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Team:Cornell/notebook
From 2014.igem.org
Notebook
Week 1 (June 2 - June 8)
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Wetlab Overview
Transformation efficiency and protocols were tested - heat shock did not work well, and we came to the conclusion to stick with electroporation. The first day of wetlab training began on the 7th! We started working on amplification of metallothionein genes - so far nixA and GST-PMT appear to be working.
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Drylab Overview
Today was the first drylab meeting for the new project! We discussed the mechanics and optimization of general filtration systems. We also started looking for the best way to make hollow fiber reactors the focal point of our filtration system.
Week 2 (June 9 - June 15)
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Wetlab Overview
Obtained transformants of pA14F and pC14T heat shocks and both E/B and E/D were successfully heat shocked into DH5a. Ran into problems later in the week with heat shocked plates from overgrowth and contamination; switched to electroporating of C+F and E+B.
Drylab Overview
We began the design process for our filtration system by choosing our ideal target: runoff streams that feed contaminated water into natural rivers. By basing our assumptions around this, we were able to sketch out some functional requirements for our system, such as minimum flow rate, power consumption, materials, etc. We divvied up the system into subparts to research and report back next week.
Week 3 (June 16 - June 22)
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Wetlab Overview
This week we ligated various parts (F+A, F+C, E+B, and E+D), transformed, ran colony PCRs, and submitted them for sequencing. Most of our attempts were unsuccessful either due to failed ligations or contamination. We also made T for future minipreps.
Drylab Overview
After researching hollow fiber reactors, we found that our assumptions from the last meeting were too liberal. We scaled down all our numbers around a slower flow rate. We discussed our findings on tubing materials, pipe fittings, power sources, and pump options. We sketched out a rough sketch of our system, which included a pump, multiple fiber reactors, larger filters to prevent debris from entering, and a solar panel and battery as power sources.
Week 4 (June 23 - June 29)
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Wetlab Overview
Cloning and troubleshooting continues. E+D, F+C, E+D, E+B4, and E+D11 sequencing results came in negative. The restriction cocktail method was used on F+C and F+A because mRFP kept religating back into the backbone. Plates were successful, but colony PCRs showed they were negative. Repeat cloning. We are facing problems with contamination of lead transporter and R plate. Submitting F+C3 for sequencing. We are also working on transforming off the AA and AB kit plate.
Drylab Overview
After contacting several fiber reactor manufacturers for product quotes, we quickly discovered our hypothetical multi-reactor system was insanely expensive. Since we didn’t want Eric to have to sell an organ to pay for our filtration system, we scaled it down again to a one or two fiber reactor system so it was more feasible.
Week 5 (June 30 - July 6)
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Wetlab Overview
Transformants gave negative signals; many gels lacked proper bands in correct locations. Growth assay looked good for mercury although concentration needs to be increased for nickel.
Drylab Overview
Dan Levine, a drylab member from the 2012 Cornell iGEM team, met with us to help plan our project and pass down ancient drylab design wisdom. He had a unique technique for brainstorming, which was to spend five minutes writing down any ideas you have, regardless of how farfetched, and then share them with the rest of the team. This approach worked extremely well. We had an extensive, positive discussion about our project and decided to completely overhaul our original design. The overall structure of our system was changed to some sort of drum to collect contaminated water, which would then be moved to and filtered in an attached box. We also changed the targeted water source to outflow from a factory, which would fall into the collecting drum.
Week 6 (July 7 - July 13)
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Wetlab Overview
We gathered the data for an assay testing the growth of cells in different heavy metals. In addition, we ligated each the lead transporter (R), and nickel (AA) and mercury (AB) inducible promoters with H. Unfortunately, our transformations did not seem to work for reasons like incomplete digests and inefficient stocks.
Drylab Overview
We found a pump deep in the box of drylab components that have accumulated over the years and decide to test it out. We gutted “the Box” from the 2012 team’s project in order to use it as housing for our own filtration system. Unfortunately, the flow was too slow for us to salvage it for our project, but we decided to order new parts in order to begin assembling our own Box.
