scholarly journals Subunit structures of sonicated .ALPHA. and .BETA.-ovomucin and their molecular weights estimated by sedimentation equilibrium.

1978 ◽  
Vol 42 (5) ◽  
pp. 957-961 ◽  
Author(s):  
Shigeru HAYAKAWA ◽  
Yasushi SATO
1999 ◽  
Vol 270 (2) ◽  
pp. 286-295 ◽  
Author(s):  
Robert Fairman ◽  
William Fenderson ◽  
Mark E. Hail ◽  
Youling Wu ◽  
Shyh-Yu Shaw

1970 ◽  
Vol 118 (3) ◽  
pp. 467-474 ◽  
Author(s):  
P. H. Lloyd ◽  
A. R. Peacocke

Solutions of crystalline β-lactamase I and β-lactamase II, prepared by Kuwabara (1970), were examined in the ultracentrifuge and their sedimentation coefficients, diffusion coefficients, molecular weights and heterogeneity determined. Each sample was shown to consist of a major component comprising at least 97% of the material and a minor component of much higher molecular weight. The molecular weights of the major components were 27800 for β-lactamase I and 35600 for β-lactamase II. Emphasis is placed on a straightforward practical way of analysing the sedimentation-equilibrium results on mixtures of two macromolecular components rather than on a strict theoretical solution. Appendices describe the theory of systems at both chemical and sedimentation equilibrium and the procedure for calculating the combined distribution of two components.


Biochemistry ◽  
1969 ◽  
Vol 8 (6) ◽  
pp. 2609-2615 ◽  
Author(s):  
Elton P. Katz ◽  
Camille J. Francois ◽  
Melvin J. Glimcher

1939 ◽  
Vol 12 (4) ◽  
pp. 789-793 ◽  
Author(s):  
W. Harold Smith ◽  
Henry J. Wing

Abstract Some investigators believe that rubber consists of associated molecules, and others accept Staudinger's view that long-chain molecules are formed by polymerization. Pummerer, Andriessen and Gündel have obtained a molecular weight as low as 600. Meyer and Mark believe that it is approximately 5,000, although they calculated on the basis of osmotic pressures values as high as 350,000. They, as well as Pummerer, consider that rubber is an associated colloid and that high molecular weights are caused by aggregates, sometimes called micelles. Staudinger, however, considers that the long-chain rubber molecule itself has a molecular weight of 200,000 or even 350,000, and that products with lower values, which may be formed in rubber, result from degradation. if the molecules are small it might be possible to distil them if their vapor pressure could be sufficiently increased, but none would distil without decomposition if the molecules are very large. Because the vapor pressure of rubber below its decomposition temperature is low, it appeared of interest to attempt to distil the material in a molecular still. Paraffin wax and sugar, both substances of relatively high molecular weight, have been successfully distilled in this type of apparatus. Subsequent to the work described in this paper, the molecular weight of sol rubber prepared at this Bureau was determined by Kraemer and Lansing of E. I. du Pont de Nemours & Co., Inc. They used the Svedberg method of sedimentation equilibrium in an ultracentrifuge with ethereal solutions of sol rubber. The temperature of the solutions during determinations was approximately 10° C, and an average value of 460,000 was obtained. There was evidenced of a mixture of molecular species.


1969 ◽  
Vol 114 (4) ◽  
pp. 819-825 ◽  
Author(s):  
David A. Swann

Physical and chemical methods were used to characterize hyaluronic acid before (fraction HAIIBI) and after (fraction HA-AA) treatment with ascorbic acid. Fraction HA-AA was recovered with an almost quantitative yield and was shown to be chemically identical with fraction HAIIBI by all the methods used. These two materials, however, differed markedly in their molecular sizes and degree of polydispersity. By using sedimentation, diffusion and sedimentation-equilibrium analyses, weight-average molecular weights of about 1·2×106 and 6·5×104 respectively were obtained for fractions HAIIBI and HA-AA. It is concluded from these results that hyaluronic acid has a molecular weight of about 65000 and that the polysaccharide chain of this molecule is not depolymerized by ascorbic acid. It is further proposed that hyaluronic acid molecules in the matrix of connective tissues are present either in an aggregated form or as subunits of heterogeneous macromolecules, and that it is the linkages responsible for the organization of these structures which are broken by ascorbic acid.


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