Difference between revisions of "Team:Bielefeld-CeBiTec/Results/unnatural base pair/preservation system"

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             <p class="figure subtitle"><b>Figure 1: </b><br> A: Average OD<SUB>600</SUB> of the three biological replicates for each cultiva-tion volume in the 12 well plate over the cultivation period. B: Average OD<SUB>600</SUB> of the three biological replicates of each volume in the 24 well plate over the cultivation period. C: Average OD<SUB>600</SUB> of the three bio-logical replicates of each cultivation volume in the 48 well plate over the cultivation period.</p>
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             <p class="figure subtitle"><b>Figure (1): </b><br> A: Average OD<SUB>600</SUB> of the three biological replicates for each cultivation volume in the 12 well plate over the cultivation period. B: Average OD<SUB>600</SUB> of the three biological replicates of each volume in the 24 well plate over the cultivation period. C: Average OD<SUB>600</SUB> of the three biological replicates of each cultivation volume in the 48 well plate over the cultivation period.</p>
 
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         Figures 1 shows that cultivation is possible in all well plates. The lowest OD<SUB>600</SUB> is consistently achieved by the highest volume with values at 2.271, 2.027 and 1.286 using the 12 well plate, 24 well plate and 48 well plate, respectively. The highest OD<SUB>600</SUB> is associated with the lowest volume with values of 2.629, 2.416 and 1.889 using the 12 well plate, 24 well plate and 48 well plate, respectively.  
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         Figure 1 shows that cultivation is possible in all well plates. The lowest OD<SUB>600</SUB> is consistently achieved by the highest volume with values at 2.271, 2.027 and 1.286 using the 12 well plate, 24 well plate and 48 well plate, respectively. The highest OD<SUB>600</SUB> is associated with the lowest volume with values of 2.629, 2.416 and 1.889 using the 12 well plate, 24 well plate and 48 well plate, respectively.  
 
Irrespective of volume, the highest OD<SUB>600</SUB> values were reached using the 12 well plate. Specifically, the OD<SUB>600</SUB> value of 2.271 using 3 mL in the 12 well plate is still higher than the OD<SUB>600</SUB> value of 2.027 using 1 mL in the 24 well plate.  
 
Irrespective of volume, the highest OD<SUB>600</SUB> values were reached using the 12 well plate. Specifically, the OD<SUB>600</SUB> value of 2.271 using 3 mL in the 12 well plate is still higher than the OD<SUB>600</SUB> value of 2.027 using 1 mL in the 24 well plate.  
 
After determining the best plate and volume to perform cultivations with, we investigated the influence of the rpm by cultivating three biological replicates at 500, 600, and 700 rpm in the 12 well plate in 1 mL.
 
After determining the best plate and volume to perform cultivations with, we investigated the influence of the rpm by cultivating three biological replicates at 500, 600, and 700 rpm in the 12 well plate in 1 mL.
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             <p class="figure subtitle"><b>Figure 2: </b><br> Growth curves of the three replicates of <i>E.coli</i> BL21 (DE3) in LB<sub>CM25</sub> at 350, 500, 600, and 700 rpm, respectively. The DNA concentration was measured under the optimal condition of 600 rpm and 1 mL volume.</p>
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             <p class="figure subtitle"><b>Figure (2): </b><br> Growth curves of the three replicates of <i>E.coli</i> BL21 (DE3) in LB<sub>CM25</sub> at 350, 500, 600, and 700 rpm, respectively. The DNA concentration was measured under the optimal condition of 600 rpm and 1 mL volume.</p>
 
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         <h3> <i>codA</i> </h3>
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         <h3> <i>Cytosine Deaminase <i>cod</i>A</i> </h3>
 
          
 
          
 
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             <p class="figure subtitle"><b>Figure 3: </b><br> Design of the flanking sequences for the deletion of <i>codA</i>.</p>
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             <p class="figure subtitle"><b>Figure (3): </b><br> Design of the flanking sequences for the deletion of <i>codA</i>.</p>
 
