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DNA Absorbance Quantitation Using BMG LABTECH´s POLARstar Omega Microplate Reader

Franka Ganske, BMG LABTECH, Offenburg, Germany, 01/2008

 

  • Rapid method to measure DNA using absorbance 260 nm
  • High degree of linearity to measure DNA (0.1 to 100 µg/mL)
  • New data analysis software, MARS, with integrated extinction coefficients for dsDNA, ssDNA and RNA

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Introduction

One of the most common methods to measure DNA concentration is using absorbance 260 nm (A260) due to the fact that nucleic acids have an absorption maximum at this UV wavelength. Although a relatively simple and time-honored method, absorbance 260 suffers from low sensitivity and interference from nucleotides and single-stranded nucleic acids. Furthermore, compounds commonly used in the preparation of nucleic acids absorb at 260 nm leading to abnormally high quantitation levels(1). However, these interference and preparation compounds also absorb at 280 nm (i.e. proteins) leading to the calculation of DNA purity by performing ratio DNA absorbance measurements at A260/ A280.

Absorbance 260 / 280 = 1.7 to 2.0 for “pure” DNA

Therefore, constructing a ratio between these two absorbance wavelengths can provide an estimate of sample purity. As a general rule any preparations with an A260/A280 greater than approximately 1.7 is called “pure” (1, 2).

The DNA absorbance measurement is governed by Beer’s Law.

A = εbc

Where A is absorbance, ε is the molar extinction coefficient, b is the path length, and c is the analyte concentration. With the spectrometer, the POLARstar Omega (Figure 1) easily measures DNA and its impurities. The integrated path length correction and the new data analysis software, MARS, allow for fast determination of DNA concentration in samples. Alternative methods to measure DNA than absorbance are new fluorescent techniques that are much more sensitive and specific for DNA. The PicoGreen® dsDNA Quantitation Reagent from Molecular Probes® for example is a highly sensitive fluorescent assay that can routinely measure DNA in the 100 pg range or lower with optimization (3).


Fig. 1: BMG LABTECH’s POLARstar Omega multidetection microplate reader with fast absorbance spectrometer easily measures dna at absorbance 260 nm.

Material and Methods

All materials were obtained through normal distribution channels from the manufacturers stated.

  • UV-Star plates, 96-well, Greiner Bio-One, Cat. No. 655801, Frickenhausen, Germany
  • Deoxyribonucleic acid (DNA), Activated from calf thymus, lyophilized powder, Cat. No. D-4522, Sigma-Aldrich, Munich, Germany
  • Distilled water
  • POLARstar Omega, BMG LABTECH, Offenburg, Germany

In addition, consumables such as pipette tips and microcentrifuge tubes were used as needed from various manufacturers. The DNA from calf thymus was solved in distilled water to a final concentration of 1 mg/mL. From this stock solution further dilutions were performed yielding different DNA standards ranging from 0.1 to 100 µg/mL. Four replicates of 350 µL aliquots of each standard were pipetted into the 96-well UV plate. Additionally, 16 replicates of 350 µL aliquots of distilled water were pipetted into the plate to serve as a blank. The prepared 96-well plate was inserted into the instrument and was read in the POLARstar Omega using the spectrometer. There are two possibilities for the measurement. You can either choose to select up to eight specific wavelengths (in this case two wavelengths at absorbance 260 and 280 nm) or you can measure a spectrum of the sample. An example of a DNA absorbance spectral range using different concentrations of DNA is given in Figure 2.


Fig. 2: DNA Absorbance spectrum of different concentrations of calf thymus DNA recorded on the POLARstar Omega. Detection range is between 220 and 310 nm and resolution was set at 1 nm and Absorbance 260 and 280 nm are used.

Results and Discussion

The measured DNA data was evaluated using the new data analysis software, MARS, from BMG LABTECH. The average value of the blank measurement was subtracted from the measurements made at each concentration and the results plotted. A linear regression fit was performed on the standard values (Figure 3).


Fig. 3: Linear regression fit performed on the DNA absorbance standard curve in the concentration range from 0.1 to 100 µg/mL. An R2-Value of 0.99988 was obtained indicating a high degree of linearity throughout the concentration range.

The DNA absorbance standard curve allows the back calculation of unknown samples. Sensitivity of < 0.3 µg/mL DNA (or about 0.1 µg DNA/well) was observed for measurements with selected 260 nm wavelength and spectrum measurements.

A further option in the new MARS data analysis software is the possibility to measure DNA concentration of unknown samples without a DNA absorbance standard curve. Based on the knowledge that 50 µg of double stranded DNA show an OD value of 1.0, the concentration is automatically calculated without the necessity of pipetting standards into the microplate. It should be taken into account that this method only works well when the path length correction feature is activated. As double stranded and single stranded DNA or RNA have different extinction coefficients there are different MARS templates available for these different nucleic acids (Table 1).

Table 1: Extinction coefficients of different nucleic acids that can be used with absorbance 260 measurements and Beer’s law.

Conclusion

Because of its spectrometer, the POLARstar Omega offers easy handling for DNA absorbance measurements by simply selecting the absorbance 260 nm wavelength or by measuring a spectrum which covers the absorbance maximum. Furthermore, with the help of the new data analysis software, MARS, it is possible to determine different nucleic acid concentrations depending on the extinction coefficient. The ratio of Absorbance 260 / 280 indicates how pure the DNA sample is and it can be measured just as easy and within the same measurement time as Absorbance 260 alone. A full DNA absorbance spectrum in the range of 220 - 1000 nm helps to identify impurities and it can be measured within one second per well.

References

  1. Sambrook, J., Fritsch, E.F. and Manniatis, T. (1989) Molecular Cloning. A Laboratory Manual. Second Edition, Cold Spring Harbor Laboratory Press, Cold Spring Harbour
  2. Steffan, R.J., Goksoyr, J., Bej, A.K. and Atlas, R.M. (1988) Recovery of DNA from Soils and Sediments. Appl. Environ. Microbiol. 54 (12) 2908-2915.
  3. Angersbach, S. and Earp, R. (2004), Molecular Probes PicoGreen® Assay Performed on BMG LABTECH POLARstar OPTIMA Microplate Reader, BMG LABTECH,