Team:British Columbia/Notebook

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==May 28==
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<map name="sponsormap">
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<area shape="rect" coords="10,5,220,70" href="https://2012.igem.org/Team:British_Columbia/LabNotebook" />
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<area shape="rect" coords="10,90,220,155" href="https://2012.igem.org/Team:British_Columbia/BiobrickConstruction" />
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<area shape="rect" coords="10,170,220,235" href="https://2012.igem.org/Team:British_Columbia/DSZNotebook" />
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<area shape="rect" coords="10,250,220,310" href="https://2012.igem.org/Team:British_Columbia/ConsortiaDynamics" />
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<area shape="rect" coords="10,330,220,390" href="https://2012.igem.org/Team:British_Columbia/ConsortiaTunability" />
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</map>
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Started making first batch of DH5α and EPI300 competent cells. See [[Team:British_Columbia/Protocols/Competent Cell Production | Competent Cell Production]].
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<div id="sponsormap"><img align="left" src="https://static.igem.org/mediawiki/2012/a/a0/Ubcigemnotebookmenu.jpg" usemap="#sponsormap" alt="UBC iGEM 2012 notebook"> </div>
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- [[User:Tingchiawong|Tingchiawong]]
 
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==May 30==
 
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Continued production of competent cells.  OD<sub>600</sub> values were monitored as cells grew until when it reached 0.420 for DH5α and 0.443 for EPI300, upon which they were iced immediately. 
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</div><div id=note><p align=center><font face=arial narrow size=5><b>Welcome to our Notebook!</b></font></p><font face=arial narrow>
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Our Notebook is sorted by sub-project. Please use the menu to navigate through our Notebook entries and follow our progress over the year.</br> </br>  
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- [[User:Tingchiawong|Tingchiawong]]
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<b>UBC iGEM Life</b> chronicles the conferences, socials and life outside-of-the-lab of our team.</br></br>  
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<b>Biobrick Construction</b> describes how our team build our parts and improved existing parts from the Parts Registry.</br></br>  
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==May 31==
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<b>Bio-Desulfurization</b> recounts the steps our team took to distribute and assess the efficiency of the DSZ bio-desulfurization pathway in a microbial consortia.</br></br>
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<b>Consortia Dynamics</b> details our team's efforts in measuring population ratios within microbial consortia based on fluorescence readings.</br></br>  
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Finished production of the competent cell protocol that was initiated on May 28.  Competent cells were not flash-frozen with liquid nitrogen, but were placed directly into the -80ºC freezer.  Samples of each cells were transformed then plated for verification.
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<b>Consortia Tunability</b> elucidates our team's progress in creating easily tunable microbial consortia based on interdependent auxotrophies.
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</div>
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- [[User:Tingchiawong|Tingchiawong]]
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</html>
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==June 1==
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Competent cells worked.  Plates of competent cells grew on antibiotic plates.
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- [[User:Tingchiawong|Tingchiawong]]
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Made 2 bottles of 400 mL M9 + glucose media.
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==June 5==
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Made EPI 300, BL21, and DH5α competent cells with plasmid pIJ790 in them.
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-Ruichen
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==June 6==
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Learned how to electrophorese cells with biobricks (1-7B, 2-17F, 2-14N, 2-9B, 3-13M, 3-14E, 4-3I, 5-1A, 5-12O), and plated them on plates to grow colonies.
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Tested kanamycin (Kan) plates with control.
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-Ruichen
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==June 7==
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Retreated the plates previously spread, KAN plates worked and most of them grew into colonies or covered plates completely. (advised to spread the plates with 50µl recovered cells instead 100µl in the future for better colony identification).
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Made more 10µg/ml ampicillin (Amp) and 34µg/ml chloramphenicol (Chlor), and more agar plates of Amp and Chlor (half bagful respectively).
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Electrophoresed 1-1N, 2-2K, 1-5P, 2-21O using DH5α, and plated them.
