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Team:UPO-Sevilla/Project/Notebook
From 2011.igem.org
Notebook
WetLab
- Basic Flip Flop
Week 1
Week 2
Week 3
Week 4
Week 5
Week 6
Week 7
Week 8
Week 9
- Improving Flip Flop (Yolanda Gonzalez and Felix Reyes)
Week 1
This week we have finished the complete sequence of our bistable improved by proteolysis and asRNA.
At the beginning we used a temperature-sensitive mutant of the GFP, but finally we decided to use the wild type because we want to be sure that the improvement in the speed of the signal fall is because of the asRNA/proteolysis mechanism.
In order to choose the restriction sites that will make our construct modular and more versatile (for example going from a 1-2 bistable to a 1-0 bistable), we had to scan our sequence looking for restriction sites already present, so we chose those enzymes that weren’t already present both in the sequence and in the iGEM standard plasmid. In a second optimization step we selected enzymes share buffer for double digestions.
Week 2
This week we have designed a plasmid construct that will express our antisense RNA. This is regulated by Prm promoter. By having it on a plasmid we will have an easy control of the whole antisense system by comparing strains containing or not-containing it.
At first, we decided to use only the first 16 nt of the sequence of the asRNA because it was said to give a greater inhibition in our article (Small RNA Binding to 50 mRNA Coding Region Inhibits Translational Initiation, Bouvier et al.). However, when we where analyzing the kind of terminator they used we discovered that in the complete sequence the terminator was included, and it was a ρ independent one. The fact that the 16 nt asRNA was more effective was proven by chemical synthesis of the asRNA, and it was non-suitable for us as we want to express the asRNA in vivo. So finally we decided to include in the plasmid the complete asRNA sequence shown in the paper.
For the correct operation of our bistable we need a double ΔrybB-ΔSspb E. coli mutant. We have been sent ΔClpX (control strain) and ΔSspb mutants, and this week we have left the bacteria growing with the pKD46 plasmid in order to delete the rybB gene using the λ red protocol (Wanner et al.).
Finally, we have grown strains with the iGEM plasmids pSB4C5, pSB4K5, pSB1T3 and pSB4A5 (expressing RFP) and the pMP01226 Apr lineage expressing GFP.
Week 3
This week we have made minipreps of the following plasmids: pKD46, pSB4A5, pSB4K5, pSB1T3, pSB4C5, pKD3, pKD4 and pSB1C3. We have digested the pSB4A5, pSB4K5, pSB1T3 and pSB4C5 iGEM plasmids with EcoRI and PstI in order to get them ready-to-clone our synthetic DNA.
To obtain the double ΔrybB-ΔSspb E. coli mutant, we transformed ΔClpX (as we will use the double ΔrybB-ΔClpx mutants as a control) and ΔSspb mutants with the λ red plasmid (pKD46 plasmid with ampicillin resistance) by a heat shock transformation protocol. After transformation, we left the cells growing in ampicillin selective medium and we used as negative control ΔSspb and ΔClpx mutants that hadn’t been transformed. Next day, we observed colonies onto the experiment plates, but not in the negative controls. Two positive colonies of each strain carrying the λ red plasmid were inoculated to make glycerol stocks.
We digested the pKD4 and pSB1C3 plasmids with PstI and pKD3 plasmid with SphI in order to have them linear to check purity and concentration by electrophoresis. We carried out the electrophoresis with the pKD3, pKD4 and pSB1C3 plasmid (digested and not digested); digested pSB4A5, pSB4K5, pSB1T3 and pSB4C5 plasmids, and not digested pSB4A5 plasmid.
Besides we amplify pKD3 and pKD4 markers in order to electropore that fragments according to Wanner et al. protocol.
Week 4
Finally our plasmids are already digested and purified, ready to be cloned with the synthetic DNA. The worst part of this process is that during the purifying step, we always lose a great amount of DNA. we obtain, however, enough linearized plasmids.
This week we tried the transformation. We expected our transformation to be successful but despite our expectations, we obtained no colonies. Besides, something unusual occurred, our SspB strain was not able to continue growing when the culture had got a DO = 0.3 (this kept happening every time we tried to repeat that protocol). At the end of the week, after some analysis, we concluded that our SspB could be transfected with a phage, so we will execute some assays to determinate it.
