1986
DOI: 10.1016/0167-7012(86)90034-5
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Determination of the nucleotide composition of a deoxyribonucleic acid by high-performance liquid chromatography of its enzymatic hydrlysate: a review

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Cited by 60 publications
(25 citation statements)
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“…DNAs were extracted according to the method of Auling et al (1986). After enzymic hydrolysis, the GjC content was determined by HPLC analysis of the component nucleosides (Kaneko et al, 1986). The HPLC apparatus was equipped with a Waters pump (model 510), a model U6K injector, a column oven, a UV detector (Waters 484) and a reversedphase column (250i4 mm ; hypersil C18 ; 5 µm particles).…”
Section: Methodsmentioning
confidence: 99%
“…DNAs were extracted according to the method of Auling et al (1986). After enzymic hydrolysis, the GjC content was determined by HPLC analysis of the component nucleosides (Kaneko et al, 1986). The HPLC apparatus was equipped with a Waters pump (model 510), a model U6K injector, a column oven, a UV detector (Waters 484) and a reversedphase column (250i4 mm ; hypersil C18 ; 5 µm particles).…”
Section: Methodsmentioning
confidence: 99%
“…The guanine-plus-cytosine (G + C) content of DNA was determined by using a high-performance liquid chromatograph method (12,31). Heat-denatured DNA was digested into nucleosides by using nuclease P, (EC 3.1.30.1; Yamasa Shoyu Co., Ltd., Choshi, Japan) and bacterial alkaline phosphatase (EC 3.1.3.1; Sigma (Chemical Co., St. Louis, Mo.).…”
Section: Methodsmentioning
confidence: 99%
“…Purified DNA was dissolved in Nuclease P1 buffer (40 mM sodium acetate, 2 mM ZnSO % , pH 5n3). Determination of the GjC content was done by HPLC as described previously (Kaneko et al, 1986).…”
Section: Sample Collection Bacterial Strains and Cultural Conditionsmentioning
confidence: 99%