Difference between revisions of "Team:IISER-Mohali-INDIA/Demonstrate"

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Next, SOE1 PCR was performed using primers 5 and 8 to get an 891 bp amplified fragment.  
 
Next, SOE1 PCR was performed using primers 5 and 8 to get an 891 bp amplified fragment.  
 
Then, SOE2 PCR was performed using primers 5, primer 10 and the template SOE1 (891bp) fragment to amplify the 1783 bp fragment.
 
Then, SOE2 PCR was performed using primers 5, primer 10 and the template SOE1 (891bp) fragment to amplify the 1783 bp fragment.
The cloning of this SOE2 PCR fragment was attempted in the low copy number plasmid pZS21MCS, at SalI and BamHI sites. But due to problems with digestion of vector, we were not able to clone in pZS21MCS plasmid.  
+
The cloning of this SOE2 PCR fragment was attempted in the low copy number plasmid pZS21MCS, at SalI and BamHI sites, but due to problems with digestion of the vector, we were not able to clone in pZS21MCS plasmid.  
Therefore, construct 2 was finally cloned at SalI and BamHI site of pRC10 (modified ptrc99a) which is intermediate copy number plasmid.
+
Therefore, construct 2 was finally cloned at SalI and BamHI sites of pRC10 (modified ptrc99a) which is an intermediate copy number plasmid.
The <i>E. coli</i> transformants were screened for positive clones of construct 2 by restriction digestion and obtained positive clone 9 and shown in agraose gel below.
+
The <i>E. coli</i> transformants were screened for positive clones of construct 2 by restriction digestion and a positive clone 9 was obtained as shown in the image below.
 
</h4>
 
</h4>
 
<center><table><tr><td><img src="https://static.igem.org/mediawiki/2017/2/26/T--IISER-Mohali-INDIA--results1.jpg" alt="Screening of transformants containing construct 2 by resriction digestion with SalI and BamHI"></td></tr></table></center>
 
<center><table><tr><td><img src="https://static.igem.org/mediawiki/2017/2/26/T--IISER-Mohali-INDIA--results1.jpg" alt="Screening of transformants containing construct 2 by resriction digestion with SalI and BamHI"></td></tr></table></center>
<h3>2.Cloning of module 2:</h3>
+
<h3>2. Cloning of module 2:</h3>
<h4>For cloning of construct 1 of module II, Pmar-RBS4- ToxR-terminator 4  
+
<h4>Construct 1--> Pmar - RBS4 - ToxR - terminator 4.</h4>
The first PCR was performed with primer 11 and 12 using the template <i>E. coli</i> genome to amplify the pmar-RBS4. The size of PCR product is 524 bp.
+
<h4>The first PCR was performed with primers 11 and 12 using the template <i>E. coli</i> genome to amplify the pmar - RBS4. The size of the PCR product is 524 bp.
The second PCR was performed with primer 13 and 14 using the template K641009 to amplify ToxR. The size of PCR product is 1441 bp.
+
The second PCR was performed with primers 13 and 14 using the template K641009 to amplify ToxR. The size of this PCR product is 1441 bp.
Third PCR was performed using the primers 15 and 16 using the template pVenus to amplify terminator (271 bp). (for PCR conditions and reaction mixture, refer notebook).
+
The third PCR was performed using the primers 15 and 16 using the template pVenus to amplify terminator (271 bp). For PCR conditions and reaction mixture, refer notebook.
Then SOE1 PCR was performed using primer 11 and 14 to get 1965 bp amiplified fragment.  
+
Next, SOE1 PCR was performed using primers 11 and 14 to get a 1965 bp amplified fragment.  
Then SOE2 PCR was performed using using primer 11 and 16 using the template SOE1 (1965bp) and third pcr amplified fragment (271 bp) to amplify 2236 bp fragment.
+
Then, SOE2 PCR was performed using primer 11, primer 16, template SOE1 (1965bp) and third PCR amplified fragment (271 bp) to amplify the 2236 bp fragment.
This SOE2 PCR frament was tried to clone in low copy number plasmid pACYC177, at XhoI and XmaI site (high copy number plasmid).
+
This SOE2 PCR fragment was attempted to be cloned in low copy number plasmid pACYC177, at XhoI and XmaI sites (high copy number plasmid).
 
