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Pyropheophytin a accompanies pheophytin a in darkened light grown cells of Euglena [PDF]
Rüdiger, W. +4 more
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Glutamate dehydrogenase-malate dehydrogenase complex
Archives of Biochemistry and Biophysics, 1979Abstract Kinetic and Sephadex gel filtration epxeriments indicate that in the presence of palmitoyl-CoA, glutamate dehydrogenase forms a complex with mitochondrial malate dehydrogenase. In this complex, palmitoyl-CoA is bound to glutamate dehydrogenase but is not bound to malate dehydrogenase.
L A, Fahien, E, Kmiotek, L, Smith
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Stability of dehydrogenases III. malate dehydrogenases
Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 1982Cytoplasmic and mitochondrial malate dehydrogenases from pig and chicken were studied by chemical modification of amino groups, hybridization of immobilization. Determination of thermal stability was used to characterize the different species. Modification of amino groups was found to decrease thermal stability especially when neutralization of the ...
J, Müller, C, Klein
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Heterogeneity of supernatant malate dehydrogenase
Biochimica et Biophysica Acta (BBA) - Enzymology, 1968Abstract A way was found to demonstrate electrophoretically that the supernatant portion of pig heart malate dehydrogenase ( l -malate:NAD oxidoreductase, EC 1.1.1.37) is heterogeneous. Other pig organs displayed the same pattern of supernatant malate dehydrogenase forms.
R J, Kulick, F W, Barnes
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Stabilization of halophilic malate dehydrogenase
Journal of Molecular Biology, 1989Malate dehydrogenase from the extreme halophile, Halobacterium marismortui, is stable only in highly concentrated solutions of certain salts. Previous work has established that its physiological environment is saturated in KCl; it remains soluble is saturated NaCl or KCl solutions; also it unfolds in solutions containing less than 2.5 M-NaCl or -KCl ...
G, Zaccai +4 more
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Malate dehydrogenase in leaf peroxisomes
Biochimica et Biophysica Acta (BBA) - Enzymology, 1969Abstract The technique of isopycnic centrifugation of leaf homogenates has allowed a separation of chloroplasts, mitochondria, and peroxisomes according to their respective densities. Chlorophyll, cytochrome c oxidase, and glycolate oxidase, respectively, were used as markers for these organeles. Malate dehydrogenase ( l -malate; NAD oxidoreductase,
R K, Yamazaki, N E, Tolbert
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