Also, we discovered that SspB and ClpX have an F’ plasmid. It’s extremely important to remove it since there is a strong LacI gene on it. We think the best way to achieve it would be: first, continue with the deletion protocol; and then we’ll check the loss of F’ plasmid as the plasmid won’t have been selected.
Furthermore, in the middle of the week, a synthetic device arrived, the asRNA device, (hurrah!) and now we are trying to clone it with the plasmid.
Week 5
As we prognosticated before, our SspB is infected with a phage according to our assays (we could see calves!). So we decided to start from the beginning with the SspB strain… Meanwhile we focused on the ClpX strain and we carry out the protocol one more time. Thank God (or whoever it is) we acquired some colonies! Now, we have to check it by PCR after holidays (just a couple of weeks to rest).
The ligation of the iGEM vectors and asRNA device was unsuccessful, so that we will try it again in September.
Week 6
After three weeks, we return to work with renewed energy! We start checking the hypothetical ClpX RybB strain. We make the PCR very carefully, designing the proper controls and putting our hopes in it. What a relief that at least one of the 20 colonies tested was positive! We got a ClpX /RybB strain! The next step is to remove the selective marker used to provoke the delection. We will express a flipase which recombines FRT sequences. These FRT sequences are flanking the marker, so in this way, the strain will be sensitive to this marker.
We try again the ligation step but we won’t be able to see the results until next week. Once again, we tried the electro-transformation and this failed again. No more words…
Week 7
Besides, since we had ran out of fragments to electropore our bacteria, we amplifyed the pKD3 and pKD4 markers. We tried to electroporate the bacteria with the fragments at the end of the week. On Monday we will see the results (hopefully positive, this would be the last time we will try that protocol).
Also we checked three possible positive colonies which could have lost the marker (cloramfenicol resistance) and the F’plasmid. We have no results yet, next week we will obtain full details about our final strain.
Week 8
Week 9
- Epigenetic Flip Flop (Paola Gallardo)
New year, new project. This time, let's try to make an epigenetic switch!
Before the end of the classes and during the spring, this sub-team has outlined the project by organizing weekly meetings to discuss about the design of our project and the strategies to carry it out.
Week 1 (July, 4-8)
Initial contact with the lab. First of all, it is necessary to amplify some vectors that will be used in the construction of the modules, Pnmt1(41X) and Purg1, as well as two constructions that have been gently sent from the Dr. Attila Becskei from the University of Zurich. On the other hand, I have designed some primers that will be used later.
There are still lots of things to do.
Week 2 (July, 11-15)
Short week. The order of synthesized part tetR-CSD has just arrived to the Lab, so I can start to build up the compaction proteins modules. First of all, I have had to transform the plasmids into E. coli. Also, I made a PCR to amplify swi6 from the genome of Schizosaccharomyces pombe, and sir3, from a plasmid. The objective was to get enough DNA of these parts and, by using appropriate restriction sites that were introduced into the designed primes, start assembling the fusion proteins for this module. Next week we will see if the experiments have worked out as expected.
Week 3 (July, 18-22)
This week I have started to assemble the DNA fragments that will be used for the compaction protein modules, so firstly, I have had to made sure that all its parts were available. I set up an inocula of the E. coli previously transformed with the tetR-CSD plasmid and made a miniprep. At the same time, I checked the results of the PCR of sir3 and swi6. I have just been lucky with the last one.
I have repeated the PCR to get sir3 from the plasmid, using different conditions: I modified the initial concentration of the DNA template and reduced the annealing temperature), but the result was again negative. Then, I have launched a new strategy and cut the plasmid containing sir3 gene with restriction endonucleases to purify the entire gene and use it late as template for a new PCR. This strategy also allows me to check that the plasmid was the right one.
In the meantime, I have made sequential cuts of tetR-CSD, pPnmt1(41X) and swi6, all the components of the compaction module, apart from the slippery sir3. However, we have got some bad news. The rest of the synthesized parts that we had order will be delayed at least four weeks. Desperation!!! Let's do it old-style way, amplifying the parts with primers and assembling them with DNA ligase!
