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Open AccessJournal ArticleDOI

Reexamination of the Association Between Melting Point, Buoyant Density, and Chemical Base Composition of Deoxyribonucleic Acid

J. De Ley
- 01 Mar 1970 - 
- Vol. 101, Iss: 3, pp 738-754
TLDR
In this paper, the base composition of deoxyribonucleic acid (DNA) was calculated by regression and correlation analysis and treated statistically by using only sets of data on DNA determined with the same strains.
Abstract
The equations currently used for the calculation of the chemical base composition of deoxyribonucleic acid (DNA), expressed as moles per cent guanine plus cytosine (% GC), from either buoyant density (ρ) or midpoint of thermal denaturation (Tm) were recalculated by using only sets of data on DNA determined with the same strains. All available information from the literature was screened and supplemented by unpublished data. The results were calculated by regression and correlation analysis and treated statistically. From the data on 96 strains of bacteria, it was calculated that% GC = 2.44 (Tm – 69.4). Tm appears to be unaffected by the substitution of cytosine by hydroxymethylcytosine. This equation is also valid for nonbacterial DNA. From the data on 84 strains of bacteria, the relation% GC = 1038.47 (–1.6616) was calculated. The constants in this equation are slightly modified when data on nonbacterial DNA are included. Both correlations differ only slightly from those currently used, but now they lean on a statistically sound basis. As a control, the relation between ρ and Tm was calculated from data of 197 strains; it agrees excellently with the above two equations.

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Citations
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A new purple bacterium that oxidizes sulfide to extracellular sulfur and sulfate

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Chryseobacterium takakiae sp. nov., a member of the phylum Bacteroidetes isolated from Takakia lepidozioides.

TL;DR: A Gram-stain-negative, rod-shaped and non-endospore-forming bacterium, isolated from Takakia lepidozioides collected from the Gawalong glacier in Tibet, China and characterized using a polyphasic taxonomic approach is considered to represent a novel species of the genus Chryseobacterium.
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A microanalytical procedure for determination of the base composition of DNA.

TL;DR: A new procedure for the determination of the percentage guanine plus cytosine values of microquantities of DNA is described, and a method for purification of bacterial DNA is detailed in the present work.
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Cytological and deoxyribonucleic acid-deoxyribonucleic acid hybridization studies on lactobacillus isolates from San Francisco sourdough.

TL;DR: Since these SD isolates have the characteristic phenotypic and morphological properties of the genus Lactobacillus and are not related genetically to any known species, the tentative characterization by the above workers of these isolates as a new species is substantiated.
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Diaphorobacter polyhydroxybutyrativorans sp. nov., a novel poly(3-hydroxybutyrate-co-3-hydroxyvalerate)-degrading bacterium isolated from biofilms

TL;DR: A novel Gram-stain-negative, facultatively aerobic and rod-shaped strain was isolated from the biofilms of a denitrifying reactor using poly(3-hydoxybutyrate-co-3-Hydroxyvalerate) as the sole carbon source in Beijing, PR China andylogenetic analyses revealed that strain SL-205(T) is a member of the genus Diaphorobacter.
References
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Journal ArticleDOI

Determination of the base composition of deoxyribonucleic acid from its thermal denaturation temperature.

TL;DR: The previously discovered linear relation between the base composition of DNA, expressed in percentage of guanine plus cytosine bases, and the denaturation temperature, T m, has been further investigated and it appears that the measurement of the T m is a satisfactory means of determining base composition in DNA.
Journal ArticleDOI

Determination of the base composition of deoxyribonucleic acid from its buoyant density in CsCl.

TL;DR: A comprehensive study of the buoyant density of DNA as a function of composition has been made and the linear relation previously reported has been confirmed.
Journal ArticleDOI

Physical and chemical characterization of two- and three-stranded adenine-thymine and adenine-uracil homopolymer complexes.

TL;DR: The DNA homopolymers dA and dT have been prepared enzymically using Escherichia coli DNA polymerase, and their properties have been studied, but the homopolymer pair dA:rU is not stable under any conditions of temperature and salt concentration tested.
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