Team:BYU Provo/Notebook/Cholera - Detection/Winterexp/Period3/Dailylog

From 2013.igem.org

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| colspan="3" | <font color="#333399" size="5" font face="Calibri"> '''Cholera Detection March - April Notebook: April 1 - April 14 Daily Log'''</font>
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| colspan="3" | <font color="#333399" size="5" font face="Calibri"> '''Cholera Detection March - April Notebook: April 1 - April 15 Daily Log'''</font>
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<font size="4"> '''4/1/13''' </font>
<font size="4"> '''4/1/13''' </font>
-
KK
+
-KK Our transformations worked this time and we had several beautiful lawns of E.Coli. The E. Coli did NOT fluoresce either red or green to the naked eye. We haven’t yet looked at them under UV light. Clarisse streaked several singles, and also set up two overnight colonies. Kelton and I practiced streaking to singles for the first time, using old plates. We placed our E.Coli singles in the 37 degree room to grow, along with the overnights on the shaker. Most of today we spent presenting our progress thus far. It appears that bacteriophage K139 will not be very useful to us, as we will need to use E.Coli bacteriophage lambda for our system. Dr. Grose has ordered Lambda and it is on it’s way. Our goal is to incorporate the Lambda genome as a lysogenic prophage into the genome of E.Coli, and have that prophage remain dormant until the presence of cholera’s autoreceptor triggers the phage to be excised from E.Coli’s genome and become lytic. The lysogeny/lysis balance is determined by the relative concentrations of two proteins, CRO and CI. The two proteins are mutually exclusive; if one is being expressed, then the other cannot be expressed, because they share a promoter region. Expression of CRO triggers the events that lead to replication and lysis. Expression of CI induces and maintains lysogeny. Our plan is clone the CI protein into E.Coli following the Qrr4 protein and the CRO protein following HapR.
-
Our transformations worked this time and we had several beautiful lawns of E.Coli. The E. Coli did NOT fluoresce either red or green to the naked eye. We haven’t yet looked at them under UV light. Clarisse streaked several singles, and also set up two overnight colonies. Kelton and I practiced streaking to singles for the first time, using old plates. We placed our E.Coli singles in the 37 degree room to grow, along with the overnights on the shaker. Most of today we spent presenting our progress thus far. It appears that bacteriophage K139 will not be very useful to us, as we will need to use E.Coli bacteriophage lambda for our system. Dr. Grose has ordered Lambda and it is on it’s way. Our goal is to incorporate the Lambda genome as a lysogenic prophage into the genome of E.Coli, and have that prophage remain dormant until the presence of cholera’s autoreceptor triggers the phage to be excised from E.Coli’s genome and become lytic. The lysogeny/lysis balance is determined by the relative concentrations of two proteins, CRO and CI. The two proteins are mutually exclusive; if one is being expressed, then the other cannot be expressed, because they share a promoter region. Expression of CRO triggers the events that lead to replication and lysis. Expression of CI induces and maintains lysogeny. Our plan is clone the CI protein into E.Coli following the Qrr4 protein and the CRO protein following HapR.
+
-
KP  
+
- KP We started today with each group presenting their research and game plan for the coming weeks/months. It seems like we all know, or at least have a direction, to our next plan of action. Our E. coli turned out well and we were able to single out a colony in order to prepare overnight. After further research, it is clear that we will not be able to use T phages in our E. coli as a means to destroy cholera biofilm. We have all done more research on lambda, and it appears to be our best lysogenic phage choice. It is well studied and the mechanism for turning on the lytic cycle is very well understood.
-
We started today with each group presenting their research and game plan for the coming weeks/months. It seems like we all know, or at least have a direction, to our next plan of action. Our E. coli turned out well and we were able to single out a colony in order to prepare overnight. After further research, it is clear that we will not be able to use T phages in our E. coli as a means to destroy cholera biofilm. We have all done more research on lambda, and it appears to be our best lysogenic phage choice. It is well studied and the mechanism for turning on the lytic cycle is very well understood.
+
<br>
<br>
<font size="4"> '''4/3/13''' </font>
<font size="4"> '''4/3/13''' </font>
-
- Learned about how to start an overnight liquid culture for host bacteria
+
- KK Not this Friday, but next Friday, we will have our Final Presentations. They will be done by sub-group; my sub-group is the cholera-phage approach. As part of the project, I need to attend a science seminar. Tomorrow I’ll attend the seminar by John Roth on something to do with molecular biology, then write a one-paragraph summary of HOW the presentation was done, the showsmanship of the presentation. On the day of our presentation we need to explain the background of what we have done, then go into our methods and results, then give our conclusions. Today we followed the mini-prep/Alkaline lysis procedure to purify plasmids from our overnight samples. We followed the step-by step protocol given in the kit we used. We chose to use 1 mL of our E.Coli overnight solution in our samples ... and at the end, our plasmid concentrations were low (24 ng/microL and 16ng/microL, respectively). We used the spectrophotometer in Dr. Grose’s lab to determine the concentrations of our plasmids. So, in the future, we ought to a) include Dr. Grose as we follow the protocol to ensure we are doing things correctly, and b) probably use more of the E.Coli sample to get more plasmids and hopefully a higher concentration.
-
- Learned about how to create bacterial glycerol stock
+
- KP April Today we purified the plasmids and got them ready to be sequenced. We used Dr. Grose’s spectrophotometer. We learned how to analyze the graph in order to know if we just have DNA or if there is something else in our mixture after the purification process. The bump of our graph was right over 260, so we know that we successfully purified our plasmids! The only object of concern, is the fact that we had a very low concentration of plasmids. The instructions in the kit advised 1-3 mL of E. coli potion for high copy DNA. We used 1 mL, so next time we will try 2-3 mL to see if we can get a higher concentration. We are unsure if we did something wrong, if there is something wrong with the kit, or if we just need to use more of the E. coli overnight potion. I need to become more familiar with the sequence of our plasmid, and we need to find out why our E.coli doesn’t glow. When I understand the plasmid sequence, hopefully we can know what is missing or defective in our E. coli that keeps it from glowing.
-
 
