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. Author manuscript; available in PMC: 2020 Mar 5.
Published in final edited form as: Mol Plant. 2020 Jan 14;13(3):398–413. doi: 10.1016/j.molp.2020.01.002

Table 1.

Kinetics parameters of CRY photooligomerization.

Parameters Experiment #1 Experiment #2 Sources
CRY2 30O50 (minute) 0.83 0.78 HEK 293
100O50 (minute) 0.14* 0.25* HEK 293
10F50 (μmolm−2s−1) 27.91* 28.9 HEK 293
22T½ (minute) 16.58* 18.62* HEK 293
37T½ (minute) 5.42 HEK 293
30O50 (minute) 0.17* 0.26 Arabidopsis
10F50 (μmolm−2s−1) 16.89 13.56 Arabidopsis
10T½ (minute) 8.42* Arabidopsis
22T½ (minute) 6.98* Arabidopsis
37T½ (minute) 5.46* Arabidopsis
CRY1 30O50 (minute) 1.47 1.70 Arabidopsis
100O50 (minute) 0.37* 0.38 Arabidopsis
60F50 (μmolm−2s−1) 14.90 16.21 Arabidopsis
22T½ (minute) 2.56 1.82 Arabidopsis

The table summarizes results of the experiments for the measurement of kinetics parameters of Arabidopsis CRY1 and CRY2 photooligomerization in HEK293 (Human Embryonic Kidney) cells or Arabidopsis seedlings. Symbols of parameters are the following: 30O50 or 100O50: time (minute) required to reach 50% saturation of CRY photooligomerization at the fluence rate of 30 or 100 μmolm−2s−1, respectively; 10F50 or 60F50: the fluence rate of blue light (μmolm−2s−1) required to achieve 50% CRY photooligomerization after light exposure for 10 or 60 seconds, respectively; 10T1/2, 22T1/2, or 37T1/2: time (minute) required to reach 50% saturation of CRY monomerization at the temperature of 10 °C, 22 °C, or 37 °C, respectively. Numbers with asterisk (*) indicates the measurements were means of three technical repeats, and numbers without asterisk indicates the measurements were derived from one technical repeat.