The binding of Zinc by S-Carboxymethyl Kerateine 2 from wool

1957 ◽  
Vol 10 (3) ◽  
pp. 344 ◽  
Author(s):  
JM Gillespie ◽  
PH Springell

The binding of zinc from zinc acetate solution by the S-carboxymethyl derivative of kerateine 2 (SCMK2), a soluble protein extracted from reduced wool, has been studied by the method of equilibrium dialysis over the pH range 5.5 to 8.0 using radioactive 65Zn to determine the zinc concentration. The binding increases as the pH increases from 5.5 to 7.5. The extent of binding is also a function of free zinc concentration, but it is not affected by changes in ionic strength between 0.15 and 1.0. The difference in solubility between the zinc complexes of the two protein components of SCMK2 is probably not due to the differences in the amount of zinc bound. The binding of zinc is reversible over the concentration range studied at both pH 6.0 and 7.5, and its removal is accelerated by treatment with chelating agents. Over the pH range 6.0 to 7.5 more zinc is bound by this protein than can be accounted for by histidine binding alone, assuming a 1 : 1 zinc-histidine ratio.

1976 ◽  
Vol 153 (3) ◽  
pp. 713-718 ◽  
Author(s):  
M N Jones ◽  
A Wilkinson

1. The binding of sodium n-dodecyl sulphate to β-lactoglobulin was studied in the pH range 3.5-7.0 by equilibrium dialysis, ultracentrifugation and microcalorimetry. 2. At low binding concentrations (less than 30 bound surfactants anions per protein molecule) the complexes formed aggregates in solution. 3. At higher binding concentrations aggregation does not occur at low ionic strength (0.01 mol/litre), but continues at high ionic strength (0.1 mol/litre). 4. At 25 degrees C the enthalpy of interaction of sodium n-dodecyl sulphate with β-lactoglobulin can be interpreted as the sum of the enthalpies of formation of a complex with 2 bound surfactant anions, with an enthalpy change of -9.5 kJ-mol-1 of bound surfactant, and complexes containing at least 22 bound surfactant anions, with limiting enthalpies per bound surfactant anion of -12.4 kJ-mol-1 at pH 3.5 and -3.25 kJ-mol-1 at pH 5.5. 5. The binding of surfactant and the enthalpy of interaction at pH 3.5 ARE NOT SIGNIFICANTLY AFFECTED BY THE ADDITION Of 8 M-urea. 6. The data indicate that at low binding concentrations the interaction is of an ionic nature, and is accompanied by a conformational change in the protein.


1971 ◽  
Vol 49 (4) ◽  
pp. 417-425 ◽  
Author(s):  
E. A. MacGregor ◽  
J. M. Bowness

Equilibrium dialysis was used to study the distribution of calcium or phosphate ions at equilibrium in dialysis cells containing proteoglycan or chondroitin sulfate in one compartment. A higher concentration of calcium or lower concentration of phosphate was found in the cell compartment containing the polymer than in the compartment separated from it by a semipermeable membrane. The difference in calcium concentration across the boundary represents bound calcium. The formation constant (K) for the complex of bound calcium with chondroitin sulfate was investigated and found to be affected by two main factors: ionic strength and calcium/glucuronate ratio. K decreased rapidly with increasing ionic strength up to 0.15. At low ionic strength and high Ca2+/glucuronate ratios, evidence has been obtained that more calcium is bound by the polymers than can be accounted for by the simple equilibrium system, involving the combination of one calcium per disaccharide unit period, whose operation is consistent with the K values found at low Ca/glucuronate ratios over a wide range of ionic strengths. Infrared spectra obtained at high and low Ca2+/glucuronate ratios also indicate the existence of two calcium forms of proteoglycans. Viscosity and ultracentrifugal data show that differences exist between proteoglycans in calcium and sodium solutions. The data for disaggregated proteoglycan preparations indicate that their calcium-binding properties are very similar to those of chondroitin 4-sulfate and are determined by the same factors. One aggregated puppy rib proteoglycan, however, showed significantly greater K values than chondroitin 4-sulfate; these decreased after disaggregation.


