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. 1999 Jul;181(13):3994–4003. doi: 10.1128/jb.181.13.3994-4003.1999

TABLE 4.

Characteristics of variable fluorescence (QA reduction and QA reoxidation) of PS I-less strains measured in darkness in the presence of KCNa

Genotype of strain A (KCN) (AU) A (increase) (AU) t1/2 (increase) (s) Fmax (AU) t1/2 (decay) (s)
Parent 0.39 ± 0.17 0.29 ± 0.12 35.3 ± 7.0 4.2 ± 1.0 2.5 ± 0.5
ΔndbA 0.44 ± 0.23 0.36 ± 0.20 44.3 ± 17.3 4.3 ± 1.0 2.3 ± 0.3
ΔndbB 0.38 ± 0.16 0.39 ± 0.17 44.8 ± 18.3 3.9 ± 0.7 1.8 ± 0.4
ΔndbC 0.30 ± 0.16 0.27 ± 0.06 33.7 ± 4.9 4.0 ± 1.1 2.1 ± 0.3
ΔndbA ΔndbB 0.29 ± 0.23 0.40 ± 0.28 41.4 ± 26.0 3.6 ± 1.0 1.4 ± 0.2
ΔndbA ΔndbC 0.28 ± 0.13 0.28 ± 0.23 39.8 ± 24.6 3.7 ± 1.2 1.8 ± 0.4
ΔndbB ΔndbC 0.20 ± 0.10 0.27 ± 0.12 41.6 ± 17.9 3.6 ± 1.1 1.7 ± 0.4
ΔndbA ΔndbB ΔndbC 0.31 ± 0.17 0.42 ± 0.37 42.0 ± 26.3 3.7 ± 1.2 1.7 ± 0.3
a

Values given are averages ± standard deviations from at least four determinations. Chlorophyll fluorescence of whole cells was measured in 10 mM HEPES–NaOH (pH 7.4) in the presence of 5 mM KCN. The amplitude of the immediate increase upon addition of KCN [A (KCN)], the amplitude and kinetics (t1/2) of the subsequent noninstantaneous and nonlinear increase in variable fluorescence [A (increase) and t1/2 (increase), respectively], the Fmax upon illumination with actinic light, and the t1/2 of decay after actinic illumination [t1/2 (decay)] are indicated. See Fig. 4 for an example of the experimental data from which these values were determined. AU, arbitrary units.