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-Ruichen
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In the afternoon, we (Ruichen, Mehul, Grace) made many more K12 competent cells, which we put into storage. (The protocol is now on the wiki.) There was also talk from Jacob and John about buying $0.50 worth of gasoline/diesel from the nearest gas station to test solvent resistance of some of our cells. I left before that happened, though. (Would have been fun to see the attendant's reaction!)
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- grace
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==June 8==
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Tried to make more EPI300 cells, though no obvious growth even after hours for the second time, and decided to leave it over night to see if there are any changes.
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Electrophoresed K12 with PIJ790 plasmid, and plated them on Chlor plates with control plates to examine the plates.
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- Ruichen
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Prepared a 96 well plate for co-culture experiments with the the following ratios:
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{| class="wikitable"
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|+ Co-culture ratios
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|-
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| GFP||RFP||YFP||0.5G/0.5R||O.67G/0.33R||0.33G/0.67R||0.5G/0.5Y||O.67G/0.33Y||0.33G/0.67Y||0.5R/0.5Y||O.67R/0.33Y||0.33R/0.67Y||
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|-
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| GFP||RFP||YFP||0.5G/0.5R||O.67G/0.33R||0.33G/0.67R||0.5G/0.5Y||O.67G/0.33Y||0.33G/0.67Y||0.5R/0.5Y||O.67R/0.33Y||0.33R/0.67Y||
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|-
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| GFP||RFP||YFP||0.5G/0.5R||O.67G/0.33R||0.33G/0.67R||0.5G/0.5Y||O.67G/0.33Y||0.33G/0.67Y||0.5R/0.5Y||O.67R/0.33Y||0.33R/0.67Y||
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|-
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| ||||||||||||||||||||||||||
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|-
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| 0.33G,R,Y||0.33G,R,Y|||0.33G,R,Y|||||||||||||||||||||
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| Media||Media||Media||||||||||||||||||||||
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|}
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All cells were derived from EPI300, and were grown in M9 media to allow for accurate OD measurements. a total of 10 uL culture in each case was added to 190 uL M9 media.
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However, the plate reader was later found to be broken. The plate was placed in the 4° cold room until such time that the experiment could be done.
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The wells were plated by GFP first, then RFP, the YFP. There was a slight accident that involved losing some of the YFP culture, but enough was recovered to fill the plates. It is likely that the GFP cultures spent over 30 minutes in the plate before the YFP was added, so some readings may not accurately reflect the ratios shown above. 
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-Jacob
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Miniprepped biobricks 12O, 5P, 17F, 13M, 14N, 14E using the QIAGEN Spin Miniprep Kit provided by the Hallam lab. We had planned to miniprep 7B also, but a slight accident caused there to be less than 1.5 mL in the microcentrifuge tube. It will be done sometime later, after regrowing a culture
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-grace
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==June 9==
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The EPI300 did grow!
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- [[User:Ruichen|Ruichen]]
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Bought $1 of 91 octane (no ethanol) gas from the Shell on 10th. It's in a red jerrycan in the flammables cabinet near our bench.
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[[User:JohnHenry|JohnHenry]] 14:31, 9 June 2012 (CDT)
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Experiment plan for week of June 10-16th:
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'''1) Kill Switch Assay for Colicin E7, Colicin E2, BamH1, H<sub>2</sub>O<sub>2</sub>'''
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''Colicin E7:''
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There is currently a plate of K12 cells with protein immunity and Colicin E7. Lysis protein (cuts the immunity gene to allow for Colicin E7 production) will be transformed into K12 (Sat). Cultures will be set up for both the protein immunity+Colicin E7 and the Lysis (Sun). The two cultures will be mixed and grown up to correct OD then plated (Mon). Plates will be checked for growth (Tues).
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''Colicin E2, BamH1, H<sub>2</sub>O<sub>2</sub>:''
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There are currently plates of K12 cells with Colicin E2 and H<sub>2</sub>O<sub>2</sub>s. Colonies will be picked and cultures will be set up for each of these (Sat). The cultures will be grown to correct OD and induced then plated (Sun). Colicin E2 is induced low concentration of ampicillin, BamH1 is induced with arabinose, and H<sub>2</sub>O<sub>2</sub> is induced with 2nM of AHL. Plates will be checked for growth (Mon). BamH1 will be transformed into K12 cells and plated (Sat). Same steps will be taken as above and plates will be checked for growth (Tues).
