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. 2017 Jan 17;83(3):e02952-16. doi: 10.1128/AEM.02952-16

TABLE 1.

Decay kinetics of flash-induced variable fluorescence in Synechocystisa

Time (h) Fast-phase T1 (μs)/A1 (%) Middle-phase T2 (ms)/A2 (%) Slow-phase T3 (s)/A3 (%) A0 (%)
Without DCMU
    0 128 ± 29/36.3 ± 2.8 1.3 ± 0.5/38.8 ± 0.3 0.06 ± 0.04/17.7 ± 5.8 7.2 ± 2.7
    0.5 206 ± 11/38.0 ± 1.3 3.2 ± 0.1/37.6 ± 0.5 0.60 ± 0.11/16.1 ± 0.5 8.4 ± 0.3
    1.5 242 ± 5/39.4 ± 2.6 3.3 ± 0.1/37.8 ± 0.4 1.82 ± 0.33/15.7 ± 2.3 7.1 ± 0.9
    3 226 ± 4/39.1 ± 1.9 2.8 ± 0.2/38.8 ± 0.4 1.71 ± 0.48/15.8 ± 1.8 6.3 ± 0.7
    6 198 ± 14/39.2 ± 0.2 2.6 ± 0.1/38.2 ± 0.4 0.99 ± 0.33/14.7 ± 0.6 7.9 ± 0.4
    12 136 ± 9/37.8 ± 0.3 3.9 ± 0.3/37.3 ± 0.2 0.50 ± 0.30/15.8 ± 0.8 9.5 ± 1.0
With DCMU
    0 0.96 ± 0.02/92.0 ± 1.2 8.0 ± 1.2
    0.5 0.96 ± 0.00/91.7 ± 1.0 8.3 ± 0.6
    1.5 1.06 ± 0.02/91.6 ± 1.1 8.4 ± 1.1
    3 1.01 ± 0.03/91.1 ± 0.5 8.9 ± 0.5
    6 1.05 ± 0.11/88.9 ± 1.9 11.1 ± 1.9
    12 1.15 ± 0.24/86.9 ± 2.6 13.1 ± 2.6
a

Synechocystis cells were treated with 70.4 mM (4×) NO2 for the indicated periods of time, and relaxation of the flash-induced fluorescence yield with or without 20 μM DCMU was measured. The curves were analyzed in terms of three exponential components (fast, middle, and slow phases).