Week 4 (July, 25-29)
I began this week trying to clone into the pREP41X vector the parts of two compaction modules (tetR-CSD, tetR-Swi6). I transformed E. coli DH5α with the ligation products. The following day, I used a new method for screening recombinant clones, colony cracking, but I didn't obtain positive results. So, I tried with minipreps and digestions, but results were negatives too. I followed the same protocol, but digestions didn't work.
I changed again the PCR conditions to get sir3 and made a gradient PCR, but it didn't work either. To make sure that the template was the correct one, I made analytic cuts of it, with different restriction enzymes. After two tries, results were conclusive. What's wrong? New primers.
Apart from that, obtained Tadh1-tetOn (ADH1 terminator with a variable number of tetR operator sites repetitions). For doing that PCR conditions had to be optimized (annealing temperature, template concentration, extension time, …).
Week 5 (August, 1-5)
I digested again tetR-CSD with the appropriate restriction enzymes, XhoI and XmaI, but and electrophoresis with the digestion products demonstrated that there wasn't cuts. Analysis of tetR-CSD DNA sequence showed that restriction sites were lost. A site-directed mutagenesis was order to recover restriction sites.
I made analytic digestions of pPR013 and pPR074, obtaining coherent results.
I also amplified and purified Swi6 using an optimized PCR reaction, in order to use it when needed. Amplification of sir3 with new primers gave no results. So, I need to optimize the PCR conditions.
At last, we received another synthesized part: tetO2. I transformed DH5α E. coli with this part and the following day I inoculated isolated colonies to make minipreps.
In the meantime, I began to construct the Purg-GFP-Tadh1 module, a positive control of the designed module containing the tetO flanking sequences. This construction will be integrated into the genome of S. pombe at the leu1 locus by homologous recombination.
In other hand, I ligated the fragment containing the Tadh1-tetOn obtained by PCR into pGEM-T vector and transformed it in E.coli. Colonies will be screened after the holiday break.
Week 6 (September, 2)
When I came back from holidays, I found the rest of synthesis parts (GFP·tetO4 and tetR·CSD) over my table. I used the standard protocol to transform them into E coli.
I made digestions of tetO2·Tadh1 and Purg with BglII restriction enzyme.
Week 7 (September, 5-9)
Colonies of transformation plates were quite strange. I set up inocula of them and repeated the transformation protocol. Some of the inocula didn't grow up, maybe because of selection of satellite colonies in ampicillin plates. I made minipreps and digestions of them, to get tetR·CSD (XhoI/XmaI), tetR (XhoI/BamHI) and GFP·tetO4 (PacI/AscI). I also digested pREP41X plasmid with XhoI and XmaI, in order to ligate tetR·CSD and tetR+Swi6 between pnmt41X promoter and nmt1 terminator. However, the result of the ligation was not positive possibly because the plasmid was not properly digested.
I made an electrophoresis and I tried to purify TAdh1·tetO2 and Purg from agarose gel, but TAdh1·tetO2 fragment migrates with bromophenol, so I had to repeat this process again. Then, I proceeded to ligate them o/n while keeping my fingers crossed, and transformed ligation product in DH5α the following day. There appeared colonies in spread petri plates. Colonies cracking didn't work, so I set up inocula to do minipreps next day. After an immeasurable colonies screening, I obtained two positive clones (19 and 35), Tadh1·tetO2·Purg is ready.
Digestion of Tadh1·tetO2·Purg with AscI and PacI is made to introduce the next component of this module, GFP·Tadh1·tetO4. I had the same problem: plasmid was not totally digested and control religation plate was plenty of colonies. Lesson learned: if you don't give enough time to a reaction, you'll be wasting your time.
Week 8 (September, 12-16)
Due to last week result, I made a new ligation reaction of Tadh1·tetO2·Purg plus GFP·Tadh1·tetO4, but I obtained the same results: the same number of colonies in religation plate and ligation plates.
I kept on trying to clone tetR·CSD and tetR+Swi6 into the pREP41X vector, by digestion, precipitation of DNA, ligation and transformation, but the last step always failed.
Finally, I obtained sir3 gene by PCR, and also swi6, but they were lost in their purification.
