Daviso Eugenio, Diller Anna, Gast Peter, Alia A, Lugtenburg Johan, Müller Marc G, Matysik Jörg
Appl Magn Reson. 2010 Mar;38(1):105-116. doi: 10.1007/s00723-009-0103-6. Epub 2009 Dec 3.
Photochemically induced dynamic nuclear polarization magic-angle spinning nuclear magnetic resonance (photo-CIDNP MAS NMR) allows for the investigation of the electronic structure of the photochemical machinery of photosynthetic reaction centers (RCs) at atomic resolution. For such experiments, either continuous radiation from white xenon lamps or green laser pulses are applied to optically dense samples. In order to explore their optical properties, optically thick samples of isolated and quinone-removed RCs of the purple bacteria of Rhodobacter sphaeroides wild type are studied by nanosecond laser-flash (13)C photo-CIDNP MAS NMR using excitation wavelengths between 720 and 940 nm. Action spectra of both the transient nuclear polarization as well as the nuclear hyperpolarization, remaining in the electronic ground state at the end of the photocycle, are obtained. It is shown that the signal intensity is limited by the amount of accessible RCs and that the different mechanisms of the photo-CIDNP production rely on the same photophysical origin, which is the photocycle induced by one single photon.
光化学诱导动态核极化魔角旋转核磁共振(photo-CIDNP MAS NMR)能够在原子分辨率下研究光合反应中心(RCs)光化学机制的电子结构。对于此类实验,可将来自白色氙灯的连续辐射或绿色激光脉冲应用于光学致密样品。为了探究其光学性质,利用720至940纳米之间的激发波长,通过纳秒激光闪光(13)C photo-CIDNP MAS NMR对球形红细菌野生型紫色细菌的分离且去除醌的RCs的光学厚样品进行了研究。获得了瞬态核极化以及在光循环结束时保留在电子基态的核超极化的作用光谱。结果表明,信号强度受可及RCs数量的限制,并且photo-CIDNP产生的不同机制依赖于相同的光物理起源,即由单个光子诱导的光循环。