Department of Chemistry and Biochemistry, Arizona State University, 85287-1604, Tempe, AZ, USA.
Photosynth Res. 1996 Mar;47(3):207-18. doi: 10.1007/BF02184282.
The optical properties of a methyl ester homolog of bacteriochlorophylld (BChld M ) and bacteriochlorophyllc (BChlc) in H2O, hexanol-saturated H2O and methanol were studied by absorption, fluorescence emission, and circular dichroism (CD). In H2O, BChld M spontaneously forms an aggregate similar to that formed in hexane, with absorption maximum at 730 nm and fluorescence emission at 748 nm. For the pigment sample in hexanol-saturated H2O, while the absorption peaks at 661 nm, only slightly red-shifted compared to the monomer, the fluorescence emission is highly quenched. When diluted 2-3 fold with H2O, the absorption returns to around 720 nm, characteristic of an aggregate. The CD spectrum of the H2O aggregate exhibits a derivative-shaped feature with positive and negative peaks, while the amplitude is lower than that of chlorosomes. The Fourier transform infrared spectra of BChld M aggregates in H2O and hexane were measured. A 1644 cm(-1) band, indicative of a bonded 13(1)-keto group, is detected for both samples. A marker band for 5-coordinated Mg was observed at 1611 cm(-1) for the two samples as well. To study the kinetic behavior of the samples, both single-photon counting (SPC) fluorescence and transient absorption difference spectroscopic measurements were performed. For BChld M in hexanol-saturated H2O, a fast decay component with a lifetime of 10 to 14 ps was detected using the two different techniques. The fast decay could be explained by the concentration quenching phenomenon due to a high local pigment concentration. For the pigment sample in H2O, SPC gave a 16 ps component, whereas global analysis of transient absorption data generated two fast components: 3.5 and 26 ps. The difference may arise from the different excitation intensities. With a much higher excitation in the latter measurements, other quenching processes, e.g. annihilation, might be introduced, giving the 3.5 ps component. Finally, atomic force microscopy was used to examine the ultrastructure of BChld M in H2O and hexanol-saturated H2O. Pigment clusters with diameters ranging from 15 to 45 nm were observed in both samples.
研究了在 H2O、己醇饱和 H2O 和甲醇中细菌叶绿素 d(BChld M)和细菌叶绿素 c(BChlc)甲酯同系物的光学性质,通过吸收、荧光发射和圆二色性(CD)进行研究。在 H2O 中,BChld M 自发形成类似于在己烷中形成的聚集体,其吸收最大值为 730nm,荧光发射为 748nm。对于在己醇饱和 H2O 中的色素样品,尽管与单体相比,吸收峰仅略微红移至 661nm,但荧光发射被高度猝灭。当用水稀释 2-3 倍时,吸收回到约 720nm,特征为聚集体。H2O 聚集体的 CD 光谱表现出具有正负峰的导数形状,但其幅度低于类囊体。还测量了 BChld M 聚集体在 H2O 和己烷中的傅里叶变换红外光谱。两个样品均检测到 1644cm(-1) 带,表明存在键合的 13(1)-酮基。两个样品的 5 配位 Mg 的标记带也观察到在 1611cm(-1)。为了研究样品的动力学行为,进行了单光子计数(SPC)荧光和瞬态吸收差光谱测量。对于在己醇饱和 H2O 中的 BChld M,使用两种不同的技术检测到具有 10 至 14ps 寿命的快速衰减分量。快速衰减可以通过由于高局部色素浓度而导致的浓度猝灭现象来解释。对于 H2O 中的色素样品,SPC 给出了 16ps 分量,而瞬态吸收数据的全局分析则产生了两个快速分量:3.5 和 26ps。差异可能来自不同的激发强度。在后一种测量中,由于激发强度高,可能引入了其他猝灭过程,例如湮灭,从而产生 3.5ps 分量。最后,使用原子力显微镜检查了 BChld M 在 H2O 和己醇饱和 H2O 中的超微结构。在两个样品中都观察到直径在 15 至 45nm 之间的色素簇。