Symons M, Swysen C, Sybesma C
Biochim Biophys Acta. 1977 Dec 23;462(3):706-17. doi: 10.1016/0005-2728(77)90112-8.
An analysis has been made of the spectrum of the carotenoid absorption band shift generated by continuous illumination of chromatophores of the GlC-mutant of Rhodopseudomonas sphaeroides at room temperature by means of three computer programs. There appears to be at least two pools of the same carotenoid, only one of which, comprising about 20% of the total carotenoid content, is responsible for the light-induced absorbance changes. The 'remaining' pool absorbs at wavelengths which were about 5 nm lower than those at which the 'changing' pool absorbs. This difference in absorption wavelength could indicate that the two pools are influenced differently by permanent local electric fields. The electrochromic origin of the absorbance changes has been demonstrated directly; the isosbestic points of the absorption difference spectrum move to shorter wavelengths upon lowering of the light-induced electric field. Band shifts up to 1.7 nm were observed. A comparison of the light-induced absorbance changes with a KCl-valinomycin-induced diffusion potential has been used to calibrate the electrochromic shifts. The calibration value appeared to be 137 +/- 6 mV per nm shift.
借助三个计算机程序,对室温下球形红假单胞菌GlC突变体的色素细胞连续光照产生的类胡萝卜素吸收带位移光谱进行了分析。似乎至少有两个相同类胡萝卜素池,其中只有一个(约占类胡萝卜素总量的20%)负责光诱导的吸光度变化。“其余”的池在比“变化”池吸收波长约低5nm的波长处吸收。吸收波长的这种差异可能表明这两个池受到永久局部电场的影响不同。吸光度变化的电致变色起源已得到直接证明;降低光诱导电场时,吸收差光谱的等吸收点移向更短波长。观察到高达1.7nm的带位移。将光诱导的吸光度变化与KCl-缬氨霉素诱导的扩散电位进行比较,以校准电致变色位移。校准值似乎为每纳米位移137±6mV。