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Dynamic instabilities and mechanism of the electrochemical oxidation of thiosulfate.

The electrochemical oxidation of thiosulfate is revealed to have two distinct oscillatory regimes in both linear potential and galvanic voltammograms, where various nonlinear behaviors such as period-2, mixed-mode and quasi-periodic oscillations, and chaos are observed under potentiostatic or galvanostatic conditions. Electrochemical impedance spectroscopy and iR compensation characterization indicate that, depending on the operating conditions, the system could be either a strictly potentiostatic oscillator or an S-shaped negative differential resistance oscillator. Chronoamperometry measurements reveal that the first oscillatory process involves a single-electron transfer, whereas within the second oscillatory regime the average number of electrons transferred is around 3.8. Measurements with capillary electrophoresis and chemical methods illustrate that the oxidation products include S2O6(2-), S4O6(2-), S5O6(2-), S3O6(2-), and SO4(2-).

Journal Article↗

Kinetics of Maize Leaf Elongation : III. Silver Thiosulfate Increases the Yield Threshold of Salt-Stressed Plants, but Ethylene Is Not Involved.

The involvement of ethylene in the short-term responses of maize (Zea mays L.) leaf elongation to salinity was investigated. Leaf elongation rates (LER) were monitored with linear variable differential transformers. Salinity (80 mm NaCl) rapidly inhibited LER. Pretreatment with 4 mm silver thiosulfate (STS), an inhibitor of ethylene action, decreased LER of salt-stressed plants, but not that of controls. Investigation of the growth parameters affected by the interaction of STS and salinity indicated that the yield threshold was increased and the cell wall extensibility was decreased. All other growth parameters controlling cell elongation were unaffected. Further investigation indicated that ethylene production may not be involved in this reponse because treatments with 10 mum aminoethoxyvinylglycine, an ethylene biosynthesis inhibitor, did not affect the growth of salt-stressed plants, and no increase in ethylene production was detected in salt-stressed plants compared with controls. No changes in sensitivity to ethylene were evident because LER of both control and salt-stressed plants were inhibited to the same extent with exposure to 1.2 ppm ethylene. The above evidence indicated that ethylene was not involved in the short-term LER responses of salt-stressed maize.

Journal Article↗

A novel five-coordinate cadmium phenanthroline thiosulfate.

The structure of the novel cadmium phenanthroline thiosulfate poly[[(1,10-phenanthroline-kappa(2)N,N')cadmium(II)]-micro(3)-thiosulfato-kappa(3)S:S:O], [Cd(S(2)O(3))(C(12)H(8)N(2))](n), with a pentacoordinated Cd centre, is reported. It forms linear chains built up around a 2(1) axis and is isostructural with the known bipyridine homologue. The structure is also compared with a previously reported closely related monoaqua monohydrated phase, where the Cd(2+) cation is hexacoordinated. The incidence of weak C-H.O interactions in the determination of its general packing properties is discussed.

Journal Article↗

Tetraaqua(3,4,7,8-tetramethyl-1,10-phenanthroline-kappa2N,N')zinc(II) thiosulfate.

In the title complex of zinc(II) with 3,4,7,8-tetramethyl-1,10-phenanthroline (tmph), viz. [Zn(C16H16N2)(H2O)4](S2O3), the metal atom has a monomeric octahedral ZnN2O4 complex environment comprising two N-atom donors from the tmph group and four aqua O-atom donors. The complex cation is connected to four thiosulfate anions through a compact hydrogen-bonding network involving all coordinated aqua H-atom donors and all the outer acceptors (O and S) of the anion.

Anti-Inflammatory Agents, Non-Steroidal↗

Crystallization, preliminary crystallographic analysis and phasing of the thiosulfate-binding protein SoxY from Chlorobium limicola f. thiosulfatophilum.

The 22 kDa SoxYZ protein complex from the green sulfur bacterium Chlorobium limicola f. thiosulfatophilum is a central player in the sulfur-oxidizing (Sox) enzyme system of the organism by activating thiosulfate for oxidation by SoxXA and SoxB. It has been proposed that SoxYZ exists as a heterodimer or heterotetramer, but the properties and role of the individual components of the complex thus far remain unknown. Here, the heterologous expression, purification, and the crystallization of stable tetrameric SoxY are reported. Crystals of SoxY diffract to 2.15 A resolution and belong to space group C222(1), with unit-cell parameters a = 41.22, b = 120.11, c = 95.30 A. MIRAS data from Pt(2+)- and Hg(2+)-derivatized SoxY crystals resulted in an interpretable electron-density map at 3 A resolution after density modification.

