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Supply and consumption of glucose 6-phosphate in the chloroplast stroma

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What this work says

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

inferredcites →https://doi.org/10.1006/abbi.1997.0499openalex-snapshot

Oxidation–Reduction Properties of the Regulatory Site of Spinach Phosphoribulokinase

inferredcites →https://doi.org/10.1007/978-94-017-9032-1openalex-snapshot

Non-Photochemical Quenching and Energy Dissipation in Plants, Algae and Cyanobacteria

inferredcites →https://doi.org/10.1007/978-94-017-9032-1_18openalex-snapshot

Control of Non-Photochemical Exciton Quenching by the Proton Circuit of Photosynthesis

inferredcites →https://doi.org/10.1007/s00425-003-1128-yopenalex-snapshot

Maltose is the major form of carbon exported from the chloroplast at night

inferredcites →https://doi.org/10.1007/s00425-005-1507-7openalex-snapshot

Photoinhibition of photosystem I

inferredcites →https://doi.org/10.1007/s004250050513openalex-snapshot

On the role of chloroplastic phosphoglucomutase in the regulation of starch turnover

inferredcites →https://doi.org/10.1016/0003-9861(73)90077-5openalex-snapshot

Two isoenzymes each of glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase in spinach leaves

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/10.1016/0005-2728(69)90048-6openalex-snapshot

Free energy changes and metabolic regulation in steady-state photosynthetic carbon reduction

inferredcites →https://doi.org/10.1016/0006-291x(60)90201-1openalex-snapshot

The inhibition of phosphoglucose isomerase by D-erythrose 4-phosphate

inferredcites →https://doi.org/10.1016/0076-6879(95)52025-2openalex-snapshot

[23] Measurement of equilibrium midpoint potentials of thiol/disulfide regulatory groups on thioredoxinactivated chloroplast enzymes

inferredcites →https://doi.org/10.1016/0304-4165(85)90004-2openalex-snapshot

A possible rate-limiting function of chloroplast hexosemonophosphate isomerase in starch synthesis of leaves

inferredcites →https://doi.org/10.1016/0926-6585(65)90170-6openalex-snapshot

Spectrophotometric characteristics of chlorophylls a and b and their phenophytins in ethanol

inferredcites →https://doi.org/10.1016/j.bbabio.2015.02.008openalex-snapshot

Diverse mechanisms for photoprotection in photosynthesis. Dynamic regulation of photosystem II excitation in response to rapid environmental change

inferredcites →https://doi.org/10.1016/j.bbabio.2015.07.012openalex-snapshot

Redox regulation of the antimycin A sensitive pathway of cyclic electron flow around photosystem I in higher plant thylakoids

inferredcites →https://doi.org/10.1016/j.envres.2005.01.003openalex-snapshot

Redox activity of airborne particulate matter at different sites in the Los Angeles Basin

inferredcites →https://doi.org/10.1016/j.febslet.2009.07.035openalex-snapshot

Redox regulation of chloroplastic glucose‐6‐phosphate dehydrogenase: A new role for f‐type thioredoxin

inferredcites →https://doi.org/10.1016/j.jplph.2012.05.008openalex-snapshot

Expression of Arabidopsis plastidial phosphoglucomutase in tobacco stimulates photosynthetic carbon flow into starch synthesis

inferredcites →https://doi.org/10.1016/s0021-9258(17)45210-0openalex-snapshot

Spontaneous and Enzymatically Catalyzed Anomerization of Glucose 6-Phosphate and Anomeric Specificity of Related Enzymes

inferredcites →https://doi.org/10.1016/s0021-9258(18)57258-6openalex-snapshot

THE ISOLATION AND PROPERTIES OF PHOSPHOGLUCOMUTASE

inferredcites →https://doi.org/10.1016/s0021-9258(18)91416-xopenalex-snapshot

A Kinetic Study of the Phosphoglucomutase Pathway

inferredcites →https://doi.org/10.1016/s0021-9258(18)93559-3openalex-snapshot

The Effect of pH and Temperature on the Kinetic Parameters of Phosphoglucose Isomerase

inferredcites →https://doi.org/10.1016/s0021-9258(19)85788-5openalex-snapshot

Kinetic mechanism of glucose-6-phosphate dehydrogenase from the lactating rat mammary gland. Implications for regulation.

