Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Method enabling detection of single-stranded DNA ligation activity
KTH, School of Biotechnology (BIO).
2017 (English)In: Archives of industrial biotechnology, Vol. 1, no 1, p. 35-40Article in journal (Refereed) Published
Abstract [en]

The enzyme DNA ligase is an essential tool in many different applications in the field of biotechnology. For these applications the DNA quality can be crucial for the final result. In this paper we present a new method that can be used for specific studies of DNA ligases and for simultaneous analyzes of DNA quality. More specifically, a simple, fast and sensitive method for detection of single-stranded DNA (ssDNA) ligase activity is presented. The new method is based on real-time detection of nucleotide incorporation over the ligation site catalyzed by a DNA polymerase. The ratio between the incorporation signal after and before the ligation site gives an estimate of the ligation efficiency. To further increase the robustness of the assay the exact amount of unligated product can be easily estimated in a separate assay using a 3’-end blocked oligonucleotide functioning as template. Produced circular DNA can be cleaned from unligated DNA by exonuclease I treatment and the quality of the circle can be easily analyzed by a simple sequencing procedure. If the ssDNA used for the ligation reaction contains truncated fragments this will be observed by uneven signals during the analysis. The new method can be a useful tool for researchers working with both basic and applied projects in the field of biotechnology.

Place, publisher, year, edition, pages
2017. Vol. 1, no 1, p. 35-40
Keywords [en]
Pyrosequencing, DNA sequencing, DNA ligase, Luciferase, Single-Stranded DNA, Circular single-Stranded DNA, Alkaline phosphatase, Exonuclease I, Inorganic pyrophosphatase
National Category
Other Industrial Biotechnology
Research subject
Biotechnology; Biotechnology
Identifiers
URN: urn:nbn:se:kth:diva-219475OAI: oai:DiVA.org:kth-219475DiVA, id: diva2:1163394
Note

QC 20180123

Available from: 2017-12-06 Created: 2017-12-06 Last updated: 2018-01-24Bibliographically approved

Open Access in DiVA

fulltext(1016 kB)6 downloads
File information
File name FULLTEXT01.pdfFile size 1016 kBChecksum SHA-512
6792f6b71a1c2d1b8ff601db266a442fb14c68e39c079d8520e5b3d3778711b52e5aeaa571c0c80031a36191d36dea8fd60285bc54899cd35d937900b1a73048
Type fulltextMimetype application/pdf

Other links

Länk till artikel

Search in DiVA

By author/editor
Nyrén, Pål
By organisation
School of Biotechnology (BIO)
Other Industrial Biotechnology

Search outside of DiVA

GoogleGoogle Scholar
Total: 6 downloads
The number of downloads is the sum of all downloads of full texts. It may include eg previous versions that are now no longer available

urn-nbn

Altmetric score

urn-nbn
Total: 61 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf