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Showing 1 to 8 of 8 for “"DCCD"”.

  1. Double-Change Covering Designs with Block Size k = 4

    A double-change covering design (dccd) is an ordered set of blocks with block size k is an ordered collection of b blocks, B = {B1,B2, · · · ,Bb}, each an unordered subset of k distinct elements from [v] = {1, 2, · · · , v}, which obey: (1) each block differs from the previous block by two …

    siu-theses Repository record for Double-Change Covering Designs with Block Size k = 4 (opens in a new tab)

  2. Properties of Conductance and Inhibition of Proton Channels: M2 from Influenza A Virus and Fo from Escherichia coli ATP Synthase

    … deletion strain, the single-hit hypothesis of DCCD inhibition of passive proton flux through Fo was examined. A DCCD-induced reduction in ATP synthase activity correlates with a reduction in the total initial slope, the number of functional Fo per µg protein, and the single channel proton flux. …

    byu Repository record for Properties of Conductance and Inhibition of Proton Channels: M2 from Influenza A Virus and Fo from Escherichia coli ATP Synthase (opens in a new tab)

  3. Guard Cell Regulation of Stomatal Response: Chloroplast Function and Abscisic Acid Metabolism in Guard Cells of Commelina Communis and Vicia Faba

    … activity, DBMIB-sensitive electron transport and DCCD-sensitive relaxation of the electric field associated with photophosphorylation. These results indicate that guard cell chloroplasts, although reported to lack Calvin-Benson cycle enzymes, are photosynthetically competent with respect to …

    uiuc Repository record for Guard Cell Regulation of Stomatal Response: Chloroplast Function and Abscisic Acid Metabolism in Guard Cells of Commelina Communis and Vicia Faba (opens in a new tab)

  4. Proton-atpase in fish gills

    … by other proton-ATPase blockers such as DCCD, DES,PCMBS and Bafilomycins. It was concluded, therefore, that the NEM-sensitive ATPase activity was generated by a proton-translocating ATPase. Since this NEM-sensitive ATPase was also sensitive to the plasma membrane ATPase inhibitor …

    ubc Repository record for Proton-atpase in fish gills (opens in a new tab)

  5. Study on polypeptides of cyanobacterial photosystem 2

    … to be related , in terms of homology, to a 20kDa DCCD-binding protein of plants which is thought to be a LHC protein.

    cent-lancashire Repository record for Study on polypeptides of cyanobacterial photosystem 2 (opens in a new tab)

  6. Die außergewöhnliche Diversität der der Proteolipide in Archaea: Multimere und monomere Rotoren mit sechs bis dreizehn Ionenbindestellen in A1AO-ATPasen

    … von E. coli DK8 betrug 150 mU/mg Protein. 13. DCCD und der für archäelle ATPasen spezifische Inhibitor DES hemmten das Enzym. Die I50-Wert betrugen 0,5 mM/mg Protein, beziehungsweise 200 nmol/mg Protein. 14. Die Synthese von AhaA, AhaB, AhaC, AhaE, AhaH, AhaK, und zum ersten Mal auch des …

    lmu-germany Repository record for Die außergewöhnliche Diversität der der Proteolipide in Archaea: Multimere und monomere Rotoren mit sechs bis dreizehn Ionenbindestellen in A1AO-ATPasen (opens in a new tab)

  7. Intrinsic uncoupling in the ATP synthase of Escherichia coli. Studies on WT and ε-truncated mutants

    … as well. First of all, we have shown that the DCCD-sensitive ATP hydrolysis activity of E.coli internal membranes was strongly inhibited by ADP and Pi, with a half-maximal effect in the submicromolar range for ADP and at 140 µM for Pi. In contrast to this monotonic inhibition, however, the …

    bologna Repository record for Intrinsic uncoupling in the ATP synthase of Escherichia coli. Studies on WT and ε-truncated mutants (opens in a new tab)

  8. Molecular Modulation of a-Subunit VISIT-DG Sequence Residue Asp-350 in the Catalytic sites of <em>Escherichia coli</em> ATP Synthase.

    <p>ATP Synthase is the fundamental means of cellular energy production in animals, plants, and almost all microorganisms. In order to understand the mechanism of ATP catalysis, critical amino acid residues involved in Pi binding have to be identified. The αVISIT-DG sequence at the interface of α/β …

    etsu Repository record for Molecular Modulation of a-Subunit VISIT-DG Sequence Residue Asp-350 in the Catalytic sites of <em>Escherichia coli</em> ATP Synthase. (opens in a new tab)