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RESPIRATORY PATHWAYS IN THEMYCOPLASMAI
Author(s) -
Susan Smith,
P. J. Van Demark,
J. Fabricant
Publication year - 1963
Publication title -
journal of bacteriology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.652
H-Index - 246
eISSN - 1067-8832
pISSN - 0021-9193
DOI - 10.1128/jb.86.5.893-897.1963
Subject(s) - biology , nicotinamide adenine dinucleotide , flavin adenine dinucleotide , biochemistry , nicotinamide adenine dinucleotide phosphate , reductase , thiamine pyrophosphate , mycoplasma gallisepticum , nicotinamide , dehydrogenase , oxidase test , enzyme , cofactor , mycoplasma , nad+ kinase , microbiology and biotechnology
Smith , S. L. (Cornell University, Ithaca, N.Y.), P. J.Van Demark, and J. Fabricant . Respiratory pathways in theMycoplasma . I. Lactate oxidation byMycoplasma gallisepticum . J. Bacteriol.86: 893–897. 1963.—Resting cells ofMycoplasma gallisepticum 293 required the addition of nicotinamide adenine dinucleotide, thiamine pyrophosphate, and flavine mononucleotide for the maximal rate of sodium lactate oxidation. Inhibitor studies, as well as spectrophotometric and chemical assays, indicate that the pathway of electron transport to oxygen during lactate oxidation does not involve heme catalysts, and is mediated by flavin-linked enzyme systems. The presence of reduced nicotinamide adenine dinucleotide-specific lactic dehydrogenase, menadione reductase, ferricyanide reductase, and reduced nicotinamide adenine dinucleotide oxidase activities was detected in cell-free extracts. No cytochromec reductase or reduced nicotinamide adenine dinucleotide peroxidase activity was detected in these extracts.

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