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...
Guardado en:
Autores principales: | , , , , |
---|---|
Formato: | JOUR |
Materias: | |
Acceso en línea: | http://hdl.handle.net/20.500.12110/paper_03276309_v46_n4_p265_RiosdeMolina |
Aporte de: |
id |
todo:paper_03276309_v46_n4_p265_RiosdeMolina |
---|---|
record_format |
dspace |
spelling |
todo:paper_03276309_v46_n4_p265_RiosdeMolina2023-10-03T15:24:58Z Porphyrinogen carboxylyase. Studies on the existence of isoenzymes. Ríos de Molina, M.C. Chaufan, G. Iglesias, S. Billi de Catabbi, S. San Martín de Viale, L.C. isoenzyme porphyrin porphyrinogen animal article comparative study enzymology isolation and purification liver metabolism rat Animals Isoenzymes Liver Porphyrinogens Porphyrins Rats 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. Fil:Ríos de Molina, M.C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Chaufan, G. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Iglesias, S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Billi de Catabbi, S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:San Martín de Viale, L.C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_03276309_v46_n4_p265_RiosdeMolina |
institution |
Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-134 |
collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
topic |
isoenzyme porphyrin porphyrinogen animal article comparative study enzymology isolation and purification liver metabolism rat Animals Isoenzymes Liver Porphyrinogens Porphyrins Rats |
spellingShingle |
isoenzyme porphyrin porphyrinogen animal article comparative study enzymology isolation and purification liver metabolism rat Animals Isoenzymes Liver Porphyrinogens Porphyrins Rats Ríos de Molina, M.C. Chaufan, G. Iglesias, S. Billi de Catabbi, S. San Martín de Viale, L.C. Porphyrinogen carboxylyase. Studies on the existence of isoenzymes. |
topic_facet |
isoenzyme porphyrin porphyrinogen animal article comparative study enzymology isolation and purification liver metabolism rat Animals Isoenzymes Liver Porphyrinogens Porphyrins Rats |
description |
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. |
format |
JOUR |
author |
Ríos de Molina, M.C. Chaufan, G. Iglesias, S. Billi de Catabbi, S. San Martín de Viale, L.C. |
author_facet |
Ríos de Molina, M.C. Chaufan, G. Iglesias, S. Billi de Catabbi, S. San Martín de Viale, L.C. |
author_sort |
Ríos de Molina, M.C. |
title |
Porphyrinogen carboxylyase. Studies on the existence of isoenzymes. |
title_short |
Porphyrinogen carboxylyase. Studies on the existence of isoenzymes. |
title_full |
Porphyrinogen carboxylyase. Studies on the existence of isoenzymes. |
title_fullStr |
Porphyrinogen carboxylyase. Studies on the existence of isoenzymes. |
title_full_unstemmed |
Porphyrinogen carboxylyase. Studies on the existence of isoenzymes. |
title_sort |
porphyrinogen carboxylyase. studies on the existence of isoenzymes. |
url |
http://hdl.handle.net/20.500.12110/paper_03276309_v46_n4_p265_RiosdeMolina |
work_keys_str_mv |
AT riosdemolinamc porphyrinogencarboxylyasestudiesontheexistenceofisoenzymes AT chaufang porphyrinogencarboxylyasestudiesontheexistenceofisoenzymes AT iglesiass porphyrinogencarboxylyasestudiesontheexistenceofisoenzymes AT billidecatabbis porphyrinogencarboxylyasestudiesontheexistenceofisoenzymes AT sanmartindevialelc porphyrinogencarboxylyasestudiesontheexistenceofisoenzymes |
_version_ |
1782030088549695488 |