Redesigning the QA binding site of Photosystem II allows reduction of exogenous quinones
Strategies to harness photosynthesis from living organisms to generate electrical power have long been considered, yet efficiency remains low. Here, we aimed to reroute photosynthetic electron flow in photosynthetic organisms without compromising their phototrophic properties. We show that 2,6-dimet...
Saved in:
Published in: | Nature communications Vol. 8; no. 1; p. 15274 |
---|---|
Main Authors: | , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
London
Nature Publishing Group UK
03-05-2017
Nature Publishing Group Nature Portfolio |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Strategies to harness photosynthesis from living organisms to generate electrical power have long been considered, yet efficiency remains low. Here, we aimed to reroute photosynthetic electron flow in photosynthetic organisms without compromising their phototrophic properties. We show that 2,6-dimethyl-
p
-benzoquinone (DMBQ) can be used as an electron mediator to assess the efficiency of mutations designed to engineer a novel electron donation pathway downstream of the primary electron acceptor Q
A
of Photosystem (PS) II in the green alga
Chlamydomonas reinhardtii
. Through the use of structural prediction studies and a screen of site-directed PSII mutants we show that modifying the environment of the Q
A
site increases the reduction rate of DMBQ. Truncating the C-terminus of the PsbT subunit protruding in the stroma provides evidence that shortening the distance between Q
A
and DMBQ leads to sustained electron transfer to DMBQ, as confirmed by chronoamperometry, consistent with a bypass of the natural Q
A
°
−
to Q
B
pathway.
Devices that harness electron flow from photosynthetic organisms generally compromise host photosynthesis. Here, the authors show that, by redesigning the Q
A
site of Photosystem II, it is possible to reroute electrons to an exogenous quinone while maintaining endogenous photosynthetic electron transfer in a green alga. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Deceased. Present address: School of Chemistry, The University of New South Wales, Sydney, New South Wales 2052, Australia (G.L.) Present address: Biodiversity Research Center, Academia Sinica, Taipei 11529, Taiwan (H.-Y.F.) |
ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/ncomms15274 |