Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Of nucleotides

Oligonucleotides contain about 50 or fewer nucleotides held together by phosphodiester links polynucleotides can contain thousands of nucleotides... [Pg.1188]

Section 28 15 A rough draft of the sequence of nucleotides that make up the human genome has been completed There is every reason to believe that the increased knowledge of human biology it offers will dramatically affect the practice of medicine... [Pg.1189]

DNA from a gene contains hundreds to thousands of nucleotide units for which the sequence is needed in order to interpret its code. Sequencing methods require only small amounts (5 (tg) of purified DNA, which can be produced by cloning. Automated sequencers are available that can daily sequence DNA containing hundreds of nucleotide units. [Pg.329]

Genes are constructed from sets of deoxyribonucleic acids (DNA), which in turn consist of chains of nucleotides. These chains occur in matched pairs, twisted around each other (a double helix). [Pg.421]

A chain of nucleotides containing only deoxyribose as the sugar is a DNA. Similarly, RNA possesses chains nucleotides having only ribose as the sugar and is therefore a ribonucleic acid. [Pg.422]

Xanthine oxidase, mol wt ca 275,000, present in milk, Hver, and intestinal mucosa (131), is required in the cataboHsm of nucleotides. The free bases guanine and hypoxanthine from the nucleotides are converted to uric acid and xanthine in the intermediate. Xanthine oxidase cataly2es oxidation of hypoxanthine to xanthine and xanthine to uric acid. In these processes and in the oxidations cataly2ed by aldehyde oxidase, molecular oxygen is reduced to H2O2 (133). Xanthine oxidase is also involved in iron metaboHsm. Release of iron from ferritin requires reduction of Fe " to Fe " and reduced xanthine oxidase participates in this conversion (133). [Pg.387]

Cellular protein biosynthesis involves the following steps. One strand of double-stranded DNA serves as a template strand for the synthesis of a complementary single-stranded messenger ribonucleic acid (mRNA) in a process called transcription. This mRNA in turn serves as a template to direct the synthesis of the protein in a process called translation. The codons of the mRNA are read sequentially by transfer RNA (tRNA) molecules, which bind specifically to the mRNA via triplets of nucleotides that are complementary to the particular codon, called an anticodon. Protein synthesis occurs on a ribosome, a complex consisting of more than 50 different proteins and several stmctural RNA molecules, which moves along the mRNA and mediates the binding of the tRNA molecules and the formation of the nascent peptide chain. The tRNA molecule carries an activated form of the specific amino acid to the ribosome where it is added to the end of the growing peptide chain. There is at least one tRNA for each amino acid. [Pg.197]

Nucleic Acids. Nucleic acids are polynucleotides that is, they are condensation polymers of nucleotide monomers. A nucleotide is a three-component system, ie, a combination of a sugar, a phosphate, and a nitrogenous base residue. Adenosine monophosphate is an example ... [Pg.94]

Polymerization of nucleotides occurs through the sugar and phosphate groups so that the polymers consist of a sugar-phosphate backbone having pendent bases. [Pg.94]

The o-nitrobenzyl and p-nitrobenzyl ethers can b prepared and cleaved by many of the methods described for benzyl ethers. The p-nitrobenzyl ether is also prepared from an alcohol and p-nitrobenzyl alcohol (trifluoroacetic anhydride, 2,6-lutidine, CH2CI2, 67% yield). In addition, the o-nitrobenzyl ether can be cleaved by irradiation (320 nm, 10 min, quant, yield of carbohydrate " 280 nm, 95% yield of nucleotide ). The p-nitrobenzyl ether has been cleaved by electrolytic reduction (—1.1 V, DMF, R4N X, 60% yield) and by reduction with Na2S204 (pH 8-9, 80-95% yield). These ethers can also be cleaved oxidatively (DDQ or electrolysis) after reduction to the aniline derivative. ... [Pg.56]

Exonucleases. Like the endonucleases they are restriction enzymes which act at the 3 or 5 ends of linear DNA by hydrolysing off the nucleotides. Although they are highly specific for hydrolysing nucleotides at the 3 or 5 ends of linear DNA, the number of nucleotides cleaved are time dependent and usually have to be estimated from the time allocated for cleavage. Commercially available exonucleases are used without further purification. [Pg.533]