</h4>
 
</h4>
<h4>The E. coli transformants were screened for positive clones of construct 2 by restriction
+
<h4>The <i>E. coli</i> transformants were screened for positive clones of construct 2 by restriction
digestion and obtained positive clone in lane 2,3,4,6,7,8,9,10 and 11 are shown in agraose gel
+
digestion and positive clones were obtained in lane 2,3,4,6,7,8,9,10 and 11 as shown in image below:</h4>
below.</h4>
+
  
 
<center><table><tr><td><img src="https://static.igem.org/mediawiki/2017/7/72/T--IISER-Mohali-INDIA--rslstss.png" alt="Flow chart"></td></tr></table></center>
 
<center><table><tr><td><img src="https://static.igem.org/mediawiki/2017/7/72/T--IISER-Mohali-INDIA--rslstss.png" alt="Flow chart"></td></tr></table></center>
 
<center><table><tr><td><img src="https://static.igem.org/mediawiki/2017/3/31/T--IISER-Mohali-INDIA--CS4.png" alt="Flow chart"></td></tr></table></center>
 
<center><table><tr><td><img src="https://static.igem.org/mediawiki/2017/3/31/T--IISER-Mohali-INDIA--CS4.png" alt="Flow chart"></td></tr></table></center>
<h4>For cloning of construct 2, Pctx-RBS5- chromoprotein I- RBS6-TetR- terminator5.</h4>
+
<h4>Construct 2--> Pctx - RBS5 - chromoprotein I - RBS6 - TetR - terminator5.</h4>
 
<center><table><tr><td><img src="https://static.igem.org/mediawiki/2017/6/63/T--IISER-Mohali-INDIA--CS5.png" alt="Flow chart"></td></tr></table></center>
 
<center><table><tr><td><img src="https://static.igem.org/mediawiki/2017/6/63/T--IISER-Mohali-INDIA--CS5.png" alt="Flow chart"></td></tr></table></center>
<h4>Two PCR reactions were performed.
+
<h4>Two PCR reactions were performed. The first PCR reaction was performed with primers 17 and 18 to amplify the Pctx. The size of PCR product is 180 bp.
First PCR reaction is performed with primer 17 and 18 to amplify the Pctx. The size of PCR product is 180 bp.
+
The second PCR reaction was performed with primers 19 and 20 using the template K1343022 to amplify the RBS5 - chromoprotein I - RBS6 - TetR - terminator5. The size of PCR product is 1645 bp.
Second PCR reaction is performed with primer 19 and 20 using the template K1343022 to amplify the RBS5- chromoprotein I- RBS6-TetR- terminator5. The size of PCR product is 1645 bp.
+
Thirdly, SOE PCR was performed using the primers 17 and 20 to amplify 1825 bp (for PCR conditions and reaction mixture, refer notebook).
Third SOE PCR was performed using the primers 17 and 20 to amplify 1825 bp (for PCR conditions and reaction mixture, refer notebook).
+
Finally, construct II of module II was cloned at BamHI and AatII site of pACYC177 plasmid.
Final construct II of module II was cloned at BamHI and AatII site of pACYC177.
+
The <i>E. coli</i> transformants were screened for positive clones of construct 2 by PCR and obtained positive clone 4,6,7,8 and 10 shown in image below:</h4>
The <i>E. coli</i> transformants were screened for positive clones of construct 2 by PCR and obtained positive clone 4,6,7,8 and 10 shown in agraose gel below.</h4>
+
 
<center><table><tr><td><img src="https://static.igem.org/mediawiki/2017/a/a2/T--IISER-Mohali-INDIA--results2.jpg" alt="Flow chart"></td></tr></table></center>
 
<center><table><tr><td><img src="https://static.igem.org/mediawiki/2017/a/a2/T--IISER-Mohali-INDIA--results2.jpg" alt="Flow chart"></td></tr></table></center>
<h4>To check the sensitivity of the <i>mar</i> promoter, we used an <i>E. coli</i> strain (taken from C.R. Rao’s lab), which contains <i>mar</i> cis-element cloned upstream of the Venus reporter gene (a fast folding variant of yellow fluorescent protein) integrated at the <i>attλ</i> site. We monitored the induction of fluorescence in the reporter strain with increasing amount of salicylate as shown in the figure below.</h4>
+
<h4>To check the sensitivity of the <i>mar</i> promoter, we used an <i>E. coli</i> strain (taken from C.R. Rao’s lab), which contains a <i>mar</i> cis-element cloned upstream of the Venus reporter gene (a fast folding variant of yellow fluorescent protein) integrated at the <i>attλ</i> site. We monitored the amount of fluorescence in the reporter strain with increasing amount of salicylate as shown in the figure below:</h4>
 
