Influence of Chemically Disrupted Photosynthesis on Cyanobacterial Thylakoid Dynamics in Synechocystis sp. PCC 6803

Laura Roxana Stingaciu, Hugh M. O’Neill, Michelle Liberton, Himadri B. Pakrasi, Volker S. Urban

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11 Scopus citations

Abstract

The photosynthetic machinery of the cyanobacterium Synechocystis sp. PCC 6803 resides in flattened membrane sheets called thylakoids, situated in the peripheral part of the cellular cytoplasm. Under photosynthetic conditions these thylakoid membranes undergo various dynamical processes that could be coupled to their energetic functions. Using Neutron Spin Echo Spectroscopy (NSE), we have investigated the undulation dynamics of Synechocystis sp. PCC 6803 thylakoids under normal photosynthetic conditions and under chemical treatment with DCMU (3-(3,4-dichlorophenyl)-1,1-dimethylurea), an herbicide that disrupts photosynthetic electron transfer. Our measurements show that DCMU treatment has a similar effect as dark conditions, with differences in the undulation modes of the untreated cells compared to the chemically inhibited cells. We found that the disrupted membranes are 1.5-fold more rigid than the native membranes during the dark cycle, while in light they relax approximately 1.7-fold faster than native and they are 1.87-fold more flexible. The strength of the herbicide disruption effect is characterized further by the damping frequency of the relaxation mode and the decay rate of the local shape fluctuations. In the dark, local thicknesses and shape fluctuations relax twice as fast in native membranes, at 17% smaller mode amplitude, while in light the decay rate of local fluctuations is 1.2-fold faster in inhibited membranes than in native membranes, at 56% higher amplitude. The disrupted electron transfer chain and the decreased proton motive force within the lumenal space partially explain the variations observed in the mechanical properties of the Synechocystis membranes, and further support the hypothesis that the photosynthetic process is tied to thylakoid rigidity in this type of cyanobacterial cell.

Original languageEnglish
Article number5711
JournalScientific Reports
Volume9
Issue number1
DOIs
StatePublished - Dec 1 2019

Funding

Neutron beam time for this research at ORNL’s Spallation Neutron Source was allocated through the Scientific User Facilities Division, Office of Basic Energy Sciences, U.S. Department of Energy. SANS data were previously obtained using resources at the High Flux Isotope Reactor sponsored by the Scientific User Facilities Division, Office of Basic Energy Sciences and by the Office of Biological and Environmental Research, U.S. Department of Energy. The authors acknowledge M. Cochran for technical support, R. Moody and Dr. K. Weiss for biochemistry lab support and Dr. P. Zolnierczuk for automatization of light cell sample environment and advise on statistical errors calculation. M.L., H.B.P., H.O.N., and V.S.U. were supported by Photosynthetic Antenna Research Center (PARC) under Award Number DE-SC 0001035; L.R.S. was supported by Juelich Research Center FZJ-JCNS1.

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