Experiment Rationale

To investigate the behaviour of the lamda-cI thermoinducible promoter and show that when temperature is low (at 28 degrees Celsius), there is low fluorescence output. This shows that the genome deletion module is repressed. When temperature is raised to 42 degrees Celsius, fluorescence increases, indicating that the repression is lifted. We are looking at both absorbance and fluorescence data. This analysis serves to characterize the construct [http://partsregistry.org/wiki/index.php/Part:BBa_K200022 BBa_K200022], submitted by Harvard last year.

Summary of method

In order to characterize the thermoinducible promoter, absorbance (optical density) and fluoresence data were recorded over time for:

• Cells containing the BBa_K200022 construct: The thermoinducible promoter.
• Positive control cells: Containing the [http://partsregistry.org/Part:BBa_I13522 BBa_I13522], acting as a baseline comparison by constitutively expressing GFP.
• Negative control cells: These contain the thermoinducible promoter on its own ( [http://partsregistry.org/Part:BBa_K098995 BBa_K098995]) with no GFP attached to it.

Absorbance data

Understanding of the fluorescence data requires normalization with cell growth data, in the form of optical density (absorbance).

28 degrees Celsius

Figure 1: Absorbance at 28 degrees Celsius

42 degrees Celsius

Figure 2: Absorbance at 42 degrees Celsius
Plotting raw absorbance data on its own does not provide sufficient information about the effects of temperature on our system. Therefore, further analysis is required. This includes recording the variation in absorbance of the blank well (containing only the M9 medium) and normalizing absorbance data against the latter to spot ay possible trends in growth rate variations at different temperatures.

Variation in absorbance of the blank

Calculation of growth rate of the population for varying blank levels

Conclusion