{"title":"疏水相互作用色谱法研究质粒DNA和大肠杆菌核酸的保留。","authors":"M M Diogo, J A Queiroz, D M Prazeres","doi":"10.1023/a:1016361721316","DOIUrl":null,"url":null,"abstract":"<p><p>This work presents studies on the interactions of supercoiled plasmid DNA and Escherichia coli genomic DNA (gDNA) and RNA, with an hydrophobic interaction chromatography (HIC) gel, obtained by derivatisation of Sepharose CL-6B with 1,4-butanediol diglycidyl ether. Nucleic acids purified from E. coli were injected separately in the above HIC column and eluted with 1.5 M (NH4)2SO4 in the buffer. The column was able to separate single-stranded from double-stranded nucleic acids. RNA and denatured gDNA were retarded in a different way due to the interactions of the exposed hydrophobic bases with the ligands. Supercoiled plasmid DNA, on the contrary, eluted in the flowthrough.</p>","PeriodicalId":9179,"journal":{"name":"Bioseparation","volume":"10 4-5","pages":"211-20"},"PeriodicalIF":0.0000,"publicationDate":"2001-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1023/a:1016361721316","citationCount":"45","resultStr":"{\"title\":\"Studies on the retention of plasmid DNA and Escherichia coli nucleic acids by hydrophobic interaction chromatography.\",\"authors\":\"M M Diogo, J A Queiroz, D M Prazeres\",\"doi\":\"10.1023/a:1016361721316\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>This work presents studies on the interactions of supercoiled plasmid DNA and Escherichia coli genomic DNA (gDNA) and RNA, with an hydrophobic interaction chromatography (HIC) gel, obtained by derivatisation of Sepharose CL-6B with 1,4-butanediol diglycidyl ether. Nucleic acids purified from E. coli were injected separately in the above HIC column and eluted with 1.5 M (NH4)2SO4 in the buffer. The column was able to separate single-stranded from double-stranded nucleic acids. RNA and denatured gDNA were retarded in a different way due to the interactions of the exposed hydrophobic bases with the ligands. Supercoiled plasmid DNA, on the contrary, eluted in the flowthrough.</p>\",\"PeriodicalId\":9179,\"journal\":{\"name\":\"Bioseparation\",\"volume\":\"10 4-5\",\"pages\":\"211-20\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2001-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1023/a:1016361721316\",\"citationCount\":\"45\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Bioseparation\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1023/a:1016361721316\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bioseparation","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1023/a:1016361721316","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 45
摘要
这项工作介绍了超螺旋质粒DNA与大肠杆菌基因组DNA (gDNA)和RNA相互作用的研究,用一种疏水相互作用色谱(HIC)凝胶,由Sepharose CL-6B与1,4-丁二醇二缩水甘油醚衍生而成。大肠杆菌纯化的核酸分别注射到上述HIC柱中,用1.5 M (NH4)2SO4在缓冲液中洗脱。该柱能够分离单链和双链核酸。由于暴露的疏水碱基与配体的相互作用,RNA和变性dna以不同的方式被阻滞。相反,超螺旋质粒DNA在流动中被洗脱。
Studies on the retention of plasmid DNA and Escherichia coli nucleic acids by hydrophobic interaction chromatography.
This work presents studies on the interactions of supercoiled plasmid DNA and Escherichia coli genomic DNA (gDNA) and RNA, with an hydrophobic interaction chromatography (HIC) gel, obtained by derivatisation of Sepharose CL-6B with 1,4-butanediol diglycidyl ether. Nucleic acids purified from E. coli were injected separately in the above HIC column and eluted with 1.5 M (NH4)2SO4 in the buffer. The column was able to separate single-stranded from double-stranded nucleic acids. RNA and denatured gDNA were retarded in a different way due to the interactions of the exposed hydrophobic bases with the ligands. Supercoiled plasmid DNA, on the contrary, eluted in the flowthrough.