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  • 1
    ISSN: 1432-072X
    Keywords: Osmoadaptation ; Hypoosmotic shock ; Stretch-activated channels ; K+ release ; Glutamate release ; Trehalose release ; K+ uptake ; Glutamate uptake ; Amino-acid pool ; Accute osmotic stress ; Escherichia coli
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The influence of hypoosmotic shock on the solute content of growing Escherichia coli K-12 cells was investigated at 37°C. Within 20 s after the shock the cells had released most of their osmolytes K+, glutamate and trehalose. This release was specific and not due to rupture of the cell membrane, since under these conditions i) the cells neither lost protein nor ATP, ii)[14C]-labeled sucrose did not enter the cytoplasm from the periplasm, and iii) except for their glutamate and aspartate level, which decreased, the amino acid pool of alanine, lysine and arginine of the cells remained approximately constant. Within a minute after the shock the cells started to reaccumulate parts of their previously released glutamate, aspartate and K+, but not trehalose and resumed growth within 10 min after the shock. Experiments with K+-transport mutants showed that none of the genetically-identified K+ transport systems is involved in the K+-release process. Reaccumulation of K+ took place via the uptake systems TrkG and TrkH. The possibility is discussed that the exit of solutes after hypoosmotic shock occurs via several stretch-activated channels, which each allow the release of a specific osmolyte.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-072X
    Keywords: Osmoadaptation ; Potassium uptake ; Glutamate synthesis ; Trehalose synthesis ; Internal pH ; Membrane potential ; Protonmotive force ; Proline uptake ; ProP system ; acr A-mutant ; Escherichia coli
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The sequence of events following the addition of 0.5 M NaCl to cells of Escherichia coli growing in a minimal mineral medium was investigated. Immediately after upshock the cells took up a large amount of K+ and synthesized approximately half the equivalent amount of glutamate concomitantly. After 30 min the cells started to synthesize trehalose, and after 2 h they had replaced most of their initial osmoprotectants by the carbohydrate. Cell trehalose was rapidly replaced by proline, taken up from the medium when added to the osmoadapting cells. The initial rate of this proline uptake was extremely rapid, and with rates observed of up to 0.6 mmolxmin-1xg-1 of cell protein it was approximately ten times faster than that reported in the literature for non-growing cells. These results indicate that for osmoadaptation of growing cells of E. coli the uptake of proline has priority over the synthesis of trehalose, which in its turn is preferred above K+ and glutamate as osmoprotectants. We observed that two mutants with unknown lesions, but which are known to be impaired in osmoadaptation, were inhibited in replacing K+ and glutamate by trehalose, indicating that this is the basis for their defect in osmoadaptation. Further experiments revealed that neither internal pH nor the membrane potential nor the transmembrane protonmotive force are likely to be involved in osmoadaptation in E. coli. However, during osmoadaptation a high internal potassium concentration appeared to stimulate the derepression of proline-uptake systems (mainly system ProP).
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The electron transfer step of the reduction of Mn(acac)3 and Co(acac)3 by Fe(II) in acetonitrile is preceded by the one-ended dissociation of an acac ligand and the formation of a binuclear bridged complex. After the electron transfer has taken place through the bridging ligand, the complex dissociates into the products M(acac)2 (M = Mn, Co) and Fe(acac)2+. These primary reaction products could not be identified, since the transfer of acac from M(acac)2 to Fe(acac)2+ is too rapid, producing ultimately Fe(acac)3 and M2+. The M(III)-oxygen cleavage is accelerated by M(acac)2. Furthermore, the dissociation of the binuclear intermediate is catalyzed by the M(acac)3 reactant. Mn(acac)3 is reduced more than a thousand times faster than Co(acac)3.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 11 (1979), S. 1-9 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction between tris(acetylacetonato)magnanese(III) and hexa(N,N-dimethylformamide)iron(III) perchlorate in acetonitrile proceeds in two stages. The first stage corresponds to the reaction of pentacoordinated Fe(DMF)53+ with Mn(acac)3, and the rate-determining step of the second stage consists mainly in the elimination of a DMF ligand from Fe(DMF)63+ to yield Fe(DMF)53+ which reacts rapidly with the manganese complex. The formation of Fe(DMF)53+ is catalyzed by Mn(acac)3, this catalytic effect being decreased by manganese products. The rate-determining step for the formation of Fe(acac)3 is the transfer of the first acetylacetonate to yield Fe(acac)2+. The final products of iron depend on the ratio of reactant concentrations. With Mn or Fe in excess, Fe(acac)3 or Fe(acac)2+ are mainly produced.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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