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Nat Commun ; 9(1): 2008, 2018 05 22.
Article in English | MEDLINE | ID: mdl-29789614

ABSTRACT

The Calvin-Benson-Bassham (CBB) cycle is presumably evolved for optimal synthesis of C3 sugars, but not for the production of C2 metabolite acetyl-CoA. The carbon loss in producing acetyl-CoA from decarboxylation of C3 sugar limits the maximum carbon yield of photosynthesis. Here we design a synthetic malyl-CoA-glycerate (MCG) pathway to augment the CBB cycle for efficient acetyl-CoA synthesis. This pathway converts a C3 metabolite to two acetyl-CoA by fixation of one additional CO2 equivalent, or assimilates glyoxylate, a photorespiration intermediate, to produce acetyl-CoA without net carbon loss. We first functionally demonstrate the design of the MCG pathway in vitro and in Escherichia coli. We then implement the pathway in a photosynthetic organism Synechococcus elongates PCC7942, and show that it increases the intracellular acetyl-CoA pool and enhances bicarbonate assimilation by roughly 2-fold. This work provides a strategy to improve carbon fixation efficiency in photosynthetic organisms.


Subject(s)
Acyl Coenzyme A/metabolism , Carbon Dioxide/metabolism , Escherichia coli/genetics , Glyceric Acids/metabolism , Photosynthesis/genetics , Synechococcus/genetics , Acetyl Coenzyme A/metabolism , Bacterial Proteins/genetics , Bacterial Proteins/metabolism , Escherichia coli/metabolism , Glyoxylates/metabolism , Metabolic Engineering/methods , Synechococcus/metabolism , Transgenes
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