A PCR was run on the amilCP with His-tag the results is shown in figure 15. Well number 4 and 5 was amilCP with His-tag (BBa_K2355002) and it showed clear bands at 1065 bp.

Below two pictures of amilCP with His-tag (BBa_K2355002) is displayed see figure 16. The left picture is amilCP with His-tag spun down in LB media. The picture on the right is a picture of amilCP with His-tag after the lysis procedure by sonication. It is clear that the expression of the blue/purple color is very strong. In conclusion the amilCP has been successfully modified by adding a His-tag without compromising the protein.

AmilCP with His-tag purification test

To test whether the amilCP with His-tag worked as expected, we purified two solutions of amilCP; one with His-tagged amilCP, and one with just amilCP. Cells producing the His-tagged amilCP were lysed in accordance with the cell lysis protocol before being used in this experiment. The non His-tagged amilCP producing cells were not lysed because they secreted the amilCP out of the cells and into the media.

Both solutions of amilCP were diluted to an equal absorbance before the solutions were loaded onto Ni-NTA columns to be purified. The purification is based on loading the columns, washing away residual proteins, and eluting the target protein.

As shown in table 1 below, the vast majority of amilCP without His-tag seems to run right through the column, as high concentrations can be detected in the flow through after adding the samples to the column. In addition, the absorbance of the eluant is not far from that of the blank, indicating that no amilCP was retained in the column and eluted. It seems like it makes no difference to run the sample through the column multiple times before washing and eluting, which makes sense if the amilCP is not bound to the column.

Table 2 shows a different pattern for the His-tagged amilCP. For the His-tagged amilCP, the flow-through after sample loading yields concentrations of amilCP that are lower or equal to that of the eluates. The number of times the sample is run through the column seems to make a big difference, especially in the 2nd elution, where it seems there are a linear correlation between the number of times cell lysate were loaded onto the column, and the concentration of eluted amilCP with His-tag.

The difference between the purification of amilCP with and without His-tag is illustrated by figure 16. It is clear that amilCP without His-tag just runs directly through the column, whereas the His-tagged amilCP actually binds to the column and elutes as expected.

From these results we can conclude that our his-tag purification of amilCP has worked.

AmilCP degradation by venom

The amilCP without His-tag (BBa_K592009) was obtained from Biosensor. Apparently the cells had produced an excessive amount of amilCP and exported it out of the cells. This means that it was not necessary to lyse the cells. A simple spin down of the cells left the amilCP in the supernatant and it was used for the amilCP degradation experiment.

AmilCP were incubated with the three different snake venoms: Bitis arietans, Bitis gabonica and Naja nigricollis.

After 70 min of incubation time at 37°C, a spectrophotometer was used to measure the absorbance at 588 nm. There was no loss of amilCP during the incubation with snake venom. The reason for the slight fluctuation could be small pipetting errors, or that the spectrophotometer did not have an optimal readout at 588 nm. The results of the experiment is shown in table 3.

Since the measured absorbance was not lower that the control with no venom, it is clear from table 3 that the amilCP was not degraded by any of the three snake venoms. In conclusion this means that it is safe to use amilCP as a reporter molecule in our device with snake venom.

Test of lacZ degradation by venom

As in the test for amilCP stability in venom, the reporter enzyme β-galactosidase, which is used in the composite part (BBa_K2355313), was incubated in venom to test whether or not venom incubation would degrade or otherwise interfere with the activity of the enzyme. After 70 minutes of incubation at 37°C, the activity of venom-incubated lacZ was measured using ONPG (1.5 mg/mL) and a spectrophotometer. The result can be seen in figure 17.

The activity of β-galactosidase is not decreased in the presence of the chosen snake venoms as seen in figure 17, suggesting that it is not degraded by the protease activity of the venoms. This makes it a suitable candidate as an amplification molecule for our device.

Assembly of linkers derived from substrate screening and literature

The linkers found by screening was ordered as oligonucleotides from IDT. The oligos were annealed to each other by heating it up to 94°C for 2 minutes and then gradually cooled. The linker part BBa_K2355001 was ordered as a gBlock from IDT. The linkers were assembled by digestion, ligation and transformation.

For verification a digestion of the purified plasmid was made. All linkers were single digested first with EcoRI and then with PstI. Uncut plasmid was also run on the gel to see the difference between cut and uncut.

All linkers obtained from the substrate screening has a length of 24 nucleotides. The oligos that we received had a total length of 60 bp because of the desired restriction sites at the ends. When the linkers are assembled correctly into the plasmid backbone (pSB1C3) and cut with either EcoRI or PstI the length obtained is 2094 bp.

The only linker not obtained by the substrate screening BBa_K2355001 has a length of 72 bp. When assembled correctly into the plasmid backbone (pSB1C3) and cut with either EcoRI or PstI the length obtained is 2142 bp.
The uncut plasmid will run faster in the gel due to the supercoiled structure. The results of the digest is displayed in figure 18, figure 19, figure 20 and figure 21.

TFrom the digestion it seems that the assembly of the linkers had succeeded. To confirm it we decided to run a PCR with the iGEM verification primers: BBa_G00100 and BBa_G00101. The expected bands for the ten small linkers are supposed to be 338 bp and for the one large linker it is 386 bp which corresponds well to the gel pictures displayed in figure 22 and 23.

