Abstract

Flexible color adaptation to available ecological niches is vital for the photosynthetic organisms to thrive. Hence, most purple bacteria living in the shade of green plants and algae apply bacteriochlorophyll a pigments to harvest near infra-red light around 850–875 nm. Exceptions are some Ca2+-containing species fit to utilize much redder quanta. The physical basis of such anomalous absorbance shift equivalent to ~5.5 kT at ambient temperature remains unsettled so far. Here, by applying several sophisticated spectroscopic techniques, we show that the Ca2+ ions bound to the structure of LH1 core light-harvesting pigment–protein complex significantly increase the couplings between the bacteriochlorophyll pigments. We thus establish the Ca-facilitated enhancement of exciton couplings as the main mechanism of the record spectral red-shift. The changes in specific interactions such as pigment–protein hydrogen bonding, although present, turned out to be secondary in this regard. Apart from solving the two-decade-old conundrum, these results complement the list of physical principles applicable for efficient spectral tuning of photo-sensitive molecular nano-systems, native or synthetic.

Highlights

  • Most purple bacteria employing bacteriochlorophyll a (BChl) as the main pigment chromophore have evolved to harvest near infra-red light around 875 nm [3]

  • We studied the spread of the light-harvesting 1 (LH1) exciton state manifold in wild type core complexes of Trv. 970 and Tch. tepidum saturated with Ca2+ and the change of the bandwidth upon the Ca2+ depletion by applying a fluorescence anisotropy excitation spectroscopy technique developed in refs. [13,14,15]

  • A set of two samples was studied: one with natural containment of Ca2+, and another where the ions were deliberately depleted by ethylenediaminetetraacetic acid (EDTA) treatment

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Summary

Introduction

The depletion of the 16 Ca2+ in the C-terminal domain of LH1 protein complexes results in a blue-shift of the absorption band. We studied the spread of the LH1 exciton state manifold (shortly, the exciton bandwidth) in wild type core complexes of Trv. 970 and Tch. tepidum saturated with Ca2+ and the change of the bandwidth upon the Ca2+ depletion by applying a fluorescence anisotropy excitation spectroscopy technique developed in refs.

Results
Conclusion
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