The process of extracting and purifying plasmid DNA from bacterial cells. It is a fundamental technique in molecular biology and biotechnology, pivotal for applications like gene cloning, DNA sequencing, and recombinant protein production. The aim is to obtain plasmid DNA in a pure form, separate from chromosomal DNA and other cellular components.
Automation involves robotic systems and specialized equipment for tasks like pipetting, mixing, and sample transferring.
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In cloning, a gene of interest is inserted into a plasmid vector, which is then introduced into bacteria for propagation. Once isolated, the plasmid DNA can be cut with restriction enzymes and ligated with new DNA fragments, enabling the study or manipulation of specific genes. This application is vital for research in genetics, drug development, and the creation of genetically modified organisms.
After isolating plasmid DNA containing the gene of interest, it is used as a template for sequencing reactions. This allows researchers to determine the exact sequence of nucleotides within the gene, essential for understanding genetic variations, disease mechanisms, and for developing targeted therapies. Plasmid-based sequencing is particularly important in projects like genome mapping, gene expression analysis, and identification of genetic mutations.
Plasmid isolation is critical in recombinant protein production, a process widely used in biotechnology and pharmaceutical industries. In this workflow, a gene coding for a desired protein is cloned into a plasmid, which is then used to transform bacterial or eukaryotic cells. These cells express the protein, which can then be harvested and purified. This approach is fundamental for producing enzymes, vaccines, and therapeutic proteins. The ability to produce high-purity proteins in large quantities hinges on the successful isolation of plasmids carrying the target gene.
This technique involves lysing bacterial cells with a solution containing sodium hydroxide (NaOH) and Sodium Dodecyl Sulfate (SDS). NaOH denatures both chromosomal and plasmid DNA, while SDS disrupts the cell membrane. The addition of a neutralization solution, typically potassium acetate, allows the plasmid DNA to renature and stay in solution, while genomic DNA and proteins precipitate. After centrifugation, the plasmid DNA is left in the supernatant, ready for further purification.
After lysing cells and neutralizing the lysate, it is passed through a silica-based column. The DNA binds to the silica under high-salt conditions, while impurities are washed away. Plasmid DNA is then eluted with a low-salt buffer or water. This method is effective for obtaining high-purity plasmid DNA, suitable for sensitive applications like cloning and sequencing.
Phenol-Chloroform Extraction is a traditional method for DNA extraction. Following cell lysis, the lysate is mixed with phenol and chloroform. DNA remains in the aqueous phase, separating from proteins and lipids in the organic phase after centrifugation. The aqueous phase containing DNA is collected, and DNA is precipitated with alcohol and re-suspended in a buffer. This method requires careful handling due to toxic solvents and is more labor-intensive than other methods.
Opentrons helps you automate plasmid isolation with open-source protocols for the OT-2 and Opentrons Flex
Propagate bacteria that contain the plasmid of interest. A bacterial strain harboring the desired plasmid is grown in a suitable culture medium, often containing an antibiotic to ensure only plasmid-containing bacteria grow.
Collect the bacterial cells for subsequent lysis. Once the bacterial culture has reached the desired density, the cells are harvested, typically by centrifugation. The supernatant is discarded, leaving a pellet of bacterial cells.
Prepare the bacterial cells for lysis. The bacterial pellet is resuspended in a resuspension buffer. This buffer may contain Tris-Cl (for pH stabilization), EDTA (to chelate divalent cations and inhibit DNases), and RNase (to degrade RNA).
Lyse the bacterial cells and release the plasmid DNA:
Precipitate cellular debris and genomic DNA, allowing plasmid DNA to remain in solution:
Separate plasmid DNA from the cleared lysate:
The OT-2 is a bench-top liquid handler designed to be accessible and flexible enough to automate many common applications.
Our team of experts can help figure out if automation is right for you. Book a virtual demo to discuss your workflow needs with an expert.
