Cryo-EM structure of the spinach cytochrome b6 f complex at 3.6 Å resolution
The cytochrome b 6 f (cyt b 6 f ) complex has a central role in oxygenic photosynthesis, linking electron transfer between photosystems I and II and converting solar energy into a transmembrane proton gradient for ATP synthesis 1 – 3 . Electron transfer within cyt b 6 f occurs via the quinol...
Gespeichert in:
Veröffentlicht in: | Nature (London) 2019-11, Vol.575 (7783), p.535-539 |
---|---|
Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | The cytochrome
b
6
f
(cyt
b
6
f
) complex has a central role in oxygenic photosynthesis, linking electron transfer between photosystems I and II and converting solar energy into a transmembrane proton gradient for ATP synthesis
1
–
3
. Electron transfer within cyt
b
6
f
occurs via the quinol (Q) cycle, which catalyses the oxidation of plastoquinol (PQH
2
) and the reduction of both plastocyanin (PC) and plastoquinone (PQ) at two separate sites via electron bifurcation
2
. In higher plants, cyt
b
6
f
also acts as a redox-sensing hub, pivotal to the regulation of light harvesting and cyclic electron transfer that protect against metabolic and environmental stresses
3
. Here we present a 3.6 Å resolution cryo-electron microscopy (cryo-EM) structure of the dimeric cyt
b
6
f
complex from spinach, which reveals the structural basis for operation of the Q cycle and its redox-sensing function. The complex contains up to three natively bound PQ molecules. The first, PQ1, is located in one cyt
b
6
f
monomer near the PQ oxidation site (Q
p
) adjacent to haem
b
p
and chlorophyll
a
. Two conformations of the chlorophyll
a
phytyl tail were resolved, one that prevents access to the Q
p
site and another that permits it, supporting a gating function for the chlorophyll
a
involved in redox sensing. PQ2 straddles the intermonomer cavity, partially obstructing the PQ reduction site (Q
n
) on the PQ1 side and committing the electron transfer network to turnover at the occupied Q
n
site in the neighbouring monomer. A conformational switch involving the haem
c
n
propionate promotes two-electron, two-proton reduction at the Q
n
site and avoids formation of the reactive intermediate semiquinone. The location of a tentatively assigned third PQ molecule is consistent with a transition between the Q
p
and Q
n
sites in opposite monomers during the Q cycle. The spinach cyt
b
6
f
structure therefore provides new insights into how the complex fulfils its catalytic and regulatory roles in photosynthesis.
A 3.6 Å resolution cryo-electron microscopy structure of the dimeric cytochrome
b
6
f
complex from spinach reveals the structural basis for operation of the quinol cycle and its redox-sensing function. |
---|---|
ISSN: | 0028-0836 1476-4687 |
DOI: | 10.1038/s41586-019-1746-6 |