Cm. Borrego et al., The molar extinction coefficient of bacteriochlorophyll e and the pigment stoichiometry in Chlorobium phaeobacteroides, PHOTOSYN R, 60(2-3), 1999, pp. 257-264
We have determined the molar extinction coefficient of bacteriochlorophyll
(BChl) e, the main light-harvesting pigment from brown-coloured photosynthe
tic sulfur bacteria. The extinction coefficient was determined using pure [
Pr,E]BChl e(F) isolated by reversed-phase HPLC from crude pigment extracts
of Chlorobium (Chl.) phaeobacteroides strain CL1401. The extinction coeffic
ients at the Soret and Q(y) bands were determined in four organic solvents.
The extinction coefficient of BChl e differs from those of other related C
hlorobium chlorophylls (BChl c and BChl d) but is similar to that of chloro
phyll b. The determined extinction coefficient was used to calculate the st
oichiometric BChl e to BChl a and BChl e to carotenoids ratios in whole cel
ls and isolated chlorosomes from Chl. phaeobacteroides strain CL1401 using
the spectrum-reconstruction method (SRCM) described by Naqvi et al. (1997)
(Spectrochim Acta A Mol Biomol Spectrosc 53: 2229-2234). In isolated chloro
somes, BChl a content was ca. 1% of the total BChl content and the stoichio
metric ratio of BChl e to carotenoids was 6. In whole cells, however, BChl
a content was 3-4%, owing to the presence of BChl a-containing elements, i.
e. FMO protein and reaction centre. An average of 5 BChl e molecules per ca
rotenoid was determined in whole cells.