inferredcites →https://doi.org/10.1016/s0140-6736(08)60073-2openalex-snapshot

Glucose-6-phosphate dehydrogenase deficiency

inferredcites →https://doi.org/10.1016/s0168-9452(97)00208-2openalex-snapshot

Competitive inhibition of spinach leaf phosphoglucose isomerase isoenzymes by erythrose 4-phosphate

inferredcites →https://doi.org/10.1016/s0969-2126(00)00104-0openalex-snapshot

Human glucose-6-phosphate dehydrogenase: the crystal structure reveals a structural NADP + molecule and provides insights into enzyme deficiency

inferredcites →https://doi.org/10.1021/bi982783vopenalex-snapshot

Oxidation-Reduction Properties of Chloroplast Thioredoxins, Ferredoxin:Thioredoxin Reductase, and Thioredoxin f-Regulated Enzymes

inferredcites →https://doi.org/10.1021/bi9916731openalex-snapshot

Oxidation−Reduction Properties of the Regulatory Disulfides of Sorghum Chloroplast Nicotinamide Adenine Dinucleotide Phosphate−Malate Dehydrogenase

inferredcites →https://doi.org/10.1034/j.1399-3054.2000.1100304.xopenalex-snapshot

Oxidation-reduction properties of thioredoxins and thioredoxin-regulated enzymes

inferredcites →https://doi.org/10.1038/nature02598openalex-snapshot

Cyclic electron flow around photosystem I is essential for photosynthesis

inferredcites →https://doi.org/10.1042/bj1680205openalex-snapshot

Midpoint redox potentials of plant and algal ferredoxins

inferredcites →https://doi.org/10.1042/bj2610457openalex-snapshot

Decreased-activity mutants of phosphoglucose isomerase in the cytosol and chloroplast of Clarkia xantiana. Impact on mass-action ratios and fluxes to sucrose and starch, and estimation of Flux Control Coefficients and Elasticity Coefficients

inferredcites →https://doi.org/10.1042/bj3180945openalex-snapshot

Starch degradation in chloroplasts isolated from C3 or CAM (crassulacean acid metabolism)-induced Mesembryanthemum crystallinum L

inferredcites →https://doi.org/10.1046/j.1365-3040.1999.00440.xopenalex-snapshot

Intramolecular deuterium distributions reveal disequilibrium of chloroplast phosphoglucose isomerase

inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00840.xopenalex-snapshot

Molecular characterization of a novel glucose‐6‐phosphate dehydrogenase from potato (Solanum tuberosum L.)

inferredcites →https://doi.org/10.1073/pnas.0810955106openalex-snapshot

Genomic basis for stimulated respiration by plants growing under elevated carbon dioxide

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/10.1074/jbc.m111.237438openalex-snapshot

Biochemical Characterization and Homology Modeling of Methylbutenol Synthase and Implications for Understanding Hemiterpene Synthase Evolution in Plants

inferredcites →https://doi.org/10.1093/jxb/ern008openalex-snapshot

Large-scale mRNA expression profiling in the common ice plant, Mesembryanthemum crystallinum, performing C3 photosynthesis and Crassulacean acid metabolism (CAM)

inferredcites →https://doi.org/10.1093/jxb/eru463openalex-snapshot

Photoprotection of photosystems in fluctuating light intensities

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/pcp/pch163openalex-snapshot

Enhancement of Cyclic Electron Flow Around PSI at High Light and its Contribution to the Induction of Non-Photochemical Quenching of Chl Fluorescence in Intact Leaves of Tobacco Plants

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.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.114.241091openalex-snapshot

