Search results for "Glyceric acid"

showing 7 items of 7 documents

Overexpression of the triose phosphate translocator (TPT) complements the abnormal metabolism and development of plastidial glycolytic glyceraldehyde…

2017

The presence of two glycolytic pathways working in parallel in plastids and cytosol has complicated the understanding of this essential process in plant cells, especially the integration of the plastidial pathway into the metabolism of heterotrophic and autotrophic organs. It is assumed that this integration is achieved by transport systems, which exchange glycolytic intermediates across plastidial membranes. However, it is unknown whether plastidial and cytosolic pools of 3-phosphoglycerate (3-PGA) can equilibrate in non-photosynthetic tissues. To resolve this question, we employed Arabidopsis mutants of the plastidial glycolytic isoforms of glyceraldehyde-3-phosphate dehydrogenase (GAPCp)…

0106 biological sciences0301 basic medicineMutantArabidopsisDehydrogenasePlant ScienceGlyceric Acids01 natural sciences03 medical and health sciencesGeneticsGlycolysisPlastidsPlastidGlyceraldehyde 3-phosphate dehydrogenasebiologyArabidopsis ProteinsGlyceraldehyde-3-Phosphate DehydrogenasesCell BiologyMetabolismCytosol030104 developmental biologyBiochemistryTriose phosphate translocatorbiology.proteinGlycolysis010606 plant biology & botanyThe Plant journal : for cell and molecular biology
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Phosphoglycerate Kinases Are Co-Regulated to Adjust Metabolism and to Optimize Growth

2017

[EN] In plants, phosphoglycerate kinase (PGK) converts 1,3-bisphosphoglycerate into 3-phosphoglycerate in glycolysis but also participates in the reverse reaction in gluconeogenesis and the Calvin-Benson cycle. In the databases, we found three genes that encode putative PGKs. Arabidopsis (Arabidopsis thaliana) PGK1 was localized exclusively in the chloroplasts of photosynthetic tissues, while PGK2 was expressed in the chloroplast/plastid of photosynthetic and nonphotosynthetic cells. PGK3 was expressed ubiquitously in the cytosol of all studied cell types. Measurements of carbohydrate content and photosynthetic activities in PGK mutants and silenced lines corroborated that PGK1 was the phot…

0106 biological sciences0301 basic medicinePhysiologyResearch Articles - Focus IssueMutantArabidopsisPlant ScienceGlyceric AcidsPlant Roots01 natural sciencesChloroplastGene03 medical and health sciencesCytosolGene Expression Regulation PlantArabidopsisGeneticsBIOQUIMICA Y BIOLOGIA MOLECULARMetabolomicsArabidopsis thalianaBamboo-Mosaic-VirusPlastidPhosphoglycerate kinaseGas-ChromatographybiologyArabidopsis ProteinsWild typefood and beveragesMetabolismArabidopsis-ThalianaPlant Components AerialPlants Genetically Modifiedbiology.organism_classificationHelianthus-Annuus L.3-Phosphoglycerate kinaseChloroplastPhosphoglycerate Kinase030104 developmental biologyBiochemistryMultigene FamilyMutationNicotiana-BenthamianaFISIOLOGIA VEGETALPlastics010606 plant biology & botanyPhosphorylating glyceraldehyde-3-phosphate dehydrogenaseGastric-Cancer
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On the Mechanistic Origins of the pH-Dependency in Au-Catalyzed Glycerol Electro-Oxidation: Insight from First Principles Calculations

2021

Electrocatalytic oxidation of glycerol (EOG) is an attractive approach to convert surplus glycerol to value-added products. Experiments have shown that EOG activity and selectivity depend on the electrocatalyst, but also on the electrode potential, the pH, and the electrolyte. For broadly employed gold (Au) electrocatalysts, experiments have demonstrated high EOG activity under alkaline conditions with glyceric acid as a primary product, whereas under acidic and neutral conditions Au is rather inactive producing only small amounts of dihydroxyacetone. In the present computational work, we have performed an extensive mechanistic study to understand the pH- and potential-dependency of Au-cata…

Glyceric acidchemistry.chemical_compoundReaction mechanismchemistryInorganic chemistryHydroxideDihydroxyacetoneSelectivityElectrocatalystRedoxElectrode potential
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Serine biosynthesis by photorespiratory and nonphotorespiratory pathways: and interesting interplay with unknown regulatory networks

2013

[EN] Photorespiration is a primary metabolic pathway, which, given its energy costs, has often been viewed as a wasteful process. Despite having reached the consensus that one important function of photorespiration is the removal of toxic metabolite intermediates, other possible functions have emerged, and others could well emerge in the future. As a primary metabolic pathway, photorespiration interacts with other routes; however the nature of these interactions is not well known. One of these interacting pathways could be the biosynthesis of serine, since this amino acid is synthesised through photorespiratory and non-photorespiratory routes. At present, the exact contribution of each rout…

