Scinovex
article Open Access

Determination of DNA base composition by reversed-phase high-performance liquid chromatography

FEMS Microbiology Letters · 1984 · Vol. 25(1) · pp. 125–128
Jin TámaokaKazuo Komagata

Abstract

DNA base composition was determined by reversed-phase high-performance liquid chromatography (HPLC). DNA was hydrolysed into nucleosides with nuclease P1 and bacterial alkaline phosphatase. The mixture of nucleosides was applied to HPLC without any further purification. One determination by chromatography needed 2 µg of hydrolysed nucleosides and took only 8 min. The relative standard error of nucleoside analysis was less than 1%. The system described here gives a direct and precise method for determining DNA base composition.

DNA and Nucleic Acid ChemistryPorphyrin Metabolism and DisordersDNA Repair MechanismsChromatographyHigh-performance liquid chromatographyNucleaseChemistryNucleosideDNAHydrolysisReversed-phase chromatographyComposition (language)Base (topology)
Citations
2,419
FWCI
1.18
field-weighted impact
References
18
Percentile
77%
vs. same field & year
Citations per year
Cited by
Vibrio coralliilyticus sp. nov., a temperature-dependent pathogen of the coral Pocillopora damicornis
INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · 2003 · 445 citations
Notes on the characterization of prokaryote strains for taxonomic purposes
INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · 2009 · 1,381 citations
Thermacetogenium phaeum gen. nov., sp. nov., a strictly anaerobic, thermophilic, syntrophic acetate-oxidizing bacterium.
INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · 2000 · 346 citations
Citation Network

How this paper connects to the literature. Drag to explore, click any node to open that paper.