Week 9 (September, 19-23)
Colony cracking of pREP41x + tetR-CSD and pREP41x + tetR + Swi6 didn't work, so I set up inocula of all the colonies in the plates to make an screening of them. I have made analytical digestions of the minipreps and, after two electrophoresis, it seems that I have a positive clone of thirty.
In the middle of the week, I have received the primers that will let me obtain all the parts in BioBrick standard.
- MiniTn7BB (David Caballero)
Week 1 (July, 4-8)
First week in the lab!
During the last few months we have been studying and designing a Tn7-based system to deliver BioBricks into bacterial chromosomes. Now it is time to perform the ideas and experiments we drew on paper.
We ordered the synthesis of a complete basic mini-Tn7 to avoid site-directed mutagenesis, cloning and other intermediate processes. Unfortunately, our order is delayed (22 days by now). So, this week I tried to prepare all the necessary strains and vectors in advance. Anyway, this is my first week in Fernan’s lab at CABD, so I am mostly getting familiar with the location of materials and equipment.
These were my main tasks this week:
Prepare pUC18-SfiI vector for mini-Tn7 insertion. Our mini-Tn7 was designed flanked by SfiI target sites. We plan to use a pUC18 vector, replicative in Enterobacteriaceae to maintain the mini-Tn7. I located the vector in the lab strain collection, set up an inoculum, purified the plasmid DNA, measured the concentration with the Nanodrop and digested with SfiI.
Prepare pUC18R6K-SfiI vector for mini-Tn7 insertion. The goal is to obtain a vector with an R6K replication origin, which is non-replicative in pir- strains to host the mini-Tn7 constructs. We requested a pUC18R6K-mini-Tn7T-Km vector from Herbert Schweizer's lab in Colorado State University. We will use this as a template to amplify vector sequences adding SfiI restriction sites. I had problems to get amplification in the PCR reaction (twice), so I did analytic digestions with different restriction enzymes (four different cuts). The restriction patterns are not as expected. I may have used the wrong template (maybe the tube was mislabeled). I made new mini-preps, double-checking that the strain was the right one. Next week I will try to do this again with the new miniprep DNA.
Prepare large amounts of the vectors necessaries to transpose the mini-Tn7. we will need fairly large amounts of pTNS2 (containing the Tn7 transposase complex), pUC18R6K-mini-Tn7T-Km (positive control), pBBR1MCS5 (negative control) to electroporate into the recipient strains for the transposons. I streaked the strains on selective plates, set up inocula, purified plasmid DNA and measured the concentration of the DNA, which was generally lower than expected. Also I did some checking of the pTNS2 plasmids with restriction enzymes.
Finally I started a protocol to make electro-competent cells of Escherichia coli and Salmonella typhimurium, two of the four strains we will use to characterize the behavior of mini-Tn7.
Week 2 (July, 11-15)
First of all, I need a suicide vector I can use as the mini-Tn7 delivery system. Similarly to last week, the new minipreps of pUC18R6K-mini-Tn7T-Km yielded no PCR product and the restriction pattern with five different enzyme combinations was again not what we expected. Despite our efforts, it is evident that the plasmid we received was not pUC18R6K-mini-Tn7T-Km as published. After contacting the Schweizer lab about this problem, they informed us that they had sent us a different, although similar plasmid, but unfortunately it is not suitable for our purposes. Instead, restriction analysis confirmed that the transposase-delivery plasmid pTNS2 is based on pUC18R6KT and contains an oriT for conjugative mobilization, so we decided to use this as a template. Unfortunately, our SfiI-bearing primers are not suitable for this plasmid, so we designed new primers to amplify the pUC18R6KT backbone from pTNS2.
The last set of mini-preps I did to purify pTNS2, pUC18R6KT-mini-Tn7T-Km (now discarded) and pBBR1-MCS5 had very low yield. I repeated the process and obtained somewhat more concentrated, but still low-yield preparations.
