Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: EC:1.9.3.1 (cytochrome oxidase)
8,822 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The activity of cytochrome oxidase in tissues was decreased in short-term adaptation to reduce pO2 and administration of KCN in small doses. In the former case the activities of peroxidase and catalase were increased in blood. These effects as well as administration of Na2ATP into rats led to an increase in water content in tissues, to soption of acidic vital stain (phenol red) and to decrease in the ether-soluble fraction of lipids. The alterations were accompanied by decreased permeability of cells to n-hexane (estimation by gas-liquid chromatography). The decrease in cell permeability for nonelectrolytes was apparently due to conformational alterations in protein molecule of cytoplasmic membranes.
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PMID:[Hypoxia and tissue permeability for non-electrolytes]. 19 82

Isolated bovine heart cytochrome oxidase has been extracted into n-hexane, probably in reverse micelles, by the use of asolectin and calcium. The diluted extracts are composed of particles with the hydrodynamic radius of 42 nm. Spectral characteristics of the extracted oxidase are similar to those in aqueous solutions. At the high molar ratio of water to phospholipid (W0 = 8) in an organic solvent both cytochrome a and a3 are reducible and oxygen uptake is observed. However, at low W0 (W0 = 1.8) the rate of cytochrome a reduction is decreased and reduction of cytochrome a3 is inhibited.
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PMID:Spectral and catalytic properties of cytochrome oxidase in organic solvents. 217 45

Plasma membranes were isolated and separated from thylakoid membranes by discontinuous sucrose density gradient centrifugation of crude membranes prepared by French pressure cell extrusion of lysozyme-treated Anacystis nidulans. Two distinct populations of chlorophyll-free plasma membrane vesicles were obtained exhibiting buoyant densities of 1.087 and 1.100 g/cm3 as opposed to a uniform density of 1.192 g/cm3 for thylakoid membranes. Plasma and thylakoid membranes were characteristically different also with respect to fatty acid and protein composition, cytochrome oxidase activity, and pigment content as analyzed by spectrophotometry, spectrofluorimetry, and high performance liquid chromatography. Apart from carotenoids, chlorophyll a was the only major photosynthetic pigment detected in thylakoid membranes while plasma membranes contained virtually no chlorophyll a but (besides large amounts of carotenoids) protochlorophyllide a and chlorophyllide a as revealed by solvent partition (between n-hexane and acetone or methanol), room and low temperature fluorescence emission and excitation spectra, and analytical separation and identification by high performance liquid chromatography and comparison with authentic standards. The protochlorophyllide in the plasma membrane could be transformed into chlorophyllide in the dark in vitro by incubating the membrane preparation with NADPH; NADP+ effected the reverse transition.
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PMID:Chlorophyll precursors in the plasma membrane of a cyanobacterium, Anacystis nidulans. Characterization of protochlorophyllide and chlorophyllide by spectrophotometry, spectrofluorimetry, solvent partition, and high performance liquid chromatography. 250 Dec 98

Surgical cardiac denervation was carried out in dogs under halothane anaesthesia. In a paired experimental design control biopsy specimens were obtained before surgical denervation. The dogs were allowed to recover and three weeks to elapse before the second biopsy specimen was taken. Both right and left ventricular specimens had higher in vitro oxygen consumption after denervation than before. Other specimens were immediately cooled in hexane at -60 degrees C and stored under liquid nitrogen until analysed. Succinate dehydrogenase and cytochrome oxidase activities were then measured histochemically in sequential 10 or 12 microns sections. There was no significant difference between the enzyme activities measured before or after cardiac denervation (succinate dehydrogenase 20.3(6.3) before, 19.4(4.02) pmol.H2.cm-2.s-1, after; cytochrome oxidase 223(73.4) before, 263(61.6) (measured as extinction coefficient) after). Thus the changes in oxygen consumption in the chronically denervated dog heart are not due to any lack of these mitochondrial enzymes.
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PMID:Effect of lack of noradrenaline on myocardial oxygen consumption in denervated dog hearts. 282 57

Blocks of tissue from various organs of the rat have been chilled by precipitate immersion in n-hexane cooled to -70 degrees C, and then stored at -70 degrees C. At various intervals (up to 14 days) after chilling, cryostat sections were prepared from these blocks and assayed for the activity of a variety of enzymes. Enzyme activity was measured by scanning and integration microdensitometry. With the exception of acid phosphatase and cytochrome oxidase, all enzymes assayed were stable for at least 7 days after storage at -70 degrees C and most were stable for 14 days, Storage of fresh-frozen sections at -30 degrees C in the cabinet of the cryostat, for up to 24 h, had little effect on enzyme activity.
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PMID:The influence on enzyme activity of storage of tissue blocks at -70 degrees C. 729 88