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IN VITRO STUDIES OF P(32) UPTAKE IN MOUSE LIVER MITOCHONDRIA

Isolated mouse liver mitochondria were incubated in two types of P(32)-labelled sucrose-phosphate buffers. The first contained no added ATP or oxidizable substrate. The second contained added ATP. Samples were taken at specified times, up to 60 minutes, and analyses were made of the mitochondrial TC...

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Detalles Bibliográficos
Autor principal: Edmunds, Arthur B.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1959
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2194924/
https://www.ncbi.nlm.nih.gov/pubmed/13620888
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author Edmunds, Arthur B.
author_facet Edmunds, Arthur B.
author_sort Edmunds, Arthur B.
collection PubMed
description Isolated mouse liver mitochondria were incubated in two types of P(32)-labelled sucrose-phosphate buffers. The first contained no added ATP or oxidizable substrate. The second contained added ATP. Samples were taken at specified times, up to 60 minutes, and analyses were made of the mitochondrial TCA-soluble inorganic P(32) and the total mitochondrial residue P(31) and P(32). The results of the analyses showed that when the phosphorus inhibition index (the ratio of the amount of incubation inorganic phosphorus to the square of the amount of tyrosine in the mitochondria) was high, inorganic P(32) uptake was low and vice versa. In accordance with established data, increased P(32) uptake was obtained when ATP was added. ATP was found to stabilize the turnover of TCA-insoluble residue phosphorus as well as to maintain the TCA-soluble orthophosphate pool. These results support findings regarding the inhibitory and controlling effects of incubation medium phosphate in the regulation of inorganic phosphorus uptake.
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spelling pubmed-21949242008-04-23 IN VITRO STUDIES OF P(32) UPTAKE IN MOUSE LIVER MITOCHONDRIA Edmunds, Arthur B. J Gen Physiol Article Isolated mouse liver mitochondria were incubated in two types of P(32)-labelled sucrose-phosphate buffers. The first contained no added ATP or oxidizable substrate. The second contained added ATP. Samples were taken at specified times, up to 60 minutes, and analyses were made of the mitochondrial TCA-soluble inorganic P(32) and the total mitochondrial residue P(31) and P(32). The results of the analyses showed that when the phosphorus inhibition index (the ratio of the amount of incubation inorganic phosphorus to the square of the amount of tyrosine in the mitochondria) was high, inorganic P(32) uptake was low and vice versa. In accordance with established data, increased P(32) uptake was obtained when ATP was added. ATP was found to stabilize the turnover of TCA-insoluble residue phosphorus as well as to maintain the TCA-soluble orthophosphate pool. These results support findings regarding the inhibitory and controlling effects of incubation medium phosphate in the regulation of inorganic phosphorus uptake. The Rockefeller University Press 1959-01-20 /pmc/articles/PMC2194924/ /pubmed/13620888 Text en Copyright © Copyright, 1959, by The Rockefeller Institute This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Edmunds, Arthur B.
IN VITRO STUDIES OF P(32) UPTAKE IN MOUSE LIVER MITOCHONDRIA
title IN VITRO STUDIES OF P(32) UPTAKE IN MOUSE LIVER MITOCHONDRIA
title_full IN VITRO STUDIES OF P(32) UPTAKE IN MOUSE LIVER MITOCHONDRIA
title_fullStr IN VITRO STUDIES OF P(32) UPTAKE IN MOUSE LIVER MITOCHONDRIA
title_full_unstemmed IN VITRO STUDIES OF P(32) UPTAKE IN MOUSE LIVER MITOCHONDRIA
title_short IN VITRO STUDIES OF P(32) UPTAKE IN MOUSE LIVER MITOCHONDRIA
title_sort in vitro studies of p(32) uptake in mouse liver mitochondria
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2194924/
https://www.ncbi.nlm.nih.gov/pubmed/13620888
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