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Redox poise in R. rubrum phototrophic growth drives large-scale changes in macromolecular pathways

Fig 2

Overview of cyclic photophosphorylation by the branched-cyclic Q cycle, hydrogen uptake, and primary and secondary biosynthetic pathways of Rhodospirillum rubrum included in the thermo-kinetic model.

Red dashed arrows indicate the flow of single electrons in the Q cycle unless otherwise noted, and each cytochrome C (Cyt_C) carries each, so two (2) Cyt−C proteins are required. For hydrogen uptake, note the specific redox carrier that interacts with the HupSLM [Ni-Fe] hydrogenase is not known and thus indicated by X/H2X for a general thermodynamically acceptable redox carrier, e.g., NAD(P)+/NAD(P)H. Both the oxidative and reductive versions of the TCA cycle were tested in the modeling. The reductive TCA cycle was used in the final model. The main pathways for CO2 uptake or release are highlighted in orange blocks. Metabolites (alphabetical order): 2PG - 2-phospho-glycerate, 3PG - 3-phospho-glycerate (2 indicates the formation of 2 molecules from RuBP), Ac-CoA - acetyl-CoA, KG - 2-keto-glutarate, BPG - 1,3-bisphospho-glycerate, Cit - citrate, CCA - citryl-CoA (intermediate of Citrate Synthase), CoA-SH - Coenzyme A, DHAP - dihydroxyacetone phosphate, E4P - erythrose-4-phosphate, F6P - fructose-6-phosphate, Fum - fumarate, G3P - glyceraldehyde-3-phosphate, G6P - glucose-6-phosphate, H4THF – Tetrahydrofolate, Hcy – homocysteine, Isc - isocitrate, LPS - lipopolysaccharide, Mal - malate, MCA - malyl-CoA, MmCA - methylmalyl-CoA, Oxa - oxaloacetate, PCA - propanoyl-CoA, PEP - phosphoenol-pyruvate, PHB - polyhydroxybutyrate, Pyr - pyruvate, R-CH3 - methylated methyl acceptor (R), Q/QH2 - oxidized and - reduced quinone, R5P - ribose-5-phosphate, Ru5P - ribulose-5-phosphate, RuBP - ribulose-1,5-bisphosphate, SAM – S-adenosyl-methionine, SAH – S-adenosyl-homocysteine, S7P - sedoheptulose-7-phosphate, SBP - sedoheptulose-1,7-bisphosphate, SCA - succinyl-CoA, Suc - succinate, Xu5P - xylulose-5-phosphate, - a redox carrier. All amino acids are indicated by standard 3-letter code. Enzymes (alphabetical order): ACL - acetate:CoA ligase (AMP-forming), ACON – aconitase, CLY – ATP-independent citrate lyase, CS - Citrate Synthase (with CCA intermediate) Cyt_bc1-ISP - complex of cytchrome b (heme b560 and b566 containing) cytochrome c1 (heme c containing) and Rieske iron sulfur protein (ISP, yellow), Cyt_C - bacterial cytochrome C2 (heme c containing), Eno – enolase, F0F1 - ATP synthasae, FBPA – fructose-1,6-bisphosphate aldolase, FBPase – fructose-1,6-bisphosphotase, FRD – fumarate reductase, FUM – fumarase, GAPDH – glyceraldehyde-3-phosphate dehydrogenase, GPI – glucose-6-phosphate isomerase, HupSLM - Uptake hydrogenase complex of small, large, and medium subunits, IDH – isocitrate dehydrogenase, KGOR – 2-keto-glutarate:ferredoxin oxidoreductase (-KG synthase), MDH – malate dehydrogenase, NAD-ME – NAD-dependent malic enzyme, ODC – oxaloacetate decarboxylase, PEP-CK – phosphoenol-pyruvate carboxykinase, PFK – phosphofructokinase, PFOR – pyruvate-ferredoxin oxidoreductase (pyruvate synthase), PGK – 3-phosphoglycerate kinase, PGM – 3-phosphoglycerate mutase, PK – pyruvate kinase, PRK – phosphoribulokinase, RC(P870) - Type II photosynthetic reaction center with characteristic P870 pigment for photo-oxidation of , RPE – ribulose-5-phosphate epimerase, RPI – ribose-5-phosphate isomerase, RubisCO – ribulose-1,5-bisphosphate oxygenase/carboxylase, SBPase – sedoheptulose-1,7-bisphosphate phosphatase, SCS – succinyl-CoA synthetase, TKT – transketolase, TPI – triose-phosphate isomerase.

Fig 2

doi: https://doi.org/10.1371/journal.pcbi.1013015.g002