+
-
- Made fresh LB and concentrated top agar stock
+
-
: [[Team:BYU_Provo/Notebook/SmallPhage/Winterexp/Period1/Exp/4.3 Top Agar Stock Preparation|4.3 Top Agar Stock Preparation]]
+
-
 
+
-
<br>
+
-
 
+
-
<font size="4"> '''4/4/13''' </font>
+
-
 
+
-
- T7 arrived
+
-
 
+
-
- Overnight liquid culture for bacterial host started by Dr. Grose
+
<br>
<br>
Line 61: Line 48:
<font size="4"> '''4/5/13''' </font>
<font size="4"> '''4/5/13''' </font>
-
- Background research on phiX174: the only phage we have in stock
+
- KP Today we made a plan of exactly what we need to do in the next week and coming months. Our biggest priority at this time is sequencing the plasmid from last years iGEM team. I was reading in the iGEM registry, and I saw that there is a pIG78 A and B. We tried A, but we haven’t tried B. On Monday we will try to transfer B into E. Coli and see if B works better than A. Next week our goal is to completely sequence the plasmid to see if something is missing or incorrect. I also need to do more research to understand better what last years team did and also the specifics of how we are going to set up our phage and how we are going to induce the lytic cycle in the presence of cholera.
-
- Performed [[Team:BYU_Provo/Notebook/SmallPhage/Winterexp/Period1/Exp/3.20 Phage Viability Test|3.20 Phage Viability Test]]
+
- KK Today we set out some long-term priorities for what we should do from here on out. Our priorities: 1. Determine is the QS circuit working? We aren’t getting RFP right now … what’s wrong? a. We need to determine what primers were used to amplify the HapR and Qrr4 out of cholera b. What is the difference between pIG78 A and pIG78 B? There are two plasmids that are the same? We hope to KNOW the answers to these questions by Thursday 2. Clone CI behind Qrr4 promoter; determine where in plasmid and order primers order primers 3. Clone CRO behind HapR promoter DONE by Mid-May 4. Modify tails of phage (after C1 and CRO steps complete) DONE by summer 5. If possible, use selectable marker on phage to purify many E. Coli that have prophage incorporated into the genome. So these are the steps we set out, we need to discuss with Dr. Grose where we should be the C1 and CRO genes, because the plasmid is already very full. Personally, I need to understand the plasmid we’re using, the Lambda repression circuit, and the Lambda tail proteins better.
<br>
<br>
-
<font size="4"> '''3/21/13''' </font>
+
<font size="4"> '''4/8/13''' </font>
-
- Checked up on results for [[Team:BYU_Provo/Notebook/SmallPhage/Winterexp/Period1/Exp/3.20 Phage Viability Test|3.20 Phage Viability Test]]
+
- KK The other cholera-subgroup is successfully growing biofilm. They have found that cholera biofilm grows best in a salty solution (their best imitation of seawater) at 37 C. Today we set up a quick experiment to see how our pIG78d+ E.Coli would respond to the presence of cholera. Using a cholera sample that was NOT growing much biofilm (the sample had been grown in normal LB at 30 C), we set up 5 test tubes. 1. 4 mL plain LB 2. 4 mL plain LB + 500 microL V.Cholerae solution 3. 4 mL plain LB + pIG78D DH5alpha E.Coli 4. 4 mL plain LB + 100 microL V. Cholerae solution + pIG78D DH5alpha E.Coli 5. 4 mL plain LB + 500 microL V. Cholerae solution + pIG78D DH5alpha E.Coli
 +
We set the overnight tubes in 30 C room on the shaker. Also, we set up two E.Coli overnights for miniprep on Wednesday.
 +
As part of our presentation on Friday we plan to present the results of whether our plasmid is functioning to detect cholera or not and why. We are still waiting for the sequencing results to come back to us. We also will present the research we have done on Lambda.
-
<br>
+
- KP I worked with kendall to set up an overnight so that we can do a mini-prep tomorrow to continue our sequencing of our plasmid. After we completed our overnight prep, we set up an experiment to test to ability of our plasmid to give off a color response to cholera. We prepared the 5 tubes that Kendall explained above, we then put them in the 30 C room overnight and we will check on them tomorrow.
-
 
+
-
<font size="4"> '''3/22/13''' </font>
+
-
 
+
-
- Discussed results from tittering experiment (preliminary experiment 1)
+
-
 
+
-
: Contamination mostly likely resulted from the step involving suspending phage in LB – obvious contamination in the LB bottle
+
-
 
+
-
: One of the stock phage solution had contamination as well
+
-
 
+
-
- Discussed step of attack with Dr. Grose
+
-
 
+
-
: Decided to go with T7, if necessary Qbeta
+
-
 
+
-
: Need to learn to make top agar at various concentrations
+
-
 
+
-
: Need to do more background research and decide whether to assemble phage capsid in vitro (plasmid + E coli) or do direct mutagenesis of phage genome
+
-
 
