首页> 外文期刊>The journal of physical chemistry, A. Molecules, spectroscopy, kinetics, environment, & general theory >Femtosecond Spectroscopy of the primary charge separation in reaction centers of chloroflexus aurantiacus with selective excitation in the Q(Y) and soret bands
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Femtosecond Spectroscopy of the primary charge separation in reaction centers of chloroflexus aurantiacus with selective excitation in the Q(Y) and soret bands

机译:飞秒光谱法分析桔小叶绿藻反应中心中的初级电荷,并在Q(Y)和soret带中进行选择性激发

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摘要

The primary charge separation and electron-transfer processes of photosynthesis occur in the reaction center (RC). Isolated RCs of the green filamentous anoxygenic phototrophic bacterium Chloroflexus aurantiacus were studied at room temperature by using femtosecond transient absorption spectroscopy with selective excitation. Upon excitation in the Q(Y) absorbance band of the bacteriochlorophyll (BChl) dimer (P) at 865 nm, a 7.0 +/- 0.5 ps kinetic component was observed in the 538 nm region Q(X) band of the bacteriopheophytin (BPheo)), 750 nm region Q(Y) band of the BPheo), and 920 nm region (stimulated emission of the excited-state of P), indicating that this lifetime represents electron transfer from P to BPheo. The same time constant was also observed upon 740 nm or 800 nm excitation. A longer lifetime (300 +/- 30 ps), which was assigned to the time of reduction of the primary quinone, Q(A), was also observed. The transient absorption spectra and kinetics all indicate that only one electron-transfer branch is involved in primary charge separation under these excitation conditions. However, the transient absorption changes upon excitation in the Soret band at 390 nm reveal a more complex set of energy and electron-transfer processes. By comparison to studies on the RCs of the purple bacterium Rhodobacter sphaeroides, we discuss the possible mechanism of electron-transfer pathway dependence on excitation energy and propose a model of the Cf. aurantiacus RC that better explains the observed results.
机译:光合作用的一次电荷分离和电子转移过程发生在反应中心(RC)中。通过使用选择性激发的飞秒瞬态吸收光谱,在室温下研究了绿色丝状产氧光养细菌Chloroflexus aurantiacus的分离的RC。在865 nm处的细菌叶绿素(BChl)二聚体(P)的Q(Y)吸收带中激发后,在细菌脱镁叶绿素(BPheo)的538 nm区域Q(X)带中观察到7.0 +/- 0.5 ps的动力学成分),BPheo的750 nm区域Q(Y)带和920 nm区域(P激发态的受激发射),表明该寿命表示电子从P转移到BPheo。在740 nm或800 nm激发下也观察到相同的时间常数。还观察到更长的寿命(300 +/- 30 ps),这归因于伯醌Q(A)的还原时间。瞬态吸收光谱和动力学都表明在这些激发条件下一次电荷分离中仅涉及一个电子转移分支。但是,在390 nm的Soret谱带中激发后的瞬态吸收变化揭示了一组更复杂的能量和电子转移过程。通过与对紫色细菌球形红细菌的RC的研究进行比较,我们讨论了电子传输途径依赖于激发能的可能机理,并提出了Cf模型。 aurantiacus RC可以更好地解释观察到的结果。

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