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Pentose Phosphate Pathway Reactions in Photosynthesizing Cells

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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/msb.20145228openalex-snapshot
Non‐enzymatic glycolysis and pentose phosphate pathway‐like reactions in a plausible Archean ocean
inferredcites →https://doi.org/10.1007/bf00017756openalex-snapshot
Short-term responses of Photosystem I to heat stress
inferredcites →https://doi.org/10.1007/bf00384257openalex-snapshot
Some relationships between the biochemistry of photosynthesis and the gas exchange of leaves
inferredcites →https://doi.org/10.1007/bf00384921openalex-snapshot
Changes in specific radioactivities of corn-leaf metabolites during photosynthesis in 14CO2 and 12CO2 at normal and low oxygen
inferredcites →https://doi.org/10.1007/bf00384922openalex-snapshot
Changes in specific radioactivities of sunflower leaf metabolites during photosynthesis in 14CO2 and 12CO2 at normal and low oxygen
inferredcites →https://doi.org/10.1007/bf00386231openalex-snapshot
A biochemical model of photosynthetic CO2 assimilation in leaves of C3 species
inferredcites →https://doi.org/10.1007/bf00390292openalex-snapshot
Changes in specific radioactivity of sunflower leaf metabolites during photosynthesis in 14CO2 and 12CO2 at three concentrations of CO2
inferredcites →https://doi.org/10.1007/bf00392238openalex-snapshot
Effect of temperature on the CO2/O2 specificity of ribulose-1,5-bisphosphate carboxylase/oxygenase and the rate of respiration in the light
inferredcites →https://doi.org/10.1007/bf02139287openalex-snapshot
The path of carbon in photosynthesis
inferredcites →https://doi.org/10.1007/s004250050226openalex-snapshot
Reduced sedoheptulose-1,7-bisphosphatase levels in transgenic tobacco lead to decreased photosynthetic capacity and altered carbohydrate accumulation
inferredcites →https://doi.org/10.1007/s11120-006-9113-5openalex-snapshot
The metabolic significance of octulose phosphates in the photosynthetic carbon reduction cycle in spinach
inferredcites →https://doi.org/10.1007/s11120-006-9114-4openalex-snapshot
A re-investigation of the path of carbon in photosynthesis utilizing GC/MS methodology. Unequivocal verification of the participation of octulose phosphates in the pathway
inferredcites →https://doi.org/10.1007/s11120-009-9420-8openalex-snapshot
Photosynthetic electron transport and proton flux under moderate heat stress
inferredcites →https://doi.org/10.1007/s11120-011-9651-3openalex-snapshot
Peroxisomal hydroxypyruvate reductase is not essential for photorespiration in Arabidopsis but its absence causes an increase in the stoichiometry of photorespiratory CO2 release
inferredcites →https://doi.org/10.1007/s11120-018-0600-2openalex-snapshot
Discovery of the canonical Calvin–Benson cycle
inferredcites →https://doi.org/10.1016/0003-9861(89)90441-4openalex-snapshot
Chloroplast glucose-6-phosphate dehydrogenase: Km shift upon light modulation and reduction
inferredcites →https://doi.org/10.1016/0005-2744(71)90051-9openalex-snapshot
Chloroplast and cytoplasmic enzymes II. Pea leaf triose phosphate isomerases
inferredcites →https://doi.org/10.1016/0020-711x(87)90239-4openalex-snapshot
The pentose pathway: A random harvest
inferredcites →https://doi.org/10.1016/j.cell.2011.05.022openalex-snapshot
Riboneogenesis in Yeast
inferredcites →https://doi.org/10.1016/j.plantsci.2016.12.004openalex-snapshot
Induction of cyclic electron flow around photosystem I during heat stress in grape leaves
inferredcites →https://doi.org/10.1016/j.ymben.2020.09.003openalex-snapshot
