Porphyrinogen carboxylyase. Studies on the existence of isoenzymes.

Porphyrinogen carboxylyase from normal rat liver was subjected to purification methods. Two different purification protocols were used. In both cases, the initial steps consisted in obtaining a liver homogenate, followed by centrifugation, salt precipitation and phosphate gel absorption. Scheme I co...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autor principal: Ríos de Molina, M.C
Otros Autores: Chaufan, G., Iglesias, S., Billi de Catabbi, S., San Martín de Viale, L.C
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 1996
Acceso en línea:Registro en Scopus
Handle
Registro en la Biblioteca Digital
Aporte de:Registro referencial: Solicitar el recurso aquí
LEADER 03437caa a22005177a 4500
001 PAPER-3427
003 AR-BaUEN
005 20230518203253.0
008 190411s1996 xx ||||fo|||| 00| 0 eng|d
024 7 |2 scopus  |a 2-s2.0-0030325438 
024 7 |2 cas  |a porphyrin, 24869-67-8; porphyrinogen, 4396-11-6; Isoenzymes; Porphyrinogens; Porphyrins 
040 |a Scopus  |b spa  |c AR-BaUEN  |d AR-BaUEN 
100 1 |a Ríos de Molina, M.C. 
245 1 0 |a Porphyrinogen carboxylyase. Studies on the existence of isoenzymes. 
260 |c 1996 
270 1 0 |m Ríos de Molina, M.C. 
506 |2 openaire  |e Política editorial 
520 3 |a Porphyrinogen carboxylyase from normal rat liver was subjected to purification methods. Two different purification protocols were used. In both cases, the initial steps consisted in obtaining a liver homogenate, followed by centrifugation, salt precipitation and phosphate gel absorption. Scheme I consisted in then submitted the preparation to DEAE-cellulose, followed by Sephacryl S-200 and Phenyl-sepharose sequential column chromatographies. Scheme II involved an affinity column followed by a Sephadex G-75 gel filtration column. In both cases, the enzyme was stored at -20 degrees C until its assay. The addition of 2mM dithiotreytol to the incubation media or to the enzyme extract before storage, did not help improve the activity nor the stability of the enzyme. Those fractions containing the maximal enzyme activity, detected using Uroporphyrinogen III or Pentacarboxy-porphyrinogen III as substrate, were not always present in the same tubes for the different columns employed. In addition, the degree of purification obtained in some steps was different according to the substrate employed. The results suggest the existence of at least two isoenzymes for rat liver porphyrinogen carboxy-lyase.  |l eng 
593 |a Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Argentina 
690 1 0 |a ISOENZYME 
690 1 0 |a PORPHYRIN 
690 1 0 |a PORPHYRINOGEN 
690 1 0 |a ANIMAL 
690 1 0 |a ARTICLE 
690 1 0 |a COMPARATIVE STUDY 
690 1 0 |a ENZYMOLOGY 
690 1 0 |a ISOLATION AND PURIFICATION 
690 1 0 |a LIVER 
690 1 0 |a METABOLISM 
690 1 0 |a RAT 
690 1 0 |a ANIMALS 
690 1 0 |a ISOENZYMES 
690 1 0 |a LIVER 
690 1 0 |a PORPHYRINOGENS 
690 1 0 |a PORPHYRINS 
690 1 0 |a RATS 
700 1 |a Chaufan, G. 
700 1 |a Iglesias, S. 
700 1 |a Billi de Catabbi, S. 
700 1 |a San Martín de Viale, L.C. 
773 0 |d 1996  |g v. 46  |h pp. 265-275  |k n. 4  |p Acta Physiol Pharmacol Ther Latinoam  |x 03276309  |w (AR-BaUEN)CENRE-1948  |t Acta physiologica, pharmacologica et therapeutica latinoamericana : órgano de la Asociación Latinoamericana de Ciencias Fisiológicas y [de] la Asociación Latinoamericana de Farmacología 
856 4 1 |u https://www.scopus.com/inward/record.uri?eid=2-s2.0-0030325438&partnerID=40&md5=16c26c137aa18d2211cf5592fd479a34  |y Registro en Scopus 
856 4 0 |u https://hdl.handle.net/20.500.12110/paper_03276309_v46_n4_p265_RiosdeMolina  |y Handle 
856 4 0 |u https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03276309_v46_n4_p265_RiosdeMolina  |y Registro en la Biblioteca Digital 
961 |a paper_03276309_v46_n4_p265_RiosdeMolina  |b paper  |c PE 
962 |a info:eu-repo/semantics/article  |a info:ar-repo/semantics/artículo  |b info:eu-repo/semantics/publishedVersion