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Sensing

Overview

The Idea of this module was to transform the bacterium with a plasmid that would contain a promoter which senses a specific signal. Once this promoter senses the signal, it would initiate transcription of an enzyme which degrades the nanocapsule, thus releasing its contents. We decided to use pH as the specific trigger that activates the promoter. As a proof of principle, we inserted three different promoters into three plasmids in front of the bio brick BBa_I746916 which encodes superfolded GFP. Then we transformed cells with these plasmids and let them grow in media with different pHs in order to check the expression.

Figure 1: A Graphical summary of what the sensing module contained. Each promoter was inserted into the same plasmid in front of GFP

Experiments

We chose the following three pH sensitive promoters:
1.) Hya-promoter, isolated from the Escherichia Coli K-12 MG1655 strain
2.) Cad-promoter, isolated from the Escherichia Coli K-12 MG1655 strain
3.) BioBrick BBa_J23119, a constitutive promoter that was made by the 2006 Berkley team.

Figure 2: Sequence of the Hya promoter

Figure 3: Sequence of the Cad promoter

Figure 4: Sequuence of the constitutive promoter BBa_J23119

We digested the Plasmid containing the biobrick BBa_I746908 which would serve us as backbone for our constructs in order to qualitatively asses if it was indeed the expected plasmid.

Figure 5: Sequuence of the constitutive promoter BBa_J23119

All the promoters were isolated by PCR and then assembled into the pSB1C3 Plasmid in front of the superfolded GFP.

Figure 6: PCRs of the three Backbones

Figure 7: PCRs of the Hya and the Cad promoter

Figure 8: PCR of the constitutive promoter BBa_J23119

Then each of the constructs was used to transform DH5-alpha competent cells, which were first plated and then incubated into media with different pHs. 

We used four media:
1.) LB-Chloramphenicol with 10X MOPS+HCl, with a final pH of 5
2.) LB-Chloramphenicol with 10X MOPS, with a final pH of 6
3.) LB-Chloramphenicol without any buffer, with a final pH of 7
4.) LB-Chloramphenicol with 10X HEPES, with a final pH of 8.5

For each medium we measured the OD of the cells. This helped us to establish if a low expression of GFP was really due to the fact that the promoters did not work or simply that the cells were dying before they could initiate transcription and translation of the proten. It also would tell us if an increase of fluorescence was only due to an accumulation of bacteria or to the actual acumulation of GFP.

OD measurements

Figure 9: OD measurements of Bacteria with the hya promoter in different media

Figure 10: OD measurements of Bacteria with the cadpromoter in different media

Figure 11: OD measurements of Bacteria with the constitutive promoter in different media

GFP expression was measured using a plate reader where we made three replicates of each promoter with each pH. Then, the average for each replicate was calculated and used to establish a curve depicting GFP expression within each medium.

Hya Promoter

Figure 12: Normalized Fluorescence at pH 5.5

Figure 13: Normalized Fluorescence at pH 6.5

Figure 14: Normalized Fluorescence at pH 7.0

Figure 15: Normalized Fluorescence at pH 8.5

Cad Promoter

Figure 16: Normalized Fluorescence at pH 5.5

Figure 17: Normalized Fluorescence at pH 6.5

Figure 18: Normalized Fluorescence at pH 7.0

Figure 19: Normalized Fluorescence at pH 8.5

Constitutive Promoter

Figure 20: Normalized Fluorescence at pH 5.5

Figure 21: Normalized Fluorescence at pH 6.5

Figure 22: Normalized Fluorescence at pH 7.0

Figure 23: Normalized Fluorescence at pH 8.5

The Cells were also looked at under a microscope to qualitatively study their GFP expression.

Hya Promoter

Figure 24: FRAC_image, exposure: 400ms, Multiplier 1, pH 6.5

Figure 25: FRAC_image, exposure: 400ms, Multiplier 1, pH 8.5

Figure 26: FRAC_image, exposure: 550ms, Multiplier 1, pH 7

Cad Promoter

Figure 27: FRAC_image, exposure: 400ms, Multiplier 50, pH 6.5

Figure 28: FRAC_image, exposure: 400ms, Multiplier 50, pH 8.5

Figure 29: FRAC_image, exposure: 400ms, Multiplier 50, pH 7

Constitutive Promoter (Positive Control)

Figure 30:FRAC_image, exposure: 400ms, Multiplier 1, pH 6.5

Figure 31: FRAC_image, exposure: 400ms, Multiplier 1, pH 8.5

Figure 32: FRAC_image, exposure: 400ms, Multiplier 1, pH 7

Expected outcome:

The Promoters Hya and Cad were supposed to initiate transcription upon external acidification, which would then cause the bacteria to express superfolded GFP and turn bright green. The biobrick BBa_J23119, being a constitutive promoter, would turn the bacteria green independently of their medium.