Loss of Cytosolic Phosphoglucose Isomerase Affects Carbohydrate Metabolism in Leaves and Is Essential for Fertility of Arabidopsis

inferredcites →https://doi.org/10.1104/pp.114.4.1413openalex-snapshot

In Vivo and in Vitro Studies of Glucose-6-Phosphate Dehydrogenase from Barley Root Plastids in Relation to Reductant Supply for NO2- Assimilation

inferredcites →https://doi.org/10.1104/pp.123.1.319openalex-snapshot

Mutation of Arabidopsis Plastid Phosphoglucose Isomerase Affects Leaf Starch Synthesis and Floral Initiation

inferredcites →https://doi.org/10.1104/pp.53.6.835openalex-snapshot

Inactivation of Pea Leaf Chloroplastic and Cytoplasmic Glucose 6-Phosphate Dehydrogenases by Light and Dithiothreitol

inferredcites →https://doi.org/10.1104/pp.59.6.1146openalex-snapshot

Role of Orthophosphate and Other Factors in the Regulation of Starch Formation in Leaves and Isolated Chloroplasts

inferredcites →https://doi.org/10.1104/pp.66.5.815openalex-snapshot

Inhibition by Catalase of Dark-mediated Glucose-6-Phosphate Dehydrogenase Activation in Pea Chloroplasts

inferredcites →https://doi.org/10.1104/pp.83.2.399openalex-snapshot

Subcellular Metabolite Levels in Spinach Leaves

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.104.029124openalex-snapshot

The Arabidopsis Plastidic Glucose 6-Phosphate/Phosphate Translocator GPT1 Is Essential for Pollen Maturation and Embryo Sac Development

inferredcites →https://doi.org/10.1105/tpc.112.106989openalex-snapshot

Metabolic Fluxes in an Illuminated Arabidopsis Rosette

inferredcites →https://doi.org/10.1111/j.1365-3040.2011.02336.xopenalex-snapshot

ROS and redox signalling in the response of plants to abiotic stress

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.2011.04535.xopenalex-snapshot

Alternative targeting of Arabidopsis plastidic glucose‐6‐phosphate dehydrogenase G6PD1 involves cysteine‐dependent interaction with G6PD4 in the cytosol

inferredcites →https://doi.org/10.1111/j.1399-3054.2010.01437.xopenalex-snapshot

Photoinhibition of photosystem I

inferredcites →https://doi.org/10.1111/j.1432-1033.1974.tb03531.xopenalex-snapshot

Two Isoenzymes of Glucosephosphate Isomerase from Spinach Leaves and Their Intracellular Compartmentation

inferredcites →https://doi.org/10.1111/j.1438-8677.2010.00349.xopenalex-snapshot

The role of plastidial glucose‐6‐phosphate/phosphate translocators in vegetative tissues of Arabidopsis thaliana mutants impaired in starch biosynthesis

inferredcites →https://doi.org/10.1111/j.1742-4658.2012.08610.xopenalex-snapshot

The cofactor preference of glucose‐6‐phosphate dehydrogenase from Escherichia coli– modeling the physiological production of reduced cofactors

inferredcites →https://doi.org/10.1111/pce.12495openalex-snapshot

Acclimation of metabolism to light in A rabidopsis thaliana: the glucose 6‐phosphate/phosphate translocator GPT 2 directs metabolic acclimation

inferredcites →https://doi.org/10.1146/annurev.pp.31.060180.002013openalex-snapshot

Role of Light in the Regulation of Chloroplast Enzymes

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Applying an NMR-based metabolomic workflow to unveil strawberry molecular mechanisms in vernalization

inferred← citeshttps://doi.org/10.1016/j.plantsci.2019.110303openalex-snapshot

The plastid phosphorylase as a multiple-role player in plant metabolism

inferred← citeshttps://doi.org/10.1016/j.plaphy.2022.09.005openalex-snapshot

Metabolic regulation of α-Ketoglutarate associated with heat tolerance in perennial ryegrass

inferred← citeshttps://doi.org/10.1038/s41540-025-00505-1openalex-snapshot

Plant cold acclimation and its impact on sensitivity of carbohydrate metabolism

inferred← citeshttps://doi.org/10.1104/pp.19.01184openalex-snapshot

Glycogen Metabolism Supports Photosynthesis Start through the Oxidative Pentose Phosphate Pathway in Cyanobacteria

inferred← citeshttps://doi.org/10.1111/ppl.12962openalex-snapshot

Balancing energy supply during photosynthesis – a theoretical perspective

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.3390/plants14060978openalex-snapshot

Chloroplast Functionality at the Interface of Growth, Defense, and Genetic Innovation: A Multi-Omics and Technological Perspective

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