THE ACCELERATING EFFECT OF MANGANOUS IONS ON PHAGE ACTION

Dilute solutions of MnCl2 or MnSO4 accelerate the lytic effect of phage upon susceptible staphylococci. Under the conditions of our experiments the manganese-containing mixtures lysed regularly 0.5 hour sooner than the controls. The effect is shown to be due to a lowering of the lytic threshold, i....

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Main Authors: Krueger, A. P., West, N. S.
Format: Online
Language:English
Published: The Rockefeller University Press 1935
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2141421/
id pubmed-2141421
recordtype oai_dc
spelling pubmed-21414212008-04-23 THE ACCELERATING EFFECT OF MANGANOUS IONS ON PHAGE ACTION Krueger, A. P. West, N. S. Article Dilute solutions of MnCl2 or MnSO4 accelerate the lytic effect of phage upon susceptible staphylococci. Under the conditions of our experiments the manganese-containing mixtures lysed regularly 0.5 hour sooner than the controls. The effect is shown to be due to a lowering of the lytic threshold, i.e. the quantity of phage/bacterium requisite for lysis; Mn++ reduces the ratio from 54 to about 12. In the presence of Mn++ phage distribution is altered and in growing phage-bacteria mixtures the extracellular phage concentration is increased by manganese to approximately 4 times that occurring in the absence of manganese. There appears to be no enhancement of phage formation nor any affect on the rate of bacterial growth. As would be anticipated, for any given initial phage concentration the end titre after completion of lysis is less in the presence of manganese than in its absence. This is due to the reduced lytic threshold produced by Mn++, there consequently being less phage needed to bring about lytic destruction of the bacteria. The Rockefeller University Press 1935-09-20 /pmc/articles/PMC2141421/ /pubmed/19872916 Text en Copyright © Copyright, 1935, 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/).
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Krueger, A. P.
West, N. S.
spellingShingle Krueger, A. P.
West, N. S.
THE ACCELERATING EFFECT OF MANGANOUS IONS ON PHAGE ACTION
author_facet Krueger, A. P.
West, N. S.
author_sort Krueger, A. P.
title THE ACCELERATING EFFECT OF MANGANOUS IONS ON PHAGE ACTION
title_short THE ACCELERATING EFFECT OF MANGANOUS IONS ON PHAGE ACTION
title_full THE ACCELERATING EFFECT OF MANGANOUS IONS ON PHAGE ACTION
title_fullStr THE ACCELERATING EFFECT OF MANGANOUS IONS ON PHAGE ACTION
title_full_unstemmed THE ACCELERATING EFFECT OF MANGANOUS IONS ON PHAGE ACTION
title_sort accelerating effect of manganous ions on phage action
description Dilute solutions of MnCl2 or MnSO4 accelerate the lytic effect of phage upon susceptible staphylococci. Under the conditions of our experiments the manganese-containing mixtures lysed regularly 0.5 hour sooner than the controls. The effect is shown to be due to a lowering of the lytic threshold, i.e. the quantity of phage/bacterium requisite for lysis; Mn++ reduces the ratio from 54 to about 12. In the presence of Mn++ phage distribution is altered and in growing phage-bacteria mixtures the extracellular phage concentration is increased by manganese to approximately 4 times that occurring in the absence of manganese. There appears to be no enhancement of phage formation nor any affect on the rate of bacterial growth. As would be anticipated, for any given initial phage concentration the end titre after completion of lysis is less in the presence of manganese than in its absence. This is due to the reduced lytic threshold produced by Mn++, there consequently being less phage needed to bring about lytic destruction of the bacteria.
publisher The Rockefeller University Press
publishDate 1935
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2141421/
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