+
-
:: Need to correspond with the isolation team
+
-
 
+
-
- Sequencing will be for individual genes to cut down cost
+
-
 
+
-
: Need to design primers and get to know the genome of the phage
+
-
 
+
-
- Learnt about Mega5 to compare genome and protein sequence
+
<br>
<br>
-
<font size="4"> '''3/25/13''' </font>
+
<font size="4"> '''4/10/13''' </font>
-
- Reported on past week and plans for this week
+
- KK Results from our overnight cholera preps: The first three tubes from the left are controls, one with pure LB, one with cholera + LB (which was grown at 30 degrees by the other subgroup), and one with E.Coli + LB, respectively. The fourth and fifth tubes have cholera, E.Coli, and LB. The fourth has a slightly greater number of cholera (500 microL of cholera-saturated broth) compared to the fifth (100 microL of cholera-saturated broth). These are the results after two days of shaker-incubation at 30 degrees C, when the cultures are viewed under UV light. We went over the quorum-sensing circuit with Dr. Grose. The Cqss membrane receptor phosphorylates Lux U, which cascades phosphorylation to LuxO. LuxO, when phosphorylated, binds to the Qrr4 promoter, activating transcription of Qrr4 mRNA. Qrr4 mRNA interferes with HapR, so there is no protein HapR. HapR is a repressor whose binding site is at the promoter for GFP. When Qrr4 eliminates HapR, there is no repression of the expression of GFP. Thus, GFP should be ON when Cholera is NOT present. The reverse is also true. In the presence of Cholera autoinducer, CQSS acts as a phophatase on LuxU, which does the same to LuxO, which does NOT activate Qrr4 mRNA which does NOT degrade HapR which represses transcription of GFP. Thus GFP should NOT glow in the presence of cholera.
-
: From last week: titering experiment
+
Our results in these test tubes aren’t exactly in agreement with what we want.
-
: This week
+
-
:: Learn to make top agar at various concentrations
+
-
:: Background research to determine in vitro assembly vs altering genome – look into specific techniques
+
-
:: Comparing genome of phage and decide on possible site-directed mutagenesis options
+
-
- Start working on designing our site directed mutagenesis
+
- KP Today we worked on our presentation for Friday and we also went over the quorum sensing with Dr. Grose.
-
: Qbeta vs MS2
+
-
:: Look for places where sequences are significantly different
+
-
:: Might be worthwhile to look at capsid structure to identify the regions where interactions between subunits take place
+
-
 
+
-
: Qbeta vs T7 major
+
-
:: No real consensus – more worthwhile to compare capsid protein sequence of T7 with those that have similar size to it
+
-
 
+
-
: T7 major vs minor
+
-
:: Minor is longer, but not necessary – the tail overhang is due to ribosome moving two codons downstream instead of three
+
-
:: Suggest we can direct mutation to the poly-U site and prevent ribosome slippage
+
-
 
+
-
: Qbeta major vs minor
+
-
:: Just continue transcribing after it reaches the stop codon. What does the stop codon code for?
+
-
 
+
-
- Research into in-vitro assembly vs direct mutation of phage genome
+
-
: It seems that we’ll need to clone the genome of the phage into a plasmid and let it assemble in an E coli
+
-
: Using chemicals we can induce random mutations in phage – might be worthwhile if selection in agar is not working as well.
+
<br>
<br>
-
<font size="4"> '''3/27/13''' </font>
+
<font size="4"> '''4/12/13''' </font>
-
 
+
-
- More research on genome of enterobacteria phage
+
-
: Generation of the major and minor capsid in Q beta
+
