Team:SJTU-BioX-Shanghai/Results

From 2009.igem.org

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=Results overview=
=Results overview=
==Detection of bacterial growth activity==
==Detection of bacterial growth activity==
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[[Image:SJTU09_Result_eukaryotic4.png|left|thumb|165px|relB]]
[[Image:SJTU09_Result_eukaryotic4.png|left|thumb|165px|relB]]
[[Image:SJTU09_Result_eukaryotic5.png|left|thumb|165px|relE]]
[[Image:SJTU09_Result_eukaryotic5.png|left|thumb|165px|relE]]
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==Parts & devices==
 
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;Go to [http://partsregistry.org/cgi/partsdb/pgroup.cgi?pgroup=iGEM2009&group=SJTU-BioX-Shanghai PartsRegistry] to see our submited parts.
 
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Almost all of our parts have been detected after enzyme digestion. The following DNA Electrophoresis pictures prove our parts to be accurate and reliable.
 
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[[Image:SJTU09_Result_html_47688d36.png|center]]
 
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#Lane2: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K185000 BBa_K185000] RelE toxin+Rbs30 311bp OK
 
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#Lane3: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K185001 BBa_K185001] Arabinose-induced RelE Generator 1791bp Failed
 
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#Lane4: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K185002 BBa_K185002] Lon Protease+Double terminater 2492bp OK
 
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#Lane5: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K185003 BBa_K185003] RelE toxin+Lon proteas 2827bp OK
 
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#Lane6: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K185004 BBa_K185004] RelE toxin+Double terminator 443bp OK
 
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[[Image:SJTU09_Result_html_m3e71a479.png|center]]
 
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#Lane3: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K185028 BBa_K185028] RelB+Double-terminator 395bp OK
 
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[[Image:SJTU09_Result_html_78756540.png|center|thumb|500px]]
 
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#Lane3: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K185007 BBa_K185007] Promoter116+RBS34+lLacI+Double-terminator+Plac+RBS31 1514bp OK
 
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#Lane5: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K185016 BBa_K185016] Promoter118+RBS34+LacI+Double-terminator+Plac+RBS31 1514bp OK
 
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#Lane15: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K185018 BBa_K185018] Promoter118+QPI+RBS30+RelB+Double-terminator 1454bp OK
 
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#Lane17: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K185036 BBa_K185036] Promoter110+QPI+RBS34+RelB+Double-terminator 1433bp OK
 
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#Lane20: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K185011 BBa_K185011] Promoter116+QPI+RBS31+RelB+Double-terminator 1435bp OK
 
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[[Image:SJTU09_Result_html_m41139464.png|center]]
 
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#Lane13: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K185053 BBa_K185053] Promoter116+RBS34+LacI+Double-terminator+pPlac+RBS31+RelE+RBS30+Lon protease+Double terminator 4347bp OK
 
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[[Image:SJTU09_Result_html_51e6b685.png|center]]
 
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#Lane10: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K185012 BBa_K185012] Promoter116+RBS34+LacI+Double-terminator+Plac+RBS34 1347bp OK
 
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#Lane12: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K185019 BBa_K185019] Promoter118+RBS34+LacI+Double-terminator+Plac+RBS34 1512bp OK
 
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[[Image:SJTU09_Result_html_m33466830.png|center|thumb|500px]]
 
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#Lane 2&3: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K185045 BBa_K185045] Composite J23110+Q01121 1416bp OK
 
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#Lane 4&5: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K185046 BBa_K185046] Composite J23110+Q01121 1416bp OK
 
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#Lane 6&7: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K185042 BBa_K185042] Composite J23110+Q04510 1030bp OK
 
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#Lane 8&9: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K185043 BBa_K185043] Composite J23116+Q04510 1030bp OK
 
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#Lane 10&11 [http://partsregistry.org/wiki/index.php?title=Part:BBa_K185044 BBa_K185044] Composite J23118+Q04510 1030bp OK
 
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[[Image:SJTU09_Result_html_m6dee86aa.png|center|thumb|500px]]
 
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#Lane 5&6&7: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K185037 BBa_K185037] Composite J23116+Q04510+B0031 1052bp OK
 
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#Lane 8-12: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K185038 BBa_K185038] Composite J23116+Q04510+B0034 1050bp OK
 
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#Lane 15&17&18&19: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K185039 BBa_K185039] J23118+Q04510+B0030 1053bp OK
 
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#Lane 20&21: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K185040 BBa_K185040] J23118+Q04510+B0031 1052bp OK
 
