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The Cellular Transport of Magnesium in Rat Liver 总被引:1,自引:0,他引:1
The bidirectional transport of Mg in rat liver was studied using slices labeled with 28Mg in a closed two-compartment system under steady-state conditions. The influx (Kbs) and efflux (Ksb) transfer coefficients governing transport between the extracellular phase and a rapidly exchanging cell fraction were 0.074 and 0.019 per min, respectively. An increased extracellular concentration of Mg++ caused a 30% decrease in Kbs and a 31% increase in Ksb. A decreased extracellular Mg++ had an opposite effect. At 0°C, both transfer coefficients were reduced by 65%. Increased pH and NaCN increased transport, whereas Ca++ reduced transport. Reduced pH, altered Na+:K+ ratio, Sr++, glucose deletion, iodoacetate, ethanol, and lactate had no significant influence. Dinitrophenol reduced Ksb but had no effect on Kbs. These data support the thesis that the intracellular concentration of Mg is in part regulated by a reciprocal change in the influx transfer coefficient and a parallel change in the efflux transfer coefficient in response to altered extracellular concentrations of Mg++. The qualitative and quantitative similarities of Mg and Ca transport in this system suggest that Mg and Ca share a common transport mechanism which is primarily dependent upon the binding of these divalent cations to macromolecular ligands within the cell membrane or within the cell. 相似文献
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987.
A Ahmed 《Biochimica et biophysica acta》1968,166(1):218-228
988.
1. A number of yeast species were examined for the presence of β-glucanases. Extracts obtained by cell disruption of Saccharomyces cerevisiae, Fabospora fragilis and Hansenula anomala hydrolysed laminarin and pustulan with the production of glucose. Enzymic activities were also detected in the culture fluids of F. fragilis and H. anomala grown aerobically in buffered mineral medium with glucose as the carbon source. 2. F. fragilis and H. anomala possessed approximately sevenfold higher β-(1→3)-glucanase activity than S. cerevisiae. 3. Intracellular exo-β-glucanase from baker's yeast was purified 344-fold from the dialysed cell extract. 4. Exo-β-glucanase from F. fragilis was purified 114-fold from the dialysed culture fluid and 423-fold from the dialysed intracellular extract. The purified extracellular and intracellular enzymes had similar properties and essentially the same specific activity, 79 enzyme units/mg. of protein. 5. Extracellular exo-β-glucanase of H. anomala was purified 600-fold. 6. The optimum pH of the enzymes from F. fragilis, S. cerevisiae and H. anomala was 5·5 in each case. Chromatographic evidence indicated that the three enzymes remove glucosyl units sequentially from laminarin as well as pustulan. 7. The ratio of activities towards laminarin and pustulan remained constant during purification of the exo-β-glucanase obtained from the three species, suggesting a single enzyme. Additional evidence for its unienzymic nature are: (i) the two activities were destroyed at exactly the same rate on heating of the purified enzyme from F. fragilis at three different temperatures; (ii) the competitive inhibitor glucono-δ-lactone gave the same value of Ki when tested with either substrate; (iii) quantitative application of the `mixed-substrate' method with the purified enzyme of S. cerevisiae gave data that were in excellent agreement with those calculated on the assumption of a single enzyme. 8. The purified exo-β-glucanases of the different species of yeast had different kinetic constants. The ratios of maximal velocities and Km values with laminarin and pustulan differed markedly. Comparison of Vmax. and Km values suggests that the rapid release of spores from asci in F. fragilis might be explained in terms of an enzyme with higher maximal velocity and higher affinity to the ascus wall than that present in baker's yeast. 9. The estimated molecular weights for exo-β-glucanases from F. fragilis, S. cerevisiae and H. anomala were 22000, 40000 and 30000 respectively. 相似文献
989.
990.
Mechanism of repression of methionine biosynthesis in Escherichia coli. II. The effect of metJ mutations on the free amino acid pool 总被引:2,自引:0,他引:2
Summary Ethionine-resistant mutants (metJ mutants) were isolated and characterized as constitutive in the biosynthesis of methionine. Such mutations resulted in marked differences or alterations in the free amino acid pool. In some strains the levels of threonine and histidine were elevated by as much as 13 and 22 times that of the wild type level. The possibility that structural modifications of methionyl-tRNA were giving rise to constitutive methionine biosynthesis and the apparent aberrations in the free amino acid pool, was in large part ruled out by a comparison of the mobilities of wild type and mutant methionyl-tRNA on benzoylated DEAE-cellulose columns. The results obtained are consistent with the view that the product of the metJ locus is a repressor protein which is directly involved in the repression of the methionine genes. 相似文献