4.6 Article

Analysis of bacterial plasmid DNA by solid-phase microextraction

Journal

ANALYTICAL METHODS
Volume 7, Issue 17, Pages 7202-7207

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c5ay00532a

Keywords

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Funding

  1. Chemical Measurement and Imaging Program at the National Science Foundation [CHE-1413199]
  2. University of Toledo College of Graduate Studies
  3. Division Of Chemistry
  4. Direct For Mathematical & Physical Scien [1602091] Funding Source: National Science Foundation

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The extraction and preconcentration of DNA is a critical step in the analysis of microorganisms. In this study, a polymeric ionic liquid (PIL) sorbent coating was applied for the preconcentration of plasmid DNA (pDNA) from bacterial cells using solid-phase microextraction (SPME). PIL-based SPME devices were prepared by ultraviolet photoinitiated polymerization of a dicationic ionic liquid (IL)-based cross-linker and IL monomer on a nitinol support. pDNA was extracted from buffered aqueous solution using the PIL-based sorbent coating followed by the amplification of a target gene by polymerase chain reaction (PCR). Extraction conditions for the method were optimized based on the relative intensities of PCR amplicon bands visualized on an agarose gel. Compared to a commercial polyacrylate sorbent coating, the PIL sorbent coating extracted greater quantities of pDNA. With an extraction time of 5 min, the PIL-based SPME technique was capable of preconcentrating a sufficient amount of template pDNA from a 20 ng mL(-1) solution to allow detection of the amplicon on an agarose gel. Sequence analysis demonstrated that the sequence of the pDNA was unaltered following PIL-based SPME. The developed method was successfully employed for the analysis of pDNA from two different E. coli transformants in a dilute aqueous solution.

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