Promiscuous phosphoketolase and metabolic rewiring enables novel non-oxidative glycolysis in yeast for high-yield production of acetyl-CoA derived products
inferredcites →https://doi.org/10.1016/s0021-9258(18)71280-5openalex-snapshot
THE MECHANISM OF PENTOSE PHOSPHATE CONVERSION TO HEXOSE MONOPHOSPHATE
inferredcites →https://doi.org/10.1016/s0021-9258(19)52402-4openalex-snapshot
THE PATH OF CARBON IN PHOTOSYNTHESIS
inferredcites →https://doi.org/10.1016/s0021-9258(19)52464-4openalex-snapshot
THE ENZYMATIC CONVERSION OF 6-PHOSPHOGLUCONATE TO RIBULOSE-5-PHOSPHATE AND RIBOSE-5-PHOSPHATE
inferredcites →https://doi.org/10.1021/ja01100a526openalex-snapshot
THIAMINE PYROPHOSPHATE, A COENZYME OF TRANSKETOLASE
inferredcites →https://doi.org/10.1021/ja01128a524openalex-snapshot
THE ENZYMATIC FORMATION OF SEDOHEPTULOSE PHOSPHATE FROM PENTOSE PHOSPHATE
inferredcites →https://doi.org/10.1021/ja01150a543openalex-snapshot
SEDOHEPTULOSE IN PHOTOSYNTHESIS BY PLANTS1
inferredcites →https://doi.org/10.1021/ja01150a545openalex-snapshot
IDENTIFICATION OF RIBULOSE IN C14O2 PHOTOSYNTHESIS PRODUCTS1
inferredcites →https://doi.org/10.1021/ja01160a080openalex-snapshot
The Path of Carbon in Photosynthesis. V. Paper Chromatography and Radioautography of the Products1
inferredcites →https://doi.org/10.1021/ja01636a012openalex-snapshot
The Path of Carbon in Photosynthesis. XXI. The Cyclic Regeneration of Carbon Dioxide Acceptor1
inferredcites →https://doi.org/10.1023/a:1006149317411openalex-snapshot
Heat sensitivity of chloroplasts and leaves: Leakage of protons from thylakoids and reversible activation of cyclic electron transport
inferredcites →https://doi.org/10.1034/j.1399-3054.2000.1100303.xopenalex-snapshot
Investigating the role of the thiol-regulated enzyme sedoheptulose-1,7-bisphosphatase in the control of photosynthesis
inferredcites →https://doi.org/10.1038/nchembio.1786openalex-snapshot
A pentose bisphosphate pathway for nucleoside degradation in Archaea
inferredcites →https://doi.org/10.1042/bcj20190234openalex-snapshot
Plastidic glucose-6-phosphate dehydrogenases are regulated to maintain activity in the light
inferredcites →https://doi.org/10.1042/bcj20200480openalex-snapshot
Source of 12C in Calvin–Benson cycle intermediates and isoprene emitted from plant leaves fed with 13CO2
inferredcites →https://doi.org/10.1042/bst20170245openalex-snapshot
The importance of the photosynthetic Gibbs effect in the elucidation of the Calvin–Benson–Bassham cycle
inferredcites →https://doi.org/10.1071/pp01091openalex-snapshot
Respiration in the light measured by 12 CO 2 emission in 13 CO 2 atmosphere in maize leaves
inferredcites →https://doi.org/10.1073/pnas.1319485111openalex-snapshot
Isotopically nonstationary 13 C flux analysis of changes in Arabidopsis thaliana leaf metabolism due to high light acclimation
inferredcites →https://doi.org/10.1073/pnas.1418223112openalex-snapshot
Activation of cyclic electron flow by hydrogen peroxide in vivo
inferredcites →https://doi.org/10.1074/jbc.272.43.26985openalex-snapshot
Identification of the Cysteine Residues Involved in Redox Modification of Plant Plastidic Glucose-6-phosphate Dehydrogenase
inferredcites →https://doi.org/10.1093/jxb/50.330.1openalex-snapshot
New insights into the structure and function of sedoheptulose-1,7-bisphosphatase; an important but neglected Calvin cycle enzyme
inferredcites →https://doi.org/10.1093/jxb/erp374openalex-snapshot
Metabolic turnover analysis by a combination of in vivo13C-labelling from 13CO2 and metabolic profiling with CE-MS/MS reveals rate-limiting steps of the C3 photosynthetic pathway in Nicotiana tabacum leaves
