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Pyrenoid loss in Chlamydomonas reinhardtii causes limitations in CO2 supply, but not thylakoid operating efficiency

Accepted version
Peer-reviewed

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Authors

Caspari, OD 
Meyer, MT 
Tolleter, D 
Wittkopp, TM 
Cunniffe, NJ 

Abstract

The pyrenoid of the unicellular green alga Chlamydomonas reinhardtii is a microcompartment situated in the centre of the cup-shaped chloroplast, containing up to 90% of cellular Rubisco. Traversed by a network of dense, knotted thylakoid tubules, the pyrenoid has been proposed to influence thylakoid biogenesis and ultrastructure. Mutants that are unable to assemble a pyrenoid matrix, due to expressing a vascular plant version of the Rubisco small subunit, exhibit severe growth and photosynthetic defects and have an ineffective carbon-concentrating mechanism (CCM). The present study set out to determine the cause of photosynthetic limitation in these pyrenoid-less lines. We tested whether electron transport and light use were compromised as a direct structural consequence of pyrenoid loss or as a metabolic effect downstream of lower CCM activity and resulting CO₂ limitation. Thylakoid organization was unchanged in the mutants, including the retention of intrapyrenoid-type thylakoid tubules, and photosynthetic limitations associated with the absence of the pyrenoid were rescued by exposing cells to elevated CO₂ levels. These results demonstrate that Rubisco aggregation in the pyrenoid functions as an essential element for CO₂ delivery as part of the CCM, and does not play other roles in maintenance of photosynthetic membrane energetics.

Description

Keywords

Carbon-concentrating mechanism, Chlamydomonas, reinhardtii, chlorophyll fluorescence, chloroplast, electrochromic shift, electron transport rate, green algae, photosynthesis, pyrenoid, Rubisco

Journal Title

Journal of Experimental Botany

Conference Name

Journal ISSN

0022-0957
1460-2431

Volume Title

68

Publisher

Oxford University Press
Sponsorship
Biotechnology and Biological Sciences Research Council (BB/I024518/1)
Isaac Newton Trust (1106(ai))
Biotechnology and Biological Sciences Research Council (BB/M007693/1)
BBSRC (1090746)
We wish to gratefully acknowledge financial support to ODC by Wolfson College, the Cambridge Philosophical Society and the TH Middleton Fund (Department of Plant Sciences) toward research-related travel, which was crucial to enable this collaborative study. This work was supported by the Biotechnology and Biological Sciences Research Council (PhD studentship 1090746 to ODC and BB/M007693/1 to MTM and HG). The work was also supported by NSF grant MCB 0951094 and US Department of Energy Grants DE-FG02-07ER64427, DE- FG02-12ER16338 awarded to ARG.