Holzforschung ◽  
2009 ◽  
Vol 63 (6) ◽  
Author(s):  
Kim Granholm ◽  
Pingping Su ◽  
Leo Harju ◽  
Ari Ivaska

Abstract Chelation of thermomechanical pulp (TMP) was studied in this work. The desorption of Mn, Fe, and Mg due to their impact on peroxide bleaching was investigated. The desorption experiments were performed with EDTA, citric acid, oxalic acid, and formic acid as chelating agents at different pH. Chelation experiments with EDTA were carried out at pH 3–11. Sodium dithionite was used as the reducing agent in studying chelation with EDTA in a reducing environment. Mn was very effectively desorbed with EDTA from TMP at pH <10 and the reducing environment further improved the removal of all the studied metal ions from TMP with EDTA. Citric acid also removed Mn effectively from TMP at pH 5. The thermodynamic stability constants of different metal chelates do not present the correct picture of how strongly the metal ions are bound by the chelating agents in different conditions. But by means of the side reaction coefficients (α M(L)-coefficients) it is also theoretically possible to evaluate and compare the real binding strengths between the metal ions and different chelating agents at varying pH values and other solution conditions. In this study, a theory is given for the calculation of side reaction coefficients. Values of the α M(L)-coefficients, for the pH range 0–14, are presented for EDTA, DTPA, and also for some other new potential environmentally friendly chelating agents.


2018 ◽  
Vol 107 (1) ◽  
pp. 39-54
Author(s):  
Chunli Wang ◽  
Xiaoyu Yang ◽  
Jiangang He ◽  
Fangxin Wei ◽  
Zhong Zheng ◽  
...  

Abstract To explore the diffusion behavior of 75Se(IV) in Beishan granite (BsG), the influences of temperature, oxygen condition and ionic strength were investigated using the through-diffusion experimental method. The effective diffusion coefficient De of 75Se(IV) in BsG varied from 4.21×10−14 m2/s to 3.19×10−13 m2/s in our experimental conditions, increased with increasing temperature. The formation factor Ff of BsG was calculated to be nearly constant in the range of temperatures investigated, suggesting that the inner structure of BsG had no significant change in the temperature range of 20–55°C. Meanwhile, the De values of 75Se(IV) in BsG under anaerobic condition was significantly larger than that under aerobic condition, which may be attributed to the difference in the sorption characteristics and species distribution of Se and pH values. Moreover, the diffusion of 75Se(IV) was promoted with ionic strength increased from 0.01 M to 0.1 M, and then decreased at 0.5 M, mainly due to the combined effects of reduced double layers with increased ionic strength and increase of the solution viscosity at higher ionic strength.


1975 ◽  
Vol 21 (8) ◽  
pp. 1236-1246 ◽  
Author(s):  
W. M. Spira ◽  
J. M. Goepfert

An enterotoxin synthesized during exponential growth by Bacillus cereus produces fluid accumulation in rabbit ileal loops, alters vascular permeability in the skin of rabbits, and kills mice when injected intravenously. All activities are eluted simultaneously from a Sephadex G-75 column and are distinct from the hemolysin and egg yolk turbidity factor of B. cereus. The enterotoxin is a true exotoxin. It interacts with intestinal receptor sites in a highly transient manner in the ileal loop system. Rabbit immune serum produced against the culture fluids from one strain of B. cereus neutralized the three biological activities in all other strains tested except strain B-6-ac for which none of the activities were neutralized.Enterotoxin proved to be unstable under a wide variety of conditions; ionic strength was especially critical. Enterotoxin was most stable in a pH range of 5.0 to 10.0, but lost activity rapidly outside this range. Alkylation provided some protection of enterotoxin activity in crude preparations but failed to protect activity during purification procedures. It did not appear to affect critically the enterotoxin molecule itself, since elution profiles on Sephadex G-75 chromatography were unchanged after alkylation.


2018 ◽  
Vol 73 (9-10) ◽  
pp. 345-351 ◽  
Author(s):  
Alena Komersová ◽  
Markéta Kovářová ◽  
Karel Komers ◽  
Václav Lochař ◽  
Alexander Čegan

AbstractThe dependence of the activity of acetylcholinesterase from electric eel at a pH value range of 4.8–9.8 (phosphate buffer), regarding acetylcholine and acetylthiocholine hydrolysis, was determined at 25 °C, ionic strength of 0.11 M, and initial substrate concentration of 4 mM. At a pH range of 4.8–9.8, the dependencesA(pH) form a sigmoid increasing curve with the maximum catalytic activity at a pH range 8–9.5. For acetylcholine hydrolysis, the kinetic reason for such an increase inAconsists mainly of an increase in the rate constantk2(Michaelis-Menten) model with increasing pH of the reaction mixture. For acetylthiocholine hydrolysis, the kinetic explication of the determined dependenceA(pH) is more complicated.


