4.7 Article

Pyrenoid loss impairs carbon-concentrating mechanism induction and alters primary metabolism in Chlamydomonas reinhardtii

Journal

JOURNAL OF EXPERIMENTAL BOTANY
Volume 68, Issue 14, Pages 3891-3902

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/jxb/erx121

Keywords

Carbon-concentrating mechanism; Chlamydomonas; photosynthesis; proteomics; pyrenoid; tandem mass spectrometry

Categories

Funding

  1. University of Cambridge
  2. BBSRC [BB/M007693/1]
  3. BBSRC [BB/M007693/1, BB/I024518/1] Funding Source: UKRI
  4. Biotechnology and Biological Sciences Research Council [BB/M007693/1, BB/I024518/1] Funding Source: researchfish

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Carbon-concentrating mechanisms (CCMs) enable efficient photosynthesis and growth in CO2-limiting environments, and in eukaryotic microalgae localisation of Rubisco to a microcompartment called the pyrenoid is key. In the model green alga Chlamydomonas reinhardtii, Rubisco preferentially relocalises to the pyrenoid during CCM induction and pyrenoid-less mutants lack a functioning CCM and grow very poorly at low CO2. The aim of this study was to investigate the CO2 response of pyrenoid-positive (pyr+) and pyrenoid-negative (pyr-) mutant strains to determine the effect of pyrenoid absence on CCM induction and gene expression. Shotgun proteomic analysis of low-CO2-adapted strains showed reduced accumulation of some CCM-related proteins, suggesting that pyr-has limited capacity to respond to low-CO2 conditions. Comparisons between gene transcription and protein expression revealed potential regulatory interactions, since Rubisco protein linker (EPYC1) protein did not accumulate in pyr-despite increased transcription, while elements of the LCIB/LCIC complex were also differentially expressed. Furthermore, pyr-showed altered abundance of a number of proteins involved in primary metabolism, perhaps due to the failure to adapt to low CO2.Carbon- This work highlights two-way regulation between CCM induction and pyrenoid formation, and provides novel candidates for future studies of pyrenoid assembly and CCM function.

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