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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 All available information from the literature was screened and supplemented by unpublished data.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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Separation of Kluyvera and Buttiauxella by Biochemical and Nucleic Acid Methods

TL;DR: It is suggested that production of indole and lysine decarboxylase and fermentation of sucrose in 2 days could differentiate Kluyvera from Buttiauxella.
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Ribosomes, polyribosomes, and deoxyribonucleic acid from thermophilic mesophilic, and psychrophilic clostridia.

TL;DR: Analysis of deoxyribonucleic acid (DNA) from four species of Clostridium, including two thermophiles, a mesophile, and a psychrophile, revealed no obvious relationship between growth temperature and DNA base composition.
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Two Burkholderia strains from nodules of Dalbergia odorifera T. Chen in Hainan Island, southern China

TL;DR: Results show that both Burkholderia strains 8111 and 8201 are able to form functional nodules on D. odorifera and are potentially beneficial inoculants for seedling propagation to be used in large scale D. smelledifera plantations.
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Dyadobacter endophyticus sp. nov., an endophytic bacterium isolated from maize root

TL;DR: The results of physiological and biochemical tests and the differences in the fatty acid profiles allowed the clear phenotypic differentiation of strain 65T from closely related species of the genus Dyadobacter.
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Deoxyribonucleic Acid Hybridization Studies Among Some Strains of Group D and Group N Streptococci

TL;DR: The results indicate that DNA-DNA hybridization studies may be useful in placing atypical strains in a particular species if screening of physiologic properties is used to separate these strains into groups resembling S. faecalis, S. Faecium, and S. lactis.
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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