Search results for "Guano"

showing 10 items of 193 documents

Presence of phosphorylatedO-ribosyl-adenosine In T-ψ-stem of yeast methlonine initiator tRNA

1989

We report in this paper on isolation and characterization of two unknown nucleosides G* and [A*] located in the T-psi-stem of yeast methionine initiator tRNA, using the combined means of HPLC protocols, real time UV-absorption spectrum, and post-run mass spectrometry by electron impact or fast atom bombardment. The G* nucleoside in position 65 was identified as unmodified guanosine. The structure of the unknown [A*] in position 64 was characterized as an isomeric form of O-ribosyl-adenosine by comparison of its chromatographic, UV-spectral and mass spectrometric properties with those of authentic O-alpha-ribofuranosyl-(1"----2')-adenosine isolated from biosynthetic poly(adenosine diphosphat…

Poly Adenosine Diphosphate RiboseAdenosineRNA Transfer MetIon chromatographySaccharomyces cerevisiaeGuanosineSaccharomyces cerevisiaeBiologyChromatography DEAE-CelluloseGas Chromatography-Mass Spectrometrychemistry.chemical_compoundMethionineGeneticsmedicinePhosphorylationChromatography High Pressure LiquidGuanosineAdenosine diphosphate riboseNucleosidesRNA Transfer Amino Acid-SpecificFast atom bombardmentbiology.organism_classificationAdenosineYeastchemistryBiochemistryNucleic Acid ConformationNucleosidemedicine.drugNucleic Acids Research
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Stereoselective Metabolic Activation of Dibenzo[a,l]Pyrene in the Human Mammary Carcinoma Cell Line MCF-7 Results in Formation of (-)-antiand (+)-syn…

1996

Abstract Dibenzo[a,l]pyrene (DB[a,l]P) is an important polycyclic aromatic hydrocarbon because of possible human exposure and its exceptionally high carcinogenicity in rodents. We examined the metabolism of DB[a,l]P and the formation of DB[a,l]P-DNA adducts in the human mammary carcinoma cell line (MCF-7). Analysis of the DNA adducts by 33P-postlabeling, immobilized boronate chromatography, HPLC and TLC demonstrated that DB[a,l]P is stereoselectively metabolized to specific optical isomers of DB[a,l]P-11,12-diol-13,14-epoxide (DB[a,l]PDE). The major anti-DB[a,l]PDE adduct formed in DB[a,l]P-treated MCF-7 cells resulted from reaction of (-)-anti-DB[a,l]PDE with DNA whereas the two major syn-…

Polymers and PlasticsChemistryStereochemistryOrganic ChemistryDiolAdductchemistry.chemical_compoundDeoxyadenosineMaterials ChemistryPyreneDeoxyguanosineheterocyclic compoundsStereoselectivitysense organsCarcinogenDNAPolycyclic Aromatic Compounds
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Spectroscopic Studies of Oligonucleotide Adducts and Base Sequence Preference of Adducts Formed by the Stereoisomers of 7,8-Dihydroxy-9,10-epoxy-7,8,…

1996

Abstract 5′-d(CCTATAGATATCC) has been reacted with BPDE and the adducts derived from binding of BPDE to the exocyclic amino group of deoxyguanosine (dG) were studied with spectroscopic methods. The major dG-adducts of (+)- and (-)-anti-BPDE and a minor adduct of (+)-syn-BPDE showed the characteristics of trans-adducts. The major products formed with (+)- and (-)-syn-BPDE exhibit cis-adduct characteristics. Annealing of BPDE-modified oligonucleotides to complementary or partially complementary strands results in reduced fluorescence intensity in several cases and in others the intensity is markedly increased. These differences demonstrate that the adduct microenvironment is strongly influenc…

Polymers and PlasticsOligonucleotideStereochemistryOrganic ChemistryEpoxyPhotochemistryAdductchemistry.chemical_compoundchemistryDuplex (building)visual_artpolycyclic compoundsMaterials Chemistryvisual_art.visual_art_mediumPyreneDeoxyguanosineThermal stabilityBase sequencePolycyclic Aromatic Compounds
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Changes in the proteome of sea urchin Paracentrotus lividus coelomocytes in response to LPS injection into the body cavity.