Week 7 (July 14 - July 20)
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Wetlab Overview
We are troubleshooting some problems with gel purification and smearing on the gel when we visualize it. Our new stocks of competent cells also appear to be bad. Sequencing of R+H returned a portion of a random promoter region of Enterococcus, so this will have to be remade. We are in the process of creating many different BioBrick parts, such as AB1+H, F, AC+H, AB2+H, AC1S+H, AB2S+H, AC+H, AA + H, which are all at various stages of the cloning process.
Lead Subteam
R was cultured, miniprepped and quantified. R and H were digested, gel purified and quantified. The pSB1C3 backbone was dephosporylated, and the R and H digests were ligated and transformed.
Mercury Subteam
Our first objective is to place the synthesized mercury gene pA14AG into the pSB1C3 backbone. This will be done by digesting pA14AG and pC14H (mRFP in pSB1C3 backbone) with EcoRI and PstI, ligating them, and transforming them. The resulting colonies should contain pA14AG+pC14H (pC14I). pC14I will then be placed upstream of the metallothionein construct pC14AI. This week liquid cultures of pC14H were made from glycerol stock, which were then miniprepped. pA14AG and pC14H were both digested with EcoRI-HF/PstI-HF and gel purified. The gel was good – the pA14AG band was around 800 bp and the pC14H band was around 2000 bp. The concentrations were around 10 ng/μL and they were not worth ligating. Next week we will try re-digesting and re-ligating.
Nickel Subteam
We started out by making glycerol stocks for cultures containing our plasmids pA14AF and pA14AG and miniprepping pA14AF for cloning into the psB1C3 backbone.
Reporters Subteam
The goal of the reporter subteam is to put the reporter (pc14H, which is mRFP) into pc14AA (the nickel inducible promter) and pc14AB (the mercury inducible promoter). Later, we will get a third vector (pc14AC, nixA) that we will also have to put our promoter inside. This week, we made glycerol stocks of pc14AA and pc14AB. We also used glycerol stocks to make cultures of pc14H (mRFP; this is our insert), and later miniprepped these cultures, as well as pre-existing cultures of pc14AA and pc14AB.
Metallothionein Subteam
This week, AH insert was rehydrated and tranformed, to be prepared in the future.
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Drylab Overview
We ordered our fiber reactor!
Week 8 (July 21 - July 27)
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Lead Subteam
T was miniprepped. New plates were made. Cultures of the putative transformants were made, but the transformation proved unsuccessful. R and H cultures were grown and miniprepped, but the concentrations were low. New cultures of R and H were subsequently made. A culture of T was made.
Mercury Subteam
The double digests of pA14AG and pC14H were redone and new pC14H minipreps made. We increased the amount of DNA used in each digest in hopes of increasing the concentration of the gel purified bands. The gel did not turn out well so we had to re-digest. These newly digested pA14AG and pC14H were run on a gel and gel purified. In the meantime, the gel purified pA14AG and pC14H from last week were ligated (even though the concentrations for each were low) to see if the ligation would work. This ligation was transformed but once plated, there was a lawn of cells – it appears the antibiotic had degraded. The most recent digests turned out to have good concentrations so the backbone was dephosphorylated and ligated with the insert. Transformation and plating of this new ligation produced colonies! Colony cells were grown in liquid cultures, miniprepped, digest screened, and sent to sequencing.
Nickel Subteam
We went through numerous iterations of miniprepping pA14AF and pC14H, digesting both with EcoRI and PstI, gel purifying the insert from pA14AF and backbone from pC14H, dephosphorylating the backbone, ligating, and transforming. By the end of the week, one of the transformations yielded colonies! Here’s hoping…
Reporters Subteam
This week we almost completed one iteration of the cloning cycle. We digested, cleaned, and ligated pc14AA, pc14AB, and pc14H. We transformed the ligations for a total of 6 plates plates (4 pc14AA +pc14H and 6 pc14B + pc14H). We were able to culture 3 colonies from each of the pc14AA+pc14H plates for a total of 12 cultures, and we miniprepped these cultures for digest screening.
