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THE PRODUCTION OF HYDROGEN PEROXIDE BY HIGH OXYGEN PRESSURES
Hydrogen peroxide is formed in solutions of glutathione exposed to oxygen. This hydrogen peroxide or its precursors will decrease the viscosity of polymers like desoxyribonucleic acid and sodium alginate. Further knowledge of the mechanism of these chemical effects of oxygen might further the unders...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
1958
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2194850/ https://www.ncbi.nlm.nih.gov/pubmed/13525677 |
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author | Gilbert, Daniel L. Gerschman, Rebeca Ruhm, K. Barclay Price, William E. |
author_facet | Gilbert, Daniel L. Gerschman, Rebeca Ruhm, K. Barclay Price, William E. |
author_sort | Gilbert, Daniel L. |
collection | PubMed |
description | Hydrogen peroxide is formed in solutions of glutathione exposed to oxygen. This hydrogen peroxide or its precursors will decrease the viscosity of polymers like desoxyribonucleic acid and sodium alginate. Further knowledge of the mechanism of these chemical effects of oxygen might further the understanding of the biological effects of oxygen. This study deals with the rate of solution of oxygen and with the decomposition of hydrogen peroxide in chemical systems exposed to high oxygen pressures. At 6 atmospheres, the absorption coefficient for oxygen into water was about 1 cm./hour and at 143 atmospheres, it was about 2 cm./hour; the difference probably being due to the modus operandi. The addition of cobalt (II), manganese (II), nickel (II), or zinc ions in glutathione (GSH) solutions exposed to high oxygen pressure decreased the net formation of hydrogen peroxide and also the reduced glutathione remaining in the solution. Studies on hydrogen peroxide decomposition indicated that these ions act probably by accelerating the hydrogen perioxide oxidation of glutathione. The chelating agent, ethylenediaminetetraacetic acid disodium salt, inhibited the oxidation of GSH exposed to high oxygen pressure for 14 hours. However, indication that oxidation still occurred, though at a much slower rate, was found in experiments lasting 10 weeks. Thiourea decomposed hydrogen peroxide very rapidly. When GSH solutions were exposed to high oxygen pressure, there was oxidation of the GSH, which became relatively smaller with increasing concentrations of GSH. |
format | Text |
id | pubmed-2194850 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1958 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21948502008-04-23 THE PRODUCTION OF HYDROGEN PEROXIDE BY HIGH OXYGEN PRESSURES Gilbert, Daniel L. Gerschman, Rebeca Ruhm, K. Barclay Price, William E. J Gen Physiol Article Hydrogen peroxide is formed in solutions of glutathione exposed to oxygen. This hydrogen peroxide or its precursors will decrease the viscosity of polymers like desoxyribonucleic acid and sodium alginate. Further knowledge of the mechanism of these chemical effects of oxygen might further the understanding of the biological effects of oxygen. This study deals with the rate of solution of oxygen and with the decomposition of hydrogen peroxide in chemical systems exposed to high oxygen pressures. At 6 atmospheres, the absorption coefficient for oxygen into water was about 1 cm./hour and at 143 atmospheres, it was about 2 cm./hour; the difference probably being due to the modus operandi. The addition of cobalt (II), manganese (II), nickel (II), or zinc ions in glutathione (GSH) solutions exposed to high oxygen pressure decreased the net formation of hydrogen peroxide and also the reduced glutathione remaining in the solution. Studies on hydrogen peroxide decomposition indicated that these ions act probably by accelerating the hydrogen perioxide oxidation of glutathione. The chelating agent, ethylenediaminetetraacetic acid disodium salt, inhibited the oxidation of GSH exposed to high oxygen pressure for 14 hours. However, indication that oxidation still occurred, though at a much slower rate, was found in experiments lasting 10 weeks. Thiourea decomposed hydrogen peroxide very rapidly. When GSH solutions were exposed to high oxygen pressure, there was oxidation of the GSH, which became relatively smaller with increasing concentrations of GSH. The Rockefeller University Press 1958-05-20 /pmc/articles/PMC2194850/ /pubmed/13525677 Text en Copyright © Copyright, 1958, by The Rockefeller Institute for Medical Research 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 Gilbert, Daniel L. Gerschman, Rebeca Ruhm, K. Barclay Price, William E. THE PRODUCTION OF HYDROGEN PEROXIDE BY HIGH OXYGEN PRESSURES |
title | THE PRODUCTION OF HYDROGEN PEROXIDE BY HIGH OXYGEN PRESSURES |
title_full | THE PRODUCTION OF HYDROGEN PEROXIDE BY HIGH OXYGEN PRESSURES |
title_fullStr | THE PRODUCTION OF HYDROGEN PEROXIDE BY HIGH OXYGEN PRESSURES |
title_full_unstemmed | THE PRODUCTION OF HYDROGEN PEROXIDE BY HIGH OXYGEN PRESSURES |
title_short | THE PRODUCTION OF HYDROGEN PEROXIDE BY HIGH OXYGEN PRESSURES |
title_sort | production of hydrogen peroxide by high oxygen pressures |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2194850/ https://www.ncbi.nlm.nih.gov/pubmed/13525677 |
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