Search results for "PHOSPHATE"

showing 10 items of 1874 documents

Purification and characterization of the catabolic ?-acetolactate synthase from Leuconostoc mesenteroides subsp. cremoris

1995

The α-acetolactate synthase from Leuconostoc mesenteroides subsp. cremoris was purified to homogeneity in SDS-PAGE. The enzyme is a trimer of 3×55,000 Da. It was unstable but could be preserved by addition of pyruvate and thiamine pyrophosphate in the buffer. The enzyme exhibits Michaelis-Menten kinetics, and Km for pyruvate is 10 mM. Three intermediates in glucose metabolism (ATP, 3-phosphoglycerate, and phosphoenolpyruvate) exhibit a noncompetitive inhibition towards the enzyme. This enzyme does not require any divalent metal ion for activity. The α-acetolactate synthase from Leuconostoc mesenteroides subsp. cremoris is not inhibited by the branched-chain amino acids (valine, leucine, and…

Acetolactate synthasebiologyATP synthaseGeneral Medicinebiology.organism_classificationApplied Microbiology and BiotechnologyMicrobiologychemistry.chemical_compoundNon-competitive inhibitionchemistryBiochemistryBiosynthesisValineLeuconostoc mesenteroidesbiology.proteinIsoleucineThiamine pyrophosphateCurrent Microbiology
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Application of the General Model "Biological Nutrient Removal Model No.1" to upgrade two full-scale WWTPs

2012

In this paper, two practical case studies for upgrading two wastewater treatment plants (WWTPs) using the general model BNRM1 (Biological Nutrient Removal Model No. 1) are presented. In the first case study, the Tarragona WWTP was upgraded by reducing the phosphorus load to the anaerobic digester in order to minimize the precipitation problems. Phosphorus load reduction was accomplished by mixing the primary sludge and the secondary sludge and by elutriating the mixed sludge. In the second case study, the Alcantarilla WWTP, the nutrient removal was enhanced by maintaining a relatively low dissolved oxygen concentration in Stage A to maintain the acidogenic bacteria activity. The VFA produce…

AcidogenesisBiological nutrient removalWATER TREATMENT PLANTSAerobic bacteriachemistry.chemical_elementActivated sludge modelPhosphatesWater PurificationWASTE-WATERBNRM1Environmental ChemistryAnaerobiosisOrganic ChemicalsWaste Management and DisposalTECNOLOGIA DEL MEDIO AMBIENTEWater Science and TechnologyCALIBRATIONSewagePhosphorusEnvironmental engineeringGeneral MedicineModels TheoreticalASM2DAerobiosisACTIVATED-SLUDGE MODELActivated sludge modelsEnhanced biological phosphorus removalWastewaterchemistrySIMULATIONPlant-wide mathematical modellingEnvironmental scienceSewage treatmentWater treatmentSanitary EngineeringWWTP upgrading
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Isoquercitrin and polyphosphate co-enhance mineralization of human osteoblast-like SaOS-2 cells via separate activation of two RUNX2 cofactors AFT6 a…

2014

Isoquercitrin, a dietary phytoestrogen, is a potential stimulator of bone mineralization used for prophylaxis of osteoporotic disorders. Here we studied the combined effects of isoquercitrin, a cell membrane permeable 3-O-glucoside of quercetin, and polyphosphate [polyP], a naturally occurring inorganic polymer inducing bone formation, on mineralization of human osteoblast-like SaOS-2 cells. Both compounds isoquercitrin and polyP induce at non-toxic concentrations the mineralization process of SaOS-2 cells. Co-incubation experiments revealed that isoquercitrin (at 0.1 and 0.3μM), if given simultaneously with polyP (as Ca(2+) salt; at 3, 10, 30 and 100μM) amplifies the mineralization-enhanci…

Activating transcription factorBiochemistryProto-Oncogene Protein c-ets-103 medical and health sciences0302 clinical medicineCalcification PhysiologicPolyphosphatesCell Line TumormedicineHumansSaos-2 cells030304 developmental biologyPharmacology0303 health sciencesOsteoblastsbiologyATF6OsteoblastDrug SynergismActivating Transcription Factor 6RUNX2medicine.anatomical_structureBiochemistryGene Expression Regulation030220 oncology & carcinogenesisOsteocalcinbiology.proteinAlkaline phosphataseCalciumQuercetinSignal transductionBiochemical pharmacology
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Modeling ATP protonation and activity coefficients in NaClaq and KClaq by SIT and Pitzer equations.