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<h3> Design of a Plasmid for the Retention of Unnatural Base Pairs </h3>
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Given that selection and screening of the transformants were not possible with our experimental design, we designed a plasmid which would kill or inhibit growth of the wrong colonies. Our initial design focused on the use of <i>ccd</i>B, but given that <i>ccd</i>B cannot be handed in, we decided to use levansucrase of <i>Bacillus subtilis</i>, encoded by <i>sac</i>B instead. Therefore, a mRFP-<i>sac</i>B fusion protein was constructed (BBa_K2201017). BBa_J23100 was used as a promoter and BBa_B0034 was used as a strong RBS, followed by BBa_E1010. Between mRFP and <i>sac</i>B, a linker consisting of four alanines was used. As a backbone, pSB3C5 was used. Given that this plasmid was designed to eventually carry an unnatural base pair, a low-copy plasmid was the better choice for a higher stability of the unnatural base pair.
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The idea behind this construct is the following: in the initial plasmid, mRFP and <i>sac</i>B are in-frame, meaning that cells turn red when incubated in standard media such as LB, but die or grow weakly when cultivated in media supplemented with sucrose. This is due to the toxic effect of levansucrase, which unfolds when cells are cultivated in sucrose supplemented media.
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<img class="figure image" src="https://static.igem.org/mediawiki/2017/e/e2/T--Bielefeld-CeBiTec--mRFPsacB-construct.jpeg">
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<p class="figure subtitle"><b>Figure (4): Fusionprotein of mRFP and sacB. Shown is the linker between the two sequences.</b><br> A flexible 4xAla linker was used between mRFP and <i>sac</i>B. </p>
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The linker between mRFP and <i>sac</i>B represents the insertion site for the fragment containing the unnatural base pair. This insertion, if successful, leads to a frameshift of the downstream located <i>sac</i>B, leading to loss of function. Therefore, cells can only survive in sucrose supplemented media if the fragment containing the unnatural base pair was successfully incorporated. This provides an easy screening method, since cells that turn red and survive in sucrose supplemented media most likely inserted the fragment containing the unnatural base pair into the plasmid. Having the coding sequences of both proteins in one frame has one big advantage: given that <i>sac</i>B is prone to loss-of-function mutations, contaminations can be easily distinguished by color. Furthermore, cells with mutations in the promotor region would also survive, since they would not express <i>sac</i>B, but not turn red. Therefore, this two-layered system allows to visually check if a culture either is contaminated, has a mutation in the promotor region, or if the correct plasmid is present.
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<p class="figure subtitle"><b>Figure (5): Method for selection of the correct plasmids in liquid cultures. </b><br> If the assembly was successful, cells turn red and survive in sucrose supplemented media. The cells die if the assembly was not successful, since <i>sac</i>B can be expressed.</p>
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To test the effect of sucrose on growth of the cells, a cultivation was performed of <i>E.&nbsp;coli</i> BL21(DE3) harboring BBa_K2201017. The cultivations were carried out in a 12 well plate in 1 mL of LB media supplemented with different concentrations of sucrose. Three biological replicates were cultivated for each condition and three technical replicates taken for each measurement point.
  
