scholarly journals Evidence that circularly dichroic chlorophyll forms a-682 and a-710 are oriented at right angles to the thylakoid membranes of whole chloroplasts, and that the circular dichroism is light-dependent

1975 ◽  
Vol 148 (3) ◽  
pp. 487-497 ◽  
Author(s):  
R P Gregory

Chloroplasts from the pea (Pisum sativum L.) suspended in iso-osmotic buffered medium were oriented by flow in specially constructed cuvettes and examined for circular dichroism (c.d.). In one cuvette the flow was transverse to the direction of the light-path, but the other cuvette was designed so that flow and the light-path were coaxial. The induced orientation is such that the chloroplasts appear to move edgewise. C.d. was maximum when the light-path lay in the plane of the chloroplast disc. The intense c.d. of intact chloroplasts ascribed by Gregory & Raps [Biochem. J. (1974) 142, 193-201] to bulk chlorophyll a was found to contain two components, one the split-exciton type centred at 682nm and the other a simple maximum at 700-710 nm. The chlorophyll a-710 form was distinguished by its greater dependence on chloroplast orientation. The preferred direction of the transition moment in both chlorophyll forms was at right angles to the plane of the chloroplast, that is, at right angles to the plane of the thylakoids. This is in conflict with several reports based on polarization of fluorescence. It is suggested that the present effect is due to thylakoid-thylakoid interaction. Evidence for this is the reversible diminution in the c.d. signal caused by illumination in the presence of electron-transport reagents. It is argued that the c.d. is an indicator of chlorophyll movement, or changes in the thylakoid-thylakoid distance, possibly related to ion movement, affecting energy transfer between photosynthetic units.

Nature ◽  
1969 ◽  
Vol 224 (5224) ◽  
pp. 1108-1110 ◽  
Author(s):  
GWENDOLYN M. SHERMAN

Biochemistry ◽  
1988 ◽  
Vol 27 (7) ◽  
pp. 2430-2434 ◽  
Author(s):  
Gyozo Garab ◽  
Richard C. Leegood ◽  
David A. Walker ◽  
John C. Sutherland ◽  
Geoffrey Hind

1981 ◽  
Vol 36 (6) ◽  
pp. 735-738 ◽  
Author(s):  
Harald Lehner ◽  
Corinna Krauss ◽  
Hugo Scheer

Abstract The applicability of solvent induced circular dichroism (SICD) for the conformational analysis of bile pigments has been investigated. The S-(-)-ethyl lactate induced rotational strengths for octaethylbilindion (4) and its dihydroderivative 5 are remarkably high. Related compounds, e.g. the isomeric purpurines 1 and 2 and formyltripyrrinon 3 exhibit an optical activity which is smaller by more than one order of magnitude. 1-3 are essentially free from steric strain so that a flat arrangement of the chromophore is most likely. On the other hand the closed conformations of 4 and 5 experience considerable steric repulsion of their terminal rings, so that a helical topology is energetically favoured. This distinction is reflected in the magnitude of the SICD observed and demonstrates its applicability for the conformational analysis of bile pigments.


1973 ◽  
Vol 26 (11) ◽  
pp. 2401 ◽  
Author(s):  
CJ Hawkins ◽  
GA Lawrance

The preparations of pentaamminecobalt(III) complexes of a series of asymmetric unidentate amines are reported. The circular dichroism spectra for the (S)-amines show negative Cotton effects under the 1A1g → 1T1g absorption band, which are somewhat solvent dependent but independent of temperature down to -190�C. The vicinal effect from 1- cyclohexylethylamine was comparable to that from analogous aromatic compounds, but the simpler alkyl derivatives were found to impose smaller rotational strengths on the d-d transitions. The lack of measurable c.d. in the visible region for tetraammine((S)-butane-1,3- diamine)cobalt(III) is reported and discussed in the light of the other studies.


Sign in / Sign up

Export Citation Format

Share Document