Both of the verification methods showed that all 11 linkers submitted are present in the backbone (pSB1C3).

We also decided to send the linkers for sequencing the results of the sequencing is available here.

In conclusion the assembly of all linkers succeeded.

Assembly of composite part

An unregistered composite part was ordered as an IDT gBlock. The gBlock was assembled by digestion, ligation and transformation. It was done in several attempts with different protocols. The parameters that were changed during the troubleshooting was the ligation ratio, incubation temperature and time. Unfortunately despite these alterations the assembly was unsuccessful.

The composite part BBa_K2355302 was ordered as an IDT gBlock but delivered very late in the process. It was assembled by digestion, ligation and transformation.
The first verification of the part was done by digestion of the purified plasmid. Six colonies were chosen and digested with EcoRI and PstI the desired bands were 2029 bp and 2658 bp. The results of the digestion is shown in figure 24.

None of the digestions gave the expected bands. Therefore, a PCR was also run on BBa_K2355302 with iGEM verification primers: BBa_G00100 and BBa_G00101. But showed no bands of the expected length.

The results of the digestion and PCR showed that the assembly of BBa_K2355302 had not worked.

Assembly of composite lacZ part (BBa_2355313)

Using basic digestion/ligation based assembly of parts, we were able to assemble a composite part, consisting of a coding sequence for ScAvidin with BBa_B0030 RBS, and the coding sequence for an empirical protein linker. This has been confirmed by sequencing. We were also able to attach a promoter (BBa_R0010) to this composite part, and we were able to PCR-amplify a lacZ coding sequence to prepare the BBa_I732005 lacZ part for assembly using the RFC[25] standard.

However, while assembling the lacZ part with the RBS + ScAvidin + linker part, we might have encountered some STAR activity from our restriction enzymes, as the finalised lacZ part only contains fractions of the ScAvidin molecule, in contrast to the intermediates, where all of the ScAvidin was present.

The finalised composite lacZ plasmid was digested with BseRI to verify that the Scavidin part + RBS was there. If inserted correctly, two bands would be visible at ~6000 bp and ~1000 bp respectively. The bands on the gel (see figure 26) fit quite nicely with this description, except for the ~1000 bp band, which looks to be ~2000 bp long. However, since the plasmid only is about 7000 bp in length, it made no sense for such a large band to appear, and we assumed that the Scavidin would be inserted correctly, or the 6000 bp band wouldn’t appear. It thus appeared like the lacZ composite part was assembled correctly, but after sequencing the part, it was apparent that the positive result from the BseRI digest were due to the BseRI sites from Scavidin being recombined within the plasmid.

Test of composite lacZ part: ScAvidin binding to biotin

To test if our composite lacZ part was able to attach to biotinylated beads, a cell lysate from BBa_K2355313 transformants was added to tubes containing biotinylated magnetic beads. After separation on a magnetic separation rack, the supernatant was removed from tubes, and tubes were washed with washing buffer (PBS TWEEN-20 0.05%) a couple of times. For each washing cycle, samples were put aside for testing. The different samples were tested by adding ONPG, and measuring the activity of β-galactosidase. A plot of the measured average β-galactosidase for each purification step is shown in figure 27. Along with samples of washing buffer, the biotinylated beads themselves were measured for β-galactosidase activity, both before (Beads 1) and after (Beads 2) the washing steps.

Figure 27 shows that first fraction, which is the supernatant from the first magnetic separation following the addition of cell lysate to the beads, has the highest enzymatic activity of all the fractions measured, indicating that most of the β-galactosidase is washed out immediately, and not bound to the biotin beads. This is true for both the lacZ device with and without ScAvidin, which suggests that the ScAvidin of the composite lacZ part doesn’t work as intended. The fractions from the secondary and tertiary washing steps showed an enzyme activity close to zero; as did the enzyme activity of the isolated beads.

The fact that the lacZ part with ScAvidin didn’t bind to the biotin beads underlines the fact that a fully working ScAvidin might not be present at in the composite lacZ part.

Comparison of composite part with β-galactosidase

To test if our composite lacZ part (BBa_K2355313) would be cleaved by the snake venom, we used the biotinylated beads from the ScAvidin-binding experiment, and incubated them in snake venom for approx. 70 minutes. Besides having solutions of snake venom in Brij (0.01%), human blood serum was used to make solutions of snake venom that would emulate the blood samples of patients being envenomed by snakes.

As with the ScAvidin binding experiment, the presence of β-galactosidase is determined by measuring the conversion of ONPG in a spectrophotometer.

Figure 28 shows the result of the β-galactosidase activity measurements for the venom solutions with human blood serum.

As seen in figure 28, no noticeable activity is observed in any of the venom solutions. Ideally, we would have seen more β-galactosidase activity in the solutions with venoms that are able to cleave the empirical linker (i.e. the two Bitis venoms) as the venoms would have cleaved the linker, thus releasing the β-galactosidase into the supernatant that we were collecting in this experiment. The test with Brij-diluted venom had the same profile as figure 28, with no β-galactosidase activity from the venom solutions.

Since the ScAvidin binding experiment demonstrated an insignificant amount of ScAvidin binding to biotinylated beads, the concentrations of our composite lacZ part on the beads were probably too low for us to measure any cleavage of the linker sequence.