Saccharomyces cerevisiae porphobilinogenase: Some physical and kinetic properties

1. 1. Properties of porphobilinogenase (PBGase), the enzyme complex converting porphobilinogen (PBG) into uroporphyrinogens, were studied in a wild strain, D273-10B and a mutant, B231, of Saccharomyces cerevisiae 2. 2. A well-defined maximum of enzyme activity was observed for the mutant strain afte...

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Autor principal: Araujo, L.S
Otros Autores: Lombardo, M.E, Rossetti, ]M.V, Batlle, A.M.d.C
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 1989
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PH
Acceso en línea:Registro en Scopus
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024 7 |2 cas  |a magnesium, 7439-95-4; porphobilinogenase, 9055-40-7; sodium, 7440-23-5; Ammonia-Lyases, EC 4.3.1.; Magnesium, 7439-95-4; porphobilinogenase, EC 5.-; Sodium, 7440-23-5 
040 |a Scopus  |b spa  |c AR-BaUEN  |d AR-BaUEN 
100 1 |a Araujo, L.S. 
245 1 0 |a Saccharomyces cerevisiae porphobilinogenase: Some physical and kinetic properties 
260 |c 1989 
270 1 0 |m Batlle, A.M.d.C.; Centro de Investigaciones sobre Porfirinas y Porfirias, CIPYP (CONICET-FCEN, UBA), Ciudad Universitaria, Pabellon II, 2do. Piso, 1428 Buenos Aires, Argentina 
506 |2 openaire  |e Política editorial 
504 |a Araujo, Lombardo, Rossetti, Batlle, Porphobilinogenase activity in a wild strain and its haem mutant of Saccharomyces cerevisiae (1987) Revta argent., 19, pp. 109-120 
504 |a Arrese, Carvajal, Robison, Sambunaris, Panek, Mattoon, Cloning of the δ-aminolevulinic acid synthase structural gene in yeast (1983) Curr. Genet., 7, pp. 175-183 
504 |a Batlle, Llambias, Wider de Xifra, Tigier, Porphyrin biosynthesis in the soybean callus tissue system—XV. The effect of growth conditions (1975) Int. J. Biochem., 6, pp. 591-606 
504 |a Bilinski, Litwinska, Lukaszkiewicz, Rytka, Simon, Labbe-Bois, Characterization of two mutant strains of Saccharomyces cerevisiae deficient in coproporphyrinogen 3-oxidase activity (1981) J. gen. Microbiol., 122, pp. 79-87 
504 |a Clement, Kohashi, Piper, Rat liver purification uroporphyrinogen III cosynthetase (1982) Archs Biochem. Biophys., 214, pp. 657-663 
504 |a Cornford, Transformation of porphobilinogen into porphyrins by preparations from human erythrocytes (1964) Biochem. J., 91, pp. 64-73 
504 |a Fumagalli, Rossetti, Juknat de Geralnik, Kotler, Batlle, Estudios sobre la PBGasa de hígado de cerdo (1982) An. Asoc. quím. argent., 70, pp. 375-382 
504 |a Juknat, Biosintesis de porfirinógenos (1983) Ph.D. Thesis, , University of Buenos Aires 
504 |a Juknat, Kotler, Koopmann, Batlle, Porphobilinogenase from Rhodopseudomonas palustris (1989) Comp. Biochem. Physiol., 92 B, pp. 291-295 
504 |a Labbe-Bois, Urban-Grimal, Volland, Camadro, Dehoux, About the regulation of protoheme synthesis in the yeast Saccharomyces cerevisiae (1983) Mitochondria, 523, p. 534 
504 |a Llambías, Batlle, Porphyrin biosynthesis in soybean-callus—V. The porphobilinogen deaminase-uroporphyrinogen cosynthetase system (1970) Kinetic studies, 220, pp. 552-559. , Biochim. biophys. Acta 
