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Query: UMLS:C0847097 (acidity)
 15,165 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The acidity in aqueous solutions following release of acid components from glass ionomer, silicate, zinc phosphate and zinc polycarboxylate cements has been registered by pH measurements. One brand of each type was studied. Initial setting was accomplished at two different temperatures; 23 degrees C and in the interval from 23 degrees C to about 60 degrees C. In the latter case external heat was transferred to the samples by infrared radiation for a period of 2 min. The highest acidity was associated with the silicate specimen, while the lowest acidity was recorded for the zinc polycarboxylate specimen. Exposure to infrared radiation resulted in a reduced acidity for all types of cements. The effect of infrared exposure was most pronounced for the silicate specimens, resulting in a reduction of acid release by a factor of about 10 compared to the nontreated samples. The resistance to acid release was found to be improved by a factor of about 5 for the glass ionomer and about 3 for the zinc phosphate cement treated in a similar way. Clinically, it seems possible considerably to reduce the risk of pulpal injuries associated with the insertion of silicate restorations by using a moderate infrared radiation treatment. Furthermore, the susceptibility of glass ionomer cements to a high initial erosion should be reduced by the use of such a technique. After exposure of the glass ionomer and silicate specimens to infrared radiation at the temperature interval applied, the samples had a more glossy, tooth-like appearance compared to the nonexposed samples, improving the aesthetic properties.
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PMID:Initial acidity of dental cements. 658 21

Three types of luting cements were compared for acidity, disintegration, and film thickness. The pH during setting of the two types of polycarboxylate cements exceeded 6 after 5 hours; that of the water-settable polycarboxylate cement was the highest, almost reaching neutral. The zinc phosphate cement reached pH 3.4 after 5 hours and 5.5 after 24 hours. All cements tested showed remarkably greater disintegration in the lactic acid solution than in the distilled water. The disintegration of the water-settable zinc polycarboxylate cement in distilled watter was about half that of the other cements. The disintegration in the lactic acid solution was approximately the same for all cements tested. The film thickness was smallest with the water-settable zinc polycarboxylate cement.
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PMID:Comparison of three luting agents. 692 80

The acidity constant of protonated 2-[bis(2-hydroxyethyl)amino]-2(hydroxymethyl)-1,3-propanediol (Bistris) has been measured. The influence of hydroxo groups on the basicity of Bistris and related bases is discussed. The interaction of Bistris with the metal ions (M2+) Mg2+, Ca2+, Sr2+, Ba2+, Mn2+, Co2+, Ni2+, Cu2+, Zn2+, Cd2+, and Pb2+ was studied by potentiometry and spectrophotometry in aqueous solution (I = 1.0 M, KNO3; 25 degrees C) and the stability constants of the M(Bistris)2+ complexes were determined. Unexpectedly Ca(Bistris)2+ is the most stable among the alkaline earth ion complexes (log KCaCa(Bistris) = 2.25; the corresponding values for the Mg2+, Sr2+ and Ba2+ complexes are 0.34, 1.44 and 0.85, respectively). The ions of the 3d series follow the Irving-Williams sequence: log KMnMn(Bistris) = 0.70, for Cu2+, 5.27 and Zn2+ 2.38. Ternary complexes containing ATP4- as a second ligand were also investigated: the values for delta log KM (= log KM(ATP)M(ATP)(Bistris) -log KMM(Bistris) are in general negative (e.g. delta log KCa = -0.40 or delta log KCu = -1.65), thus indicating that the interaction of Bistris with M(ATP)2- is somewhat less pronounced tan with M2+. However, even in mixed-ligand systems, complex formation may still be considerable, hence great reservations should be exercised in employing Bistris as a buffer in systems containing metal ions. Moreover, in several cases delta log KM is relatively high [for Mg2+-ATP4- -Bistris even positive], indicating some cooperativity between the coordinated ligands, possibly hydrogen-bond formation. Distributions of the complexes in dependence on pH are given, and the structures of the binary M(Bistris)2+ and the ternary M(ATP) (Bistris)2- complexes are discussed. The participation of Bistris hydroxo groups in complex formation is evident.
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PMID:Metal ion/buffer interactions. Stability of binary and ternary complexes containing 2-[bis(2-hydroxyethyl)amino]-2(hydroxymethyl)-1,3-propanediol (Bistris) and adenosine 5'-triphosphate (ATP). 739 53