- KP We had our presentation today. It was good practice and I learned some things to improve on in the future. There was some confusion on the quorum sensing, because we thought that HapR was a repressor and that it shouldn’t glow green in the presence of cholera. It turn out that it is the other way around and that it should glow green in the presence of cholera and red in the absence of cholera. That still doesnt explain why our tests are glowing green in the absence of cholera. We will have to work backwards and find out exactly what it is that we have. I feel that we have a clearer view of what we need to do. Also, I need to do more research other than wikipedia on lambda phage and its lytic and lysogenic cycles, because in our presentation, I said that that lambda enters the lytic cycle when it is in a cell that is healthy and lysogenic cycle when the cell is in trouble. That is what it says on wikipedia. Anyway, when I said that, I was told that I was wrong and that it is the other way around. I will look into that. We also hopefully got our quorum sensing system worked out now. All we need to do (once we figure out what we actually have in our plasmids) is add the cro transcription site after the GFP, and in the presence of cholera more cro will be produced and lambda will enter the lytic cycle!
-
: Capsid protein information research
+
-
: Capsid protein sequence comparison
+
-
- Outlined protocol for producing stock top agar
+
- KK Today was our presentation in class. This is the link to our powerpoint presenation: https://docs.google.com/presentation/d/14mUxVrUdTvNXaPGifXZs_lpXeMrFd-4CxSZ9o1bPqYo/edit#slide=id.p Our presentation gave a background for our project - though we ought to have been clearer WHY we want to use phage - and also the work that we’ve accomplished thus far in our group. We went a long time over in our presentation; it took a long time to explain the quorum sensing circuit, Lambda, and other things. Dr Grose sent an email with several suggestions for presentations in the future. They include being more concise with our time management and better coordinating within our group so that we don’t end up repeating ourselves. In the future we will be expected to be more polished presenters.
-
: [[Team:BYU_Provo/Notebook/SmallPhage/Winterexp/Period1/Exp/4.3 Top Agar Stock Preparation|4.3 Top Agar Stock Preparation]]
+
<br>
<br>
-
<font size="4"> '''3/29/13''' </font>
+
<font size="4"> '''4/15/13''' </font>
-
- Worked on our first team presentation.
+
- KP Today we started out by getting photographed. We also watched the phage group’s presentations. It seems as if they have a good start to their project. We didn’t have too much time to do our own experiments, but we did set up an overnight to do mini-prep tomorrow, and we streaked out our plates of lambda phage.
 +
- KK The three phage groups presented today. I realized how very quickly each of our groups has specialized to the point that I have to concentrate deeply to understand what seems to be second nature to members of the phage group. That’s good! It means each of our groups is moving along nicely. The objective of the phage project is to make a library of sizes - the biggest and smallest phage capsids possible using phages that have already been well characterized and approved for medicinal purposes. One group is working on selecting for the largest phage possible, one for the smallest, and another group is developing a method to purify both phages as they are made. Afterwards, we laid out singles of our three E.Coli strains with Lambda prophage incorporated into its genome. Tomorrow Kelton and I are going to go in and check on them after our Intro to Medicine class.
<br>
<br>

