Divalent cations and

The site preference of several transition-metal ions is discussed in References 4 and 24. The occupation of the sites is usually denoted by placing the cations on B-sites in stmcture formulas between brackets. There are three types of spinels normal spinels where the A-sites have all divalent cations and the B-sites all trivalent cations, eg, Zn-ferrite, [Fe ]04j inverse spinels where all the divalent cations are in B-sites and trivalent ions are distributed over A- and B-sites, eg, Ni-ferrite, Fe Fe ]04 and mixed spinels where both divalent and trivalent cations are distributed over both types of sites,... 

Kimura and coworkers [17], Diamond [18], and Damien et al. [19] have described that the polymeric calix-[4]arenes have been used as ionophores in ion selective electrodes for Na (based on calixarene esters and amides) and for Na and Cs (based on p-alkylcalixarene acetates). The electrodes are stated to function as poten-tiometric sensors as well, having good selectivity for primary ion, virtually no response to divalent cations, and being stable over a wide pH range. 

The results from such occluders show that Na channels differ in structure between their internal and external surfaces, have binding sites for a variety of monovalent and divalent cations, and are pharmacologically different despite very similar physiological actions in nerve, muscle, and mammalian cardiac cells. 

The mechanism of acquired resistance in Pseudomonas aeruginosa is different. Chromosomal mutations result in the increase of a specific outer membrane protein with a concomitant reduction in divalent cations. Polymyxins bind to the outer membrane at sites normally occupied by divalent cations, and therefore it is thought that a reduction in these sites will lead to decreased binding of the antibiotic with a consequent decreased susceptibility of the cell. 

Setting times and hydrolytic stability of these cements are given in Table 8.3. In some cases the speed of reaction was very high, and practical cements could not be formed from ZnO or CaO even when these oxides were deactivated by heating. All the faster-setting cements exhibited good hydrolytic stability. The stability of the complexes between divalent cations and PVPA was found by a titrametric procedure to follow the order Mg Ca < Cu Zn (Ellis Wilson, 1991). This result was... 

Klancke, J. W., Determination of monovalent and divalent cations and chloride in the carbacephalosporin loracarbef by ion chromatography, /. Chromatogr., 637, 63, 1993. 

Some strains of P. aeruginosa are resistant to benzalkonium chloride and, in fact, can be grown in solutions concentrated in this agent. This has caused great concern because of the virulent nature of this organism in ocular infections, as discussed previously. Thus, it was an important finding in 1958 that the acquired resistance could be eliminated by the presence of ethylenediaminetetracetic acid (sodium edetate) in the formulation. This action of EDTA has been correlated with its ability to chelate divalent cations, and it is commonly used as a preservative aid [125]. The use of disodium EDTA, where compatible, is recommended in concentrations up to 0.1%. 

To use liposomes as delivery systems, drug is added during the formation process. Flydrophilic compounds usually reside in the aqueous portion of the vesicle, whereas hydrophobic species tend to remain in the lipid proteins. The physical characteristics and stability of lipsomal preparations depend on pH, ionic strength, the presence of divalent cations, and the nature of the phospholipids and additives used [45 47],... 

Alkaline phosphatases [AP, orthophosphoric-monoester phosphorylase (alkaline optimum) EC 3.1.3.1] represent a large family of almost ubiquitous isoenzymes found in organisms from bacteria to animals. In mammals, there are two forms of AP, one form present in a variety of tissues and another form found only in the intestines. They share common attributes in that the phosphatase activity is optimal at pH 8-10, is activated by the presence of divalent cations, and is inhibited by cysteine, cyanides, arsenate, various metal chelators, and phosphate ions. Most conjugates created with AP utilize the form isolated from calf intestine. 

Salt activation falls into two classes with respect to the valency of the cation component. With divalent cations and at pH 6, maximum activation is produced at about 0.03 M concentration. At higher concentrations with the same pH, suppression of activity occurs. Monovalent cations in general produce maximum activation at pH 6 in 0.10 M concentration and do. not suppress activity below molarities of 1.0. Maximum activity is obtained at a lower pH and lower concentration of divalent cations than monovalent. The maximum activity obtained at the optimum salt concentration for a given pH value is, within experi-... 

Thus, calcium-dependent hydrolases show clear structural and catalytic similarities with metallohydrolases, both in the role played by a divalent cation and in the mechanism of H20 activation. 

Thus, cosolvents can be used as perturbing tools and as probes for conformation change after careful, comparative analysis of their effects compared to those induced by various physiological agents, such as protons, monovalent and divalent cations, and other ligands which act to regulate equilibria and rate processes. 

F17. Frei, J., Multiplicity and specificity of UDP-glucuronyltransferase. I. Effect of divalent cations and EDTA on the activity of UDP-glucuronyltransferase assayed with bilirubin, 4-methylumbelliferone and p-nitrophenol. Emymol. Biol. Clin. 11, 385-401 (1970). 

Although the acidic antibiotics do not show the high selectivity characteristic of the neutral ones, there is still some preference, a strong one for monovalent as compared with divalent cations, and within the monovalent cations a variation from one acid to another. Monensin prefers sodium to potassium. The larger nigeridn, (X7), prefers potassium to sodium its silver, potassium, and sodium salts are isomorphous and anhydrous. Crystal structure determinations on the silver salt were carried out independently by workers in the U.S.A. (78) and in Japan... 

Figure 7.2 Schematic representation of alginate cross-linking with divalent cations and the chemical structure of the constituent repeat units, guluronate (G) and mannuronate (M). Carboxylate groups present along the backbone (largely from the G residues) interact with multivalent cations to yield metal ion cross-linked gels.

Are properties of the molecule of interest regulated by divalent cations and do chelators as EDTA therefore affect them ... 

Ferrite compounds with the inverse spinel structure are similar to magnetite, with different ions substituting for the iron atoms. As with FeO (cf. Figure 6.62), the oxygen ions have no permanent magnetic moment. Tetrahedral sites in the FCC oxygen array are occupied by half of the trivalent cations, and octahedral sites are occupied equally by divalent cations and the remaining trivalent cations. 

The ready availability of the transketolase (TK E.C. 2.2.1.1) from E. coli within the research collaboration in G. A. Sprenger s group suggested the joint development of an improved synthesis of D-xylulose 5-phosphate 19, which was expensive but required routinely for activity measurements [27]. In vivo, transketolase catalyzes the stereospecific transfer of a hydroxyacetyl nucleophile between various sugar phosphates in the presence of a thiamine diphosphate cofactor and divalent cations, and the C2 donor component 19 offers superior kinetic constants. For synthetic purposes, the enzyme is generally attractive for its high asymmetric induction at the newly formed chiral center and high kinetic enantioselectivity for 2-hydroxyaldehydes, as well as its broad substrate tolerance for aldehyde acceptors [28]. 

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