504 |a Llambías, Batlle, Studies on the porphobilinogen deaminase-uroporphyrinogen cosynthetase system of cultured soya-bean cells. (1971) Biochem J, 121, pp. 327-340 
504 |a Llambías, Batlle, Porphyrin biosynthesis—VIII. Avian erythrocyte porphibilinogen deaminase-uroporphyrinogen III cosynthetase (1971) Its purification, properties and the separation of its components, 227, pp. 180-191. , Biochim. biophys. Acta 
504 |a Lowry, Rosebrough, Farr, Randall, Protein measurement with the Folin phenol reagent (1951) J. biol. Chem., 193, pp. 265-275 
504 |a Mattoon, Malamud, Brunner, Braz, Carvajal, Lancanshire, Panek, Regulation of heme formation and cytochrome biosynthesis in normal and mutant yeast (1978) Biochemistry and Genetics of Yeast, Pure and Applied Aspects, pp. 317-337. , M. Bacila, B. Horecker, A.O.M. Stoppani, Academic Press, New York 
504 |a Moore, Labbe, Assays for ALA and PBG determination (1964) Clin. Chem., 10, pp. 1105-1109 
504 |a Rimington, Spectral-absorption coefficients of some porphyrins in the Soret-band region. (1960) Biochem J, 75, pp. 620-623 
504 |a Rossetti, Batlle, Polypirrol intermediates in porphyrin biosynthesis (1977) Studies with Euglena gracilis, 8, pp. 277-283. , Int. J. Biochem 
504 |a Rossetti, Lombardo, Juknat de Geralnik, Araujo, Batlle, Porphyrin biosynthesis in Euglena gracilis—V. Soluble and particulate PBG-ase (1986) Comp. Biochem. Physiol., 85 B, pp. 451-458 
504 |a Rossetti, Araujo, Lombardo, Correa Garcia, Batlle, Porphyrin biosynthesis in Euglena gracilis—VI. The effect of growth conditions on porphobilinogenase activity and further properties (1987) Comp. Biochem. Physiol., 87 B, pp. 593-600 
504 |a Rykta, Bilinski, Labbe-Bois, Modified uroporphyrinogen decarboxylase activity in yeast mutant which mimics porphyria cutanea tarda (1984) Biochem J., 218, pp. 405-413 
504 |a Sancovich, Batlle, Grinstein, Porphyrin biosynthesis—VI. Separation and purification of porphobilinogen deaminase and uroporphyrinogen isomerase from cow liver (1969) Porphobilinogenase as an allosteric enzyme, 191, pp. 130-143. , Biochim. biophys. Acta 
504 |a Sancovich, Ferramola, Batlle, Grinstein, Preparation of porphobilinogen (1970) Methods in Enzymology, 17 A, pp. 220-222. , H. Tabor, C.W. Tabor, Academic Press, New York 
504 |a Sancovich, Ferramola, Batlle, Kivilevich, Grinstein, Studies on cow liver porphobilinogen deaminase (1976) Acta physiol. latinoam., 26, pp. 376-386 
504 |a Sanders, Mied, Briquet, Hernández-Rodríguez, Gottal, Mattoon, Regulation of mitochondrial biogenesis: yeast mutants deficient in synthesis of δ-aminolevulinic acid (1973) J. molec. Biol., 80, pp. 17-39 
504 |a Urban-Grimal, Labbe-Bois, Genetic and biochemical characterization of mutants of Saccharomyces cerevisiae blocked in six different steps of heme biosynthesis (1981) Molec. Gen. Genet., 183, pp. 85-92 
504 |a Wider de Xifra, Batlle, Tigier, δ-aminolaevulinate synthetase in extracts of cultured soybean cells (1971) Biochimica et Biophysica Acta (BBA) - Enzymology, 235, pp. 511-517 
