Team:BCCS-Bristol/Wetlab/signal soil

From 2010.igem.org

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=Signal Visibility in Soil=
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==Motivation==
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=Signal Visibility in Soil=
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{{:Team:BCCS-Bristol/newtoc}}
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==Motivation==
 
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For this project to work it was essential that a signal could actually be detected when in soil. To test this we mixed ''E. coli'' constitutively expressing GFP in soil and imaged and photographed them under a stereo-microscope, mimicking the CCD-based method we envision farmers using to detect fluorescence were this project to be used commercially.
For this project to work it was essential that a signal could actually be detected when in soil. To test this we mixed ''E. coli'' constitutively expressing GFP in soil and imaged and photographed them under a stereo-microscope, mimicking the CCD-based method we envision farmers using to detect fluorescence were this project to be used commercially.
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==Experiment==
==Experiment==
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The soil cultures were left overnight at 37°C.
The soil cultures were left overnight at 37°C.
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Soil samples viewed under fluorescence microscope. Controls used were as follows:
Soil samples viewed under fluorescence microscope. Controls used were as follows:
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==Results and Conclusion==
==Results and Conclusion==
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All test soil samples showed growth of ''E.coli'' expressing GFP. As might have been expected, a significant increase in growth was observed in the sterile samples when compared to the non-sterile samples at similar dilutions of bacteria/g soil, suggesting our lab-safe MG1655s had been out-competed by more robust wild-type bacteria strains.
All test soil samples showed growth of ''E.coli'' expressing GFP. As might have been expected, a significant increase in growth was observed in the sterile samples when compared to the non-sterile samples at similar dilutions of bacteria/g soil, suggesting our lab-safe MG1655s had been out-competed by more robust wild-type bacteria strains.
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Click [https://2010.igem.org/Team:BCCS-Bristol/Wetlab/Lab_photos/First_GFP_Experiment here] for some example images from the test.
Click [https://2010.igem.org/Team:BCCS-Bristol/Wetlab/Lab_photos/First_GFP_Experiment here] for some example images from the test.
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It quickly became clear that using 'E. coli' spread freely in the soil was not going to yield a strong enough signal to detect from relatively low tech equipment attached to the back of a tractor. It was because of this that we invented the bead method of spreading our bacteria.
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It quickly became clear that using <i>E. coli</i> spread freely in the soil was not going to yield a strong enough signal to detect from relatively low tech equipment attached to the back of a tractor. It was because of this that we invented the bead method of spreading our bacteria.

Latest revision as of 19:09, 27 October 2010

Signal Visibility in Soil

Motivation

Contents

For this project to work it was essential that a signal could actually be detected when in soil. To test this we mixed E. coli constitutively expressing GFP in soil and imaged and photographed them under a stereo-microscope, mimicking the CCD-based method we envision farmers using to detect fluorescence were this project to be used commercially.



Experiment

Sample soil taken from local source (team member's garden). 6 x ~15g aliquots of soil were placed in 50mL centrifuge tubes, taking care to avoid including wildlife. 3 of the tubes were then sterilised using an autoclave. Meanwhile, a 1 in 10 dilution of the overnight culture of MG1655 cells + [http://partsregistry.org/Part:BBa_I13522 BBa_I13522] was found to have an A600 value of ~0.5, roughly translating as 2.5x109 cells/mL in the original culture. The following table lists the rough figures for the 6 soil experiments set up. The lines notated with "S" were for the sterilised tubes, the lines notated with "N" were for the non-sterilised tubes:

S1 ~107 cells/g soil 100μL cell culture plus 900μL LB added to soil
S2 ~106 cells/g soil 100μL 1/10 dilution of cell culture plus 900μL LB added to soil
S3 ~105 cells/g soil 100μL 1/100 dilution of cell culture plus 900μL LB added to soil
N1 ~107 cells/g soil 100μL cell culture plus 900μL LB added to soil
N2 ~106 cells/g soil 100μL 1/10 dilution of cell culture plus 900μL LB added to soil
N3 ~105 cells/g soil 100μL 1/100 dilution of cell culture plus 900μL LB added to soil

The soil cultures were left overnight at 37°C.

Soil samples viewed under fluorescence microscope. Controls used were as follows:

A 200μL aliquot of pure water
A 200μL aliquot of cell culture expressing GFP
A sample of the unsterilised soil
A sample of the unsterilised soil with a 200μL aliquot of cell culture applied 10 minutes before visualisation


Results and Conclusion

All test soil samples showed growth of E.coli expressing GFP. As might have been expected, a significant increase in growth was observed in the sterile samples when compared to the non-sterile samples at similar dilutions of bacteria/g soil, suggesting our lab-safe MG1655s had been out-competed by more robust wild-type bacteria strains.

Click here for some example images from the test.

It quickly became clear that using E. coli spread freely in the soil was not going to yield a strong enough signal to detect from relatively low tech equipment attached to the back of a tractor. It was because of this that we invented the bead method of spreading our bacteria.