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'''2) Solvent Tolerance Assay'''
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Cultures of K12 cells with 3I plasmid will be set up (9am on Sun) in gasoline and pentane. OD will be checked every hour for 12 hours or less until stable phase (Sun). Protocol is on the TU Delft 2010 page [https://2010.igem.org/Team:TU_Delft#page=Notebook/protocols&anchor=Protocol_for_growth_of_E.coli_K12_on_alkanes].
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'''3) PCR RFP, YFP, GFP on to pcc1 fosmid'''
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There will be a PCR tutorial on Thursday 6pm with the primers for putting the RFP, YFP, and GFP from the biobrick on to pcc1 fosmids.
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- Marianne
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Wanted to start the solvent tolerance assay today, but previous protocols required 12 hours and by the time we got the gasoline, it was already 12. We decided to wait a day. In the mean time, we started some cultures and plates for a few kill switches that could also be assayed. The cultures were of a H2O2 producing strain, and another strain that expressed the colicin E2 operon, which is inducible under low (10 uG/mL) concentrations of B-lactam antibiotics, such as ampicillin (http://www.sciencemag.org/content/305/5690/1629.full#F2). Despite documentation of plating of the BAMHI kil switch, the plates were unable to be found, so another transformation was done, along with a transformation for the lysis gene from the colicin E7 operon. The colicin E7 toxin and immunity protein have already been grown in cultures.
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The tentative plan is to see if the two cultures interact by the lysis gene cleaving the E7/immunity complex, causing cell death. There was no one who knew how to use the plate reader in the lab today, so the co-culture experiments were further put on hold. It should be noted that the kill switches, unless otherwise noted, have been transformed into K12 E. coli cells, which are RecA positive, allowing the SOS promoter to work.
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- Jacob
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==June 11==
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Started kill switch assays on colicin E2 and BamHI. Colicin E2 is on the SOS promoter, which is best switched on by mitomycin. However, we currently do not have access to mitomycin or any of its closely related derivatives, so, judging by the previous;y mentioned paper, it might be able to be induced by b-lactam antibiotics in low concentrations.
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Procedure outline:
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Dilute 1:100 22A, 3C and wt strains in 25 mL LB. Measure OD every hour. At start of exponential phase, add arabinose to 0.01% or amp to 4 ug/mL to strain+control. Plate 25 uL 2 hours later, mid exponential phase. Details to follow.
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The plate reader is still broken, with no estimated repair date.
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-Jacob
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Transformed biobricks 7C, 22C, and 20K into K12, 8G into BL21 pIJ790, 7C into EPI300 pIJ790, and 14C into DH5α pIJ790 for miniprep.  After recovery, the cells were plated in the following manner: 22C and 20K on LB + Kan, 14C and 8G on LB + Amp, and 7C (both the K12 and EPI300 cells) on LB + Chlor.  Different cells were chosen to test out the newly made competent cells. Only the K12 cells have been verified.  7C was transformed into K12 after, in addition to EPI300 pIJ790, because the 7C biobrick has Chlor resistance, which mimics the marker on pIJ790.
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Quantified previously miniprepped biobricks using the nanodrop spectrophotometer.
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- [[User:Tingchiawong|Tingchiawong]]
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==June 12==
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Checked plates from Jacob's June 11 kill switch assay.  Every single plate (3C+, 3C-, 22A+, and 22A- in both 5 uL and 10 uL plating quantities) grew a lawn.  Only 3C+ and 3C- plates had a few distinguishable colonies.
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Checked plates of the cells transformed on June 11 by Ting-Chia and started 3 mL cultures for miniprepping. Only the DH5α pIJ790 and EPI300 pIJ790 transformed with the 14C and 7C biobricks, respectively, did not seem show any growth upon the first check.  It was unclear as to whether there were actually any 7C (EPI300 pIJ790) colonies growing, so both plates were returned to the 37ºC room to incubate.  For the other plates that did show growth, single colonies were picked and inoculated in 3 mL starter cultures for miniprep.  Cells were incubated at 37ºC at first, then at 30ºC to grow overnight.
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QIAprep Miniprep kit from Qiagen was used to miniprep 4-3I, 2-3C, and 3-22A.  The cells used were previously inoculated cultures that were stored at 4ºC.  DNA product was stored in sterile dH2O and frozen in the -20ºC freezer.
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We received plates of ''Rhodococcus'' sp. strain JVH1, ''Rhodococcus rhodochrous'' IGTS8 (ATCC 53968), and ''Baillus sphaericus'' IGTS9 (ATCC 53969) from Dr. Jonathan Van Hamme of Thompson Rivers University today.  Single colonies were picked and inoculated in 3 mL LB at 37ºC at first, then at 30ºC to grow overnight.  Plates were then parafilm-sealed and stored at 4ºC.