2020

Background The immune system of echinoderm sea urchins is characterised by a high degree of complexity that is not completely understood. The Mediterranean sea urchin Paracentrotus lividus coelomocytes mediate immune responses through phagocytosis, encapsulation of non-self particles, and production of diffusible factors including antimicrobial molecules. Details of these processes, and molecular pathways driving these mechanisms, are still to be fully elucidated. Principal findings In the present study we treated the sea urchin P. lividus with the bacterial lipopolysaccharide (LPS) and collected coelomocytes at different time-points (1, 3, 6 and 24 hours). We have shown, using label-free q…

ProteomicsLipopolysaccharidesProteomeHydrolasesBiochemistry0302 clinical medicineParacentrotusMedicine and Health SciencesSea urchinCoelomocyteImmune ResponseCytoskeleton0303 health sciencesPhagocytesMultidisciplinarybiologyChemistryQREukaryotaAnimal ModelsCell biologyEnzymesEchinodermExperimental Organism Systems030220 oncology & carcinogenesisProteomeParacentrotusMedicineProtein Interaction NetworksCellular Structures and OrganellesNetwork AnalysisResearch ArticleEchinodermsComputer and Information Sciencesfood.ingredientScienceImmunologyLipopolysaccharideEndocytosisResearch and Analysis MethodsParacentrotus lividusLymphatic System03 medical and health sciencesfoodPhagocytosisbiology.animalHeat shock proteinDNA-binding proteinsAnimalsProtein Interactions030304 developmental biologyPhagocytosiAnimalOrganismsBiology and Life SciencesProteinsCell Biologybiology.organism_classificationInvertebratesCytoskeletal ProteinsGuanosine TriphosphataseProtein-Protein InteractionsPhagocyteImmune SystemSea UrchinsAnimal StudiesEnzymologyParacentrotuPLoS ONE
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Hydrogen bonding patterns of 7,9-dimethylguanine and its transplatinum(II) complexes

2002

Methylation at the N7 position is one of the most frequently naturally occurring modifications of guanosine. This alteration drastically changes the hydrogen bonding and acid–base properties of the guanine nucleobase. Here we show on the example of the model nucleobase 7,9-dimethylguanine that due to blockage of N7 of the purine ring, new hydrogen bonding patterns occur on the minor groove binding face of this nucleobase involving the ring nitrogen N3 and the exocyclic amino group N2H2. The free 7,9-dimethylguaninium ion and several transplatinum(II) complexes of the this ligand are presented and discussed. Methylation at N7 drastically changes the acid–base and hydrogen bonding properties …

Purine10120 Department of ChemistryTransplatinumLigandStereochemistryGuanineHydrogen bond1604 Inorganic ChemistryInorganic chemistryGuanosineRing (chemistry)Nucleobase complexeNucleobaseIonHydrogen bondsInorganic Chemistrychemistry.chemical_compoundchemistryModified nucleobaseSettore CHIM/03 - Chimica Generale E Inorganica540 ChemistryMaterials ChemistryPhysical and Theoretical Chemistry1606 Physical and Theoretical Chemistry2505 Materials Chemistry
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Differential changes in purine nucleotides after Doxorubicin treatment of human cancer cells in vitro

2002

The present investigation was performed to elucidate the role of purine nucleotides as potential indicators of chemosensitivity of malignant tumors. Drug-sensitive (s) and -resistant (r) tumor cell lines grown as monolayers (s: T47D, MCF-7 wild-type; r: NCI/ADR-RES, MCF-7/MDR) or as multicellular spheroids (T47D; NCI/ADR-RES) were exposed to 0.1, 1.0, and 10.0 microM Doxorubicin for up to 24 h. Purine nucleotides were assayed using HPLC and with some selected spheroids using imaging bioluminescence. The data show that in the time frame of the experiments reproducible and statistically significant changes in the nucleotides only occur at the highest drug concentration investigated. Under the…

PurineCancer ResearchOligomycinGTP'Antineoplastic AgentsIn Vitro TechniquesBiologychemistry.chemical_compoundAdenosine TriphosphateIn vivoSpheroids CellularTumor Cells CulturedmedicineHumansNucleotideDoxorubicinATP Binding Cassette Transporter Subfamily B Member 1Chromatography High Pressure Liquidchemistry.chemical_classificationBiological activityMolecular biologyDrug Resistance MultipleIn vitroOncologyBiochemistrychemistryDoxorubicinDrug Resistance NeoplasmLuminescent MeasurementsGuanosine Triphosphatemedicine.drugInternational Journal of Oncology
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IV. An Improved Separation Method for Twenty two Compounds Related to Purine and 6-Thiopurine Metabolism Using High-Pressure Liquid Cation-Exchange C…

