Lack of leaf carbonic anhydrase activity eliminates the C 4 carbon-concentrating mechanism requiring direct diffusion of CO 2 into bundle sheath cells.

Autor: DiMario RJ; School of Biological Sciences, Washington State University, Pullman, Washington, USA., Giuliani R; School of Biological Sciences, Washington State University, Pullman, Washington, USA., Ubierna N; School of Biological Sciences, Washington State University, Pullman, Washington, USA., Slack AD; Department of Crop Sciences, University of Illinois Urbana-Champaign, Urbana, Illinois, USA., Cousins AB; School of Biological Sciences, Washington State University, Pullman, Washington, USA., Studer AJ; Department of Crop Sciences, University of Illinois Urbana-Champaign, Urbana, Illinois, USA.
Jazyk: angličtina
Zdroj: Plant, cell & environment [Plant Cell Environ] 2022 May; Vol. 45 (5), pp. 1382-1397. Date of Electronic Publication: 2022 Mar 02.
DOI: 10.1111/pce.14291
Abstrakt: Carbonic anhydrase (CA) performs the first enzymatic step of C 4 photosynthesis by catalysing the reversible hydration of dissolved CO 2 that diffuses into mesophyll cells from intercellular airspaces. This CA-catalysed reaction provides the bicarbonate used by phosphoenolpyruvate carboxylase to generate products that flow into the C 4 carbon-concentrating mechanism (CCM). It was previously demonstrated that the Zea mays ca1ca2 double mutant lost 97% of leaf CA activity, but there was little difference in the growth phenotype under ambient CO 2 partial pressures (pCO 2 ). We hypothesise that since CAs are among the fastest enzymes, minimal activity from a third CA, CA8, can provide the inorganic carbon needed to drive C 4 photosynthesis. We observed that removing CA8 from the maize ca1ca2 background resulted in plants that had 0.2% of wild-type leaf CA activity. These ca1ca2ca8 plants had reduced photosynthetic parameters and could only survive at elevated pCO 2 . Photosynthetic and carbon isotope analysis combined with modelling of photosynthesis and carbon isotope discrimination was used to determine if ca1ca2ca8 plants had a functional C 4 cycle or were relying on direct CO 2 diffusion to ribulose 1,5-bisphosphate carboxylase/oxygenase within bundle sheath cells. The results suggest that leaf CA activity in ca1ca2ca8 plants was not sufficient to sustain the C 4 CCM.
(© 2022 John Wiley & Sons Ltd.)
Databáze: MEDLINE
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