Changes in supramolecular organization of cyanobacterial thylakoid membrane complexes in response to far-red light photoacclimation

MacGregor-Chatwin, Craig; Nürnberg, Dennis J.; Jackson, Philip J.; Vasilev, Cvetelin; Hitchcock, Andrew; Ho, Ming-Yang; Shen, Gaozhong; Gisriel, Christopher J.; Wood, William H.J.; Mahbub, Moontaha; Selinger, Vera M.; Johnson, Matthew P.; Dickman, Mark J.; Rutherford, Alfred William; Bryant, Donald A.; Hunter, C. Neil

doi:10.1126/sciadv.abj4437

Title: Changes in supramolecular organization of cyanobacterial thylakoid membrane complexes in response to far-red light photoacclimation

Journal Article · Wed Feb 09 00:00:00 EST 2022 · Science Advances

DOI:https://doi.org/10.1126/sciadv.abj4437· OSTI ID:1871338

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Univ. of Sheffield (United Kingdom); Diamond Light Source (United Kingdom)
Imperial College, London (United Kingdom); Freie Univ. Berlin (Germany)
Univ. of Sheffield (United Kingdom)
Pennsylvania State Univ., University Park, PA (United States); National Taiwan Univ., Taipei (Taiwan)
Pennsylvania State Univ., University Park, PA (United States
Arizona State Univ., Tempe, AZ (United States); Yale Univ., New Haven, CT (United States)
Imperial College, London (United Kingdom)
Freie Univ. Berlin (Germany)
Pennsylvania State Univ., University Park, PA (United States)

Cyanobacteria are ubiquitous in nature and have developed numerous strategies that allow them to live in a diverse range of environments. Certain cyanobacteria synthesize chlorophylls d and f to acclimate to niches enriched in far-red light (FRL) and incorporate paralogous photosynthetic proteins into their photosynthetic apparatus in a process called FRL-induced photoacclimation (FaRLiP). We characterized the macromolecular changes involved in FRL-driven photosynthesis and used atomic force microscopy to examine the supramolecular organization of photosystem I associated with FaRLiP in three cyanobacterial species. Mass spectrometry showed the changes in the proteome of Chroococcidiopsis thermalis PCC 7203 that accompany FaRLiP. Fluorescence lifetime imaging microscopy and electron microscopy reveal an altered cellular distribution of photosystem complexes and illustrate the cell-to-cell variability of the FaRLiP response.

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Research Organization:: Pennsylvania State Univ., University Park, PA (United States)

Sponsoring Organization:: USDOE Office of Science (SC), Basic Energy Sciences (BES); National Science Foundation (NSF); H2020 European Research Council

Grant/Contract Number:: SC0001035; MCB-1613022; 854126

OSTI ID:: 1871338

Journal Information:: Science Advances, Vol. 8, Issue 6; ISSN 2375-2548

Publisher:: AAASCopyright Statement

Country of Publication:: United States

Language:: English

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