inferredcites →https://doi.org/10.1093/jxb/err038openalex-snapshot
Evaluating a new method to estimate the rate of leaf respiration in the light by analysis of combined gas exchange and chlorophyll fluorescence measurements
inferredcites →https://doi.org/10.1093/jxb/ert400openalex-snapshot
Substantial roles of hexokinase and fructokinase in the effects of sugars on plant physiology and development
inferredcites →https://doi.org/10.1093/jxb/erv484openalex-snapshot
The glucose 6-phosphate shunt around the Calvin–Benson cycle
inferredcites →https://doi.org/10.1093/plphys/kiab076openalex-snapshot
The metabolic origins of non-photorespiratory CO2 release during photosynthesis: a metabolic flux analysis
inferredcites →https://doi.org/10.1104/pp.010576openalex-snapshot
The Plastidic Pentose Phosphate Translocator Represents a Link between the Cytosolic and the Plastidic Pentose Phosphate Pathways in Plants
inferredcites →https://doi.org/10.1104/pp.105.062141openalex-snapshot
In Vivo Respiratory Metabolism of Illuminated Leaves
inferredcites →https://doi.org/10.1104/pp.105.070490openalex-snapshot
Chloroplastic NAD(P)H Dehydrogenase in Tobacco Leaves Functions in Alleviation of Oxidative Damage Caused by Temperature Stress
inferredcites →https://doi.org/10.1104/pp.106.081174openalex-snapshot
Carbon Balance and Circadian Regulation of Hydrolytic and Phosphorolytic Breakdown of Transitory Starch
inferredcites →https://doi.org/10.1104/pp.108.2.609openalex-snapshot
Enzymatic Evidence for a Complete Oxidative Pentose Phosphate Pathway in Chloroplasts and an Incomplete Pathway in the Cytosol of Spinach Leaves
inferredcites →https://doi.org/10.1104/pp.112.3.1245openalex-snapshot
Effect of High Temperature on Photosynthesis in Beans (I. Oxygen Evolution and Chlorophyll Fluorescence)
inferredcites →https://doi.org/10.1104/pp.125.2.982openalex-snapshot
Photosynthetic Capacity Is Differentially Affected by Reductions in Sedoheptulose-1,7-Bisphosphatase Activity during Leaf Development in Transgenic Tobacco Plants
inferredcites →https://doi.org/10.1104/pp.19.00256openalex-snapshot
A Cytosolic Bypass and G6P Shunt in Plants Lacking Peroxisomal Hydroxypyruvate Reductase
inferredcites →https://doi.org/10.1104/pp.83.2.399openalex-snapshot
Subcellular Metabolite Levels in Spinach Leaves
inferredcites →https://doi.org/10.1104/pp.83.4.772openalex-snapshot
Comparison of the Activities and Some Properties of Pyrophosphate and ATP Dependent Fructose-6-Phosphate 1-Phosphotransferases of Phaseolus vulgaris Seeds
inferredcites →https://doi.org/10.1104/pp.90.2.385openalex-snapshot
Low Oxygen Inhibition of Photosynthesis Is Caused by Inhibition of Starch Synthesis
inferredcites →https://doi.org/10.1105/tpc.10.1.105openalex-snapshot
Molecular Characterization of a Carbon Transporter in Plastids from Heterotrophic Tissues: The Glucose 6-Phosphate/Phosphate Antiporter
inferredcites →https://doi.org/10.1105/tpc.108.063925openalex-snapshot
A Chloroplastic UDP-Glucose Pyrophosphorylase from Arabidopsis Is the Committed Enzyme for the First Step of Sulfolipid Biosynthesis
inferredcites →https://doi.org/10.1105/tpc.112.106989openalex-snapshot
Metabolic Fluxes in an Illuminated Arabidopsis Rosette
inferredcites →https://doi.org/10.1105/tpc.17.00256openalex-snapshot
The Photorespiratory Metabolite 2-Phosphoglycolate Regulates Photosynthesis and Starch Accumulation in Arabidopsis
inferredcites →https://doi.org/10.1111/brv.12140openalex-snapshot
The return of metabolism: biochemistry and physiology of the pentose phosphate pathway
