Difference between revisions of "Part:BBa K863010"

Team TecCEM Characterization, Colorimetric Assay and Purification

TecCEM Characterization, colorimetric assay and purification

For the characterization of the Laccase BBa_K863010 we conducted an IPTG induction experiment in which we used the transformation of the Laccase in E. coli BL21. We thought that we could use another strain called SoluBL21 but results were not successful as no expression was found. We verified the presence of the protein through an SDS-PAGE with a gel concentration of 12% and found a visible band with a mass of around 50 kDa. This can be seen in figure 1. 

Figure 1. The lanes correspond to the following. M: Molecular weight marker; 1: Total protein after induction; 2: Total protein before induction; 3: Protein found in the Culture Medium after induction; 4: Cytoplasmic soluble fraction; 5: Inclusion bodies of the insoluble fraction; 6: Concentrated Culture Medium after induction. The band observed in lanes 1, 3 and 6 weighs around 48 kDa and corresponds to the expected size. 

We found that the protein was mostly found on the culture medium but can also be found on the cytoplasmic soluble fraction. The band that was appreciated in figure 1. indicates that there’s an expression of the Laccase after it’s induction with IPTG so our results and experience using this part was different from what 2019 PuiChing Macau’s team reported previously. 

To prove that the Laccase was being expressed, we conducted a colorimetric assay involving three colorants that act as a substrate: methylene blue, malachite green and rose bengal. We based this experiment upon the findings of D. Singh et al. (2014) [1], in which they used agar plates with these colorants to determine the expression of Laccases in a medium. The first assays we conducted were only to find out if there was any color change with the presence of our extracted Laccase either from the cytoplasmic soluble fraction or from the culture medium. We used Citrate Buffer and found a change of color in different samples of Laccase after its purification using Ni Affinity. We also verified that the effect we saw wasn’t related to a change in pH. The results are available in figure 2. 

Figure 2. In section a) we can see the change of color of the substrates used (methylene blue, malachite green and rose bengal from left to right). a)-I. corresponds to the cytoplasm soluble fraction while a)-II. corresponds to the secreted protein from the culture medium. In section b) we can see that the pH remained unchanged throughout the assay. 

After this first assay, we decided that we had to establish a purification protocol through which we could get the most enzyme possible. We used a Ni Affinity Column and a system of recollection of the different phases. We collected the enzyme from both the culture medium and the cytoplasmic soluble fraction and measured the absorbance of the fractions collected at 280 nm. In total, we got 21 fractions for the cytoplasm proteins and 20 fractions for the culture medium. The purification conditions were established using a growing elution buffer concentration. These conditions are shown in figures 3 and 4.

Figure 3. Chromatogram of the purification of the cytoplasmic soluble fraction showing the spike of absorbance in an elution volume of around 15 mL to 20 mL (with a percentage of elution buffer of around 30 to 50%); corresponding to the fractions containing the Laccase. 

>

Figure 4. Chromatogram of the purification of the culture medium showing the spike of absorbance in an elution volume of 12 mL to 20 mL (with a percentage of elution buffer of around 16% to 50%); corresponding to the fractions containing the Laccase. 

Finally, we conducted a last assay in which we first quantified the amount of protein recovered through a BCA quantification protocol. Using this protocol and with the elaboration of a BCA curve, we estimated that we recovered 0.334 µg/mL of Laccase in the culture medium while for the cytoplasmic soluble fraction we obtained 0.1298 µg/mL of Laccase. This was consistent with the results we got from the chromatograms. 

For the final colorimetric assay we conducted, we quantified the activity of the Laccase obtained from the purification. We compared it with a Commercial Laccase from Sigma belonging to Trametes versicolor and used the spectrophotometer to measure methylene blue, malachite green and rose bengal at 664, 617 and 562 nm respectively. Since we didn’t quite have the exact concentration of colorants in our samples, we limited to measure the activity as a percentage of degradation of each colorant where a 100% of substrate would be the absorbance of the control of the blue, green and rose colorants and the enzymatic degradation would be expressed as the loss of color. The results can be seen below.

Figure 5. Percentage of degradation of Methylene Blue through time for the Laccase in the culture medium (blue), soluble fraction (orange), purified culture medium (yellow), purified soluble fraction (light blue) and the Laccase from Trametes versicolor (gray).

Figure 6. Percentage of degradation of Malachite green through time for the Laccase in the culture medium (blue), soluble fraction (orange), purified culture medium (yellow), purified soluble fraction (light blue) and the Laccase from Trametes versicolor (gray).

Figure 7. Percentage of degradation of Rose Bengal through time for the Laccase in the culture medium (blue), soluble fraction (orange), purified culture medium (yellow), purified soluble fraction (light blue) and the Laccase from Trametes versicolor (gray).

In the assays, we saw a similar trend for the degradation of Methylene Blue. For Malachite Green, the Laccase from Trametes versicolor had a higher degradation rate. Finally, for Rose Bengal we observed a similar trend between Trametes versicolor Laccase and the Soluble Fraction Laccase (before purification). We then reported the percentage of degradation of each sample for each colorant at the final point in time and got the next results:

Figure 8. Percentage of degradation of each Laccase at the final point in time for each colorant. 

We observed that overall, the best results were obtained by the Laccase of Trametes versicolor (as expected) followed by the soluble fraction and the purified soluble fraction. However, it is worth noting that although these results show that the commercial Laccase may have higher degradation values, it also has a higher concentration since it was prepared at 1 mg/mL (compared to the purified Laccases which had concentrations of 0.334 µg/mL in the culture medium and 0.1298 µg/mL in the soluble fraction.