Team:Tokyo Tech/Projects/making-rain/GC-Assay

From 2011.igem.org

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We made dilution series (deluted 102,103,104,105,106,107 times) of liquid isoprene (Wako Pure Chemical Industries, Ltd, Japan) diluted in chloroform.  
We made dilution series (deluted 102,103,104,105,106,107 times) of liquid isoprene (Wako Pure Chemical Industries, Ltd, Japan) diluted in chloroform.  
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The undiluted isoprene solution 1[&micro;l] is 0.654[mg]. We injected diluted isoprene into GC-MS. We tried to draw a calibration curve (Fig.2).
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The undiluted isoprene solution 1[&micro;l] is 0.654[mg]. We injected diluted isoprene into GC-MS. We tried to draw a calibration curve (Fig.1).
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<h4><calibration curve></h4>
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<h4><calibration data></h4>
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<p>We firstly made dilution series (diluted 102,103,104,105,106,107 times) of liquid isoprene (Wako Pure Chemical Industries, Ltd, Japan) diluted in chloroform. The undiluted isoprene solution 1[µl] is 0.654[mg]. We injected diluted isoprene into GC-MS, and draw a calibration curve (Fig.2)</P><br />
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<p>We firstly made dilution series (diluted 102,103,104,105,106,107 times) of liquid isoprene (Wako Pure Chemical Industries, Ltd, Japan) diluted in chloroform. The undiluted isoprene solution 1[µl] is 0.654[mg]. We injected diluted isoprene into GC-MS, and draw a calibration curve (Fig.1)</P><br />
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<img alt="Fig.2 - Calibration Data" /><br />
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<img alt="Fig.1 - Calibration Data" /><br />
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Fig.2 Dilution series of liquid isoprene diluted in chloroform were injected into GC-MS.  
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Fig.1 Dilution series of liquid isoprene diluted in chloroform were injected into GC-MS.  
Let area be the vertical axis, and amount of isoprene itself ([mg]) the horizontal axis.
Let area be the vertical axis, and amount of isoprene itself ([mg]) the horizontal axis.
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Revision as of 10:26, 4 October 2011

Tokyo Tech 2011

Rain details

Method

In order to assay the amount of isoprene produced by our E.coli, we use the Gas chromatography-mass spectrometry (GC-MS, QP-2010, SHIMADZU, Japan) for measurement. The MS uses an electron ionization method and quadrupole. Analytes were separated using a nonpolar column (Rtx-1MS: Length 30m, ID 0.25mm film thickness 0.5µm, USA) working in a constant flow mode (2.99ml min-1). The temperature program was chosen as follows: 40℃ for 7 min, increase to 280℃ at rate of 10℃ min-1, 280℃ for 5 min. The mass spectrometer worked in SIM mode, m/z 67. The retention time of isoprene is very short (about 1.06-1.10 min). But thanks to MS, isoprene could be identified.


<Quantitative Analysis>

Method

We made dilution series (deluted 102,103,104,105,106,107 times) of liquid isoprene (Wako Pure Chemical Industries, Ltd, Japan) diluted in chloroform. The undiluted isoprene solution 1[µl] is 0.654[mg]. We injected diluted isoprene into GC-MS. We tried to draw a calibration curve (Fig.1).

We firstly made dilution series (diluted 102,103,104,105,106,107 times) of liquid isoprene (Wako Pure Chemical Industries, Ltd, Japan) diluted in chloroform. The undiluted isoprene solution 1[µl] is 0.654[mg]. We injected diluted isoprene into GC-MS, and draw a calibration curve (Fig.1)


Fig.1 - Calibration Data
Fig.1 Dilution series of liquid isoprene diluted in chloroform were injected into GC-MS. Let area be the vertical axis, and amount of isoprene itself ([mg]) the horizontal axis.
Table.1 various experiments: We sampled headspace gas of solvent including isoprene or LB media with E.coli or none.
number container solvent isoprene[mg] sampling[ml] Condition from dripping isoprene to sampling
1 15ml centrifuge tube None 6.54 15 room temperature, 20minutes
2 500ml flask Water 100ml 13.1 50 room temperature, 20minutes
3 500ml flask Water 100ml 13.1 50 37℃, 20minutes
4 500ml flask LB medium 100ml 13.1 50 37℃, 20minutes
5 500ml flask LB medium 100ml 0 50 37℃, culture, 6hours
6 500ml flask LB medium 100ml 0 50 37℃, 6hours + E.coli(LT-21)

Table.1 Different conditions that used in samples` headspace gas of solvent including isoprene or LB media with E.coli or none. The condition is from dripping to sampling.


<Assay Isoprene from E.coli>

Method

E. coli BL21 (DE3) with positive control pSB3K-placIQ-ispS constructed, and other with negative control pSB3K-placIQ were grown in separate 500 ml flasks containing 100ml LB media. Cultures were grown at 37℃ and then induced using 0.5mM IPTG when OD600 of 0.6 was reached. After 5 hours of induction, 50ml of headspace gas samples were taken using absorbing material (mini-PAT including Tenax: Japan Analytical Industry Co., Ltd) and injected into GC-MS.