<center><table><tr><td><img src="https://static.igem.org/mediawiki/2017/c/cf/T--IISER-Mohali-INDIA--results3.jpg" alt="Flow chart"></td></tr></table></center>
 
<center><table><tr><td><img src="https://static.igem.org/mediawiki/2017/c/cf/T--IISER-Mohali-INDIA--results3.jpg" alt="Flow chart"></td></tr></table></center>
 
<h4>The reporter strain was grown to exponential phase (0.5 OD600) and aliquoted 200 µl into three wells each of 96-well, clear bottom, black plate. Desired amount of salicylate was added from a stock into each well. LB media with and without salicylate were used as blank. The plates were incubated at 37°C with shaking and fluorescence was measured after 40 minutes of incubation λ<sub>excitation</sub> = 515 nm and λ<sub>emission</sub>= 547 nm.
 
<h4>The reporter strain was grown to exponential phase (0.5 OD600) and aliquoted 200 µl into three wells each of 96-well, clear bottom, black plate. Desired amount of salicylate was added from a stock into each well. LB media with and without salicylate were used as blank. The plates were incubated at 37°C with shaking and fluorescence was measured after 40 minutes of incubation λ<sub>excitation</sub> = 515 nm and λ<sub>emission</sub>= 547 nm.

Revision as of 21:10, 1 November 2017

gEco
Demonstrate






1. Cloning of module 1:

Construct 1--> Ptet - RBS1 - T7 RNA polymerase - terminator 1 - terminator 2. Two PCR reactions were performed. The first PCR reaction was performed with primer 1 and 2 using the template R0040 to amplify the Ptet. The size of PCR product is 77 bp. The second PCR reaction was performed with primer 3 and 4 using the template K1450004 to amplify the RBS1 - T7 RNA polymerase - terminator 1 - terminator 2. The size of this PCR product is 2338 bp. Thirdly, SOE PCR was performed using the primers 1 and 4 (for PCR conditions and reaction mixture, refer notebook).

Flow chart

The final PCR product was attempted to be cloned at AatII and ApaI sites of pZS21MCS. However, we did not get positive results for cloning, resulting in failure to clone the construct 1. Similarly, cloning of construct 2 (PT7 - RBS2 - Chromoprotein II - RBS3 - tetR - terminator3), three PCR reactions were performed.

Flow chart

The first PCR reaction was performed with primer 5 and 6 using the template K1343022 to amplify PT7-RBS2. The size of the PCR product is 132 bp. The second PCR reaction was performed with primer 7 and 8 using the template K1033910 to amplify chromoprotein II. The size of the PCR product is 759 bp. The third PCR was performed using the primers 9 and 10 (for PCR conditions and reaction mixture, refer notebook). Next, SOE1 PCR was performed using primers 5 and 8 to get an 891 bp amplified fragment. Then, SOE2 PCR was performed using primers 5, primer 10 and the template SOE1 (891bp) fragment to amplify the 1783 bp fragment. The cloning of this SOE2 PCR fragment was attempted in the low copy number plasmid pZS21MCS, at SalI and BamHI sites, but due to problems with digestion of the vector, we were not able to clone in pZS21MCS plasmid. Therefore, construct 2 was finally cloned at SalI and BamHI sites of pRC10 (modified ptrc99a) which is an intermediate copy number plasmid. The E. coli transformants were screened for positive clones of construct 2 by restriction digestion and a positive clone 9 was obtained as shown in the image below.

Screening of transformants containing construct 2 by resriction digestion with SalI and BamHI

2. Cloning of module 2:

Construct 1--> Pmar - RBS4 - ToxR - terminator 4.

The first PCR was performed with primers 11 and 12 using the template E. coli genome to amplify the pmar - RBS4. The size of the PCR product is 524 bp. The second PCR was performed with primers 13 and 14 using the template K641009 to amplify ToxR. The size of this PCR product is 1441 bp. The third PCR was performed using the primers 15 and 16 using the template pVenus to amplify terminator (271 bp). For PCR conditions and reaction mixture, refer notebook. Next, SOE1 PCR was performed using primers 11 and 14 to get a 1965 bp amplified fragment. Then, SOE2 PCR was performed using primer 11, primer 16, template SOE1 (1965bp) and third PCR amplified fragment (271 bp) to amplify the 2236 bp fragment. This SOE2 PCR fragment was attempted to be cloned in low copy number plasmid pACYC177, at XhoI and XmaI sites (high copy number plasmid).

