4.6 Article

CAM photosynthesis: the acid test

Journal

NEW PHYTOLOGIST
Volume 233, Issue 2, Pages 599-609

Publisher

WILEY
DOI: 10.1111/nph.17790

Keywords

C-3 photosynthesis; CAM photosynthesis; carboxylate; citrate; crassulacean acid metabolism; malate; malic acid; titratable acidity

Categories

Funding

  1. Smithsonian Tropical Research Institute
  2. Oxford Martin School, University of Oxford

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Research shows that nocturnal acidification is unique to CAM species, while many C-3 species can synthesize malate during the light period, the transition to night-time malic acid accumulation requires fundamental metabolic reprogramming. The central element of the CAM pathway, even at a low level, represents a biochemical capability not seen in C-3 plants, so it is considered a discrete evolutionary innovation.
There is currently considerable interest in the prospects for bioengineering crassulacean acid metabolism (CAM) photosynthesis - or key elements associated with it, such as increased water-use efficiency - into C-3 plants. Resolving how CAM photosynthesis evolved from the ancestral C-3 pathway could provide valuable insights into the targets for such bioengineering efforts. It has been proposed that the ability to accumulate organic acids at night may be common among C-3 plants, and that the transition to CAM might simply require enhancement of pre-existing fluxes, without the need for changes in circadian or diurnal regulation. We show, in a survey encompassing 40 families of vascular plants, that nocturnal acidification is a feature entirely restricted to CAM species. Although many C-3 species can synthesize malate during the light period, we argue that the switch to night-time malic acid accumulation requires a fundamental metabolic reprogramming that couples glycolytic breakdown of storage carbohydrate to the process of net dark CO2 fixation. This central element of the CAM pathway, even when expressed at a low level, represents a biochemical capability not seen in C-3 plants, and so is better regarded as a discrete evolutionary innovation than as part of a metabolic continuum between C-3 and CAM.

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