Three Questions to Ask When Choosing a PCR Enzyme

Sometimes you only need to detect a PCR product or estimate its size, such as, when you’re genotyping mice or screening for recombinant clones. For this type of routine PCR, you should use a standard thermostable DNA polymerase (like Taq DNA polymerase) to confirm the presence or absence of target DNA.

If, however, you are performing cloning experiments or next-generation sequencing (NGS), then accuracy matters. To obtain an exact DNA copy, make sure that you are choosing a DNA polymerase that has high-fidelity. High fidelity DNA polymerases have the ability to proofread the DNA sequence being amplified through 3' to 5' exonuclease activity. When a mismatched base pair is incorporated, the DNA polymerase stalls which creates a delay in synthesis. This delay allows the mismatched nucleotide to be removed and replaced with the correct nucleotide.

An excellent choice for a DNA polymerase that preserves sequence accuracy is Thermo Scientific Phusion Plus DNA Polymerase. This enzyme features high fidelity that is >100x more accurate than Taq DNA polymerase. For even higher accuracy of sequences, Invitrogen Platinum SuperFi II DNA Polymerase is available and offers >300x than Taq DNA polymerase's fidelity.

When you’re working with long DNA templates, you need a PCR enzyme that can go the distance. In this case, choose a polymerase with a high processivity and fast extension rate. Processivity represents the number of nucleotides that can be incorporated during a single binding event by the DNA polymerase. Highly processive DNA polymerases help with amplification of long templates due to the number of nucleotides that can be processed. In addition, DNA polymerases with fast extension rates are able to amplify DNA in a shorter time. PCR enzymes with high processivity and fast extension rates will help ensure efficient DNA synthesis of long templates and cut down on your cycling time. Both Platinum SuperFi II and Phusion DNA polymerases can synthesize up to 20 kb of DNA at 15–30 sec/kb.

Maybe you are seeing bands on your gel that should not be there. These extra bands could be an example of nonspecific amplification (see Figure 1). To help achieve specific target amplification with high yields, choose a hot-start PCR enzyme like Platinum II Taq or DreamTaq Hot-Start DNA polymerases. Hot-start DNA polymerases begin amplification only when the initial denaturation step reaches 90°C. This feature helps ensure that the PCR reaction does not initiate too soon, preventing undesirable off-target products. This feature also helps prevent primer-dimers from extending, which is particularly helpful when using multiple primers for multiplex and high-throughput PCR.

There’s more to consider. Selecting the right polymerase format can simplify your workflow. PCR enzyme format options include ready-to-use master mixes, buffers with dyes for direct gel loading, and kits that assemble all the necessary components for direct PCR.

With a master mix, you can just add your template and primers, then start your PCR. If you want to further minimize pipetting steps, use a polymerase with a buffer and loading dye that allows for direct gel loading of PCR products (note: ensure the dye is compatible with downstream applications). Direct PCR kits can also help save time by allowing you to skip purification of DNA and go straight to DNA amplification. Despite these available options, if you’re looking to optimize specific components of your reaction, stick with a stand-alone DNA polymerase.

As you evaluate the level of accuracy, speed, and specificity you need for your PCR experiments, you can confidently navigate the crowded marketplace of PCR enzymes and choose the right DNA polymerase for your molecular biology applications.