4.4 Article

Differential sensitivity to oxygen among the bacteriochlorophylls g in the type-I reaction centers of Heliobacterium modesticaldum

Journal

PHOTOCHEMICAL & PHOTOBIOLOGICAL SCIENCES
Volume 20, Issue 6, Pages 747-759

Publisher

SPRINGERNATURE
DOI: 10.1007/s43630-021-00049-3

Keywords

Type-I photosystem; Optically detected magnetic resonance; Triplet state; Bacteriochlorophyll g; Oxygen sensitivity; Chlorophyll a

Funding

  1. University of Padova
  2. NSERC
  3. Photosynthetic Systems Program, Chemical Sciences, Geosciences, & Biosciences (CSGB) Division, US Department of Energy [DE-SC0010575]
  4. U.S. Department of Energy (DOE) [DE-SC0010575] Funding Source: U.S. Department of Energy (DOE)

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HbRC is the only known photosynthetic reaction center containing BChl g, which undergoes isomerization in the presence of oxygen. ODMR study reveals the characteristics of antenna triplet states in HbRCs with different conversion levels, providing useful information on the behavior of chlorophylls in the complex system.
The type-I, homodimeric photosynthetic reaction center (RC) of Heliobacteria (HbRC) is the only known RC in which bacteriochlorophyll g (BChl g) is found. It is also simpler than other RCs, having the smallest number of protein subunits and bound chromophores of any type-I RC. In the presence of oxygen, BChl g isomerizes to 8(1)-hydroxychlorophyll a(F) (Chl a(F)). This naturally occurring process provides a way of altering the chlorophylls and studying the effect of these changes on energy and electron transfer. Transient absorbance difference spectroscopy reveals that triplet-state formation occurs in the antenna chlorophylls of HbRCs but does not provide site-specific information. Here, we report on an extended optically detected magnetic resonance (ODMR) study of the antenna triplet states in HbRCs with differing levels of conversion of BChl g to Chl a(F). The data reveal pools of BChl g molecules with different triplet zero-field splitting parameters and different susceptibilities to chemical oxidation. By relating the detailed spectroscopic characteristics derived from the ODMR data to the recently solved crystallographic structure, we have tentatively identified BChl g molecules in which the probability of triplet formation is high and sites at which BChl g conversion is more likely, providing useful information about the fate of the excitation in the complex.

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