2006

Abstract The acid–base properties of Adenosine 5′-triphosphate (ATP) in NaCl and KCl aqueous solutions at different ionic strengths (0  I  / mol L − 1  ≤ 5 for NaCl aq , 0  I  / mol L − 1  ≤ 3 for KCl aq ) and at t  = 25 °C were investigated. A selection of literature data on ATP protonation constants and on activity isopiestic coefficients was performed, together with new potentiometric measurements (by ISE-H + , glass electrode). Both literature and new experimental data were used to model the dependence on ionic strength and ionic medium of ATP protonation by SIT (Specific ion Interaction Theory) and Pitzer equations. In addition to values of first and second ATP protonation constants in…

Activity coefficientMolar concentrationactivity coefficientsActivity coefficientPotentiometric titrationInorganic chemistryBiophysicsIonic bondingProtonationProtonationATP; protonation; activity coefficients; Dependence on medium and ionic strength; SIT model; Pitzer modelSodium ChlorideBiochemistryPotassium ChlorideAdenosine TriphosphateElectrochemistrySettore CHIM/01 - Chimica AnaliticaChemistryOrganic ChemistryOsmolar ConcentrationPitzer modelSIT modelATPSpecific ion interaction theoryIonic strengthDependence on medium and ionic strengthPhysical chemistryPitzer equationsBiophysical chemistry
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Novel mutations of the MET proto-oncogene in papillary renal carcinomas.

1999

Hereditary papillary renal carcinoma (HPRC) is characterized by multiple, bilateral papillary renal carcinomas. Previously, we demonstrated missense mutations in the tyrosine kinase domain of the MET proto-oncogene in HPRC and a subset of sporadic papillary renal carcinomas. In this study, we screened a large panel of sporadic papillary renal carcinomas and various solid tumors for mutations in the MET proto-oncogene. Summarizing these and previous results, mutations of the MET proto-oncogene were detected in 17/129 sporadic papillary renal carcinomas but not in other solid tumors. We detected five novel missense mutations; three of five mutations were located in the ATP-binding region of t…

AdenomaModels MolecularCancer ResearchProtein ConformationDNA Mutational AnalysisMolecular Sequence DataHereditary Papillary Renal Cell CarcinomaBiologymedicine.disease_causeTransfectionProto-Oncogene MasReceptor tyrosine kinaseMiceAdenosine TriphosphateNeoplastic Syndromes HereditaryProto-OncogenesGeneticsCarcinomamedicineMissense mutationAnimalsHumansPoint MutationAmino Acid SequencePhosphorylationCodonMolecular BiologyKidneyMutationBinding SitesSequence Homology Amino AcidPoint mutation3T3 CellsDNA NeoplasmProto-Oncogene Proteins c-metmedicine.diseaseCarcinoma PapillaryKidney NeoplasmsNeoplasm Proteinsmedicine.anatomical_structureCell Transformation NeoplasticCancer researchbiology.proteinMutagenesis Site-DirectedTyrosine kinaseProtein Processing Post-TranslationalSequence AlignmentOncogene
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Nested MWC model describes hydrolysis of GroEL without assuming negative cooperativity in binding

2002

Folding assistance and ATPase activity of GroEL are based on the existence of different conformations. In order to characterise these conformations, published data on steady state ATPase activity in the absence of GroES were reanalysed simultaneously in terms of the Nested MWC model. This model is a hierarchical extension of the symmetry-model of Monod et al. [J. Mol. Biol. 12 (1965) 88]. An unique set of GroEL specific parameters was obtained. This set was supported by comparison of predictions arising from this set of values with experimental data for hydrolysis of ATP in the presence of ADP and ATPgammaS, binding of ATPgammaS and ADP to GroEL in the absence of ATP, and binding of ATP as …

Adenosine TriphosphatasesModels Molecularchemistry.chemical_classificationChemistryHydrolysisBiophysicsCooperative bindingCooperativityChaperonin 60GroESBiochemistryGroELAnalytical ChemistryAdenosine DiphosphateFolding (chemistry)CrystallographyAdenosine TriphosphateATP hydrolysisCalibrationBiophysicsComputer SimulationNucleotideSteady state (chemistry)Molecular BiologyProtein BindingBiochimica et Biophysica Acta (BBA) - Proteins and Proteomics
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Membrane-Bound F1 ATPase from Micrococcus Sp. ATCC 398E. Purification and Characterization by Affinity Chromatography