Results:

We successully managed to isolate and amplify each of the three promoters as well as inserting them into the pSB1C3 plasmid so that they would control the expression of superfolded GFP. The transformation that followed was also successful, which was determined by sequencing the plasmid isolated from the colonies on the plate. This sequencing result showed a 100% match between the original promoter sequence and the inserted sequence that the bacteria contained. Also, the bacteria containing the biobrick pH-promoter had turned green on the plates as well as in liquid culture, which was just as expected.

References:

Journal of Bacteriology
Response of hya Expression to External pH in Escherichia coli
Paul W. King and Alan E. Przybyla
J.Bacteriol. 1990

Journal of Bacteriology
Mutational analysis and charecterization of the Escherichia coli hya operin, which encodes [NiFe] hydrogenase1
N K Menon, J Robbins, J C Wendt, K T Shanmuagam and A E Przybyla
J. Bacteriol 1991 Journal of Bacteriology
Nucleotode Sequence of the Escherichiea coli cad Operon: a system for neutralization of Low Extracellular pH
Shi-Yuan meng and George N. Bennett
J. Bacteriol 1992

Journal of Bacteriology
Regulation of the Escherichia coli cad Operon: Location of a Site Required for Acid Induction
Shi-Yuan meng and George N. Bennett
J. Bacteriol 1992

Effecting

Overview:

The goal of the effecting part of the project was to build a plasmid containing an arabinose promoter driving a tagged enzyme able to cleave gelatinase, the fabric used for our nano particles. We chose three different enzymes that would be inserted in part BBa_I746908, a pBAD promoter driving superfolder GFP, either between the promoter and GFP tag or instead of the GFP tag since it sometimes causes folding troubles. All of the constructs were planned to have a His tag as well, just in case something went wrong with the GFP tag, so we could extract and purify our expressed protein anyway.

Experiments:

The three different enzymes that we chose to use were gelatinase E (gelE) from Gram positive bacterium E. faecalis, metalloprotease 2 (MMP2) from H. sapiens and metalloprotease 9 (MMP9) from M. musculus. The genomic DNA of E. faecalis was ordered and a PCR was performed on it using Gibson primers that also added a His tag in front of the protein sequence. For MMP2 and MMP9, plasmids containing the coding sequence (CDS) of the proteins were ordered from plasmid.med.harvard.edu and the CDS were extracted in the same way as for gelatinase. In the meantime, PCRs were performed on the iGEM part BBa_I746908 to clone the backbone, add the overlap for the Gibson and, when needed, remove the GFP from the backbone (since we wanted to have a construct for each protein where GFP was replaced directly by the CDS). Competent cells were then transformed with the successful constructs, grown at 37C and later on activated, by adding 50ul of 20% arabinose solution to 5ml of inoculated culture, grown overnight, for 2h. A Western blot was then performed on the lysate and supernatural of the cells to check for the presence of the protein either out (if secreted as desired) or in (not secreted but at least expressed) the cells. A His-tag purification followed by SDS-PAGE were also executed.

Expected outcome:

We would expect the cells to be green and express/secrete a protein-GFP complex upon arabinose induction if everything works perfectly. The secreted protein, if correctly folded, could then break open the nano particles attached to the bacteria's surface, thus releasing the contained drug. However, we did not proceed to transform our bacteria with the coupling plasmid since the coupling section was stopped due to the lack of an antibody needed to prove that the coupling plasmid was complete.

Results:

The PCR reactions to amplify and extract the proteins CDSs and plasmid backbone were successful. We then proceeded to a Gibson assembly of the constructs that were meant to keep the GFP, for all three proteins. The Gibsons for the pBAD/araC-gelE-GFP and pBAD/araC-MMP2-GFP constructs worked, but not the one for the MMP9. We then transformed bacteria, isolated the plasmids and sent them for sequencing with the iGEM primers for the backbone and also with our own Gibson primers. This showed that the Gibson had been a success, but that a STOP codon had appeared in front of the GFP sequence, just after the linker. Indeed, the transformed bacteria did not appear green when induced with arabinose. Since a His tag had been added to the CDS of each protein using the Gibson primers, we did a Western blot with anti-his tag antibodies on the induced cell media and lysates. The result came out negative. We then proceeded to a his-tag purification of the cell lysates (Ni-NTA spin kit).