This week I attempted to prepare several batches of electro-competent cells that I will need for the project. The strains are E. coli DH5α-λpir, E. coli MC4100, and S. typhimurium LT2. The former will be used for cloning into the R6K plasmids, and the other two will be used as hosts for insertion of the miniTn7 transposons. The protocol requires growth of large (500 ml) cultures OD600=0.5, followed by repeated washes with sterile, cold water. Cells are concentrated, allocated in 40 l samples and stored at -80°C. It sounds easy, but I had to repeat the process three times due to beginner's mistakes.
I did mini-preps of two vectors expressing the Flp recombinase: pFLP2, a replicative vector which is lost spontaneously at high frecuency in Pseudomonas strains; and pCP20, which has a termosensitive replication origin that allows replication at 30°C but not at 37°C. This last vector will be used in E. coli and S. typhimurium.
Week 3 (July, 18-22)
Checking the electro-competent cells I made the week before. I electroporated my electro-competent cells with a pUC19 vector to measure their transformation frequency but I hardly obtained any colonies. Being suspicious that the pUC19 preparation may be bad, I repeated the transformation with a more recent preparation of pBluescript SK(+). I obtained approximately 107 transformants/g for the three strains. This is an acceptable frequency for MC4100 and LT2, but we need a really high transformation frequency (over 109 transformants/g) in order to perform cloning experiments with DH5α-λpir. We decided to prepare a new batch of DH5α-λpir electro-competent cells.
The mini-Tn7 was designed with a Gm resistance cassette flanked by selected restriction sites to facilitate exchange for other resistance cassettes. To construct mini-Tn7 variants with different markers, I designed primers to amplify kanamycin and chloramphenicol resistance cassettes from the vectors pSB4K5 and pSB1C3. Also, I did mini-preps of these vectors.
Another thing we would like to do with the mini-Tn7 is to generate a handful of functionally useful mini-Tn7 vectors. The idea is to insert into the BioBrick cloning site of the mini-Tn7 useful BioBricks, like reporters for gene expression measurement, inducible promoters and constitutively expressed fluorescent and bioluminiscent labels. We selected the following BioBricks:
Promoter measurement cassettes: BBa_K093005 (RBS+mRFP1), BBa_I732094 (LacZα+GFP-AAV).
Inducible promoters: BBa_I0500 (pBad/araC), BBa_I732083 (pLacIQ+RBS+tetR+STOP+ptetR).
Strain labels: BBa_I13521 (ptet+mRFP), BBa_K325909 (pBad+Lux).
This week I transformed these BioBricks in DH5α and prepared the corresponding plasmids.
In order to test the site-specific insertion of the mini-Tn7 transposons in our strains, I designed primers to amplify from the Tn7R end to the glmS gene. I took this opportunity to train my self in doing sequence comparison and analysis using common tools such as Clustal and Blast. I searched for a conserved motif to make one primer suitable for all four bacterial strains, but the conserved sequences were not long enough. In consequence, I designed two different glmS of primers, one for E. coli and S. typhimurium and another one for P. aeruginosa and P putida.
attTn7, the insertion site of the Tn7 transposon, is very well conserved in Gram-negative bacteria. However, if you want to use our mini-Tn7 based BioBrick delivery system in an organism without the attTn7, don’t worry, we plan to create a "portable" attTn7 for you. To this end, I designed primers to amplify the attTn7 site in the E. coli genome.
Week 4 (July, 25-29)
Checking DH5α-λpir electro-competent cells. I electroporated the previously prepared cells with a pBluescript SK(+) vector and I got approximately 2.5 108 transformants/μg. It was not the expected >109 transformants/μg, but it is an acceptable frequency even for cloning experiments.
Not amplifying the pUC18R6KT vector from pTNS2. This week I made a huge effort to obtain a suicide vector to deliver the mini-Tn7, but finally I did not get it. I performed at least one PCR reaction with this aim every day, changing conditions (polymerase, nucleotide concentration, DNA concentration, different primer preparations, even already made PCR mix) and PCR cycle (temperature and time of steps). In the last try I performed a gradient PCR to determine the optimum annealing temperature with a PCR mix kit where there was not much that could do wrong, but even then I did not get any amplification. Then we thought that the SfiI restriction site we added to the primers could be avoiding the annealing, so we designed new primers where some nucleotides of the SfiI restriction site were part of the complementary region of the primers and others without the SfiI tail to have a positive control for the amplification.