Latest revision as of 22:12, 5 June 2013


Cholera Detection March - April Notebook: April 1 - April 15 Daily Log




Overview
March-April
May-June
July-August
September-October

4/1/13

-KK Our transformations worked this time and we had several beautiful lawns of E.Coli. The E. Coli did NOT fluoresce either red or green to the naked eye. We haven’t yet looked at them under UV light. Clarisse streaked several singles, and also set up two overnight colonies. Kelton and I practiced streaking to singles for the first time, using old plates. We placed our E.Coli singles in the 37 degree room to grow, along with the overnights on the shaker. Most of today we spent presenting our progress thus far. It appears that bacteriophage K139 will not be very useful to us, as we will need to use E.Coli bacteriophage lambda for our system. Dr. Grose has ordered Lambda and it is on it’s way. Our goal is to incorporate the Lambda genome as a lysogenic prophage into the genome of E.Coli, and have that prophage remain dormant until the presence of cholera’s autoreceptor triggers the phage to be excised from E.Coli’s genome and become lytic. The lysogeny/lysis balance is determined by the relative concentrations of two proteins, CRO and CI. The two proteins are mutually exclusive; if one is being expressed, then the other cannot be expressed, because they share a promoter region. Expression of CRO triggers the events that lead to replication and lysis. Expression of CI induces and maintains lysogeny. Our plan is clone the CI protein into E.Coli following the Qrr4 protein and the CRO protein following HapR.

- KP We started today with each group presenting their research and game plan for the coming weeks/months. It seems like we all know, or at least have a direction, to our next plan of action. Our E. coli turned out well and we were able to single out a colony in order to prepare overnight. After further research, it is clear that we will not be able to use T phages in our E. coli as a means to destroy cholera biofilm. We have all done more research on lambda, and it appears to be our best lysogenic phage choice. It is well studied and the mechanism for turning on the lytic cycle is very well understood.

4/3/13

- KK Not this Friday, but next Friday, we will have our Final Presentations. They will be done by sub-group; my sub-group is the cholera-phage approach. As part of the project, I need to attend a science seminar. Tomorrow I’ll attend the seminar by John Roth on something to do with molecular biology, then write a one-paragraph summary of HOW the presentation was done, the showsmanship of the presentation. On the day of our presentation we need to explain the background of what we have done, then go into our methods and results, then give our conclusions. Today we followed the mini-prep/Alkaline lysis procedure to purify plasmids from our overnight samples. We followed the step-by step protocol given in the kit we used. We chose to use 1 mL of our E.Coli overnight solution in our samples ... and at the end, our plasmid concentrations were low (24 ng/microL and 16ng/microL, respectively). We used the spectrophotometer in Dr. Grose’s lab to determine the concentrations of our plasmids. So, in the future, we ought to a) include Dr. Grose as we follow the protocol to ensure we are doing things correctly, and b) probably use more of the E.Coli sample to get more plasmids and hopefully a higher concentration.

