TY - JOUR
T1 - How the formation process influences the structure of BChl c aggregates
AU - Umetsu, Mitsuo
AU - Wang, Zheng Yu
AU - Zhang, Jun
AU - Ishii, Takasada
AU - Uehara, Kaku
AU - Inoko, Yoji
AU - Kobayashi, Masayuki
AU - Nozawa, Tsunenori
PY - 1999
Y1 - 1999
N2 - The change of absorption spectra has been measured during the drying process of (31R)bacteriochlorophyll (BChl) c from diethyl ether, dichloromethane (CH2Cl2) and carbon tetrachloride (CCl4) solutions. Absorption maxima of the Q(y)(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.
AB - The change of absorption spectra has been measured during the drying process of (31R)bacteriochlorophyll (BChl) c from diethyl ether, dichloromethane (CH2Cl2) and carbon tetrachloride (CCl4) solutions. Absorption maxima of the Q(y)(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.
KW - BChl c-stacking size
KW - Chlorosomes
KW - High aggregates
KW - Ordering of BChl c molecules
KW - Time variation of absorption spectra
KW - X-ray diffraction
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U2 - 10.1023/a:1006258029191
DO - 10.1023/a:1006258029191
M3 - Article
AN - SCOPUS:0032863264
SN - 0166-8595
VL - 60
SP - 229
EP - 239
JO - Photosynthesis Research
JF - Photosynthesis Research
IS - 2-3
ER -