Team:NYMU-Taipei/Experiments/Functional Assays
From 2013.igem.org
(Difference between revisions)
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=== 2013-09-19 === | === 2013-09-19 === | ||
- | * | + | * Purpose: Measuring TrxCp+E0840 with respect to different H<sub>2</sub>O<sub>2</sub> concentrations. |
+ | * Scale: 10 shorts terms, time points retrieving in the order 1 to 2, then 10 to 3. | ||
+ | * Item: E0840, J23101+E0840, TrxCp+E0840 with 6 different H<sub>2</sub>O<sub>2</sub> concentrations (0mM, 0.01mM, 0.05mM, 0.1mM, 0.5mM, 1mM) | ||
=== 2013-09-20 === | === 2013-09-20 === |
Revision as of 23:51, 27 September 2013
National Yang Ming University
This page is a list of all the functional assays that we have done with simple results.
For a more combined and organized set of results, see our Data page.
Contents |
2013-07-29
- Scale: long term (25ml), samples retrieved from 2 to 6 hours once every 30 minutes.
- Items: E0240,E0240+H2O2, pLac+E0840, pLac+I13507, pNHaA+E0240, pLac+I13507+H2O2 on pSB1A2 backbone
- medium: M9 minimal medium
- Measuring: OD600 measured in a cuvette via spectrometer, fluorescence 485/525 (GFP) and 584/607 (RFP) in ELISA plate reader
- Results: the strength of NHaA promotor is so weak that we decided to switch our safety biobrick to the next design.
2013-08-02
- Purpose: Finding the suitable range of H2O2 concentration to test our promoters.
- Items: pLac+E0840 with 8 different H2O2 concentrations (OmM, 0.05mM, 0.1mM, 0.5mM, 1mM, 5mM, 10mM, 50mM) on pSB1A2 backbone
- Testing: Both OD600 and fluorescence 485/525 (GFP) both measured using the ELISA plate reader.
- Results:
- MG1655 dies above concentrations of 5mM H2O2
- The data measured before 3 hours seem less reliable.
2013-08-04
- Purpose: Measure the basal expressions of various promoters using smaller volume but more replicates.
- Scale: 1 long term (25ml) samples retrieved at 0, 4, 6, 8, 10, 12 hours, and 7 short terms (4ml) retrieved at 0 and 4 hours.
- Items: E0840, R0065+E0840, pLac+E0840, pNHaA+E0840, J23101+E0840, I13507, R0065+I13507, pLac+I13507, pNHaA+E0840, J23101+I13507 all on pSB1A2 backbone
- Testing: OD600 and fluorescence 490/530, 485/525 and 470/530 (all GFP) in ELISA plate reader
- Results: only R0065+E0840 ,J23101+E0840, J23101+I13507, pLac+E0840, pLac+I13507 show efficient function. This is an efficient way for creating biological replicates.
2013-08-08
- Purpose: Finding the impact of high temperature (44C) on the various promoters.
- Scale: long term, short term
- Item: E0840, J23101+E0840,R0065+E0840, pLac+E0840
- Testing: OD600, fluorescence 490/530, 485/525 and 470/530 in ELISA plate reader
- first temperature testing--suggest that plac is repressed under 44C, R0065 as well
- Results:
- The pLac promoter is highly repressed under 44C compared to at 37C, and R0065 has relatively small repression. As a result, we bagan searching for another repressible promotor in place of pLac.
- We finally settled on using the wavelength 485/525 for measuring GFP fluorescence.
2013-08-14
- Scale: long term (25ml) for 8 hours
- Item: E0840, J23101+E0840, pLac+E0840,HemHp+E0840 with 6 different H2O2 concentrations (0mM, 0.01mM, 0.05mM, 0.1mM, 0.5mM, 1mM) on pSB1A2 backbone
- Testing: OD600 and fluorescence 485/525 in ELISA plate reader
2013-08-20
- Scale: 8 short terms (2ml), sample retrieved at 4 hours
- Item: E0840, J23101+E0840, R0065+E0840, TrxC+E0840 with 7 different H2O2 concentration (0mM, 0.01mM, 0.05mM, 0.1mM, 0.5mM, 1mM, 5mM) on pSB1A2 backbone
- Testing: OD600 and fluorescence 485/525 in ELISA plate reader
- We started washing with PBS instead of M9 medium.