- KP April Today we purified the plasmids and got them ready to be sequenced. We used Dr. Grose’s spectrophotometer. We learned how to analyze the graph in order to know if we just have DNA or if there is something else in our mixture after the purification process. The bump of our graph was right over 260, so we know that we successfully purified our plasmids! The only object of concern, is the fact that we had a very low concentration of plasmids. The instructions in the kit advised 1-3 mL of E. coli potion for high copy DNA. We used 1 mL, so next time we will try 2-3 mL to see if we can get a higher concentration. We are unsure if we did something wrong, if there is something wrong with the kit, or if we just need to use more of the E. coli overnight potion. I need to become more familiar with the sequence of our plasmid, and we need to find out why our E.coli doesn’t glow. When I understand the plasmid sequence, hopefully we can know what is missing or defective in our E. coli that keeps it from glowing.


4/5/13

- KP Today we made a plan of exactly what we need to do in the next week and coming months. Our biggest priority at this time is sequencing the plasmid from last years iGEM team. I was reading in the iGEM registry, and I saw that there is a pIG78 A and B. We tried A, but we haven’t tried B. On Monday we will try to transfer B into E. Coli and see if B works better than A. Next week our goal is to completely sequence the plasmid to see if something is missing or incorrect. I also need to do more research to understand better what last years team did and also the specifics of how we are going to set up our phage and how we are going to induce the lytic cycle in the presence of cholera.

- KK Today we set out some long-term priorities for what we should do from here on out. Our priorities: 1. Determine is the QS circuit working? We aren’t getting RFP right now … what’s wrong? a. We need to determine what primers were used to amplify the HapR and Qrr4 out of cholera b. What is the difference between pIG78 A and pIG78 B? There are two plasmids that are the same? We hope to KNOW the answers to these questions by Thursday 2. Clone CI behind Qrr4 promoter; determine where in plasmid and order primers order primers 3. Clone CRO behind HapR promoter DONE by Mid-May 4. Modify tails of phage (after C1 and CRO steps complete) DONE by summer 5. If possible, use selectable marker on phage to purify many E. Coli that have prophage incorporated into the genome. So these are the steps we set out, we need to discuss with Dr. Grose where we should be the C1 and CRO genes, because the plasmid is already very full. Personally, I need to understand the plasmid we’re using, the Lambda repression circuit, and the Lambda tail proteins better.


4/8/13

- KK The other cholera-subgroup is successfully growing biofilm. They have found that cholera biofilm grows best in a salty solution (their best imitation of seawater) at 37 C. Today we set up a quick experiment to see how our pIG78d+ E.Coli would respond to the presence of cholera. Using a cholera sample that was NOT growing much biofilm (the sample had been grown in normal LB at 30 C), we set up 5 test tubes. 1. 4 mL plain LB 2. 4 mL plain LB + 500 microL V.Cholerae solution 3. 4 mL plain LB + pIG78D DH5alpha E.Coli 4. 4 mL plain LB + 100 microL V. Cholerae solution + pIG78D DH5alpha E.Coli 5. 4 mL plain LB + 500 microL V. Cholerae solution + pIG78D DH5alpha E.Coli We set the overnight tubes in 30 C room on the shaker. Also, we set up two E.Coli overnights for miniprep on Wednesday. As part of our presentation on Friday we plan to present the results of whether our plasmid is functioning to detect cholera or not and why. We are still waiting for the sequencing results to come back to us. We also will present the research we have done on Lambda.

- KP I worked with kendall to set up an overnight so that we can do a mini-prep tomorrow to continue our sequencing of our plasmid. After we completed our overnight prep, we set up an experiment to test to ability of our plasmid to give off a color response to cholera. We prepared the 5 tubes that Kendall explained above, we then put them in the 30 C room overnight and we will check on them tomorrow.