Metallothionein Subteam
Miniprepped the cultures made from the colonies of the transformed cells. After multiple digestion attempts with EcoRI and PstI, we decided to stagger our efforts. We were going to start running multiple processes of Miniprep/digestion/ligation to increase our potential for success. By the end of the week, our first ligation samples were ready for heat shocking. Luckily, the heat shocked contained colonies and we crossed our fingers that these colonies contained was we needed.
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Drylab Overview
We received most of our ordered parts earlier this week, including the fiber reactor! We tested the fiber reactor with our new pump, and the flow rate was about 0.2 mL/min. After testing the fiber reactor, we brainstormed orientations for our collecting drum and ideas for how to compactly fit the filter and piping into a protected and accessible casing.
Week 9 (July 28 - August 3)
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Lead Subteam
T and S cultures were made and miniprepped. T and R were gel purified. The T digest was dephosphorylated and ligated with R. The S ligation was transformed.
Mercury Subteam
The sequencing did not go well – we think the miniprep might have been contaminated. The minipreps of pC14I were redone and another pA14AG and pC14H ligation was done which we will transform if the sequencing of the new minipreps is again not successful. Sequencing came back as GST-YMT which is not what we were hoping for. Thus, we transformed the new ligation and redid the minipreps of pA14AG which were digested with EcoRI-HF/PstI-HF. When loading dye was added to the digested pA14AG prior to running a gel, the digest turned brown…pA14AG was digested again with EcoRI-HF/PstI-HF in two tubes and with EcoRI-HF/SpeI in two tubes but still turned brown when dye was added. We think the EB from the miniprep might have been contaminated and so grew up more pA14AG insert which were miniprepped. The first pA14AG double digest which turned brown was run on a gel. The gel did not look good however, the bands were too long.
Nickel Subteam
This week we grew up, miniprepped, and digest screened a couple colonies from the previous week’s pC14H+pA14AF transformation. The bands on the gel looked to be in the correct location, so off to sequencing they go!
The rest of the week was spent culturing, miniprepping, and digesting pC14T with EcoRI and SpeI. Our pA14AF EcoRI/SpeI digest will be the insert into the digested pC14T backbone.Reporters Subteam
Only one of the plates of pc14AB + pc14H had colonies, so we made three cultures and miniprepped them. These minipreps had very low concentrations, so we didn’t digest them, but the minipreps of pc14AA + pc14H from last week had much better concentrations, so we digested them and ran a digest screen. The digest screen was successful, so we submitted a sample for sequencing. The results of the sequencing weren’t what we were looking for, so we cultured a red culture from the plate to prepare for sequencing in order to see if there is a problem with the sequence of the promoter. We miniprepped this RFP culture, and sent it in for sequencing. Meanwhile, we also made overnight ligations of pc14AB + pc14H and transformed them into more cells using heat shock. Unfortunately, nothing grew on the pc14AB + pc14H plates so we threw them out and worked on cleaning and purifying previous pc14AB and pc14H digests.
Metallothionein Subteam
The colonies were miniprepped and sent in for sequencing… ‘lo and behold, it worked! Our construct was a complete success. The nest construct, AHH, was renamed AI. Our next task is to digest out the T7 promoter, and then subsequently submitted. Cultures of AI were made, then miniprepped. The minipreps were then digested with KpnI to cut out the T7 promoter. Again, we staggered out multiple processes. We are hoping to be able to verify a successful digestion next week with a digest screen.
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Drylab Overview
We decided to collaborate with the Outreach group to create a portfolio of future applications for our filtration system. We had a lot of fun brainstorming cool designs, the collective favorite being the idea of a water roomba. The ideas were distributed among the drylab team and each person was tasked with making a CAD model of theirs.
Week 10 (August 4 - August 10)
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Lead Subteam
Attempts to transform the ligations continued, without much success.
