The InterLab study is organized by a measurement committee of iGEM to establish better measurement techniques in the synthetic biology field. We submit our measurement results that cope with the absorbance and fluorescence related with E. coli transformed with a variety of test devices. We checked 8 plasmids, containing 2 controls and 6 test devices, and measurements were made in a plate reader with a 96 well microplate. We measured the absorbance and fluorescence of our samples using a Perkin Elmer 1420 multilabel counter.

Calibration 1: OD ₆₀₀ Reference Point - LUDOX Protocol

We used LUDOX CL-X as a single point reference to obtain a conversion factor to transform absorbance (Abs ₆₀₀) data from plate reader into acomparable OD ₆₀₀ measurement as would be obtained in a spectrophotometer.

Figure 1. Measurement of Abs ₆₀₀ and OD ₆₀₀ for LUDOX CL-X and water

Calibration 2: Particle Standard Curve - Microsphere Protocol

We prepared a dilution series of silica microspheres and measured the Abs ₆₀₀ in a plate reader. These microspheres are similar to cells in physical size and optical characteristics. This measurement was used to obtain a standardcurve of particle concentration, enabling to convert Abs ₆₀₀ measurements to an estimated number of cells.

Figure 2. Calculated particle counts from measured Abs ₆₀₀ and generation of a particle standard curve

Calibration 3: Fluorescence Standard Curve - Fluorescein Protocol

We prepared a dilution series of fluorescein in four replicates and measured the fluorescence in a 96 well plate in a plate reader. Measuring these in the plate readerenabled us togenerate astandard curve of fluorescence for fluorescein concentration.

Figure 3. Correspondence between fluorescence and fluorescein concentration

Cell Measurement

We had two plates to read at the end of procedure and one plate for each time point: 0 and 6 hours. On each plate, we read both fluorescence and absorbance. We used the generated particle standard and fluorescent curves to determine fluorescence per OD and fluorescence per particle values.

Figure 4. Measurement of raw Abs ₆₀₀ and OD ₆₀₀

Figure 5. Measurement of fluorescence per OD

Figure 6. Measurement of fluorescence per particle

Figure 7. The number of colonies and CFU/mL value in a starting sample of OD ₆₀₀ = 0.1

Colony Forming Units per 0.1 OD ₆₀₀ E. coli cultures

For the CFU protocol, we calculated colonies for our two Positive Control (BBa_I20270) cultures and our two negative Control (BBa_R0040) cultures. Our overnight cultures were diluted to yield a 0.1 OD ₆₀₀ using calculations described in iGEM 2018 InterLab Study Protocol. After a serial dilution for each overnight culture, we plated the 8*10^-3, 8*10^-4, and 8*10^-5 dilutions on LB agar with triplication. With the assumption that one bacterial cell leads to one colony, we enumerated the number of colonies on each plate and multiplied the colony count by the final dilution factor to assess a CFU/mL value for a starting sample of OD ₆₀₀.

Figure 8. Plated DH5α cells of serial dilutions for starting samples