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Light induced EPR spectra of reaction centers from Rhodobacter sphaeroides at 80K: Evidence for reduction of QB by B-branch electron transfer in native reaction centers.

机译:球形红球菌在80K时反应中心的光诱导EPR光谱:在自然反应中心中通过B分支电子转移降低QB的证据。

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摘要

Photosynthetic reaction centers (RCs) from Rhodobacter sphaeroides capture solar energy by electron transfer from primary donor, D, to quinone acceptor, QB, through the active A-branch of electron acceptors, but not the inactive B-branch. The light induced EPR spectrum from native RCs that had Fe2+ replaced by Zn2+ was investigated at cryogenic temperature (80K, 35 GHz). In addition to the light induced signal due to formation of D+•QA−• observed previously, a small fraction (~5%) of the signal displayed very different characteristics: (1) The signal was absent in RCs in which the QB was displaced by the inhibitor stigmatellin. (2) Its decay time (τ=6 s) was the same as observed for D+•QB−• in mutant RCs lacking QA, which is significantly slower than for D+•QA−• (τ=30 ms). (3) Its EPR spectrum was identical to that of D+•QB−•. (4) The quantum efficiency for forming the major component of the signal was the same as that found for mutant RCs lacking QA (Φ =0.2%) and was temperature independent. These results are explained by direct photochemical reduction of QB via B-branch electron transfer in a small fraction of native RCs.
机译:球形红球菌的光合作用反应中心(RCs)通过电子受体的活性A分支从初级供体D传递至醌受体QB的电子转移,捕获了太阳能,而惰性B分支则没有。在低温(80K,35 GHz)下,研究了用Zn 2 + 代替Fe 2 + 的天然RC的光诱导EPR光谱。除了先前观察到的由于形成D +• QA -•引起的光感应信号外,一小部分信号(约5%)显示出非常不同的特性: (1)在RCB中,信号被抑制剂stigmatellin取代了,因此没有信号。 (2)在没有QA的突变RC中,其衰减时间(τ= 6 s)与D +• QB -•所观察到的时间相同,这明显慢于D +• QA −•(τ= 30毫秒)。 (3)其EPR谱与D +• QB -•相同。 (4)形成信号主要成分的量子效率与缺少QA(Φ= 0.2%)的突变RC的量子效率相同,并且与温度无关。这些结果可以通过在少量天然RC中通过B分支电子转移对QB进行直接光化学还原来解释。

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