Mercury Subteam
We just realized that the pA14AG culture we had been using was growing in LB without ampicillin, so we grew up another culture overnight, with antibiotic in the LB this time. The pA14AG digested with EcoRI-HF/PstI-HF and with EcoRI-HF/SpeI from last week were run on a gel, the insert bands looked around .7kb so we gel purified. The concentrations were very low – 13 ng/μL for the EcoRI-HF/PstI-HF digests and 5 ng/μL for the EcoRI-HF/SpeI digests. However, the pA14AG digests with EcoRI-HF/PstI-HF were still ligated with pC14H from the metallothionein task force group and transformed. Unfortunately, the plates did not have colonies. pA14AG was again miniprepped and double digested with EcoRI-HF/PstI-HF and EcoRI-HF/SpeI. These digests were run on a gel and gel purified. The gel purified pA14AG digests had good concentrations, were ligated to the pC14H backbone, and transformed/plated. There was one colony on this plate – a LB culture was made of this colony in chloramphenicol and will be miniprepped next week. Four colonies were picked from the plate from earlier this week and LB cultures were made. These will also be miniprepped and sent for sequencing to see if we have successfully transformed pC14I.
Nickel Subteam
Sequencing came back for pC14H+pA14AF. Unfortunately it was not correct, so we needed to go back and reclone those. More cultures of pC14T were miniprepped.
Reporters Subteam
We made ligations from the digests of pc14AB and pc14H – however, we transformed them incorrectly and were unable to plate any cells. Because we ran out of ligations, we made more cultures of pc14AA and pc14AB from the glycerol stocks. We also learned that pc14H is a constitutive promoter, meaning that it will always be on (the cells will always turn red, regardless of whether or not heavy metal is present). Because of this, we started working with a new promoter this week – pc14AJ. The new promoter is a constitutive promoter (amcilCP, and it is blue!). We made a glycerol stock of pc14AJ and cultured from this stock. However, we were unable to continue with the minipreps of pc14AA, pc14AB, and pc14AJ until the beginning of the next week because the lab ran out of supplies.
Metallothionein Subteam
AI-T7 was digest screened with SacI, a few of the bands looked good, so they were purified and then sent in for sequencing. Sequencing came back a success and we had our construct AI-T7, which was renamed AK. With the quick success of this task force, we were transferred to work on creating the lead construct. Thus, we started with the same process with R, the lead insert, and H, the psB1C3 backbone. We miniprepped both pieces this week.
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Drylab Overview
We made progress on our CAD models.
Week 11 (August 11 - 17)
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Lead Subteam
The process of reculturing and religating R and T was repeated. The transformation, however, was a failure.
Mercury Subteam
pC14I cultures #1 and #3 were miniprepped and a small portion digested with EcoRI-HF/PstI-HF for a digest screen. The pA14AG insert appeared too long so this pC14I is probably not what we want. New pA14AG liquid cultures were made and miniprepped, digested with EcoRI-HF/Psti-HF, and run on a gel which did not turn out well. We had to begin the miniprepping, digesting, and gel purifying process again for pA14AG. Additionlly, new pA14 minipreps were made in case we need them again next week.
Nickel Subteam
After many, many cultures, we were finally able to get a couple of minipreps of pC14T that had good concentration. We proceeded to digest portions with EcoRI/SpeI and EcoRI/PstI for future ligations.
Reporters Subteam
Once the miniprep supplies arrived, we started making 16 minipreps…which we then lost (on the second-to-last step of the process) to the centrifuge when it refused to open. (Author’s note: as of right now, early October, the centrifuge is still sealed shut and our minipreps are still inside it). The setbacks of the previous week (losing the ligations, having to use a completely different reporter, and the stuck centrifuge) have put the reporter subteam back in square one. We miniprepped 2 cultures of pc14AA, 2 cultures of pc14AB, and 4 cultures of pc14AJ, and then digested, ligated and transformed the ligations. However, once only one plate (pc14AB + pc14AJ) had growth on it, so we made two cultures. Neither of the cultures grew, so nothing could be miniprepped.
Metallothionein Subteam
This week comprised not only of struggling to attain successful minipreps for digestions and ligations, but also to hope that the ensuing ligations will successfully have colonies. After multiple attempts at ligations and transformations, we finally had a single colony that grew that we cultured then digest screened and sent in for sequencing. Like the previous construct, these are being digested with EcoRI and PstI.
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Drylab Overview
We did a CT scan of our fiber reactor! We are hoping to do another one after extensive use and compare the two scans.