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<p class="figure subtitle"><b>Figure (6): Cultivation of <i>E.&nbsp;coli</i> BL21(DE3) in LB media supplemented with different concentrations of sucrose. </b><br> A clear difference in growth can be observed, with higher sucrose concentrations leading to weaker growth. The mRFP-SacB fusion protein does not lead to cell death, but shows bacteriostatic properties. Therefore, cells that successfully integrated the fragment containing the unnatural base pair should grow much better in the selective media and therefore overgrow cells harboring religated plasmid backbones. </p>
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The cultivations shown in figure (6) clearly show that sucrose has a significant effect on growth of strains carrying BBa_K2201017. A higher sucrose concentration leads to weaker growth, with strains cultivated in 20 % sucrose reaching only ~33 % of the OD600 of the reference strain cultivated in sucrose free media. The reference reached a final optical density of 3.233 ± 0.148, strains cultivated in media supplemented with 10 % sucrose 1.527 ± 0.055 and strains cultivated in 20 % sucrose reached a final optical density of 0.44 ± 0.05.
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Figure (7) shows a comparison of strains cultivated in media without sucrose and media supplemented with 10 % sucrose. A preculture of <i>E.&nbsp;coli</i> BL21(DE3) harboring BBa_K2201017 was prepared and cultivated overnight at 37 °C. 30 µl of this precultures were used and dropped onto LB agar plates either without or supplemented with 10 % sucrose. 50 µl of the same preculture were used to inoculate 3 mL of LB media without sucrose and 3 mL of LB media supplemented with 10 % sucrose.
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<p class="figure subtitle"><b>Figure (7): <i>E.&nbsp;coli</i> BL21(DE3) BBa_K2201017 cultivated on plates and in liquid cultures with and without 10 % sucrose. </b><br> All cultures were cultivated for 24 hours at 37 °C. <b>A)</b> Shows a drop on a LB agar plate supplemented with 10 % sucrose. <b>B)</b> Shows a drop on a LB agar plate without sucrose. A clear difference can be observed between the two drops. In presence of sucrose, <i>E.&nbsp;coli</i> BL21(DE3) BBa_K2201017 grew much weaker and did not turn red. Without sucrose, the cells grew much better and turned red. <b>C)</b> The same difference in growth and color could be observed in liquid cultures.</p>
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<h3> References </h3>
  
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Revision as of 00:05, 31 October 2017

Retention System

Pretests

Due to the high costs of our UBPs we had to carefully plan the experiments involv-ing these bases. Therefore, we carried out cultivation experiments of Escherichia coli BL21(DE3) in micro well plates, because performing experi-ments in a microscale would contribute significantly to a lower cost of the experi-ments. To cultivate at the ideal growth conditions, we performed pretests. In our ex-periments, we tested for the ideal culture volume, surface size and shaking frequency. The E. coli strain BL21(DE3) was transformed with the plasmid pSB3C5. LBCm25 plates were incubated overnight at 37 °C. Three colonies were picked and incubated in 150 mL LB media supplemented with LBCm25 overnight at 37 °C. Well-plates with 12, 24 and 48 wells were inoculated to an OD600 of 0.1 with a total of three biological replicates. Three different cultivation volumes were used to observe the cell growth in the different well plates with the different volumina.


Table 1: Used well plates and the different cultivation volumes in the particular plate. Three replicates per plate and volume were recorded at an rpm of 350.
12 Well Eppendorf 0030721012 24 Well Eppendorf 0030722019 48 Well Eppendorf 0030723015
1 mL 1 mL 0.5 mL
2 mL 2 mL 0.75 mL
3 mL 3 mL 1 mL
The cultivation was carried out in the VWR – Incubation Microplate Shaker and the OD600 measured via NanoDrop ND-1000 Spectrophotometer. Three technical replicates were measured for each sample.

Figure (1):
A: Average OD600 of the three biological replicates for each cultivation volume in the 12 well plate over the cultivation period. B: Average OD600 of the three biological replicates of each volume in the 24 well plate over the cultivation period. C: Average OD600 of the three biological replicates of each cultivation volume in the 48 well plate over the cultivation period.

Figure 1 shows that cultivation is possible in all well plates. The lowest OD600 is consistently achieved by the highest volume with values at 2.271, 2.027 and 1.286 using the 12 well plate, 24 well plate and 48 well plate, respectively. The highest OD600 is associated with the lowest volume with values of 2.629, 2.416 and 1.889 using the 12 well plate, 24 well plate and 48 well plate, respectively. Irrespective of volume, the highest OD600 values were reached using the 12 well plate. Specifically, the OD600 value of 2.271 using 3 mL in the 12 well plate is still higher than the OD600 value of 2.027 using 1 mL in the 24 well plate. After determining the best plate and volume to perform cultivations with, we investigated the influence of the rpm by cultivating three biological replicates at 500, 600, and 700 rpm in the 12 well plate in 1 mL.

