Difference between revisions of "Team:Peking/InterLab"

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             Escherichia coli strain DH5α
 
             Escherichia coli strain DH5α
 
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                 <li>1ml LUDOX</li>
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                 <li>1.5-ml Eppendorf tubes for sample storage, ice bucket with ice</li>
 
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             <br>
 
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             <h2 id = "p3">Methods</h2>
 
             <h2 id = "p3">Methods</h2>

Revision as of 07:28, 29 October 2017

Peking iGEM 2017

Interlab


The Peking iGEM 2017 team is participating in the Fourth InterLaboratory Measurement Study in synthetic biology, along with teams from around the world. We introduced eight plasmids into E. coli K-12 DH5-alpha and measured the GFP expression levels using a plate reader.

Introduction

Reliable and repeatable measurement is a key component of synthetic biology. However, there have been few opportunities to repeat the same measurements in different labs. In order to quantify the degree of variability exhibited by engineered genetic constructs across different laboratories, the measurement committee invited all iGEM teams to participate in the Interlab study, which provides researchers with a detailed protocol and data analysis form, with the aim to produce common, comparable units for measuring GFP on different plate readers.

Materials

Plasmids

  1. Positive Control (BBa_I20270): well 21B
  2. Negative Control (BBa_R0040): well 21D
  3. Test Device 1 (BBa_J364000): well 21F
  4. Test Device 2 (BBa_J364001): well 21H
  5. Test Device 3 (BBa_J364002): well 21J
  6. Test Device 4 (BBa_J364003): well 21L
  7. Test Device 5 (BBa_J364004): well 21N
  8. Test Device 6 (BBa_J364005): well 21P

Strains

Escherichia coli strain DH5α

Reagent

  • 1ml LUDOX
  • ddH2O
  • Fluorescein
  • 10ml 1xPBS

Instruments

  • Pipettes
  • 96-well plate
  • 50 ml Falcon tube (or equivalent, preferably amber or covered in foil to block light)
  • 1.5-ml Eppendorf tubes for sample storage, ice bucket with ice

Methods

At first, we used LUDOX-S40 as a single-point reference to obtain a ratiometric conversion factor to transform our absorbance readings into standard OD600 data. Simultaneously, the ratiometric conversion factor accounts for instrument differences.

Secondly, we generated a standard curve of fluorescence as a function of fluorescein concentration. We can thus use the standard curve to convert the fluorescence of GFP into a concentration of GFP.

Last and most importantly, we measured the A600 and fluorescence of green fluorescent protein. The GFP is used as a measurement marker of promoter activity, and the fluorescence/OD600 ratio is used to give an adjustment of the relative expression per cell. Furthermore, we tested some RBS devices that are intended to make gene expression more precise and reliable.

Results

Samples were prepared according to the standard protocol.The results for E. coli DH5α are shown in figures 4-8.





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