Table 1.
In vitro spectral properties of biliprotein photosensors in this study1
Photoreceptor | Affinity Tag | FDBR | SAR | 15Z λmax | 15E λmax |
---|---|---|---|---|---|
NpR5113g22 | intein-CBD | PcyA | 1.2 | 650 | 528 |
NpR5113g2 | intein-CBD | AtHY2 | 0.4 | 664 | 542 |
NpR5113g2 | poly-His | KflaHY2 | 0.5 | 650 | 530 |
NpR5113g33 | poly-His | PcyA | 0.3 | 422 | 496 |
NpR5113g23 | poly-His | PcyA | 0.4 | 650, 422 | 528, 496 |
NpR5113g23 | poly-His | KflaHY2 | 0.2 | 650, 424 | 528, 496 |
Cph1 | poly-His | PcyA | 0.2 | 660 | 704 |
Cph1 | poly-His | KflaHY2 | 0.1 | 666 | 714 |
MvirPHY1 | intein-CBD | PcyA | 0.9 | 646 | 718 |
MvirPHY1 | poly-His | KflaHY2 | 0.1 | 646 | 716 |
For NpR5113g23, values for domain 2 are reported first and values for domain 3 are derived from the photochemical difference spectrum after subtraction of signals from domain 2 (Fig. 5). Specific absorbance ratio (SAR) was calculated as the ratio of the peak absorbance of the longest-wavelength chromophore band for the 15Z photostate to the peak absorbance of the aromatic amino acid band at 280 nm. NpR5113g2 was expressed in the presence of KflaHY2 and KflaHY1, whereas other KflaHY2 expressions used KflaHY2 and cyanobacterial heme oxygenase. 2Values from Rockwell et al. (2012c). 3Values from Rockwell et al. (2012a).