Week 12 (August 18 - August 24)
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Lead Subteam
The process of reculturing and religating R and T was repeated. The transformation, however, was a failure.
Mercury Subteam
The new pA14AG minipreps were double digested with EcoRI-HF/PstI-HF and gel purified. The gel purified pA14AG from last week was ligated with pC14H which already had been double digested with EcoRI-HF/PstI-HF and dephosphorylated. This ligation was transformed into cells and plated. This process was again repeated with the newly digested pA14AG minipreps from earlier this week. There was one colony that grew on the pC14I plate which was minprepped.
Nickel Subteam
Ligations of pA14AF and pC14T were made multiple times, trying out different combinations of restriction enzymes too (EcoRI/SpeI for both and EcoRI/PstI for both). All were transformed, but colonies only seemed to grow for the EcoRI/PstI digestion enzyme combination. Regardless, colonies were grown to see if it worked.
Reporters Subteam
There was a hiatus this week because all subteam members went back home for a week of summer vacation.
Metallothionein Subteam
The sequencing didn’t come back with what we wanted, so we just have to go for a second try. More rounds of minipreps, more rounds of digestions, more round of failed gel purifications for the insert H. I’m beginning to sound like a broken record.
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Drylab Overview
We tested the large filter used for debris with our pump. It was a little difficult because without a battery, we were forced to use the gel box’s power source. Luckily, we still got the water to move completely through the filter.
Week 13 (August 25 - August 31)
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Mercury Subteam
The pC14I miniprep was digested with EcoRI-HF/PstI-HF for a digest screen and run on a gel. pC14I was then sequenced confirmed! This new biobrick consists of mercury MerT and MerP genes, Anderson promoter, and the pSB1C3 backbone. Now our objective is to place pC14I upstream of the metallothionein construct pC14AI and transform the ligated product in BL21 cells. The miniprep of pC14I that was sequence confirmed was transformed into new cells and plated to make glycerol stocks. New LB cultures of pC14AI were grown and were miniprepped.
Nickel Subteam
pC14T+pA14AF colony cultures were miniprepped and digest-screened. Unfortunately, the gel test was inconclusive, so more colonies were cultured, miniprepped, and digest-screened; this second round also led to inconclusive results.
Reporters Subteam
We transformed and plated using ligations of pc14AA + pc14AJ, pc14AB + pc14AJ, and pc14AC +pc14AJ that we’d made prior to leaving for break. Only the pc14AA + pc14AJ plate had any growth on it, despite all the plates being left in the incubator for two days, so we made a culture of this (hoping that it wasn’t contamination that we were culturing). We also cultured some more pc14AA, pc14AB, pc14AC, and pc14AJ from glycerol stocks, and were able to make cleaned digests of the four.
Metallothionein Subteam
The sequencing didn’t come back with what we wanted, so we just have to go for a second try. More rounds of minipreps, more rounds of digestions, more round of failed gel purifications for the insert H. I’m beginning to sound like a broken record.
Drylab Overview
A lot of parts came in this week. We spent the meeting putting the pieces together.
Week 14 (September 1 - September 7)
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Lead Subteam
Cultures of R and T were miniprepped. PCR’s of R were run, one with Q5 and one with Phusion. The PCR’s did not show up in a gel. A PCR of varying dilutions of R Miniprep (1 ul, 3 ul, 5 ul, 8ul - each in 200uL H2O) was run. All appeared in a gel. The PCR product was subsequently cleaned.
Mercury Subteam
The miniprepped pC14AI was digested with EcoRI-HF/PstI-HF and pC14I digested with EcoRI-HF/SpeI. pC14AI was gel purified, pC14I was dephosphorylated and was ligated to pC14AI. The length of the insert is 1076bp and backbone is about 2761bp. The pC14AI+pC14I ligation was transformed into BL21 cells and plates on chloramphenicol plates. The plates did not show colonies and the ligation was redone and transformed/plated. Liquid cultures were made of the colonies.
Nickel Subteam
We decided to redigest pA14AF and ligate with pC14T, maybe this time it will work? These ligations were then transformed and colonies grown for sequencing. Much to our pleasure, sequencing came back with positive results! We were able to construct pC14K (pC14T+pA14AF)! Glycerol stocks were made of pC14K and pC14H was religated with pA14AF.