Bacterial Proteins↗

Bacterial leaching of metal sulfides proceeds by two indirect mechanisms via thiosulfate or via polysulfides and sulfur

The acid-insoluble metal sulfides FeS2, MoS2, and WS2 are chemically attacked by iron(III) hexahydrate ions, generating thiosulfate, which is oxidized to sulfuric acid. Other metal sulfides are attacked by iron(III) ions and by protons, resulting in the formation of elemental sulfur via intermediary polysulfides. Sulfur is biooxidized to sulfuric acid. This explains leaching of metal sulfides by Thiobacillus thiooxidans.

Journal Article↗

[Synthesis and radiosensitizing activity of nitro-arylimino-diethyl-sodium thiosulfate and nitro phenylalanine derivatives].

A series of compounds was synthesized, these compounds were tested for Hela-S3 cells in vitro for radiosensitizing activity. Five of them are 2,2'-(arylimino)-diethyl-sodium thiosulfate and two of them are phenylalanine derivatives. Most of them showed various degrees of radiosensitizing activity. Among them, SER of L07 was 1.89 at 3 mmol, and had low cytotoxicity to Hela-S3 cells, ID50 was 18.8 mmol. The relationship between radiosensitizing effects and chemical structure was discussed. It offers a base for further exploration of selectively hypoxic cell radiosensitizers.

HeLa Cells↗

The catalytic mechanism of yeast thiosulfate reductase.

Thiosulfate reductase catalyzes the desulfuration of thiosulfonates while oxidizing GSH to GSSG. Kinetic studies of the enzyme-catalyzed reaction between GSH and benzenethiosulfonate have been carried out, and direct evidence for the occurrence of glutathione persulfide as an immediate product of the reaction has been obtained. The formal mechanism of this enzymic reaction has been shown to be rapid equilibrium-ordered with GSH as the leading substrate.

Glutathione↗

Effect of some enzyme inducers, fluids, and methionine-thiosulfate on induced acute aflatoxicosis in goats.

Groups of four 6- to 12-month-old male goats were injected intraruminally with a lethal dose (3 mg/kg of body weight) of aflatoxin B1 (AFB1). Drugs were administered parenterally before (pretreatment) or beginning 8 hours after goats were doses with AFB1. These drugs were phenobarbital (PB), phenylbutazone (PBZ), piperonyl butoxide (PRO), benzoflavones, water, and 5% glucose solution (D5W). Most groups given the drugs after AFB1 was administered also were given intraperitoneal injections of methionine-sodium thiosulfate (MET-TS) solution. Clinical signs of toxicosis, serum aspartate aminotransferase activities, serum bilirubin concentrations, duration of illness, mortality, and gross and microscopic pathologic findings taken together indicated that toxicosis was increased with MET-TS + PB therapy, PBZ pretreatment, PBZ therapy, benzoflavone pretreatment, benzoflavone therapy, MET-TS + benzoflavone therapy, and MET-tS + water therapy. Toxicosis was not altered appreciably by MET-TS + PBO therapy. Beneficial effects (less severe toxicosis) were produced by PB pretreatment; these effects were prolonged maintenance of strength, vigor, and appetite and (in 1 goat that recovered) absence of pathologic changes or serum bilirubin increase. Therapy with MET-TS + D5W (but not MET-TS alone) also lengthened maintenance of strength, vigor, and appetite, but did not prevent pathologic changes. The beneficial effect of MET-TS therapy reported in a previous study (AFB2 dosage of 4 mg/kg) was not observed with the 3 mg/kg lethal dose. In conclusion, therapy for acute aflatoxicosis with inducers of hepatic microsomal enzymes is ineffective (PBO) or contraindicated (PB, PBZ, benzoflavones). Therapy with D5W may be a useful adjunct to other therapeutic drugs, but multiple intraperitoneal injections of D5W may decrease survival time because of stress.

Aflatoxin B1↗

Antagonism of the lethal effects of cyanide with resealed erythrocytes containing rhodanese and thiosulfate.

A new concept has been presented for the antagonism of cyanide and possibly other chemical toxicants. Until now, only a half dozen truly specific "antidotes" were known. There are many other "antidotes" which merely prevent the absorption or enhance the elimination of a toxic compound rather than specifically destroying the substance to prevent its toxic effect. This new approach has considerable conceptual significance in toxicology, as it suggests the encapsulating other enzymes to degrade various other chemical toxicants. There are many chemical toxicants for which there are no specific antidotes, and the conceptual approach of employing erythrocyte-encapsulated enzyme provides an innovative, specific approach to antagonize the toxic and lethal effects of these chemicals.

Animals↗