inferredcites →https://doi.org/10.1111/j.1365-3040.1993.tb00907.xopenalex-snapshot
Rapid appearance of 13C in biogenic isoprene when 13CO2 is fed to intact leaves
inferredcites →https://doi.org/10.1111/j.1365-3040.2009.01934.xopenalex-snapshot
Using combined measurements of gas exchange and chlorophyll fluorescence to estimate parameters of a biochemical C 3 photosynthesis model: a critical appraisal and a new integrated approach applied to leaves in a wheat ( Triticum aestivum ) canopy
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02293.xopenalex-snapshot
Genome‐wide analysis of glucose‐6‐phosphate dehydrogenases in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02427.xopenalex-snapshot
New insights into plant transaldolase
inferredcites →https://doi.org/10.1111/j.1438-8677.1990.tb00170.xopenalex-snapshot
Light/Dark Modulation: Regulation of Chloroplast Metabolism in a New Light
inferredcites →https://doi.org/10.1111/j.1742-4658.2005.04907.xopenalex-snapshot
Revisiting the 13C‐label distribution of the non‐oxidative branch of the pentose phosphate pathway based upon kinetic and genetic evidence
inferredcites →https://doi.org/10.1111/j.1749-6632.1982.tb31198.xopenalex-snapshot
OCCURRENCE AND SIGNIFICANCE OF OCTULOSE PHOSPHATES IN LIVER
inferredcites →https://doi.org/10.1111/pbi.12676openalex-snapshot
Simultaneous stimulation of sedoheptulose 1,7‐bisphosphatase, fructose 1,6‐bisphophate aldolase and the photorespiratory glycine decarboxylase‐H protein increases CO 2 assimilation, vegetative biomass and seed yield in Arabidopsis
inferredcites →https://doi.org/10.1111/tpj.14134openalex-snapshot
Photometric screens identified Arabidopsis peroxisome proteins that impact photosynthesis under dynamic light conditions
inferredcites →https://doi.org/10.1128/jb.186.19.6360-6366.2004openalex-snapshot
Modified Pathway To Synthesize Ribulose 1,5-Bisphosphate in Methanogenic Archaea
inferredcites →https://doi.org/10.1134/s1021443716020023openalex-snapshot
Cyclic electron flow plays an important role in protection of spinach leaves under high temperature stress
inferredcites →https://doi.org/10.1139/b81-102openalex-snapshot
Inhibition of photosynthesis by low oxygen concentrations
inferredcites →https://doi.org/10.1186/1475-9292-2-11openalex-snapshot
Evolution of energy metabolism and its compartmentation in Kinetoplastida
inferredcites →https://doi.org/10.2172/915054openalex-snapshot
The Path of Carbon in Photosynthesis, XV. Ribulose andSedoheptulose
inferredcites →https://doi.org/10.3389/fpls.2019.00827openalex-snapshot
Transcriptional Regulation of the Glucose-6-Phosphate/Phosphate Translocator 2 Is Related to Carbon Exchange Across the Chloroplast Envelope
inferredcites →https://doi.org/10.3389/fpls.2020.580726openalex-snapshot
Phosphoglucoisomerase Is an Important Regulatory Enzyme in Partitioning Carbon out of the Calvin-Benson Cycle

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inferred← citeshttps://doi.org/10.1111/pce.14871openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/pce.14904openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/ppl.13602openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/tpj.16913openalex-snapshot
Wheat TaNACα18 functions as a positive regulator of high‐temperature adaptive responses and improves cell defense machinery
inferred← citeshttps://doi.org/10.1128/mbio.00654-25openalex-snapshot
Ribose-5-phosphate metabolism protects E. coli from antibiotic lethality
inferred← citeshttps://doi.org/10.1134/s1021443722060218openalex-snapshot
Plant Respiration and Global Climatic Changes
inferred← citeshttps://doi.org/10.1177/13872877261478594openalex-snapshot
