Publikationsansicht

Phenoxazinone synthase from Streptomyces antibioticus: Purification of the large and small enzyme forms (1981)

Abstract
Phenoxazinone synthase has been purified approximately 80-fold from 48-h-old cells of Streptomyces antibioticus. The purification procedure involves streptomycin sulfate and ammonium sulfate precipitations, affinity and Bio-Gel chromatography, and glycerol gradient centrifugation. Two forms of the enzyme are purified by these techniques, a large form (L) with a molecular weight of around 900,000 and a small form (S) with an Mr of about 200,000. Electrophoresis of the large and small forms on sodium dodecyl sulfate-polyacrylamide gels reveals the presence of a single polypeptide chain with a molecular weight of around 100,000. Both L and S appear to be distinct molecular forms of the enzyme since rechromatography on Bio-Gel or recentrifugation on glycerol gradients results in retention of the mobility of the form in question. These procedures do not convert L to S or S to L. The purification procedure described has been used for the preparation of phenoxazinone synthase from 12-, 18-, and 48-h cultures of S. antibioticus. These experiments have shown that the relative amounts of L and S which can be isolated depend on the age of the cells used as starting material. As the cultures age, the relative amount of L which is present increases. This result also suggests that L and S are distinct molecular entities. Antibody to a combined L plus S preparation and to L has been raised in rabbits. Anti-L antibody reacts with both L and S and is capable of completely inhibiting phenoxazinone synthase activity in crude extracts of S. antibioticus cells. Thus, the 100,000 Mr subunits of L and S must have some antigenic determinants in common, although they may not be identical in structure. Oxygen consumption during the formation of cinnabarinic acid from 3-hydroxyanthranilic acid was measured with the Clark oxygen electrode. These experiments showed that both L and S catalyze a reaction involving the consumption of 1.5 mol of oxygen per mole of phenoxazinone formed.. Peer Reviewed. http://deepblue.lib.umich.edu/bitstream/2027.42/24238/1/0000501.pdf

Details der Publikation
Download , http://www.sciencedirect.com/science/article/B6WB5-4DN45BC-SS/2/9b2a4fb1dd4d8df3e381f0a0204e91fd
http://hdl.handle.net/2027.42/24238
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=7305384&dopt=citation
http://dx.doi.org/10.1016/0003-9861(81)90429-X
Herausgeber Elsevier
Mitarbeiter Department of Cellular and Molecular Biology, Division of Biological Sciences, The University of Michigan, Ann Arbor, Michigan 48109, USA, Department of Cellular and Molecular Biology, Division of Biological Sciences, The University of Michigan, Ann Arbor, Michigan 48109, USA
Archiv University of Michigan (United States)
Keywords Public Health, Chemistry, Chemical Engineering, Biological Chemistry, Engineering, Science, Health Sciences
Sprache Englisch