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[[Image:SJTU09_Result_html_m4da2a007.png|center]]
 
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#Lane 2-8: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K185034 BBa_K185034] Device J23116+Q04510+B0034+K185048 1433bp OK
 
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[[Image:SJTU09_Result_html_m2f8f0e15.png|center]]
 
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#Lane 4: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K185005 BBa_K185005] Generator J23116+Q04510+B0034+K185048+K185005 3298bp OK
 
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[[Image:SJTU09_Result_html_6014a841.png|center|thumb|500px]]
 
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#Lane 2-9: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K185051 BBa_K185051] Composite J23110+B0034+BBa_K185008+BBa_K185009 2748bp PCR analysis (plasmid backbone added) OK
 
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[[Image:SJTU09_Result_html_2fd90b58.png|center]]
 
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#Lane 2, 4, 6, 7: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K185052 BBa_K185052] Regulatory 1342bp PCR analysis (backbone sequence added) OK
 
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[[Image:SJTU09_Result_html_2f372603.png|center|thumb|500px]]
 
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#Lane 2,3: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K185009 BBa_K185009] Device 2047bp OK
 
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[[Image:SJTU09_Result_html_m2ac05772.png|center]]
 
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#Lane 1,3,5,6: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K185031 BBa_K185031] intermediate 1104bp OK
 
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[[Image:SJTU09_Result_html_ad92060.jpg|center]]
 
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#Lane 4,5,6,7,8,9,10,11: [http://partsregistry.org/wiki/index.php?title=Part:BBa_K185033 BBa_K185033] inverter 1514bp OK
 
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Revision as of 02:46, 21 October 2009

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Project introduction. Inspired by the natural regulator of circadian bioclock exhibited in most eukaryotic organisms, our team has designed an E.coli-based genetic network with the toxin-antitoxin system so that the bacterium oscillates between two states of dormancy and activity (more...)

Contents

Results overview

Detection of bacterial growth activity

Results for Western blotting & RT-PCR

Experiments on eukaryotic cell

The circadian clock is an endogenous biological oscillator found widely throughout the tree of life. Circadian rhythms impact many behavioral and physiological processes, allowing for the anticipation of daily changes in the environment, the coordination of events that need to occur simultaneously or sequentially, and the segregation of activities that should be separated. At the organism level, these 24-hour cycles are manifested diversely, occurring in the movement of leaves and the opening of flowers, spore formation in Neurospora, and blood pressure and body temperature, as well as hunting, foraging, mating, and sleeping behavior in mammals. Clearly, because of the widespread occurrence of the circadian clock and its effects at all levels of organization, this system is an essential component of biological knowledge.

Inspired by the natural regulator of circadian bioclock exhibited in most eukaryotic organisms, our team has designed an E.coli-based genetic network with the toxin-antitoxin system so that the bacterium oscillates between the states of dormancy and activity. We want to control the circadian rhythm of bacteria using this artificial bioclock. Interestingly, we think that this system may be used in mammalian cell to realize many human practices including delaying aging, controlling the progress of cancer and curing the depression et al. Therefore, we have tried to test the relE-relB system effect in the mammalian cell line.

We have generated two constructs including pCMV-relE-flag and pIND-relB-flag (Fig. 1), the latter plasmid will be induced to express the relB protein in EcR-CHO cells (Invitrogen) when adding the Ponasterone A (Fig.2). These two plasmids were co-transfected in EcR-CHO cell line, then the expression of relB were induced and uninduced. If uninducing, the expecting result is that the cells only with relE protein will gradually show the apoptosis phenotype. However, if inducing with PA, the expression of relB will rescue the apoptosis. We can not get the final result as the limitation of time, but we will continue to conduct the experiment to identify the hypothesis if the relE-relB system indeed can be used in mammalian cell to realize the human practices.

Fig. 1 The constructs of pIND-relB-flag and pCMV-relE-flag.
pCMV-relE-flag
pIND-relB-flag


Fig. 2 The immunofluorescent assay of relB and relE in the EcR-CHO cells.
EcR-CHO cells were grown on glass slides to reach 90% confluency and transfected with relB and relE in a pIND vector and pCMV vector respectively, and after 24h fixed in 80% acetone, and were then incubated for 60min at 37°C in the PBS with anti-flag monoclonal antibody. FITC-labeled goat anti-mouse IgG (Santa Cruz Biotechnology) was used as a secondary antibody. The immunofluorescent staining signal was identified by confocal microscopy (Leica TCS SP5). The cells were stained with Evans Blue. The white scale bars represent 10μm.
Control
relB
relE