LightCellular respirationCell RespirationGene regulatory networkPlant ScienceBiologyGlyceric AcidsSerinechemistry.chemical_compoundBiosynthesisSerineBIOQUIMICA Y BIOLOGIA MOLECULARGene Regulatory NetworksPhotosynthesisEcology Evolution Behavior and Systematicschemistry.chemical_classificationPhotorespirationGeneral MedicinePlantsGlycolatesAmino acidMetabolic pathwayGlycerate pathwayPhosphorylated pathwaychemistryBiochemistryPhotorespirationGlycolysisMetabolic Networks and PathwaysFunction (biology)Glycolate pathway
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Oxygen-haemoglobin dissociation curve in hypoxic rats of first or second generation.

1993

SUMMARY 1. Albino Wistar rats were raised in a normobaric hypoxic environment (10% O2 in N2). Two generations of hypoxic rats were observed for changes in their haemoglobin-oxygen (Hb-O2) dissociation curves (ODC), 2,3-diphosphoglycerate (2,3-DPG), haemoglobin (Hb), and Hill coefficients at P50 (n50). The first generation were called (H1) and the second generation (H2). The control group (N) had a normoxic environment. 2. Thirty-five rats (13 N rats, 12 H1 rats and 10 H2 rats) were used. The 2,3-DPG was significantly higher in both hypoxic groups when compared with N rats (2.02 ± 0.51 mmol/L) but 2,3-DPG of H2 rats was significantly lower than that of H1 rats (H1 = 3.48±0.58 mmol/L and H2 =…

Malemedicine.medical_specialtyP50PhysiologyHypoxic hypoxiaOxygenepCO2HemoglobinsPhysiology (medical)Internal medicineMolemedicineAnimalsRats WistarHypoxiacomputer.programming_languagePharmacology23-DiphosphoglycerateAcid-Base EquilibriumChemistryOxygen–haemoglobin dissociation curveCarbon DioxideDiphosphoglyceric AcidsRatsOxygenEndocrinologyTissue oxygenationBiochemistryFemaleHemoglobincomputerClinical and experimental pharmacologyphysiology
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Enzymatic Synthesis and Antimicrobial Activity of Oligomer Analogues of Medicinal Biopolymers from Comfrey and Other Species of the Boraginaceae Fami…

2022

This study reports the first enzymatic synthesis leading to several oligomer analogues of poly[3-(3,4-dihydroxyphenyl)glyceric acid]. This biopolymer, extracted from plants of the Boraginaceae family has shown a wide spectrum of pharmacological properties, including antimicrobial activity. Enzymatic ring opening polymerization of 2-methoxycarbonyl-3-(3,4-dibenzyloxyphenyl)oxirane (MDBPO) using lipase from Candida rugosa leads to formation of poly[2-methoxycarbonyl-3-(3,4-dibenzyloxyphenyl)oxirane] (PMDBPO), with a degree of polymerization up to 5. Catalytic debenzylation of PMDBPO using H2 on Pd/C yields poly[2-methoxycarbonyl-3-(3,4-dihydroxyphenyl)oxirane] (PMDHPO) without loss in molecul…

RS1-441Poly[3-(34-dihydroxyphenyl)glyceric acid]Pharmacy and materia medicapoly[3-(34-dihydroxyphenyl)glyceric acid]; enzymatic polymerization; lipase; antimicrobial activity; Boraginaceae familyBoraginaceae familyPharmaceutical ScienceLipaseAntimicrobial activityArticleEnzymatic polymerization
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Differential function of the phosphoglucomutase isozymes PGM1 and PGM2

1979

A total of 13 metabolites thought to be possibly inhibitory were tested for their influence on PGM isozyme activities, each at several different concentrations. The analysis of statistical significance was based on enzyme activities obtained by densitometric measurements of starch gels. Five of the substances were found to inhibit PGM activity, three of which definitely and a further one probably led to a significantly stronger inhibition of the isozymes of the PGM2 locus than of PGM1 isozymes. They are (1) fructose-1,6-diphosphate, (2) adenosine triphosphate, (3) citrate, and (4) possibly 2,3-diphosphoglycerate. Thus, PGM1 isozymes proved to function better in hard or perhaps marginal meta…

chemistry.chemical_classificationStarchChromosome MappingLocus (genetics)BiologyDiphosphoglyceric AcidsMolecular biologyIsozymeIsoenzymeschemistry.chemical_compoundAdenosine TriphosphateEnzymeGenesPhosphoglucomutasechemistryBiochemistryPGM1FructosediphosphatesGeneticsHumansPhosphoglucomutaseCitratesAdenosine triphosphateGeneGenetics (clinical)Human Genetics
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