Figure (2):
Growth curves of the three replicates of E.coli BL21 (DE3) in LBCM25 at 350, 500, 600, and 700 rpm, respectively. The DNA concentration was measured under the optimal condition of 600 rpm and 1 mL volume.

Cultivation at 600 rpm yields the highest OD600 with a value of about 4.961 after 6.5 h. If the rpm is further increased, the cells grow badly due to an out of phase movement of the media. We finally concluded that the perfect cultivation conditions are reached in a 12 well plate with a total volume of 1 mL and shaking with 600 rpm. For analysis of the retention and preservation of the unnatural base pair, the isolation of a sufficient amount of plasmid DNA from the culture is important. In order to evaluate the plasmid concentration during the cultivation, we cultivated at 600 rpm on a 12 well plate in 1 mL. We inoculated the wells with a starting OD600 of 0.1 and conducted a plasmid isolation using 1 mL for each measurement. The highest DNA concentration was reached in the exponential phase with about 85 ng/µl in 30 µl.

Cytosine Deaminase codA

Deletion of the codA gene could be useful for our project due to its ability to transform isoG and isoC into uracile. In this case the concentration of the UBPs decreases and our plasmid carrying the UBPs could not be replicated properly. We designed three compatible constructs for the potential deletion of codA following the protocol of Jiang et al.

At first we designed our construct carrying our synthesized single guide RNA (sgRNA), which is essential for the targeting specificity. Because of the presence of the sgRNA, Cas9 could carry out a sequence-specific, double-stranded break. In the case of a repair via homology directed repair with our designed PCR-construct, codA gets deleted. Just like Jian et al., we chose pTarget as our vector. Therefore, we annealed the sgRNA oligos, cloned them into the pTarget backbone via golden gate assembly and selected positive clones via blue-white screening.

The PCR-construct responsible for the homologous recombination, and therefore the codA deletion, was generated by two PCRs. In a first step, 700 bp upstream and downstream of codA were amplified. These two fragments were then inserted into the backbone using Gibson Assembly. The homologous recombination of the neighboring sequences of codA with the plasmid bound flanks leads to a deletion of this gene.

Figure (3):
Design of the flanking sequences for the deletion of codA.

As the Crispr-Cas9 system plasmid, we conceptualized pCas, also used by Jiang et al., containing the lambda-Red system for a higher recombineering efficiency. For the codA gene deletion you need to generate E. coli BL21 DE harboring pCas, and Arabinose (10 mM) has to be added for the generation of electocompetent E. coli BL21 DE for the lambda-Red induction. For the homology directed repair, one needs to transform pTarget and the PCR fragment into the pCas harboring E. coli. Then, one needs to verify positive transformants by colony PCR and DNA sequencing.

To cure pTarget, one can inoculate a positive colony at 30 °C for 8 to 16 hours in media containing kanamycin (50 mg L-1) and IPTG (0.5 mM). For the curing of pCas, the cell can be grown overnight at 37 °C nonselectively. The challenging part of this is the biological meaning of codA because of its important role in the purine synthesis pathway. To counteract this, it is advised to supplement with uracile (Mahan et al., 2004).

Design of a Plasmid for the Retention of Unnatural Base Pairs

Given that selection and screening of the transformants were not possible with our experimental design, we designed a plasmid which would kill or inhibit growth of the wrong colonies. Our initial design focused on the use of ccdB, but given that ccdB cannot be handed in, we decided to use levansucrase of Bacillus subtilis, encoded by sacB instead. Therefore, a mRFP-sacB fusion protein was constructed (BBa_K2201017). BBa_J23100 was used as a promoter and BBa_B0034 was used as a strong RBS, followed by BBa_E1010. Between mRFP and sacB, a linker consisting of four alanines was used. As a backbone, pSB3C5 was used. Given that this plasmid was designed to eventually carry an unnatural base pair, a low-copy plasmid was the better choice for a higher stability of the unnatural base pair. The idea behind this construct is the following: in the initial plasmid, mRFP and sacB are in-frame, meaning that cells turn red when incubated in standard media such as LB, but die or grow weakly when cultivated in media supplemented with sucrose. This is due to the toxic effect of levansucrase, which unfolds when cells are cultivated in sucrose supplemented media.

