDROXIDE.

E J Cohn1, J L Hendry.   

Abstract

1. The solubility in water of purified, uncombined casein has previously been reported to be 0.11 gm. in 1 liter at 25 degrees C. This solubility represents the sum of the concentrations of the casein molecule and of the soluble ions into which it dissociates. 2. The solubility of casein has now been studied in systems containing the protein and varying amounts of sodium hydroxide. It was found that casein forms a well defined soluble disodium compound, and that solubility was completely determined by (a) the solubility of the casein molecule, and (b) the concentration of the disodium casein compound. 3. In our experiments each mol of sodium hydroxide combined with approximately 2,100 gm. of casein. 4. The equivalent combining weight of casein for this base is just half the minimal molecular weight as calculated from the sulfur and phosphorus content, and one-sixth the minimal molecular weight calculated from the tryptophane content of casein. 5. From the study of systems containing the protein and very small amounts of sodium hydroxide it was possible to determine the solubility of the casein molecule, and also the degree to which it dissociated as a divalent acid and combined with base. 6. Solubility in such systems increased in direct proportion to the amount of sodium hydroxide they contained. 7. The concentration of the soluble casein compound varied inversely as the square of the hydrogen ion concentration, directly as the solubility of the casein molecule, Su, and as the constants Ka(1) and Ka(2) defining its acid dissociation. 8. The product of the solubility of the casein molecule and its acid dissociation constants yields the solubility product constant, Su.Ka(1).Ka(2) = 2.2 x 10(-12) gm. casein per liter at 25 degrees C. 9. The solubility of the casein molecule has been estimated from this constant, and also from the relation between the solubility of the casein and the sodium hydroxide concentration, to be approximately 0.09 gm. per liter at 25 degrees C. 10. The product of the acid dissociation constants, Ka(1) and Ka(2), must therefore be 24 x 10(-12)N. 11. It is believed that these constants completely characterize the solubility of casein in systems containing the protein and small amounts of sodium hydroxide.

Entities:  

Year:  1923        PMID: 19872018      PMCID: PMC2140591          DOI: 10.1085/jgp.5.5.521

Source DB:  PubMed          Journal:  J Gen Physiol        ISSN: 0022-1295            Impact factor:   4.086


  6 in total

1.  On Amino-acids.

Authors:  H D Dakin
Journal:  Biochem J       Date:  1918       Impact factor: 3.857

2.  A New Method for Preparing Esters of Amino Acids. Composition of Caseinogen.

Authors:  F W Foreman
Journal:  Biochem J       Date:  1919-12       Impact factor: 3.857

3.  Barger's Microscopical Method of determining Molecular Weights: Part II. Its Application to Caseinogen.

Authors:  K Yamakami
Journal:  Biochem J       Date:  1920-07       Impact factor: 3.857

4.  A contribution to the chemistry of proteids: Part I. A preliminary study of a hitherto undescribed product of tryptic digestion.

Authors:  F G Hopkins; S W Cole
Journal:  J Physiol       Date:  1901-12-23       Impact factor: 5.182

5.  Caseinogen and its salts.

Authors:  W A Osborne
Journal:  J Physiol       Date:  1901-12-23       Impact factor: 5.182

6.  THE PROTECTIVE INFLUENCE OF BLOOD SERUM ON THE EXPERIMENTAL CELLFIBRIN TISSUE OF LIMULUS.

Authors:  L Loeb
Journal:  Science       Date:  1920-01-02       Impact factor: 47.728

  6 in total

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