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After 20 hours at 37ºC, the plates with 14C and 7C (EPI300 pIJ790) had colonies.  14C only had one colony, while 7C had a couple of small colonies.  The origins of the colonies were uncertain, so the plates were discarded and the cells will be transformed in K12 the next day.  Also, 13M biobrick (RFP gene), which has been verified, will be transformed into EPI300 pIJ790 and DH5α IJ790 to check if the competent cells are working properly or if they are to blame for the failed 14C and 7C plates.
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- [[User:Tingchiawong|Tingchiawong]]
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==June 13==
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Removed 3 mL overnight cultures (20K, 7C, 8G, and 22C) from the 37ºC room and stored them at 4ºC until they are miniprepped.
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- [[User:Tingchiawong|Tingchiawong]]
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Discovered a thing Joe is too cool to do:
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Update the wiki.
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- [[User:JohnHenry|JohnHenry]]
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==June 14==
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Transformed the remaining interesting kill switches without promoters into K12.  Also transformed 17F into EPI300 pIJ790 and DH5α pIJ790 cells to determine if previously failed plates were due to ineffective competent cells.  All transformed cultures were then plated onto appropriate antibiotic plates (+Amp or +Kan), along with a control for each.  An extra control plate was spread onto a Chlor plate from a batch that previously produced unclear results.  The plates were placed at 37ºC at noon and left them to grow overnight.
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Made fresh batch of LB + Amp plates, which were used for half the Amp resistant samples from above.  Check control plate tomorrow for colonies to ensure plates work.
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Grew two 250 mL cultures of EPI300 to make into competent cells.  Iced them when OD<sub>600</sub> reached 0.34 and 0.30.  Finished glycerol stocks were stored in new freezer box "iGEM 2012 Comp Cells."
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- [[User:Tingchiawong|Tingchiawong]]
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Grace mini-prepped:
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*20K (in K12)
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*7C (in K12)
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*8G (in K12)
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*22C (in BL21 w/ plasmid pIJ790)
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Ting:More EPI300 competent cells made.  Need to verify competency tomorrow.
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- [[User:JohnHenry|JohnHenry]]
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PCR Party held in the evening to start PCR experiments. PCR programmed to run overnight at keep products chilled at 4ºC until tomorrow, when gels will be ran.
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- [[User:Tingchiawong|Tingchiawong]]
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==June 15==
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A very busy day!
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1)Made 1 liter's worth of Kan plates, and about 3/4 liter's worth of chlor plates. We are now out of empty plates, and they have been placed on the list of things to buy. The Hallam lab is also out of empty plates. This is not good, for many of our knockouts are replaced by tetracycline resistance, and we have no tetracycline plates. We may have to scrounge up some from other labs. Noting that the kan plates that we used previously often grew colonies for negative controls, we increased the amount of kan stock we added from 1 mL to 1.5 mL. We have yet to test whether that is too great for the cells with the appropriate plasmid, but nothing grew on the negative test for the epi300 cells that TIng recently made.
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2)Tested epi300 cells by transforming with the rfp cassette for easy identification of whether or not the transformation was actually successful, or if other factors were in play regarding resistance. Negative controls were also employed for the newly made plates.
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*Update* many colonies on the rfp plate, but none on the negative controls. The transformation efficiency appears to be slightly lower than previous competent cells, but is still fairly high.
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3)Miniprepped the resistance cassette colonies. Previously, to do the PCR, we just picked a colony, but we thought that it would be beneficial to have a plasmid stock in case we needed to repeat the PCR.
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4)PCR with new (biobrick) primers was attempted. We received primers for the Dsz genes and also for the amino acid genes. We did not, however, receive the DszA forward primer, and decided to hold off on those experiments until later. We performed a cPCR for all the genes we had, and ran the results on the gel.