The E. coli transformants were screened for positive clones of construct 2 by restriction digestion and positive clones were obtained in lane 2,3,4,6,7,8,9,10 and 11 as shown in image below:

Flow chart
Flow chart

Construct 2--> Pctx - RBS5 - chromoprotein I - RBS6 - TetR - terminator5.

Flow chart

Two PCR reactions were performed. The first PCR reaction was performed with primers 17 and 18 to amplify the Pctx. The size of PCR product is 180 bp. The second PCR reaction was performed with primers 19 and 20 using the template K1343022 to amplify the RBS5 - chromoprotein I - RBS6 - TetR - terminator5. The size of PCR product is 1645 bp. Thirdly, SOE PCR was performed using the primers 17 and 20 to amplify 1825 bp (for PCR conditions and reaction mixture, refer notebook). Finally, construct II of module II was cloned at BamHI and AatII site of pACYC177 plasmid. The E. coli transformants were screened for positive clones of construct 2 by PCR and obtained positive clone 4,6,7,8 and 10 shown in image below:

Flow chart

To check the sensitivity of the mar promoter, we used an E. coli strain (taken from C.R. Rao’s lab), which contains a mar cis-element cloned upstream of the Venus reporter gene (a fast folding variant of yellow fluorescent protein) integrated at the attλ site. We monitored the amount of fluorescence in the reporter strain with increasing amount of salicylate as shown in the figure below:

Flow chart

The reporter strain was grown to exponential phase (0.5 OD600) and aliquoted 200 µl into three wells each of 96-well, clear bottom, black plate. Desired amount of salicylate was added from a stock into each well. LB media with and without salicylate were used as blank. The plates were incubated at 37°C with shaking and fluorescence was measured after 40 minutes of incubation λexcitation = 515 nm and λemission= 547 nm. We observed that below 1.25 mM salicylate, very little induction of fluorescence is obtained. Thus, the sensitivity of the promoter is limited to mM concentration of salicylate. To increase the sensitivity of the reporter a different strong promoter or mutations in the MarR binding site can be done. We also investigated the time kinetics of the reporter, by measuring the fluorescence of the reporter strain induced with various concentrations of the salicylate. The 200 µl aliquots of the exponentially growing reporter strain cells were induced with desired concentrations of salicylate and fluorescence was measured after every 20 minutes. As seen in the figure below, the mar promoter responds very quickly to the salicylate. As in case of 0.625 mM salicylate concentration, the minimal fluorescent signal reached saturation in 150 minutes.

Flow chart

With higher concentrations of salicylate, the response was again very quick but with greater magnitude. Saturation of fluorescence signal could not be studied with higher concentrations as the fluorescence crossed the upper-limit of the instrument. Thus, we observe that the mar promoter responds within 20 minutes to the salicylate.

Cloning of chromoprotein for selection and part submission for registry :

We select five different chromoproteins for studying their kinetics to evaluate their utility in our circuit.

We have observed that out of these five different chromoproteins, chromoprotein sequence no. 1-3 develop color very fast (24-30 hours). But chromoproteins sequence no. 4-5 develop color vey late. Hence can not be suitable for utilization in our circuit. Therefore, we select chromoprotein amilCP Blue chromoprotein and fwYellow chromoprotein for utilization circuit. Further all these chromoproteins are cloned with RBS and LacI promoter by 3A assembly and submitted in depository with accession no. (from BBa_K2320001- K2320005).

Dishes
Dishes

Software

We seek to automate the process of reading gel doc slides and give reliable band sizes as outputs in a comprehensible format with an easy-to-use software. A manual mode is also developed for graphical analysis to ease detection of fainter bands that are too close to each other to differentiate using ones eyes. The software requires minimum resources: a few Python modules, and can be adjusted to suit any gel doc machine and a variety of standard ladders. The main difficulty in differentiating very closely spaced bands, due to the inefficiency of human eyes, is done away with in this module. Furthermore, we are also working on introducing machine learning in the software to give better accuracy in this regard and also to detect extremely faint bands. The software will help students and researchers to automate the mundane and routine task of reading gel doc slides.

User Manual