The role of microglia glucose metabolism reprogramming in Alzheimer's disease treatment
inferred← citeshttps://doi.org/10.1186/s12864-026-12618-wopenalex-snapshot
Molecular and spatial integration of algal endosymbionts of the freshwater sponge, Ephydatia muelleri, throughout development in light and dark conditions
inferred← citeshttps://doi.org/10.1186/s12870-025-06515-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1242/dev.205350openalex-snapshot
Computational method to analyze linear developmental gradients reveals specific metabolite enrichment patterns in stress-tolerant maize
inferred← citeshttps://doi.org/10.12794/metadc2443184openalex-snapshot
Characterization of Fatty Acid Elongation1 (FAE1) in Thlaspi arvense
inferred← citeshttps://doi.org/10.19110/978-5-89606-709-2openalex-snapshot
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inferred← citeshttps://doi.org/10.2139/ssrn.4887238openalex-snapshot
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inferred← citeshttps://doi.org/10.32604/phyton.2025.068133openalex-snapshot
Comparative Transcriptomic Analysis of a Naturally Found Yellowish Leaf Rehmannia chingii H. L. Li Mutant and Wild Type
inferred← citeshttps://doi.org/10.3389/abp.2024.14000openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fcell.2026.1885974openalex-snapshot
Glucose metabolism in tumor-associated macrophage plasticity and cancer immunity
inferred← citeshttps://doi.org/10.3389/fmicb.2022.1000033openalex-snapshot
Endophytic nitrogen-fixing bacteria DX120E inoculation altered the carbon and nitrogen metabolism in sugarcane
inferred← citeshttps://doi.org/10.3389/fphar.2025.1642927openalex-snapshot
Potential biomarkers in early detection of gastric cancer
inferred← citeshttps://doi.org/10.3389/fpls.2022.876439openalex-snapshot
Interactions Between Carbon Metabolism and Photosynthetic Electron Transport in a Chlamydomonas reinhardtii Mutant Without CO2 Fixation by RuBisCO
inferred← citeshttps://doi.org/10.3389/fpls.2024.1439747openalex-snapshot
Integrative transcriptome and metabolome analysis reveals the mechanism of fulvic acid alleviating drought stress in oat
inferred← citeshttps://doi.org/10.3389/fpls.2025.1682825openalex-snapshot
Combined transcriptomic and proteomic analysis reveals the response mechanisms of alfalfa to freezing stress
inferred← citeshttps://doi.org/10.3389/frph.2026.1803167openalex-snapshot
The role of metabolic reprogramming in oocyte development: research progress and prospects
inferred← citeshttps://doi.org/10.3389/fviro.2024.1461375openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ani15030410openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/antiox12010065openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/biochem4020008openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/cells11233759openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/cells14221775openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/foods11223746openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms241310626openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms25168875openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms25189845openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/microorganisms13112617openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/plants10091917openalex-snapshot
Melatonin and Carbohydrate Metabolism in Plant Cells
inferred← citeshttps://doi.org/10.3390/plants11131647openalex-snapshot
Developmental Differences between Anthers of Diploid and Autotetraploid Rice at Meiosis
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