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By Alton Meister

Advances in Enzymology and similar parts of Molecular Biology is a seminal sequence within the box of biochemistry, supplying researchers entry to authoritative stories of the newest discoveries in all parts of enzymology and molecular biology. those landmark volumes date again to 1941, offering an unmatched view of the historic improvement of enzymology. The sequence bargains researchers the newest knowing of enzymes, their mechanisms, reactions and evolution, roles in advanced organic approach, and their software in either the laboratory and undefined. each one quantity within the sequence positive aspects contributions by way of best pioneers and investigators within the box from around the globe. All articles are rigorously edited to make sure thoroughness, caliber, and clarity.

With its wide variety of themes and lengthy old pedigree, Advances in Enzymology and comparable components of Molecular Biology can be utilized not just by means of scholars and researchers in molecular biology, biochemistry, and enzymology, but in addition via any scientist drawn to the invention of an enzyme, its houses, and its purposes.

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Reduced catalytically with hydrogen. 27, 1 . 5 1 1 . 6, 3 . 6, 2 . 72, 0 . 86" P:O observed TABLE V Efficiencies of Oxidative Phosphorylation in Isolated Mitochondria 377-380 380 377 377 380,384 377,379 384 377 377,378 119,121,123 378,381 382 383 Ref. 0. These data are explained on the assumption that phosphorylations occur a t different levels in the transfer of electrons between substrate and oxygen. As shown in Fig. 5, one phosphorylation is believed to occur in the trangfer of electrons between D P N H and flavoprotein, another between flavoprotein and cytochrome c, and a third during the oxidation of cytochrome c.

This was shown to be due to the fact that cysteine was converted to thiazolidine carboxylic acid, which was oxidized by the mitochondria to N-formylcysteine (Fig. 4). O : (CHa)2NCH&OOH Dimethylglycine I I CHaNHCHzCOOH Sarcosine CHzOH NHzCCOOH / + HCHO 4 NHzCHpCOOH HCHO H Serine I Glycine H H HC-CCOOH H H HC-CCOOH I NHI H8 I I L-cysteine I t S I NH HC=O N-Formylcysteine L-Thiazolidinecarboxylic acid Fig. 4. Metabolism of glycine and its methyl derivatives in mitochondria. The oxidation of the terminal carbon (C-26) of the cholesterol side chain to COz was reported by Frederickson et al.

5 1 1 . 6, 3 . 6, 2 . 72, 0 . 86" P:O observed TABLE V Efficiencies of Oxidative Phosphorylation in Isolated Mitochondria 377-380 380 377 377 380,384 377,379 384 377 377,378 119,121,123 378,381 382 383 Ref. 0. These data are explained on the assumption that phosphorylations occur a t different levels in the transfer of electrons between substrate and oxygen. As shown in Fig. 5, one phosphorylation is believed to occur in the trangfer of electrons between D P N H and flavoprotein, another between flavoprotein and cytochrome c, and a third during the oxidation of cytochrome c.

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