Figure (4): Fusionprotein of mRFP and sacB. Shown is the linker between the two sequences.
A flexible 4xAla linker was used between mRFP and sacB.

The linker between mRFP and sacB represents the insertion site for the fragment containing the unnatural base pair. This insertion, if successful, leads to a frameshift of the downstream located sacB, leading to loss of function. Therefore, cells can only survive in sucrose supplemented media if the fragment containing the unnatural base pair was successfully incorporated. This provides an easy screening method, since cells that turn red and survive in sucrose supplemented media most likely inserted the fragment containing the unnatural base pair into the plasmid. Having the coding sequences of both proteins in one frame has one big advantage: given that sacB is prone to loss-of-function mutations, contaminations can be easily distinguished by color. Furthermore, cells with mutations in the promotor region would also survive, since they would not express sacB, but not turn red. Therefore, this two-layered system allows to visually check if a culture either is contaminated, has a mutation in the promotor region, or if the correct plasmid is present.

Figure (5): Method for selection of the correct plasmids in liquid cultures.
If the assembly was successful, cells turn red and survive in sucrose supplemented media. The cells die if the assembly was not successful, since sacB can be expressed.

To test the effect of sucrose on growth of the cells, a cultivation was performed of E. coli BL21(DE3) harboring BBa_K2201017. The cultivations were carried out in a 12 well plate in 1 mL of LB media supplemented with different concentrations of sucrose. Three biological replicates were cultivated for each condition and three technical replicates taken for each measurement point.

Figure (6): Cultivation of E. coli BL21(DE3) in LB media supplemented with different concentrations of sucrose.
A clear difference in growth can be observed, with higher sucrose concentrations leading to weaker growth. The mRFP-SacB fusion protein does not lead to cell death, but shows bacteriostatic properties. Therefore, cells that successfully integrated the fragment containing the unnatural base pair should grow much better in the selective media and therefore overgrow cells harboring religated plasmid backbones.

The cultivations shown in figure (6) clearly show that sucrose has a significant effect on growth of strains carrying BBa_K2201017. A higher sucrose concentration leads to weaker growth, with strains cultivated in 20 % sucrose reaching only ~33 % of the OD600 of the reference strain cultivated in sucrose free media. The reference reached a final optical density of 3.233 ± 0.148, strains cultivated in media supplemented with 10 % sucrose 1.527 ± 0.055 and strains cultivated in 20 % sucrose reached a final optical density of 0.44 ± 0.05. Figure (7) shows a comparison of strains cultivated in media without sucrose and media supplemented with 10 % sucrose. A preculture of E. coli BL21(DE3) harboring BBa_K2201017 was prepared and cultivated overnight at 37 °C. 30 µl of this precultures were used and dropped onto LB agar plates either without or supplemented with 10 % sucrose. 50 µl of the same preculture were used to inoculate 3 mL of LB media without sucrose and 3 mL of LB media supplemented with 10 % sucrose.

Figure (7): E. coli BL21(DE3) BBa_K2201017 cultivated on plates and in liquid cultures with and without 10 % sucrose.
All cultures were cultivated for 24 hours at 37 °C. A) Shows a drop on a LB agar plate supplemented with 10 % sucrose. B) Shows a drop on a LB agar plate without sucrose. A clear difference can be observed between the two drops. In presence of sucrose, E. coli BL21(DE3) BBa_K2201017 grew much weaker and did not turn red. Without sucrose, the cells grew much better and turned red. C) The same difference in growth and color could be observed in liquid cultures.

References