The Chlamydomonas reinhardtii chloroplast envelope protein LCIA transports bicarbonate in planta

Author:

Förster Britta1ORCID,Rourke Loraine M1ORCID,Weerasooriya Hiruni N2ORCID,Pabuayon Isaiah C M2,Rolland Vivien3ORCID,Au Eng Kee1,Bala Soumi1,Bajsa-Hirschel Joanna4ORCID,Kaines Sarah1,Kasili Remmy W2ORCID,LaPlace Lillian M2ORCID,Machingura Marylou C5ORCID,Massey Baxter1ORCID,Rosati Viviana C6ORCID,Stuart-Williams Hilary1ORCID,Badger Murray R1ORCID,Price G Dean1ORCID,Moroney James V2ORCID

Affiliation:

1. The Australian National University , Canberra, ACT 2600 , Australia

2. Department of Biological Sciences, Louisiana State University , Baton Rouge, LA 70803 , USA

3. CSIRO Agriculture and Food , Canberra, ACT 2601 , Australia

4. Natural Products Utilization Research Unit, United States Department of Agriculture , University , MS 38677 , USA

5. Biology Department, Georgia Southern University , Savannah, GA 31419 , USA

6. Department of Biology, Centre for Novel Agricultural Products (CNAP), University of York , Wentworth Way, York YO10 5DD , UK

Abstract

Abstract LCIA (low CO2-inducible protein A) is a chloroplast envelope protein associated with the CO2-concentrating mechanism of the green alga Chlamydomonas reinhardtii. LCIA is postulated to be a HCO3– channel, but previous studies were unable to show that LCIA was actively transporting bicarbonate in planta. Therefore, LCIA activity was investigated more directly in two heterologous systems: an Escherichia coli mutant (DCAKO) lacking both native carbonic anhydrases and an Arabidopsis mutant (βca5) missing the plastid carbonic anhydrase βCA5. Neither DCAKO nor βca5 can grow in ambient CO2 conditions, as they lack carbonic anhydrase-catalyzed production of the necessary HCO3– concentration for lipid and nucleic acid biosynthesis. Expression of LCIA restored growth in both systems in ambient CO2 conditions, which strongly suggests that LCIA is facilitating HCO3– uptake in each system. To our knowledge, this is the first direct evidence that LCIA moves HCO3– across membranes in bacteria and plants. Furthermore, the βca5 plant bioassay used in this study is the first system for testing HCO3– transport activity in planta, an experimental breakthrough that will be valuable for future studies aimed at improving the photosynthetic efficiency of crop plants using components from algal CO2-concentrating mechanisms.

Funder

Foundation for Food & Agriculture Research

Foreign, Commonwealth & Development Office

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Physiology

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