Nucleoside Triphosphatase from the Hen’s Egg White and Vitelline Membrane

Enzyme ◽  
1978 ◽  
Vol 23 (6) ◽  
pp. 361-372 ◽  
Author(s):  
Ignace Debruyne ◽  
Jan Stockx
1931 ◽  
Vol 8 (3) ◽  
pp. 293-311
Author(s):  
MICHAEL SMITH ◽  
JAMES SHEPHERD

1. The freezing-points of white and yolk in the hen's egg gradually approach equality when the egg is kept for long periods; and the rate of the process of equilibration is rapid at first but becomes very slow as equality is more closely approached. 2. Between 0° and 25° C. the rate of equilibration has a temperature coefficient (Q 10) of from 1.5 to 2. At 25° C. equality of freezing-points is reached after about 70 days. 3. Equilibration is achieved partly by the passage of water across the vitelline membrane from white to yolk, but partly also by more complicated changes of osmotic concentration occurring more or less independently in white and yolk. 4. The recovery of hypertony by a yolk, previously diluted by immersion in water, when it is replaced in egg-white can, be explained on the basis of a temporary heterogeneity of the diluted yolk, and this explanation is supported by experimental evidence. 5. The rate of equilibration is much greater when the separated yolk is placed in mixed egg-white than in the intact egg, but since it is also greater in thin white than in thick white, and greater again in the white dialysate, the structure and viscosity of the white are probably important factors. 6. There is evidence of an appreciable resistance to water-movement both in egg-white and in egg-yolk. 7. In hypotonic or hypertonic aqueous solutions of glucose or glycerol, or in Ringer's solution, the rate of equilibration is greater than in egg-white and many times greater than in the intact egg. Water is taken up by the yolk both from hypotonic and hypertonic solutions of Ringer, within the range δ = 0.10° to 1.20° C., at a rate which increases the further the solution is removed from the point of isotony. 8. Evidence that the apparent disequilibrium in intact eggs is not a steady state maintained by a "Lebenswirkung," is afforded by: (i) the form of the equilibration curves, which strongly suggest the slow attainment of an equilibrium by diffusion, rather than a steady state terminated by death; (ii) the temperature relations of equilibration, which are consistent with the former assumption, but which do not agree at all with the effect of temperature on the viability of fertile eggs; (iii) the absence of any tendency of the yolk to maintain its hypertony when the white is concentrated by rapid evaporation; (iv) the alternative explanation for the recovery of hypertony by diluted yolks, which was the most crucial evidence for the existence of a steady state maintained by the expenditure of energy.


In a recent paper Howard (1932) claims to have shown, by three methods, that the "expected" osmotic equilibria exist between the yolk and white of a hen's egg. Johlin (1933) has criticized her technique of cryhydric measurement and re-asserted that the yolk and white of an egg hive different values for depression of freezing point. Although Needham (1931) and Meyerhof (1931) have considered the possibility of the outer layer of yolk having a lower osmotic pressure than the inner, Howard gives no experimental evidence indicating the existence of an osmotic gradient within the yolk. The methods she used being apparently incapable of showing the difference in osmotic pressure between the whole yolk and the whole white of an egg were presumably unable also to detect the osmotic gradient in the yolk. Grollman's (1931) criticisms of the Hill thermo-electric method for the measurement of vapour pressures when employed with viscous solutions were repeated by Howard, with no other evidence than that it gave results which disagreed with her own. In particular, Bateman's low vapour pressure depression found in mixtures of egg yolk and egg white are declared to be incompatible with high vapour pressure depressions for yolk. It is strange that in the differentiation of the properties of egg yolk and white so many authors should have considered the yolk as homogeneous. It is a well-known fact that the formation of an egg yolk occurs by daily deposits in the ovary of the hen. These extend over several days and that the integrity of the daily deposit is maintained more or less for many days is evidenced by observation of the spherical zones in the yolk of a frozen egg that has been sectioned. Also it is easy to withdraw from the centre of the yolk, using a fine pipette, white yolk which is different chemically from the surrounding yellow yolk. Since no membrane is known to separate these two kinds of yolk nor the daily deposit of yolk, the existence of this non-homogeneity within the yolk must be an indication of the slowness of equilibration inside a hen's egg. Hence, when one speaks of the difference in osmotic pressure of average egg white and average egg yolk, no conclusions can be drawn logically regarding the difference in osmotic pressure on opposite sides of the vitelline membrane. As the Hill thermoelectric method of measuring vapour pressure requires but small quantities of solution, it was of interest to use this micro method to study the difference in osmotic pressures of samples of yolk and white obtained on opposite sides of the membrane.


2004 ◽  
Vol 55 (8) ◽  
pp. 635-640 ◽  
Author(s):  
Kenji Yoshino ◽  
Kentaro Sakai ◽  
Yoko Mizuha ◽  
Ayako Shimizuike ◽  
Shigeru Yamamoto

1966 ◽  
Vol 124 (5) ◽  
pp. 921-952 ◽  
Author(s):  
Elliott F. Osserman ◽  
Dolores P. Lawlor

Markedly increased quantities of lysozyme have been found in the serum and urine (ranging to 2.6 g per day) of ten consecutive cases of monocytic and monomyelocytic leukemia. The enzyme has been isolated from the urine of several cases and physicochemically and immunochemically characterized. It is apparently identical to the lysozyme of normal tears, saliva, leukocytes, and serum, but structurally different from the lysozyme of hen's egg white. The activity of the human enzyme assayed with M. lysodeikticus organisms is 3 to 12 times greater than egg white lysozyme at equivalent concentrations. An agar plate method has been developed for quantitating lysozyme activity in small samples (approximately 25 µl) of serum, urine, or other biological fluids. The range and reproducibility of this method were found to be superior to previously available lysozyme assay procedures. Present evidence indicates that lysozyme is the principal, if not the sole, product of the proliferating monocytes in monocytic and monomyelocytic leukemia, and quantitation of serum and urine lysozyme should be a useful diagnostic procedure for these leukemias.


Sign in / Sign up

Export Citation Format

Share Document