1976

A chemically reactive ATP analogue, 6-[(3-carboxy-4-nitrophenyl)thio]-9-β-D-ribofuranosylpurine 5′-triphosphate (Nbs6ITP) has been synthesized. It has the ability to form stable thioether bonds between the 6-position of the purine ring and aliphatic mercapto groups. The nucleotide moiety of the reagent has been covalently bound to agarose, via iminobispropylamine and N-acetyl-homocysteine as spacer with the purpose of producing an affinity chromatography material. The affinity matrix binds solubilized F1 ATPase from a crude extract of Micrococcus sp. membranes. Afterwards the enzyme can be selectively eluted from the column at a defined ATP concentration. This method is superior to the conv…

Adenosine Triphosphataseschemistry.chemical_classificationBinding SitesChromatographybiologyStereochemistryATPaseThio-BiochemistryChromatography AffinityMicrococcuschemistry.chemical_compoundAdenosine TriphosphateMembranechemistryAffinity chromatographybiology.proteinAgaroseMoietyMagnesiumNucleotideNucleosideProtein BindingEuropean Journal of Biochemistry
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Measuring single small molecule binding via rupture forces of a split aptamer.

2011

The rupture force of a split (bipartite) aptamer that forms binding pockets for adenosine monophosphate (AMP) was measured by atomic force spectroscopy. Changes in the rupture force were observed in the presence of AMP, while this effect was absent when mutant aptamers or inosine were used. Thus, changes in the rupture force were a direct consequence of specific binding of AMP to the split aptamer. The split aptamer concept allowed the detection of nonlabeled AMP and enabled us to determine the dissociation constant on a single-molecule level.

Adenosine monophosphateChemistryAptamerForce spectroscopyGeneral ChemistryPlasma protein bindingAptamers NucleotideMicroscopy Atomic ForceBiochemistryCatalysisAdenosine MonophosphateDissociation constantCrystallographychemistry.chemical_compoundColloid and Surface ChemistrymedicineDirect consequenceSmall molecule bindingInosinemedicine.drugProtein BindingJournal of the American Chemical Society
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The compensatory regeneration of the operculum ofHydroides norvegica: Identification of the inhibiting substance

1973

In the polychete Hydroides norvegica there are two opercula with different degrees of organization: one is completely developed and functional, the other, present only in rudimentary outline. The latter only begins to develop when the functional operculum is removed. It was observed that in the whole body of the Hydroides, but particularly in the functional operculum, there is a substance which inhibits the development of the rudimental operculum. This substance was purified in order to determine its chemical nature. From preparation of opercular homogenates we chemically separated numerous fractions, each of which was tested for inhibitory activity and chemical and physical properties. The…

Adenosine monophosphateCompensatory regenerationHeat resistantbiologyGeneral MedicineAnatomybiology.organism_classificationHydroides norvegicachemistry.chemical_compoundchemistryBiochemistryvisual_artHydroidesvisual_art.visual_art_mediumAnimal Science and ZoologyWhole bodyOperculum (gastropod)Journal of Experimental Zoology
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Coordination properties of adenosine-5'-monophosphate and related ligands towards Me2Sn(IV)2+ in aqueous solution.

2002

Abstract The coordination of Me 2 Sn(IV) 2+ to adenosine-5′-monophosphate (AMP) and the related compounds d -ribose-5-phosphate (R5P), d -glucose-1-phosphate (G1P) and d -glucose-6-phosphate (G6P) in aqueous solution was investigated by means of potentiometric titration, and 1 H-, 31 P-NMR and Mossbauer spectroscopic methods in the pH range 2–11 ( I =0.1 M NaClO 4 , 298 K). The complex of AMP and Me 2 Sn(IV) 2+ precipitated at low pH was characterised by elemental analysis, FT-IR and Mossbauer spectroscopic methods. From a comparison of the p K values obtained in the presence and absence of metal ion and the stability constants for the different systems, the coordination of {N} is excluded,…

Adenosine monophosphateDenticityMagnetic Resonance SpectroscopyPotentiometric titrationInorganic chemistryMolecular Sequence DataLigandsBiochemistryInorganic ChemistryMetalchemistry.chemical_compoundSpectroscopy MossbauerDeprotonationMössbauer spectroscopySpectroscopy Fourier Transform InfraredOrganotin CompoundsAqueous solutionMolecular StructureHydrolysisGlucosephosphatesDNAHydrogen-Ion ConcentrationPhosphateAdenosine MonophosphateSolutionsCrystallographychemistryvisual_artvisual_art.visual_art_mediumPotentiometryThermodynamicsJournal of inorganic biochemistry
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