Operon flv4-flv2 Provides Cyanobacterial Photosystem II with Flexibility of Electron Transfer

A1 Journal article (refereed)


Internal Authors/Editors


Publication Details

List of Authors: Zhang PP, Eisenhut M, Brandt AM, Carmel D, Silen HM, Vass I, Allahverdiyeva Y, Salminen TA, Aro EM
Publisher: AMER SOC PLANT BIOLOGISTS
Publication year: 2012
Journal: Plant Cell
Journal acronym: PLANT CELL
Volume number: 24
Start page: 1952
End page: 1971
Number of pages: 20
ISSN: 1040-4651


Abstract

Synechocystis sp PCC 6803 has four genes encoding flavodiiron proteins (FDPs; Flv1 to Flv4). Here, we investigated the flv4-flv2 operon encoding the Flv4, Sll0218, and Flv2 proteins, which are strongly expressed under low inorganic carbon conditions (i.e., air level of CO2) but become repressed at elevated CO2 conditions. Different from FDP homodimers in anaerobic microbes, Synechocystis Flv2 and Flv4 form a heterodimer. It is located in cytoplasm but also has a high affinity to membrane in the presence of cations. Sll0218, on the contrary, resides in the thylakoid membrane in association with a high molecular mass protein complex. Sll0218 operates partially independently of Flv2/Flv4. It stabilizes the photosystem II (PSII) dimers, and according to biophysical measurements opens up a novel electron transfer pathway to the Flv2/Flv4 heterodimer from PSII. Constructed homology models suggest efficient electron transfer in heterodimeric Flv2/Flv4. It is suggested that Flv2/Flv4 binds to thylakoids in light, mediates electron transfer from PSII, and concomitantly regulates the association of phycobilisomes with PSII. The function of the flv4-flv2 operon provides many beta-cyanobacteria with a so far unknown photoprotection mechanism that evolved in parallel with oxygen-evolving PSII.

Last updated on 2019-18-08 at 04:46