Knockdown of limiting-CO sub(2)-induced gene HLA3 decreases HCO sub(3) super(-) transport and photosynthetic Ci affinity in Chlamydomonas reinhardtii

The CO sub(2)-concentrating mechanism (CCM) of Chlamydomonas reinhardtii and other microalgal species is essential for photosynthetic growth in most natural settings. A great deal has been learned regarding the CCM in cyanobacteria, including identification of inorganic carbon (Ci; CO sub(2) and HCO...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 2009-04, Vol.106 (14), p.5990-5995
Hauptverfasser: Duanmu, Deqiang, Miller, Amy R, Horken, Kempton M, Weeks, Donald P, Spalding, Martin H
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Sprache:eng
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Zusammenfassung:The CO sub(2)-concentrating mechanism (CCM) of Chlamydomonas reinhardtii and other microalgal species is essential for photosynthetic growth in most natural settings. A great deal has been learned regarding the CCM in cyanobacteria, including identification of inorganic carbon (Ci; CO sub(2) and HCO sub(3) super(-)) transporters; however, specific knowledge of analogous transporters has remained elusive in eukaryotic microalgae such as C. reinhardtii. Here we investigated whether the limiting-CO sub(2)- inducible, putative ABC-type transporter HLA3 might function as a HCO sub(3) super(-) transporter by evaluating the effect of pH on growth, photosynthetic Ci affinity, and [ super(14)C]-Ci uptake in very low CO sub(2) conditions following RNA interference (RNAi) knockdown of HLA3 mRNA levels in wild-type and mutant cells. Although knockdown of HLA3 mRNA alone resulted in only modest but high-pH-dependent decreases in photosynthetic Ci affinity and Ci uptake, the combination of nearly complete knockdown of HLA3 mRNA with mutations in LCIB (which encodes limiting-Ci- inducible plastid-localized protein required for normal Ci uptake or accumulation in low-CO sub(2) conditions) and/or simultaneous, apparently off-target knockdown of LCIA mRNA (which encodes limiting-Ci-inducible plastid envelope protein reported to transport HCO sub(3) super(-)) resulted in dramatic decreases in growth, Ci uptake, and photosynthetic Ci affinity, especially at pH 9, at which HCO sub(3) super(-) is the predominant form of available Ci. Collectively, the data presented here provide compelling evidence that HLA3 is directly or indirectly involved in HCO sub(3) super(-) transport, along with additional evidence supporting a role for LCIA in chloroplast envelope HCO sub(3) super(-) transport and a role for LCIB in chloroplast Ci accumulation.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.0812885106