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. 2011 May;55(5):2446–2450. doi: 10.1128/AAC.00808-10

Table 3.

LUV-lacticin Q interaction evaluated by blue shift of tryptophan fluorescencea

Condition Mean ± SD of fluorescence peak of lacticin Q (nm) at indicated time point (min)
1 3 10
Buffer 342.3 ± 0.3 342.9 ± 0.3 342.9 ± 0.5
PC-PG 335.7 ± 0.3 336.1 ± 0.3 336.0 ± 0.2
PE-PG-LPS 337.4 ± 1.2 336.3 ± 0.7 336.2 ± 0.4
a

Lacticin Q and LUVs were mixed in buffer A (as described in the legend to Fig. 3) at 30°C. Excitation and emission wavelengths were set at 290 and 300 to 400 nm, respectively. The fluorescence spectrum of the LUVs was subtracted from that of the LUV-lacticin Q mixture.