Team:NUS Singapore-A/InterLab
Interlab Study
Objectives
Main Objective of iGEM InterLab Study
Synthetic biology, also called engineering biology, differentiates itself from the field of biology in general through its ability to repeat and reproduce measurements and results. This reproducibility is apparent across all other engineering disciplines as well, and aids researchers in making effective comparisons for interpreting experimental controls and debugging engineered biological constructs. Through Interlab Study, iGEM’s Measurement Committee aims to achieve such reproducibility for the green fluorescent protein (GFP) in particular by developing a robust and detailed measurement protocol that anyone can follow.
The Fifth International InterLab Study Measurement
In Interlab 2018, iGEM aims to examine if it is possible to reduce lab-to-lab variability in fluorescence measurements by normalizing to absolute cell count or colony-forming units (CFUs) instead of OD. For this, we were required to measure the cell density of Escherichia coli DH5⍺ cells using two methods: by converting between absorbance of cells to the absorbance of a known concentration of beads, and by counting colony-forming units (CFUs) from the sample.
Overview
Converting between absorbance of cells to the absorbance of a known concentration of beads.
In the first method, silica beads modelled after (roughly the same shape and size of) a typical E. coli cell are used to estimate the actual amount of E. coli cells during the fluorescence measurement of the cells. In this method, silica beads were made to model a typical E. coli cell’s light scattering. As a sample of these silica beads gives a consistent and known absorbance measurement at 600 nm, absorbance measurements from a sample’s cell density can be converted into an “equivalent concentration of beads” measurement that should be more universal and comparable between different labs.
Counting colony-forming units (CFUs) from the sample.
Another way of approximating cell concentration in a sample of bacterial culture is by plating a known volume of the sample and letting colonies grow. As each bacterial colony is assumed to represent a single cell (for cells that do not stick together), the cell concentration in the sample is then directly proportional to the number of CFUs. Using a scaling factor computed from negative and positive control CFUs, the absorbance measurements can be converted to CFU.
Parts Received
| Device | Part Number | Usage |
|---|---|---|
| Negative control | BBa_R0040 | TetR repressible promoter, medium strength promoter |
| Positive Control | BBa_I20270 | Promoter MeasKit (J23151) |
| Test Device 1 | BBa_J364000 | GFP expressing constitutive device |
| Test Device 2 | BBa_J364001 | GFP expressing constitutive device |
| Test Device 3 | BBa_J364002 | GFP expressing constitutive device |
| Test Device 4 | BBa_J364007 | Expresses GFP under the control of a constitutive promoter |
| Test Device 5 | BBa_J364008 | Expresses GFP under the control of a constitutive promoter |
| Test Device 6 | BBa_J364009 | Expresses GFP under the control of a constitutive promoter |
Materials & Methods
|
Plate Reader
BioTek Synergy H1 Abs 600
|
Florescence
|
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InterLab
Bronze Medal Criterion #4
Standard Tracks: Participate in the Interlab Measurement Study and/or obtain new, high quality experimental characterization data for an existing BioBrick Part or Device and enter this information on that part's Main Page in the Registry. The part that you are characterizing must NOT be from a 2018 part number range.
For teams participating in the InterLab study, all work must be shown on this page.