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Query: UMLS:C0012739 (disseminated intravascular coagulation)
 8,673 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

In the cyanobacterium Synechococcus UTEX 625, the yield of chlorophyll a fluorescence decreased in response to the transport-mediated accumulation of intracellular inorganic carbon (CO2 + HCO3- + CO32- = dissolved inorganic carbon [DIC]) and subsequently increased to a near-maximum level following photosynthetic depletion of the DIC pool. When DIC accumulation was mediated by the active Na+-dependent HCO3- transport system, the initial rate of fluorescence quenching was found to be highly correlated with the initial rate of H14CO3- transport (r = 0.96), and the extent of fluorescence quenching was correlated with the size of the internal DIC pool (r = 0.99). Na+-dependent HCO3- transport-mediated accumulation of DIC caused fluorescence quenching in either the presence or absence of the CO2 fixation inhibitor glycolaldehyde, indicating that quenching was not due simply to NADP+ reduction. The concentration of Na+ required to attain one-half the maximum rate of H14CO3- transport, at 20 [mu]M external HCO3-, declined from 9 to 1 mM as the external pH increased from 8 to 9.6. A similar pH dependency was observed when fluorescence quenching was used to determine the kinetic constants for HCO3- transport. In cells capable of Na+-dependent HCO3- transport, both the initial rate and extent of fluorescence quenching increased with increasing external HCO3-, saturating at about 150 [mu]M. In contrast Na+-independent HCO3- transport-mediated fluorescence quenching saturated at an HCO3- concentration of about 10 [mu]M. It was concluded that measurement of chlorophyll a fluorescence emission provided a convenient, but indirect, means of following Na+-dependent HCO3- transport and accumulation in Synechococcus.
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PMID:Quenching of Chlorophyll a Fluorescence in Response to Na+-Dependent HCO3- Transport-Mediated Accumulation of Inorganic Carbon in the Cyanobacterium Synechococcus UTEX 625. 1223 26

The effects of typical organic pollutants (ethanol, acetone, ON, OP) on pH and marine carbon dioxide system were investigated in laboratory simulated experiments. The results indicated that the growth of biological carbon fixed system was promoted by ethanol and acetone of low concentration (< 0.5 mmol x L(-1)) (t = 7 d). So pH increased while DIC, HCO3(-) and p(CO2) significantly decreased compared to the controls (p <0.01). The concentrations of ethanol and acetone which resulted in the maximum decrease of carbon dioxide parameters were 0.25 mmol x L(-1) and 0.1 mmol x L(-1), respectively. When the infusion of organic pollutants were higher than the "critical concentration", the carbon dioxide parameters increased and pH decreased compared to the controls with the decrease of carbon fixation strength of alga. As for ON and OP groups, when they were in the range of experimental concentration, decreasing trends of inorganic carbon in sea water were always found. The concentration changes of DIC (DeltaDIC) under the press of the four typical organic pollutants were significantly negatively correlated with the changes of dry weight of alga (p < 0.01 or p < 0.05) and the coefficient parameters were -0.902, -0.945, -0.898 and -0.918, respectively (t = 7 d). The main controlling factor to the variation of carbon dioxided system was the adaption of biological carbon fixed system to different concentration and kind of organic pollutants.
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PMID:[Effects of typical organic pollutants on marine dioxide carbon system in simulated experiments]. 1955 94

This study deals with the ionically-driven self-assembly of oligomeric aminosilicones, judiciously protonated with a variety of organic acids. Depending on the length of the silicone and the strength of the associated acids, (inverse) water-in-silicone emulsions, small nanoparticles, or catanionic vesicles were prepared and characterized by conventional (TEM) or original (DIC optical microscopy, DOSY NMR) techniques. For chains longer than about 40 units, a specific PEG-based sulfonic acid was synthesized and used to generate a supramolecular block-like copolymer and ensure fast and efficient emulsification. In all instances, a simple impulse such as pH increase triggered phase separation of the colloidal objects.
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PMID:Supramolecular organization of protonated aminosilicones in water. 2391 58