4/10/13

- KK Results from our overnight cholera preps: The first three tubes from the left are controls, one with pure LB, one with cholera + LB (which was grown at 30 degrees by the other subgroup), and one with E.Coli + LB, respectively. The fourth and fifth tubes have cholera, E.Coli, and LB. The fourth has a slightly greater number of cholera (500 microL of cholera-saturated broth) compared to the fifth (100 microL of cholera-saturated broth). These are the results after two days of shaker-incubation at 30 degrees C, when the cultures are viewed under UV light. We went over the quorum-sensing circuit with Dr. Grose. The Cqss membrane receptor phosphorylates Lux U, which cascades phosphorylation to LuxO. LuxO, when phosphorylated, binds to the Qrr4 promoter, activating transcription of Qrr4 mRNA. Qrr4 mRNA interferes with HapR, so there is no protein HapR. HapR is a repressor whose binding site is at the promoter for GFP. When Qrr4 eliminates HapR, there is no repression of the expression of GFP. Thus, GFP should be ON when Cholera is NOT present. The reverse is also true. In the presence of Cholera autoinducer, CQSS acts as a phophatase on LuxU, which does the same to LuxO, which does NOT activate Qrr4 mRNA which does NOT degrade HapR which represses transcription of GFP. Thus GFP should NOT glow in the presence of cholera. Our results in these test tubes aren’t exactly in agreement with what we want.

- KP Today we worked on our presentation for Friday and we also went over the quorum sensing with Dr. Grose.


4/12/13

- KP We had our presentation today. It was good practice and I learned some things to improve on in the future. There was some confusion on the quorum sensing, because we thought that HapR was a repressor and that it shouldn’t glow green in the presence of cholera. It turn out that it is the other way around and that it should glow green in the presence of cholera and red in the absence of cholera. That still doesnt explain why our tests are glowing green in the absence of cholera. We will have to work backwards and find out exactly what it is that we have. I feel that we have a clearer view of what we need to do. Also, I need to do more research other than wikipedia on lambda phage and its lytic and lysogenic cycles, because in our presentation, I said that that lambda enters the lytic cycle when it is in a cell that is healthy and lysogenic cycle when the cell is in trouble. That is what it says on wikipedia. Anyway, when I said that, I was told that I was wrong and that it is the other way around. I will look into that. We also hopefully got our quorum sensing system worked out now. All we need to do (once we figure out what we actually have in our plasmids) is add the cro transcription site after the GFP, and in the presence of cholera more cro will be produced and lambda will enter the lytic cycle!

- KK Today was our presentation in class. This is the link to our powerpoint presenation: https://docs.google.com/presentation/d/14mUxVrUdTvNXaPGifXZs_lpXeMrFd-4CxSZ9o1bPqYo/edit#slide=id.p Our presentation gave a background for our project - though we ought to have been clearer WHY we want to use phage - and also the work that we’ve accomplished thus far in our group. We went a long time over in our presentation; it took a long time to explain the quorum sensing circuit, Lambda, and other things. Dr Grose sent an email with several suggestions for presentations in the future. They include being more concise with our time management and better coordinating within our group so that we don’t end up repeating ourselves. In the future we will be expected to be more polished presenters.


4/15/13

- KP Today we started out by getting photographed. We also watched the phage group’s presentations. It seems as if they have a good start to their project. We didn’t have too much time to do our own experiments, but we did set up an overnight to do mini-prep tomorrow, and we streaked out our plates of lambda phage. - KK The three phage groups presented today. I realized how very quickly each of our groups has specialized to the point that I have to concentrate deeply to understand what seems to be second nature to members of the phage group. That’s good! It means each of our groups is moving along nicely. The objective of the phage project is to make a library of sizes - the biggest and smallest phage capsids possible using phages that have already been well characterized and approved for medicinal purposes. One group is working on selecting for the largest phage possible, one for the smallest, and another group is developing a method to purify both phages as they are made. Afterwards, we laid out singles of our three E.Coli strains with Lambda prophage incorporated into its genome. Tomorrow Kelton and I are going to go in and check on them after our Intro to Medicine class.