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9 1973). [Continuous oscillations require a precisely controlled input of reducing equivalents to the system and can more easily be obtained in a cell-free extract of glycolytic enzymes (Fig. 10)]. This phenomenon of sustained oscillations in yeast cells has led to a much better understanding of metabolic regulation Yeast Extract Type TZ (72hr) 340-400m/i K- 30 min—H FIGURE 10. A sustained oscillation of NADH in an extract of cytoplasmic constituents of the Saccharomyces carlsbergensis. The oscillation was initiated by the addition of glucose.

The unit in the membrane appears to be a dimer of some 240,000 daltons, although it is shown as a monomer in the diagram of Fig. 15. The extension of the molecule beyond the membrane is rather large; it is approximately twice the membrane thickness. , 1978). 34 Brition Chance et cd. Cytochrome Oxidase in Membranes Outside Lipid Molecules 50A Membrane Inside 4H+ Of ►H20 MD 493 ß FIGURE 14. , in press). ^ 1977) and discussed in detail in this volume by G. Schatz. 0 (Wikstrom and Saari, 1976). THE FUNCTION OF CYTOCHROME OXIDASE The function of cytochrome oxidase has so far been limited to an evaluation of its effectiveness as a cytochrome c oxidase and this is the only enzymatic function that could be monitored, except for the non-enzymatic ligand binding which is unlikely to afford a functional test of electron transfer in the oxidase.

The non-constant oscillatory responses of cytoplasmic NADH afford principles of metabolic regulation and feedback control that have been generally useful in biochemistry. The alternate pathway of cytochrome oxidase so effectively utilized in yeast set the background for current studies of peroxide metabolism in liver. So let the lesson be: If you wish to make explorations of physiological and biochemical reactions in a reproducible biological system^ yeast usually can do it better. This also seems to apply to our studies of cytochrome oxidase which are described below.

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