Mini-prepping. I repeatedly had problems to get highly concentrated plasmid preparations. I used mini-prep kits, so I did not know what my mistake was. I tried different kits and Fernan supervised my work one day, but the error was not obvious. By the end of the week, when one of the solutions of the kit ran out and I had to change it, my mini-preps started to rise their concentration.
Not amplifying resistance cassettes. I tried to amplify kanamycin and chloramphenicol resistance cassettes from pSB4K5 and pSB1C3 vectors, but after three PCR reactions changing conditions I did not get an useful PCR product.
Preparing BioBricks to insert them into mini-Tn7. I set up inocula, did mini-preps of the plasmids and digested them with EcoRI and PstI restriction enzymes. The next step would be isolate from gel, but the concentration was too low to use the fragments for cloning; so I repeated the digestions with high amounts of DNA, but the results were similar. I need mini-preps with higher DNA concentrations.
Synthetizing a portable attTn7. I performed two PCR reactions changing dNTPs concentration and annealing temperature to amplify the insertion site of the Tn7 transposon from the E. coli chromosome, but I did not get any amplification. I preformed this process as a colony PCR (picking a colony to get the DNA template), so next week I will try to amplify the desire region of the E. coli chromosome by purifying the genomic DNA first.
Working on our own-designed mini-Tn7. I performed the first necessary steps to do with a synthesis order: resuspending, transformation in DH5α, plating, setting up inocula and mini-prepping (this was one of the mini-preps of the last day so I got a highly concentrated preparation).
Week 5 (August, 1-5)
Amplifying the pUC18R6KT vector from pTNS2. Using new primers I performed a gradient PCR in a Taq polymerase catalyzed reaction. This time I got the expected PCR product independently of the annealing temperature; and I isolated bands from gel. This was possible due to improved primer design, and by switching from Pfu to Taq polymerase. Finally, after innumerable problems with the template, dNTPs, enzymes, primers… I got the pUC18R6KT vector.
Amplifying resistance cassettes. I tried to amplify the kanamicin and chloramphenicol resistance cassettes in a Pfu-polymerase catalyzed PCR reaction without positive results. Again, I obtained the expected results when I switched to Taq polymerase. I isolated and purified these PCR products from an agarose gel.
Preparing BioBricks to insert them into mini-Tn7. I digested the desired BioBricks with EcoRI and PstI trying to use the highest amount of DNA possible, but the mini-preps were not concentrated enough and I could only isolate from gel a couple of BioBricks properly digested. I used the traditional alkaline lysis-ethanol precipitation plasmid DNA purification method instead of using a commercial column kit and this time I obtained really high concentration mini-preps, although they were probably less clean. I repeated the digestions with the new samples, but gel electrophoresis revealed that, even though the DNA concentration was good, a large amount of RNA was also present. I isolated and purified the BioBrick fragments that there were not masked by the RNA smear at the bottom part of the lanes.
Synthetizing a portable attTn7. I purified genomic DNA from the MC4100 E. coli strain to use it as a template to amplify attTn7, the insertion site of Tn7 transposons. The PCR reaction resulted in a PCR product of the expected size, which was isolated and purified from an agarose gel. Because the primers added the standard prefix and suffix, the attTn7 could be digested with EcoRI and PstI. This fragment was ligated with EcoRI- and PstI-digested pSB1C3 and pSB4K5, and transformed into DH5α competent cells.
Construction of plasmids containing mini-Tn7. I digested a previously prepared mini-prep of the commercial plasmid containing the synthetic mini-Tn7 construct with SfiI. The SfiI fragment containing the transposon was ligated with SfiI-digested pUC18-SfiI or PCR-amplified and SfiI-digested pUC18R6KT-SfiI, and transformed in DH5α and DH5α-λpir, respectively.
Week 6 (September, 1-2)
Checking the clones containing the portable attTn7 by colony PCR. I had transformed pSB1C3 + attTn7 and pSB4K5 + attTn7 ligations in DH5α but I only obtained colonies for the former construct. The control plates looked OK. So I tested eleven candidates by colony PCR using the pSB1C3-attTn7 plates and the standard primers for prefix and suffix. The PCR products were analyzed in an electrophoretic gel and most of them showed the expected 208 bp attTn7 band. I restreaked five positive candidates onto fresh plates.