520 3 |a 1. 1. Properties of porphobilinogenase (PBGase), the enzyme complex converting porphobilinogen (PBG) into uroporphyrinogens, were studied in a wild strain, D273-10B and a mutant, B231, of Saccharomyces cerevisiae 2. 2. A well-defined maximum of enzyme activity was observed for the mutant strain after 20 hr of growth; whilst the activity in the wild strain did not vary significantly during growth. 3. 3. Neither PBG consumption nor uroporphyrinogen formation were modified by the presence of air either in the wild or in the mutant strain. 4. 4. In both the wild and mutant strains uroporphyrinogen formation increased linearly with both protein concentration and incubation time. 5. 5. The addition of a mixture of sodium and magnesium salts to the assay system inhibited the enzyme activity of both strains by 50% without modifying the isomer composition. 6. 6. The same optimum pH (7.4) and mol. wt (50,000 ± 5000) was found for the enzyme from both strains. 7. 7. The enzyme from both the wild and mutant strains shows Michaelis-Menten kinetics when isolated from cells at either the exponential or the stationary phases of growth. Accumulation of porphyrins and δ-aminolevulinic acid occurring during the exponential phase in the mutant strain, did not modify the kinetics. © 1989.  |l eng 
536 |a Detalles de la financiación: National Council for Scientific Research 
536 |a Detalles de la financiación: Consejo Nacional de Investigaciones Científicas y Técnicas 
536 |a Detalles de la financiación: Acknowledgements--M. V. Rossetti and A. M. del C. Batlle hold posts as Scientific Researchers in the Argentine National Research Council (CONICET). M. E. Lombardo is a Research Fellow from the University of Buenos Aires. This work was supported by grants from the CONICET, the SUBCYT, Secretaria de Salud POblica del Ministerio de Bienestar Social, Banco de la Naci6n Argentina and Banco de Galicia y Buenos Aires. This paper forms part of the Doctoral Thesis of L. S. Araujo to be presented to the University of Buenos Aires for her Ph.D. Degree. We wish to express our heartfelt thanks to Professor J. Mattoon, from the Department of Biochemistry, University of Colorado, USA, for generously providing us with all the strains of S. cerevisiae and above all for his continued interest and encouragement. The technical assistance of Mrs B. Riccillo de Aprea is gratefully acknowledged. 
593 |a Centro de Investigaciones sobre Porfirinas y Porfirias, CIPYP (CONICET-FCEN, UBA), Ciudad Universitaria, Pabellon II, 2do. Piso, 1428 Buenos Aires, Argentina 
690 1 0 |a AMMONIA LYASE 
690 1 0 |a AMMONIA LYASES 
690 1 0 |a MAGNESIUM 
690 1 0 |a PORPHOBILINOGENASE 
690 1 0 |a SODIUM 
690 1 0 |a ARTICLE 
690 1 0 |a ENZYMOLOGY 
690 1 0 |a GENETICS 
690 1 0 |a KINETICS 
690 1 0 |a METABOLISM 
690 1 0 |a MOLECULAR WEIGHT 
690 1 0 |a MUTATION 
690 1 0 |a SACCHAROMYCES CEREVISIAE 
690 1 0 |a AMMONIA-LYASES 
690 1 0 |a HYDROGEN-ION CONCENTRATION 
690 1 0 |a KINETICS 
690 1 0 |a MAGNESIUM 
690 1 0 |a MOLECULAR WEIGHT 
690 1 0 |a MUTATION 
690 1 0 |a SACCHAROMYCES CEREVISIAE 
690 1 0 |a SODIUM 
690 1 0 |a SUPPORT, NON-U.S. GOV'T 
650 1 7 |2 spines  |a PH 
700 1 |a Lombardo, M.E. 
700 1 |a Rossetti, ]M.V. 
700 1 |a Batlle, A.M.d.C. 
773 0 |d 1989  |g v. 92  |h pp. 297-301  |k n. 2  |x 03050491  |w (AR-BaUEN)CENRE-2752  |t Comparative Biochemistry and Physiology -- Part B: Biochemistry and 
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