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How the formation process influences the structure of BChl c aggregates
Authors:Umetsu  Mitsuo  Wang  Zheng-Yu  Zhang   Jun  Ishii   Takasada  Uehara   Kaku  Inoko   Yoji  Kobayashi   Masayuki  Nozawa   Tsunenori
Affiliation:(1) Department of Biomolecular Engineering, Graduate School of Engineering, and Center for Interdisciplinary Science, Tohoku University, Aobayama 07, Aoba-ku, Sendai, 980-8579, Japan;(2) Research Institute for Advanced Science and Technology, Osaka Prefecture University, Gakuencho, Sakai, 593-8570, Japan;(3) Faculty of Engineering Science, Osaka University, Toyonaka, 560-0043, Japan
Abstract:The change of absorption spectra has been measured during the drying process of (31 R)bacteriochlorophyll (BChl) c from diethyl ether, dichloromethane (CH2Cl2) and carbon tetrachloride (CCl4) solutions. Absorption maxima of the Qy(0–0) transition of BChl c appear at 659 nm in diethyl ether, 680 nm in CH2Cl2 and 710 nm in CCl4. All these peaks are red-shifted to about 740 nm with formation of solid high aggregates when the solutions are completely dried. Fourier transform infrared spectra of the three solid aggregates are almost identical. However, magnetic circular dichroism and circular dichroism spectra are different and can be explained in terms of variations in stacking size of the aggregates and molecular arrangement of BChl c. Small-angle X-ray diffraction has been observed only for the aggregates treated with CH2Cl2, and the same sample gave rise to highly resolved cross polarization/magic angle spinning 13C nuclear magnetic resonance spectrum. The results suggest that molecular ordering of the solid-state BChl c aggregates is highly dependent on the formation process which is largely determined by the solvent used.
Keywords:BChl c-stacking size  chlorosomes  high aggregates  ordering of BChl c molecules  time variation of absorption spectra  X-ray diffraction
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