A modern AmpHel pH-meter permits the easy determination of dental materials pH. This new instrument has allowed, analysing seven cements and two varnishes used for pulpodentinal protection, continuously to specify this important parameter's modifications in the long run. The results of this study, conducted for six hours after cement mixing or varnishes application, certified glass ionomer cements' (Ketac-Cem, Fuji-Ionomer II) strong acidity, even higher than well known zinc phosphates' acidity is. A cavity liner's (Tubulitec) pH from an initial value of 6.07 decreased to 5.04 at sixth hour. On the contrary, much lower were the acidity of a modified ZOE (Temrex) and the one of a cavity varnish (Copalite): both showed a physiological pH from the beginning of the test.
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PMID:[Variation, over time, in the pH of the materials used for pulpal-dentinal protection. A new measurement method]. 747 77

Semi-dominant mutations in the amdA gene lead to elevated expression of the gene encoding acetamidase, amdS. These mutations also cause constitutive expression of the acetate-inducible gene, aciA. In the amdS 5' regulatory region, two cis-acting mutations, amdl66 and amdl666, have been isolated which specifically affect amdA activation of amdS. These mutations are a duplication and a triplication of an 18 bp GA-rich sequence, thought to define the amdA site of action within the amdS promoter region. Similar GA-rich sequences have also been found in the 5' region of aciA. This paper describes the cloning and initial functional characterization of the amdA gene and two of its mutant alleles. The wild-type amdA gene has been cloned by a chromosome walk from genes gatA and alcC on linkage group VII and localized by complementation of an amdA loss-of-function mutation. Transcriptional analysis reveals that the gene is expressed constitutively at low levels under growth conditions which affect expression of amdS and aciA. The gene is predicted to encode an 880-amino-acid protein which contains two C2H2 zinc fingers, a nuclear localization sequence and two transcriptional activation domains. The amdA7 semi-dominant gain-of-function mutation results in a glycine to aspartate substitution which would increase the acidity of one of these regions. Analysis of in vitro generated mutations in the 5' region of amdS using an amdS::lacZ reporter has been used to localize the site of action of AmdA. The C2H2 zinc-finger motifs identified in the protein are similar to those found in the carbon catabolite repressor protein, CreA, which also regulates amdS and recognizes sequences which overlap with the proposed site of action for AmdA.
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PMID:The positively acting amdA gene of Aspergillus nidulans encodes a protein with two C2H2 zinc-finger motifs. 759 97

WIN 22169 is a co-polymer containing approximately 11 repeating units of polyoxyethylene and diethylenetriamine pentaacetic acid (DTPA). WIN 66368, a magnetic resonance imaging (MRI) contrast agent, is the gadolinium III complex of WIN 22169. WIN 22169 has been characterized with respect to its equivalent weight, acidity constants and excess acid or base, as well as its metal ion binding constants. The logs of the equilibrium binding constants of the ligand to Gd3+, Ca2+, Zn2+ and Cu2+ were found to be 16.6, 7.47, 12.2 and 14.0. The Gd selectivity constant, a measure of the preferential binding of the ligand toward Gd3+ versus the three in vivo ions: Ca2+, Zn2+ and Cu2+, of WIN 66368 was calculated to be 7.9. This value compares favourably to that for Gd DTPA which has a Gd selectivity constant of 7.04.
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PMID:Binding constant determination of WIN 22169, a novel polymeric ligand. 781 75

The pH regulation of gene expression in Aspergillus nidulans is mediated by pacC, whose 678 residue-derived protein contains three putative Cys2His2 zinc fingers. Ten pacCc mutations mimicking growth at alkaline pH remove between 100 and 214 C-terminal residues, including a highly acidic region containing an acidic glutamine repeat. Nine pacC+/- mutations mimicking acidic growth conditions remove between 299 and 505 C-terminal residues. Deletion of the entire pacC coding region mimics acidity but leads additionally to poor growth and conidiation. A PacC fusion protein binds DNA with the core consensus GCCARG. At alkaline ambient pH, PacC activates transcription of alkaline-expressed genes (including pacC itself) and represses transcription of acid-expressed genes. pacCc mutations obviate the need for pH signal transduction.
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PMID:The Aspergillus PacC zinc finger transcription factor mediates regulation of both acid- and alkaline-expressed genes by ambient pH. 788 81

