As proof of concept, we quantified the amount of β-carotene produced by our crtEBIY BioBrick [http://parts.igem.org/Part:BBa_K2151200 K2151200] construct with different promoters. We did this by acetone extraction, followed by measuring the absorbance, shown in Figure 1A of this extraction fragment. The absorbance was measured at 454 nm because that is the peak of the β-carotene absorbance spectrum (Figure 1B).
Figure 1. β-carotene quantification in gene constructs. A: β-carotene levels were quantified after acetone extraction by measuring the absorbance and 454 nm using a spectrophotometer. The bars represent an average of the three extraction replicates of each of the gene constructs. The error bars represent the standard deviation. B: After extraction, an absorbance spectrum (334 - 550 nm) of the acetone fragment was measured using a spectrophotometer. Points on the figure, joined by a line, represent a reading from the spectrophotometer (Y-axis) at the appropriate wavelength (X-axis). The arrow indicates the peak specific to β-carotene [1]
This experiment confirmed the production of β-carotene, as the empty cells have a lower absorbance than the cells with the construct. The absorbance spectrum confirmed that K2151200 produced β-carotene, as the absorbance spectrum is highly similar to the established absorbance spectrum [1].
The levels of β-carotene produced from our crtEBIY construct were assumed to contain the promoter sequences we thought they did. After sequencing them, we found out that unfortunately they did not actually possess them. To increase the quantity of β-carotene made in the future, a promoter could be utilised.