Reporters Subteam
We digested the pc14AA + pc14AJ cells and screened them, but the first gel was inconclusive because it was warped, and the second gel showed that the bands were the incorrect lengths (the first, pc14AA was around 2000 base pairs, as it should be, but the second band, pc14AJ was around 1000 bp when it should have been closer to 700 bp). We also made 2 plates of pc14AA + pc14AJ, 3 plates of pc14AB + pc14AJ, and 1 plate of pc14AC + pc14AJ we were able to get 11 cultures from these plates. We miniprepped theses 11 cultures, and we made 12 ligations from cleaned digests left from the previous week. Towards the end of the week we plated a few pc14AA + pc14AJ and pc14AC + pc14AJ transformations.
Metallothionein Subteam
Make more cultures of R...Make more cultures of R...Also heat shocked and transformed the ligation from last week, but sadly nothing grew from the colonies. So we decided to do something new with the transformed colonies and tried colony PCRs, after running the gel of the result, we were rather disappointed (it was like watching an M. Night Shyamalan movie). The gel was too blurry and unclear have anything conclusive. So we performed another ligation and hoped that this one would work.
Drylab Overview
We bought foam to hold the box’s components in place. We carved out the shapes of the parts into three layers of foam and laid the layers in the box. It was great to see the box finally taking shape.
Week 15 (September 8 - September 14)
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Lead Subteam
Cultures of T were made from glycerol stock. Quantification of the PCR yielded poor results. The PCR was subsequently restarted. Cultures of T were miniprepped, and the R PCR was redone. The column purification of the R PCR yielded positive results. The R PCR and the T miniprep were subsequently digested. R and T were ligated and transformed. The ligations were plated with chloramphenicol. No growth appeared, so the ligation was repeated.
Mercury Subteam
pC14AI+pC14I from the plates was miniprepped and digested with EcoRI-HF/PstI-HF to run a digest screen to see if the ligation was truly of pC14AI and pC14I. The gel showed the insert to be very short and we think it may only be the mercury construct in pSB1C3. The ligation was redone, transformed/plated, and liquid cultures were made of the colonies. pC14I was also miniprepped for future use.
Nickel Subteam
Cultures were made of pC14AI and pC14K for miniprepping and future cloning. pC14AI and pA14AH were digested, but the gel for gel purification came out oddly - bands were not coming out where we would have expected them. We also digested pC14K for more cloning, but none of the digestions had measurable DNA.
Reporters Subteam
We made four cultures from the plates we made last week – 2 of pc14AA + pc14AJ and 2 of pc14AC + pc14AJ. We ran digest screens on the digested minipreps, but all the bands were the wrong length. There were a few digests remaining from the previous week, so we cleaned, dephosphorylated and ligated them to make 4 ligations (2 of pc14AB + pc14AJ, and 2 of. However, the quality of the ligations is a bit suspect because the digest concentrations were on the lower end. We transformed, plated, and cultured cells using these 4 ligations, but we were unable to miniprep them because the lab ran out of 1.5 mL tubes. We also transformed using a pc14AB + pc14AJ ligation from earlier that we’d found in the box.
Metallothionein Subteam
So there was slightly better progress this week, with the overnight ligations yielding a decent number of colonies, with all of the colonies growing in cultures, which was promising. We tried another colony PCR of the transformants again, but once again, it failed.
Drylab Overview
We tried to see the diffusion of luria broth through the fiber reactor. We combined the the LB with tonic water to see the level of fluorescence and qualitatively measure the amount of LB left in the fiber reactor.
Week 16 (September 15 - September 21)
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Lead Subteam
Colony growth was observed on the transformant plate. They were cultured, and a colony PCR was run.
Mercury Subteam
Many minipreps were made of the pC14AI+pC14I liquid cultures, digested with EcoRI-HF/PstI-HF, and run on a gel. Successful ligation would show a band at around 1.8kb and one of our bands did appear in that area – this band was gel purified and sent for sequencing. In the meantime, pC14I was miniprepped, digested with EcoRI-HF/SpeI, and column purified.