Cleaning chloramphenicol and kanamycin resistance cassettes. The gel-purified PCR products bearing resistance cassettes were digested at the flanking NcoI sites. However, we observed that these preparations did not freeze at -20, and we suspected ethanol contamination. Because of that, I discarded the digestion reactions and cleaned the DNA, analyzing the cleaning results in an agarose gel and measuring the DNA concentration.
Cleaning BioBrick mini-preps and digestions. Previous minipreps of the miniTn7 BioBrick inserts contamined with RNA were treated with RNAse and then cut with EcoRI and PstI. The digested BioBricks were isolated from gel and purified, but the resulting preparations had low DNA concentration.
Checking plasmids containing synthetic mini-Tn7 transposon. The pUC18-SfiI-miniTn7-Gm plasmid was checked by SfiI digestion with positive results. On the other hand, the selective plates from the pUC18R6KT-miniTn7-Gm ligation did not show any colonies. I checked the DNA samples used in gel and they showed the expected pattern so the problem must be in the competent cells. We planned to prepare new electro-competent and chemically competent DH5α-λpir cells.
Streaking out frozen strains. Before I went on vacation, I froze away most of the strains I had used, so I had to streak them out to work from now on.
Week 7 (September, 5-9)
Finishing the preparation of the resistance cassettes. The previously purified Cm and Km resistance cassettes were digested with NcoI. Those digested fragments are perfect to create miniTn7 variants of the basic transposon construct.
Finishing the preparation of BioBrick inserts. The BioBrick mini-preps were digested with EcoRI and PstI. As in previous digestions, all the BioBricks showed the expected size, except for BBa_I732094. We skipped this part because it was not essential for us. The DNA bands were isolated from gel and purified. These digested parts are intended for the construction of mini-Tn7 variants with specialized functions.
Checking the identity of the portable attTn7 by digestion. I performed EcoRI-PstI digestions with mini-preps from previous colony PCR positive clones. Unfortunately, the amount of DNA was too low to reach definitive conclusions; so I repeated that digestion with more DNA and an additional analytical digestion with PvuII. The restriction patterns obtained were as expected, thus confirming the presence of attTn7 in pSB1C3.
Constructing the pUC18R6KT-miniTn7-Gm. This is the central construct of the miniTn7 BioBrick tool kit, so I performed all the experiments I could in order to obtain it. I did new mini-preps of miniTn7-Gm, performed new digestions and ligations (pUC18R6KT + miniTn7-Gm) and did three different electroporations: one with previously prepared DH5α-λpir electro-competent cells, again without positive results; a second one with freshly prepared prepared DH5α-λpir electro-competent cells, obtaining only one colony; and a third electroporation with DH5α-λλpir electro-competent cells prepared with a different protocol. In the latter experiment I obtained a reasonable number of colonies on the selective plates. I set up inocula, mini-prepped and performed two different digestions (SfiI and BglI) to analyze the results. The amount of DNA was too low and because of that I could not reach any conclusions.
Characterizing pUC18-SfiI-miniTn7-Gm. The aim of this characterization is determine the orientation of the miniTn7-Gm inside pUC18-SfiI, measure the frequency of transposition in Pseudomonas putida KT2440, and check the site-specific insertion of the transposon at the end of the glmS gen. The orientation of the miniTn7 was determined by three digestion reactions (EcoRI, PstI and ScaI) and electrophoretic gel analysis. The transposition frequency was tested by conjugation and electroporation, using Pseudomonas putida KT2440 as the host. These assays demonstrated a high transposition frequency particularly by conjugation (10-4 insertions/viable cell).
Week 8 (September, 12-16)
Preparing attTn7 for sequencing. I set up a couple of inocula for freezing and sequencing, mini-prepping previously.
