Team:UNITN-Trento/Project/Ethylene
From 2013.igem.org
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+ | E. coli - Blue light circuit | ||
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+ | <img src="https://static.igem.org/mediawiki/2013/5/59/BluelightEFE.jpg" alt="e.coli_bluelight-EFE_parts"/> | ||
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+ | After having characterized Ethylene production using BBa_K1065001, we tried to put EFE under the control of a photoinducible circuit and we then tested his behaviour. We assembled the photoinducible circuit exploiting many subparts from different teams (Uppsala2011 and Berkeley 2006). The construct includes an inverter that allows ethylene production only in presence of light. | ||
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+ | <h2> | ||
+ | Photoinduced ethylene production - kinetic assay | ||
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+ | We performed a kinetic assay in order to analyze ethylene production over time using (BBa_K1065XXX). The sample was then exposed to a blue light led (470 nm) while it was connected to the micro GC (see the protocol page for the adopted method). | ||
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+ | <img src="" alt="EFE-blue_light_plot" /> | ||
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<h2>B. subtilis</h2> | <h2>B. subtilis</h2> | ||
<img src="https://static.igem.org/mediawiki/2013/8/85/Tn-2013-project_ethylene-BBa_K1065001.jpg"/> | <img src="https://static.igem.org/mediawiki/2013/8/85/Tn-2013-project_ethylene-BBa_K1065001.jpg"/> |
Revision as of 12:37, 17 September 2013
Results - Ethylene
EFE (Ethylene Forming Enzyme - 2-Oxoglutarate Oxygenase/Decarboxylase) is our keyplayer in triggering fruit ripening. It catalyzes ethylene synthesis from 2-Oxoglutarate, a TCA cycle intemediate molecule. We characterized this gene in two chassis: E. coli and B. subtilis, using different contstructs that we designed.
E. coli
In E. coli, EFE-catalyzed ethylene production was characterized using BBa_K1065001, which is a composed part with EFE under the control of an AraC-pBAD promoter.
1. Toxicity test
A toxicity test was performed inducing EFE expression with 5 mM arabinose. The growth curve was then compared to a not-induced sample.
As expected, induced samples showed a decreased growth rate.
2. Ethylene detection
Then, ethylene was detected using a Micro Gas Chromatograph (see the protocol page for the adopted methodology). The instrument was calibrated using two different air mixtures with well-defined quantities of each molecule (carbon dioxide, oxygen and ethylene).
The chromatogram clearly shows the presence of a peak corresponding to ethylene; the peak integral was converted to ppm.
Sample | Ethylene detected |
---|---|
Not induced | 0 ± 15 ppm |
Induced V = 1.5 ml | 61 ± 15 ppm |
Induced V = 3 ml | 101 ± 15 ppm |
3. Kinetic assay for ethylene production
We performed a kinetic assay in order to analyze ethylene production over time (see the protocol page for the adopted method).
Figure 3 shows how inducing the culture at O.D.600 equal to 0.8 a.u. caused a 2-fold increase in ethylene production.
E. coli - Blue light circuit
After having characterized Ethylene production using BBa_K1065001, we tried to put EFE under the control of a photoinducible circuit and we then tested his behaviour. We assembled the photoinducible circuit exploiting many subparts from different teams (Uppsala2011 and Berkeley 2006). The construct includes an inverter that allows ethylene production only in presence of light.
Photoinduced ethylene production - kinetic assay
We performed a kinetic assay in order to analyze ethylene production over time using (BBa_K1065XXX). The sample was then exposed to a blue light led (470 nm) while it was connected to the micro GC (see the protocol page for the adopted method).