Competitive inhibition as a function of pH for the metalloendoprotease thermolysin by derivatives of L-alpha-(2-hydroxyphenyl)benzenepropanoyl-L- tryptophanylglycylglycine exhibits a diagnostic bell shape. Binding is maximal between two pKa values: on the acidic limb the apparent Ki value is regulated by an unchanging enzymic ionization (pKa 5.3) which is also seen in the substrate-hydrolysis kinetics (kcat/Km), whereas the alkaline limb for inhibition varies and depends specifically on the pKa of the phenolic group in the inhibitor. Although it should be the phenolate form of the inhibitor that co-ordinates more efficiently to the active-site Zn2+, the apparent Ki shifts from pH-independent at pH values immediately below the inhibitor's pKa to progressively weaker binding at higher pH. This is explained by an anomalous acidity for the exchangeable solvent molecule that is attached to enzymic Zn2+ in the absence of substrate or inhibitor. Since OH- cannot be displaced from the enzyme as readily as H2O, a compensating pKa of 5.3 possessed by Zn(2+)-bound water rationalizes the binding characteristics, yielding the level pH profile exhibited at intermediate pH values. Recognition of the implicit heightened Lewis acidity of the metal ion in thermolysin leads to a revision of the mechanism of catalysis. The substrate amide bond becomes activated for hydrolysis by carbonyl-group co-ordination to the especially acidic Zn2+ ion (completely displacing the H2O/OH- species otherwise bound). The imidazole group of enzymic residue His-231, also discerned in the pH profile for kcat/Km from its pKa of 8, provides general-base assistance for hydration of the activated scissile linkage in the first committed step of catalysis. Additional evidence from inhibition patterns shows how substrate-binding energy may be employed in this scheme to promote hydrolysis of peptides by thermolysin.
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PMID:Binding to thermolysin of phenolate-containing inhibitors necessitates a revised mechanism of catalysis. 806 24

This study demonstrates a pH-dependent inhibition of Mg(2+)- and Ca(2+)-ATPase activities of Nostoc linckia and Chlorella vulgaris exposed to AlCl3, AlF3, NaF and AlCl3+NaF together. AlF3 and the combination of AlCl3+NaF were more inhibitory to both the enzymes as compared with AlCl3 and NaF. Toxicity of the test compounds increased with increasing acidity. Interaction of AlCl3+NaF was additive on N. linckia and C. vulgaris, respectively, at pH 7.5 and 6.8, and synergistic at pH 6.0 and 4.5. In the presence of 60 and 100 microM PO4(3-) an increased NaF concentration (in the AlCl3+NaF combination) was required to produce the same degree of inhibition in ATP synthesis and ATPase activity. Toxicity of fluoroaluminate was reduced in the presence of EDTA and citrate. Except for beryllium to some extent, combinations of cadmium, cobalt, iron, manganese, tin and zinc with fluoride were not as effective as aluminium in inhibiting the ATPase activity. The presence of a 100 kDa protein band in SDS-PAGE of both control as well as AlCl3+NaF-treated samples suggested that AlF4- inhibits the ATPase activity by acting as a functional barrier without affecting the structure of the enzyme.
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PMID:Impact of aluminium, fluoride and fluoroaluminate complex on ATPase activity of Nostoc linckia and Chlorella vulgaris. 869 79

We measured 24-h spontaneous intake of four to eight concentrations of 31 different solutions by groups of rats fed control or low-calcium diets. Relative to controls, those fed low-calcium diet had increased acceptance of one or more concentrations of sodium chloride, sodium acetate, and sodium bicarbonate, but not sodium gluconate. Differences in palatability between these sodium salts were unimportant because the rats fed low-calcium diet consumed more sodium chloride even if this was made less acceptable by adulteration with citric acid. The possibility that calcium-deprived rats have an enhanced general cation or mineral appetite was supported by findings of increased acceptance of one or more concentrations of nine of ten chloride minerals tested (aluminum chloride, ammonium chloride, ferric chloride, ferrous chloride, magnesium chloride, sodium chloride, potassium chloride, strontium chloride, zinc chloride). However, there were no differences in acceptance of any concentration of cesium chloride, magnesium sulfate, or lead acetate. Moreover, calcium-deprived rats drank more hydrochloric acid and malic acid than did controls. Thus the effect of calcium deficiency on intake was not confined to minerals. Acidity or bitterness did not appear important because there was no difference between the groups in intake of sulfuric acid, citric acid, or quinine hydrochloride. Consistent with the exacerbating effects of phosphates on calcium deprivation, deprived rats had decreased intakes of phosphates (sodium phosphate, potassium phosphate). However, they also had decreased intakes of sucrose and saccharin. It is clear that calcium deprivation does not induce a general increase in acceptance of all taste solutions, but there appears to be no simple explanation for what these animals consume.
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PMID:Acceptance of minerals and other compounds by calcium-deprived rats: 24-h tests. 876 Jan 97


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