
Introducing an algal carbon‐concentrating mechanism into higher plants: location and incorporation of key components
Author(s) -
Atkinson Nicky,
Feike Doreen,
Mackinder Luke C. M.,
Meyer Moritz T.,
Griffiths Howard,
Jonikas Martin C.,
Smith Alison M.,
McCormick Alistair J.
Publication year - 2016
Publication title -
plant biotechnology journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.525
H-Index - 115
eISSN - 1467-7652
pISSN - 1467-7644
DOI - 10.1111/pbi.12497
Subject(s) - chlamydomonas reinhardtii , chlamydomonas , arabidopsis , chloroplast , biology , arabidopsis thaliana , microbiology and biotechnology , photosynthesis , thylakoid , biochemistry , botany , gene , mutant
Summary Many eukaryotic green algae possess biophysical carbon‐concentrating mechanisms ( CCM s) that enhance photosynthetic efficiency and thus permit high growth rates at low CO 2 concentrations. They are thus an attractive option for improving productivity in higher plants. In this study, the intracellular locations of ten CCM components in the unicellular green alga Chlamydomonas reinhardtii were confirmed. When expressed in tobacco, all of these components except chloroplastic carbonic anhydrases CAH 3 and CAH 6 had the same intracellular locations as in Chlamydomonas. CAH 6 could be directed to the chloroplast by fusion to an Arabidopsis chloroplast transit peptide. Similarly, the putative inorganic carbon (Ci) transporter LCI 1 was directed to the chloroplast from its native location on the plasma membrane. CCP 1 and CCP 2 proteins, putative Ci transporters previously reported to be in the chloroplast envelope, localized to mitochondria in both Chlamydomonas and tobacco, suggesting that the algal CCM model requires expansion to include a role for mitochondria. For the Ci transporters LCIA and HLA 3, membrane location and Ci transport capacity were confirmed by heterologous expression and H 14 CO 3 ‐ uptake assays in Xenopus oocytes. Both were expressed in Arabidopsis resulting in growth comparable with that of wild‐type plants. We conclude that CCM components from Chlamydomonas can be expressed both transiently (in tobacco) and stably (in Arabidopsis) and retargeted to appropriate locations in higher plant cells. As expression of individual Ci transporters did not enhance Arabidopsis growth, stacking of further CCM components will probably be required to achieve a significant increase in photosynthetic efficiency in this species.