Nickel Subteam
In the process of constructing pC14K+pC14AI, we experienced a bit of difficulty. After multiple failed cloning experiments, we tried synthesizing the part using pC14K+pA14AH. Hopefully the second approach will work!
Reporters Subteam
Tubes arrived in the lab, so we miniprepped and digested the cultured cells from last week. The gel screen of the digests was textbook perfection for all three of pc14AA + pc14AJ, pc14AB + pc14AJ, and pc14AC + pc14AJ. We sent in samples of the minipreps for sequencing, but the results were strange – sequencing reported that only pc14AJ was in the plasmid, and that none of pc14AA, pc14AB, and pc14AC were present. Luckily earlier in the week, we’d made several ligations of all three that we’d already transformed, plated and cultured so we could still continue with miniprepping these cultures.
Metallothionein Subteam
While continuing work on R+H, we received news from high command that were to be repurposed yet again. This time we are to collect data of metal sequestrations results of e.coli containing the constructs were created. This requires that we prepare a few glycerol stocks first…
Drylab Overview
Tragedy hits the drylab world! We didn’t clean the fiber reactor thoroughly enough after last week’s experiment, resulting in the perfect environment for fungus to grow. We cleaned out the fiber reactor very, very thoroughly with water and put it in the refrigerator to stop the growth of fungus. We will keep an eye out for more fungus.
Week 17 (September 22 - September 28)
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Lead Subteam
Gel of colony PCR was run, yielding poor results. Minipreps of some of the cultures were prepared. Colony PCR’s of the R+T cultures were also run. Cultures of relevant strains were remade, and a new colony PCR was run. The cultures of these colonies were miniprepped, and one tube was sent for sequencing. The sequencing yielded unsatisfactory results.
Mercury Subteam
The miniprep of pC14AI+pC14I we had sent for sequencing ended up being Neema’s reporter and we think our whole plate was contaminated. We made more pC14AI+pC14I minipreps and digests from the same plate and ran another gel, but we still observed bands in the same region as where Neema’s reporter band was so our hypothesis was virtually confirmed. Thus, we began the entire process of miniprepping and digesting pC14AI and pC14I, gel purifying pC14AI, column purifying and dephosphorylating pC14I, ligating them together and transforming into BL21.
Nickel Subteam
Inserting pA14AH into pC14K did not seem to work judging from the digest-screen. After preparing more pC14AI for cloning, we also were going to try inserting pC14K into pC14AI. However, the gel purification step for that was bizarre and indicated our parts were shorter than what they were. Digest screens of pC14K+pA14AH minipreps also were inconclusive.
Reporters Subteam
This week, we decided to change up our digest protocol a bit – rather than digesting 3000 ng of DNA at a time and incubating the digests for 3 hours, we decided to stick to 1500 ng of DNA and incubate for 1.5 hours maximum because we thought that star activity was causing the DNA to not be digested properly when it was incubated for long periods of time. We made 2 cultures each of pc14AA, pc14AB, pc14AC, and pc14AJ, miniprepped, and digested them for the shorter period of time. When cleaning these digests, however, they smeared in the gel, so we made more cultures of the four plasmids using glycerol stocks. Additionally, we ran digest screens on the cultures from last week, but they were indicative of contamination. By the end of the week, we were able to produce 6 ligations of pc14AC + pc14AJ (we transformed and plated all 6 of these for a total of 12 plates), and we’d started up another batch of cultures from glycerol stocks in case these ligations were not any good. Unfortunately, on the last day of this week, we ran out of Pst1-HF enzyme and were unable to continue with digests because neither of our buffers worked well with both Pst1-HF and Spe1-HF.
Metallothionein Subteam
This week, we first had to make chemicompetent glycerol cell stocks of three samples: AI+R, AI+AF, and AI+AG (AF = nickel construct and AG = mercury construct). First, we took cells containing the AI construct and transformed the necessary extra plasmids in and created the glyercol stocks. So we took the AI containing cell and heat shock the necessary plasmids into the cell and made glycerol stocks of those. Simple.