Starting the characterization of attTn7. Considering that we only have achieved by then the minTn7 in pUC18SfiI vector (replicative in Enterobacteriaceae) we need to insert the attTn7 in a P. putida replicative vector to check the site-specific insertion of the miniTn7 in the attTn7. To this way the miniTn7 will be in a suicide vector and the attTn7 not. We are going to insert the attTn7 in the pBBR1-MCS4. That week I prepared mini-preps of pSB1C3-attTn7 and pBBR1-MCS4 and digested them with EcoRI and SpeI.
Constructing the pUC18R6KT-miniTn7-Gm. The previous week I could not reach any conclusions of the analytic digestions of a putative pUC18R6KT-miniTn7-Gm. I repeated the digestions with higher amounts of DNA and I realized that there were not positive results. Because of the lack of re-ligation of the vector we think it could be not well-cut. I repeated the digestions of pUC18R6KT PCR product and ligation with miniTn7-Gm. Then I performed three transformations: two with two different preparations of electro-competent DH5α-λpir cells and another with chemically competent DH5α-λpir cells. Only the plates of the chemical transformation had a reasonable number of colonies. I set up 24 inocula of the chemical transformation plates, doing replica in a Gm and Ap plate. The next day I did mini-preps only of the inocula whose replica grew (18). The mini-preps were digested with SfiI and BglI and four candidates showed the expected restriction patter. Finally I had got the main construction of the miniTn7 BioBrick tool kit.
Characterizing pUC18-SfiI-miniTn7-Gm. I preformed colony PCR to detect the site-specific insertion of the miniTn7 in the P. putida genome with 11/11 positives in conjugation product strains and 10/12 positives in electroporation product strains. Repetitions of the electroporation and conjugation to measure transposition frequency were made, but I made mistakes diluting before plating and the results were not usable.
Characterizing the resistance excision by Flp recombinase. We were to use the pFLP2 plasmid, which carried the Flp recombinase or flipase gen, to recombine the FRT cassettes who flank the Gm resistance cassette of pUC18SfiI-miniTn7BB-Gm. I followed the protocol for recombination of flipase until making dashes in different selective plates because there were growth in every dash, what means that the Gm cassette was not excised. Thus, I started again.
Creating variants of pUC18SfiI-miniTn7BB-Gm. The objective was to include BioBricks into the BCS of the miniTn7 and change its resistance cassette. I digested pUC18SfiI-miniTn7BB-Gm with EcoRI/PstI and NcoI; ligated the plasmid with previously digested and isolated BioBricks and resistance cassettes; and transformed the ligations in DH5α competent cells. The new day the number of colonies was low. Colony PCR was performed and there was just one positive: pUC18SfiI-miniTn7BB-Km.
Week 9
Our order of DNA synthesis has not arrived yet. It is a month behind-schedule by now and we are getting anxious about this delay of the DNA synthesis service. I know I must use my time in the lab despite not having all the required materials, so I made a list of all the experiments I can run without the mini-Tn7. Actually It is a long list with a fair amount of work to do. I set priorities and start from the top!
This was a less stressful week. We asked the DNA synthesis company about the 1-month delay and they claimed they had problems with the synthesis and still need two more weeks to have it ready. We are getting desperate about this! Still, I keep on preparing material in advance of the arrival of the long-awaited mini-Tn7.
Not having a better task to do, as you can see, this was primer design week for me
Back to a hard-working week. As my time in the lab passes I realize that I can perform more experiments in less time, which does not always mean to get better results. Wednesday was an incredible day: I did more of the molecular biology technics I already know, and our mini-Tn7 synthesis order arrived. I exploded with enthusiasm. These were my main tasks this week:
Last week in the lab before vacation!
This was the most successful week by now. I obtained most of the results I had been trying since I started and I went on vacation with a smile in my face.
Back to work! After three weeks on vacation it was hard to return to the lab, but I was overexcited to face the home stretch to the Regionals. In those two first days of September I mostly checked some results from August and prepared new materials.
The wiki freeze deadline is coming closer! So I have been working all the time I could, nine-ten hours a day in average, and thankfully it was a productive week.
Penultimate week before wiki freeze. I kept on focus in obtain the pUC18R6KT-miniTn7BB-Gm plasmid (main construction of the Tn7 kit) and characterize the pUC18SfiI-miniTn7BB-Gm plasmid.
DryLab
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- Bioinformatics
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- BioBrick
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- Wiki
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