- Result: the strength of TrxC promotor enhance as H2O2 concentration rises until it reach 1 mM, and the E. coli K-12 MG1655 dies at 5 mM.
2013-08-25
- Purpose: Finding the photometric and fluorometric value of the medium as background
- Item: M9 medium and PBS medium
2013-08-26
- Item: J23101+E0840, R0051+ E0840, TrxCp+E0840, Hemhp+E0840 with 7 different H2O2 concentrations (0mM, 0.01mM, 0.05mM, 0.1mM, 0.5mM, 1mM, 5mM) on pSB1A2 backbone
2013-08-27
- Purpose: Finding the reaction SufAp(K554003)+E0840 to H2O2
- Scale: 10 short terms (2 ml), sample retrieve at 4 hours
- Item: J23101+E0840, R0040+E0840, R0074+E0840, SufAp+E0840with 7 different H2O2 concentrations (0mM, 0.01mM, 0.05mM, 0.1mM, 0.5mM, 1mM, 5mM) on pSB1A2 backbone
2013-08-30
- Item: E0840, J23101+E0840, J23102+E0840, R0082+E0840
- Result: When J23101 is standardized as 1, the strength of J23102 is 1.12, and R0082 is 1.25. Since R0082 is positively regulated
- J23102 is 1.12x stronger than J23101, R0082 is 1.25x stronger than J23101. R0082 is too leaky so we chose not to use it anymore.
2013-08-31
- E0840, J23101 (replicates retrieved backwards from samples 10 till 1, thus the first time point only grew for 2hrs)
- R2=0.9757 for 40 replicates.
- J23119 J23104 K592006 are almost the same as background, thus we are doubting that it is incorrect.
2013-09-02
2013-09-05
- Purpose: Measuring NTU_Taida's parts.[Human Practice Collaboration]
2013-09-07
- Purpose: Since J23101 is taken as the standard in the reporting assay experiments, we measure the reaction of J23101 under different H2O2 concentrations.
- Scale: 10 shorts terms, time points retrieving in the order 7 to 1, then 10 to 8.
2013-09-10
- Purpose: Creating more duplicates of J23101 to standardized is value
- Scale: 10 short terms (2ml) from 3 to 7.5 hours, samples retrieved every 30 minutes.
- Item: E0840, J23101+ E0840 with 6 different H2O2 concentration (0mM, 0.05mM, 0.1mM, 0.5mM, 1mM, 2mM)
2013-09-19
- Purpose: Measuring TrxCp+E0840 with respect to different H2O2 concentrations.
- Scale: 10 shorts terms, time points retrieving in the order 1 to 2, then 10 to 3.
- Item: E0840, J23101+E0840, TrxCp+E0840 with 6 different H2O2 concentrations (0mM, 0.01mM, 0.05mM, 0.1mM, 0.5mM, 1mM)
2013-09-20
- Purpose: Knowing the reaction of our 3 new AhpCp1000 derived OxyR-induced promoters to H2O2
- Item: AhpCp1,AhpCpd1 and AhpCp2; each with three different H2O2 concentrations(OmM, 0.1mM, 1mM)
2013-09-25
- Purpose: To simplify our reporting assay protocols, we change our medium into M9 minimal medium, the E. coli K-12 MG1655 is cultivaed directly in 96-well plates.
- Item: AhpCp1+E0840, AhpCp2+E0840, SufAp+E0840, R0065+E0840,J23101+E0840, TrxC+E0840. The last two promotors aree treated with 8 different H2O2 concentrations.
- Results:The M9 minimal medium has the possibility to interferes with the H2O2, so we restore to our original protocols.
2013-09-26 - 1
- Scale: 10 short terms (2ml) from 3 to 7.5 hours, samples retrieved every 30 minutes.
- Item: AhpCp1+E0840,AhpC2+E0840, TrxC+E0840; each promoter of the three with 6 different H2O2 concentration (0mM, 0.01mM, 0.05mM, 0.1mM, 0.5mM, 1mM)
2013-09-26 - 2
- Scale: 10 short terms (2ml) from 3 to 7.5 hours, samples retrieved every 30 minutes.
- Item: AhpCp1000+E0840, AhpCp2D1+E0840; both with 6 different H2O2 concentration (0mM, 0.01mM, 0.05mM, 0.1mM, 0.5mM, 1mM)