Materials ◽  
2020 ◽  
Vol 13 (13) ◽  
pp. 2888 ◽  
Author(s):  
Giulia Pinto ◽  
Paolo Canepa ◽  
Claudio Canale ◽  
Maurizio Canepa ◽  
Ornella Cavalleri

The morphological and mechanical properties of thiolated ssDNA films self-assembled at different ionic strength on flat gold surfaces have been investigated using Atomic Force Microscopy (AFM). AFM nanoshaving experiments, performed in hard tapping mode, allowed selectively removing molecules from micro-sized regions. To image the shaved areas, in addition to the soft contact mode, we explored the use of the Quantitative Imaging (QI) mode. QI is a less perturbative imaging mode that allows obtaining quantitative information on both sample topography and mechanical properties. AFM analysis showed that DNA SAMs assembled at high ionic strength are thicker and less deformable than films prepared at low ionic strength. In the case of thicker films, the difference between film and substrate Young’s moduli could be assessed from the analysis of QI data. The AFM finding of thicker and denser films was confirmed by X-Ray Photoelectron Spectroscopy (XPS) and Spectroscopic Ellipsometry (SE) analysis. SE data allowed detecting the DNA UV absorption on dense monomolecular films. Moreover, feeding the SE analysis with the thickness data obtained by AFM, we could estimate the refractive index of dense DNA films.


2007 ◽  
Vol 4 (5) ◽  
pp. 323 ◽  
Author(s):  
Amiel Boullemant ◽  
Jean-Pierre Gagné ◽  
Claude Fortin ◽  
Peter G. C. Campbell

Environmental context. Lipophilic metal complexes, because they can readily cross biological membranes, are especially bioavailable. However, in natural waters these complexes do not necessarily exist in a free state, i.e. they may bind to the organic matter (humic substances) that is present in natural waters. It follows that the in situ bioavailability of lipophilic metal complexes will tend to be less than that measured in simple laboratory experiments. Abstract. The ability of dissolved humic substances (HS: fulvic and humic acids) to complex cationic metals is well known, but their interactions with neutral lipophilic metal complexes are little understood. In the present study, we have examined the behaviour of two such complexes ( Cd  L 2 0 -->Cd L02: L = DDC = diethyldithiocarbamate, or L = XANT = ethylxanthate) in the presence of Suwannee River Humic and Fulvic acids. Interactions between the neutral complexes and the humic substances were assessed by excitation-emission matrix (EEM) fluorescence spectroscopy at pH 5.5 and 7.0, and by equilibrium dialysis experiments (500 Da cut-off). The EEM measurements were carried out by titrating the humic substances (6.5 mg C L–1) with Cd, in the absence or presence of ligand L (1 µM DDC or 100 µM XANT). Given the very high stability constants for the complexation of cadmium by DDC and XANT and the excess ligand concentration, virtually all (>96%) of the Cd added to the L + HS matrix was calculated to be present as the neutral Cd L 2 0 -->CdL20 complex over the entire pH range tested. For both humic substances, addition of DDC or XANT alone led to shifts in the fluorescence spectra at both pH values, indicating that the DDC– and XANT– anions likely interact by electrostatic or hydrogen bonding within the humic molecules. The subsequent addition of Cd to these L + HS systems resulted in a disproportionately large enhancement of the fluorescence intensities of individual EEM peaks, this fluorescence enhancement being only slightly decreased by the shift from pH 7.0 to 5.5. We interpret this enhancement as evidence that the two neutral complexes associate with the humic substances, presumably by forming ternary complexes (Ln-Cd-HS). Hydrophobic interactions between the humic substances and the neutral complexes may also contribute, but to a lesser extent, as demonstrated by partitioning calculations based on the lipophilicity of the neutral complexes. The association of the neutral complexes with Suwannee River Humic Acid was confirmed by dialysis experiments.


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