1977

Abstract An improved method is described for the separation of 22 compounds normally related to purine and 6-thiopurine metabolism in biological materials using high-pressure liquid cation-exchange chromatography on strongly acidic exchange resin. The column (0.18 × 100 cm) is eluted with 0.4 ᴍ ammonium formate, pH 4.6, at a linear flow velocity of 5.2 cm · min-1 at 50 °C. The elution volumes of sulphate anions, allopurinol, 6-thioxanthine, adenine, adenosine, and guanosine are demonstrated additionally to further 16 purine and 6-thiopurine compounds.

PurineChromatographyChemistryElutionIon chromatographyGuanosineAllopurinolMetabolismAdenosineGeneral Biochemistry Genetics and Molecular Biologychemistry.chemical_compoundmedicineAmmonium formatemedicine.drugZeitschrift für Naturforschung C
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Extreme nucleoside concentrations in a marine annelid: a novel nucleoside storing cell in the polychaete Nereis virens.

2010

A new type of free coelomic cell was isolated from the coelomic fluid of the polychaete Nereis virens. This cell type was present only during sexual maturation and only in males with fully developed spermatozoa. In vivo acridine orange staining and electron microscopy showed that this cell type consists mainly of a large acidic vacuole with a very low proportion of cytoplasm. This cell type stores extremely high concentration of purine nucleosides reaching concentrations of >700 millimolar on a cell weight basis. The nucleoside concentrations are the highest reported from any living cell so far. Inosine (280-711 micromol/g cell mass), guanosine (8-109 micromol/g), deoxyinosine (3-26 micromo…

PurineMalePhysiologyGuanosineVacuoleBiologyBiochemistrychemistry.chemical_compoundmedicineDeoxyguanosineAnimalsInosineMolecular BiologyLife Cycle StagesGuanosineNucleotidesAcridine orangeNucleosidesPolychaetaInosinechemistryBiochemistryCytoplasmVacuolesNucleosidemedicine.drugComparative biochemistry and physiology. Part B, Biochemistrymolecular biology
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Nucleoside uptake in male germ cells of the polychaeteNereis virens

1997

Summary Uptake of inosine and guanosine was measured in male germ ceils of the polychaete Nereis virens at different stages of development. In spermatogonia I (spg I) and spermatid stages, total inosine uptake at 12°C and ambient concentrations of 100 μmol/1 was relatively low (10–50 nmol·ml of packed cell volume pcv−l·h−1). A rapid increase (150–300 nmol·ml of pcv-1·h−1) was found during transition from spg I to spg II with a subsequent decline to low values (10–30 nmol·ml of pcv−1·h−1) in spermatocyte and spermatid stages. This transient increase may be related to the proliferative activity of spg I stages leading to spg II stages, which increases the demand of purine precursors for nucle…

PurineTransition (genetics)SpermatidGuanosineSpermatocyteBiologyMolecular biologychemistry.chemical_compoundmedicine.anatomical_structurechemistryBiochemistrymedicineNucleic acidAnimal Science and ZoologyInosineNucleosideDevelopmental Biologymedicine.drugInvertebrate Reproduction & Development
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Metabolite supply in oocytes of Nereis virens: role of nucleosides

1999

Gamete development in Nereis virens and other nereidid polychaetes is organized in a simple way. Follicular tissues are absent and the germ cells develop floating freely in the coelomic fluid, which thus serves as the vehicle for the supply of substances required for oocyte growth. This overview focusses on the role of exogenous purine nucleosides for the growing oocytes. Eleocytes, a coelomic cell type which is proliferated in large amounts at the beginning of sexual maturation, supply purine nucleosides to support nucleic acid synthesis in the oocytes. Eleocytes can store large amounts of purine nucleotides (up to 50 µ mol ml−1 cell vol.) in the form of AMP and ADP. During oogenesis, thes…

Purinechemistry.chemical_classificationGuanineGuanosineBiologychemistry.chemical_compoundchemistryBiochemistryAdenine nucleotidemedicineNucleic acidNucleotideInosineNucleosidemedicine.drug
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