The interlab study is a new feature of iGEM this year. As part of the measurement track, we participated in the interlab study as described on the Interlab Study page. The purpose of this study was to measure the fluorescence of three different devices, two of which we constructed in lab from biobrick parts. The third device was simply recovered from the 2014 parts kit. Below we detail our interlab study experience and discuss what are findings mean.
Devices Measured
Figure 1. Liquid cultures of each construct
1. The first device is [http://parts.igem.org/Part:BBa_I20260 BBa_I20260], which is a composite biobrick part that contains:
A promoter, [http://parts.igem.org/Part:BBa_J23101 BBa_J23101], a downstream gene ([http://parts.igem.org/Part:BBa_E0240 BBa_E0240]), and a backbone ([http://parts.igem.org/Part:pSB1C3 pSB1C3]).
The downstream gene is also a composite of a number of biobrick parts, including an RBS - [http://parts.igem.org/Part:BBa_B0032 B0032], a GFP coding sequence - [http://parts.igem.org/Part:BBa_E0040 E0040], and a transcriptional terminator - [http://parts.igem.org/Part:BBa_B0015 B0015].
2. The second device was cloned in lab, as described in the interlab study procedure.
The device is composed of [http://parts.igem.org/Part:BBa_J23101 BBa_J23101] and [http://parts.igem.org/Part:BBa_E0240 BBa_E0240], which are the same parts as in the first device.
However, the backbone of this device is different, [http://parts.igem.org/Part:pSB3K3 pSB3K3].
3. The third device was also cloned in lab, as described in the interlab study procedure.
The device is composed of [http://parts.igem.org/Part:BBa_J23115 BBa_J23115] and [http://parts.igem.org/Part:BBa_E0240 BBa_E0240], which is the same downstream gene as in devices 1 and 2. However, the promoter sequence of device 3 is different.
This device is in [http://parts.igem.org/Part:pSB1C3 pSB1C3], the same backbone as the first device.
Protocols
Sample Preparation
First, inoculate triplicate 10 mL cultures of LB with frozen stocks of the three devices (in TOP10 cells; I20260, J23101+E0240, J23115+E0240), a cell background control (TOP10 cells), and an LB only control in a 50 mL Erlenmeyer flask. Grow for 16-18 hours at 37°C, shaking at 300rpm.
The next morning, add 10µL of each overnight culture to 10 mL of LB with three replicates of each (15 total flasks) and grow 16-18 hours at 37°C, shaking at 300rpm. Triplicate cultures were continued.
After 16-18 hours, add 80 µL of each culture to the wells of a clear-bottomed black 96-well plate.
Measurement Protocol
The fluorescence of each sample was measured using a 96-well plate as follows:
The 96-well plate was inserted into an Infinite 200 PRO Microplate Reader
Then, using the Tecan i-control the proper settings were selected and recorded.
Finally, the plate reader measured the fluorescence and the absorbance (OD600) for each well.
Sequencing Data
Add link to Sequencing data page with sequences for each. We have these, I believe.
http://parts.igem.org/Promoters/Catalog/Anderson
we sequenced our constructs, aligned them to the reference part sequences
construct 1 and 2 were consistent with the references
construct 3 was inconsistent, two point mutations--highly unlikely to be random mutations
we consulted the parts registry, sequence analysis of spring 2014 plate shows two point mutations consistent with our sequence reads
Figure 2. Fluorescence data for the three parts measured.
Data was collected using [blah plate reader and a 96 well plate blah] with ?50 ul of culture? per well [mention this briefly]. As can be seen in Figure xx, ... Make sure to mention the triplicate cultures, average values, etc...
Despite the similarities in the devices: all three contained the same coding sequence, two devices had the same backbone and two devices had the same promoter sequence, there were stark differences in the amount of fluorescence produced by the three devices...
"
