A simple method for DNA extraction from activated sludge
© 2012, Chiang Mai University. All rights reserved. A protocol for DNA extraction directly from activated sludge is described. Sludge samples were lysed by glass bead and CTAB. The extracted DNA was purified with phenol: chloroform: isoamyl alcohol mixture and precipitated in sodium acetate and isop...
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th-cmuir.6653943832-514222018-09-04T06:14:44Z A simple method for DNA extraction from activated sludge Dounghatai Singka Ladapa Kumdhitiahutsawakul Prasert Rekkriangkrai Wasu Pathom-Aree Biochemistry, Genetics and Molecular Biology Chemistry Materials Science Mathematics Physics and Astronomy © 2012, Chiang Mai University. All rights reserved. A protocol for DNA extraction directly from activated sludge is described. Sludge samples were lysed by glass bead and CTAB. The extracted DNA was purified with phenol: chloroform: isoamyl alcohol mixture and precipitated in sodium acetate and isopropanol. The proposed protocol is simple, rapid and required small sample size, yielding about 40.5 ± 1.8 μg DNA g-1sludge. The quality of DNA is good enough for successful PCR amplifications of 16S rDNA, 16S rDNA V3 region and denaturing gradient gel electrophoresis (DGGE) analysis of archaeal population. This described method can also be applied to other environmental samples such as whey and soil. 2018-09-04T06:01:43Z 2018-09-04T06:01:43Z 2012-01-01 Journal 01252526 2-s2.0-84869027526 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84869027526&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/51422 |
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Biochemistry, Genetics and Molecular Biology Chemistry Materials Science Mathematics Physics and Astronomy |
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Biochemistry, Genetics and Molecular Biology Chemistry Materials Science Mathematics Physics and Astronomy Dounghatai Singka Ladapa Kumdhitiahutsawakul Prasert Rekkriangkrai Wasu Pathom-Aree A simple method for DNA extraction from activated sludge |
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© 2012, Chiang Mai University. All rights reserved. A protocol for DNA extraction directly from activated sludge is described. Sludge samples were lysed by glass bead and CTAB. The extracted DNA was purified with phenol: chloroform: isoamyl alcohol mixture and precipitated in sodium acetate and isopropanol. The proposed protocol is simple, rapid and required small sample size, yielding about 40.5 ± 1.8 μg DNA g-1sludge. The quality of DNA is good enough for successful PCR amplifications of 16S rDNA, 16S rDNA V3 region and denaturing gradient gel electrophoresis (DGGE) analysis of archaeal population. This described method can also be applied to other environmental samples such as whey and soil. |
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Journal |
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Dounghatai Singka Ladapa Kumdhitiahutsawakul Prasert Rekkriangkrai Wasu Pathom-Aree |
author_facet |
Dounghatai Singka Ladapa Kumdhitiahutsawakul Prasert Rekkriangkrai Wasu Pathom-Aree |
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Dounghatai Singka |
title |
A simple method for DNA extraction from activated sludge |
title_short |
A simple method for DNA extraction from activated sludge |
title_full |
A simple method for DNA extraction from activated sludge |
title_fullStr |
A simple method for DNA extraction from activated sludge |
title_full_unstemmed |
A simple method for DNA extraction from activated sludge |
title_sort |
simple method for dna extraction from activated sludge |
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2018 |
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https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84869027526&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/51422 |
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