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5)Attempted to do a solvent tolerance assay, but were thwarted. As it turns out, gasoline has some rather unpleasant volatile compounds that were interpreted as dangerous. Also, the cells that we wanted to grow showed no growth for the first 5 hours. Personally, I think that while it would be nice to have the relevant data, it seems that the hurdles to test to see if the addition of the prefoldin chaperone helps our cultures grow in organic solvents to remove the sulfur compounds are too great. We may revisit the project, but right now, it seems that we should put the idea behind us.
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6)Ran the gel. Below are the results from yesterday's and today's PCR. Cameron made the gel and taped the edges of the gel box to prevent the gel from escaping. The gel itself was made to 1% agarose in 0.5% TBE, and run on a 50 well gel box. 3 uL of loading buffer were used for 8 uL (10 uL for yesterday's products) sample to increase contrast, and various ladders were tested. The negative control for today's PCR popped open during the reaction, and evaporated. Despite this, I feel fairly confident that the data is accurate.  
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Running a gel
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# Broad Range Ladder
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# Today's PCR (in Ruichen's Lab book)
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# Today's PCR (in Ruichen's Lab book)
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# Today's PCR (in Ruichen's Lab book)
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# Today's PCR (in Ruichen's Lab book)
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# Today's PCR (in Ruichen's Lab book)
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# Today's PCR (in Ruichen's Lab book)
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# Today's PCR (in Ruichen's Lab book)
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# Today's PCR (in Ruichen's Lab book)
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# Today's PCR (in Ruichen's Lab book)
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# Today's PCR (in Ruichen's Lab book)
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# Today's PCR (in Ruichen's Lab book)
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# Today's PCR (in Ruichen's Lab book)
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# empty
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# 1kb ladder
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# Mehul's Stuff metA p1002 Kan
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# Mehul's Stuff metA p1002 Kan
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# Mehul's Stuff metA p1002 Kan
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# Mehul's Stuff metA p1002 Kan
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# empty
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# Ruichen's Stuff
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# Ruichen's Stuff
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# Ruichen's Stuff
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# Ruichen's Stuff
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# Ruichen's Stuff
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# empty
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# 1kb + Ladder
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# TrpA tet
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# TrpA tet +DMSO
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# TrpA tet +MgCl2
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# TrpA tet +DMSO+MgCl2
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# ArgE tet
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# ArgE tet +DMSO
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# ArgE tet +MgCl2
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# ArgE tet +DMSO+MgCl2
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# TyrA tet
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# TyrA tet +DMSO
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# TyrA tet +MgCl2
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# TyrA tet +DMSO+MgCl2
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[[File:June15igemmyriad.png ||]]
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As you can see, we have successful bands for tyrA (from genome, biobrick primers) with no DMSO, MetA with kanamycin resistance (for knockouts), trpA with tetracycline resistance, ArgE with tetracycline resistance, and tyrA with tetracyline resistance. The 1 kb+ ladder appears the most useful in this experiment.
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-Jacob
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Latest revision as of 01:42, 4 October 2012

British Columbia - 2012.igem.org
UBC iGEM 2012 notebook

Welcome to our Notebook!

Our Notebook is sorted by sub-project. Please use the menu to navigate through our Notebook entries and follow our progress over the year.

UBC iGEM Life chronicles the conferences, socials and life outside-of-the-lab of our team.

Biobrick Construction describes how our team build our parts and improved existing parts from the Parts Registry.

Bio-Desulfurization recounts the steps our team took to distribute and assess the efficiency of the DSZ bio-desulfurization pathway in a microbial consortia.

Consortia Dynamics details our team's efforts in measuring population ratios within microbial consortia based on fluorescence readings.

Consortia Tunability elucidates our team's progress in creating easily tunable microbial consortia based on interdependent auxotrophies.

Retrieved from "http://2012.igem.org/Team:British_Columbia/Notebook"