FIGURE 1.9 (a) Amino acids build proteins by connecting the n-carboxyl C atom of one amino acid to the n-amino N atom of the next amino acid in line, (b) Polysaccharides are built by combining the C-1 of one sugar to the C-4 O of the next sugar in the polymer, (c) Nucleic acids are polymers of nucleotides linked by bonds between the 3 -OH of the ribose ring of one nucleotide to the 5 -P04 of its neighboring nucleotide. All three of these polymerization processes involve bond formations accompanied by the elimination of water (dehydration synthesis reactions). [Pg.13]

Proteins are a diverse and abundant class of biomolecules, constituting more than 50% of the dry weight of cells. This diversity and abundance reflect the central role of proteins in virtually all aspects of cell structure and function. An extraordinary diversity of cellular activity is possible only because of the versatility inherent in proteins, each of which is specifically tailored to its biological role. The pattern by which each is tailored resides within the genetic information of cells, encoded in a specific sequence of nucleotide bases in DNA. [Pg.107]

Phosphate esters of glucose, fructose, and other monosaccharides are important metabolic intermediates, and the ribose moiety of nucleotides such as ATP and GTP is phosphorylated at the 5 -position (Figure 7.13). [Pg.219]


See other pages where Of nucleotides is mentioned: [Pg.188]    [Pg.283]    [Pg.2996]    [Pg.570]    [Pg.1181]    [Pg.1183]    [Pg.334]    [Pg.210]    [Pg.235]    [Pg.235]    [Pg.240]    [Pg.243]    [Pg.243]    [Pg.245]    [Pg.197]    [Pg.209]    [Pg.122]    [Pg.140]    [Pg.184]    [Pg.255]    [Pg.296]    [Pg.296]    [Pg.320]    [Pg.359]    [Pg.386]    [Pg.289]    [Pg.1011]    [Pg.1181]    [Pg.1183]    [Pg.10]    [Pg.32]    [Pg.32]    [Pg.142]    [Pg.327]   


SEARCH



A Selection of Cyclic Hydrogen-Bonding Patterns Formed in Nucleoside and Nucleotide Crystal Structures

Additional Functions of Nucleotides

Affinity Labeling of Nucleotide-Binding Sites

Alkylation of nucleotides

Aqueous Solutions of Nucleosides, Nucleotides, Polynucleotides, and DNA

Bases of nucleic acids, nucleosides and nucleotides

Be Learned from Crossover and Nonselectivity of Cyclic Nucleotide Action in the Intact Cell

Binding sites of nucleotides and inhibitors in

Biosynthesis of Nucleotide Diphospho 6-Deoxy Sugars

Biosynthesis of Pyrimidine Nucleotides

Biosynthesis of nucleotides

Biosynthesis of purine nucleotides

CE analysis of cyclic nucleotides

Cadmium(II) Complexes of Nucleotide Analogues

Cadmium(II) Complexes of Nucleotides

Catabolism of Nucleotides

Catabolism of purine nucleotides

Catabolism of pyrimidine nucleotides

Chemical Properties of L-Amino acids and 5-Nucleotides

Complex Formation of Cadmium with Sugar Residues, Nucleobases, Phosphates, Nucleotides, and Nucleic Acids

Coordination of Purine and Pyrimidine Nucleotide Biosynthesis

Crystal structures, of carbohydrates nucleosides, and nucleotides

De novo synthesis of purine nucleotides

Determination of nucleotide sequence

Effect of D-Fructose on the Nucleotide Pool in Liver

Enzymes of Nucleotide Modification

Esters glycopyranosyl, of nucleotides

Experiment 63 HPLC Separation of Nucleotides

Experiment 64 Ultraviolet Spectra of Nucleotides

Formation of Nucleotides from Bases and Nucleosides (Salvage Pathways)

Formation of Other Pyrimidine Nucleotides

Glycosyl esters, of nucleotides

Gradient Thin-Layer Chromatography of Nucleotides

Group-Transfer Reactions of Nucleotide Coenzymes

Guanine nucleotide activation of ternary

Guanine nucleotide activation of ternary complex

Hydrogen bonding of nucleotide base pairs

Hydrolysis of nucleotides

In situ Generation of Sugar Nucleotides

Influence of MSG and 5-Nucleotides on Aroma

Influence of MSG and 5-Nucleotides on Taste

Interconversion of Sugar Nucleotides

Laboratory Synthesis of Nucleosides and Nucleotides

Metabolism of Sugars and Sugar Nucleotides

Methylation, of nucleotides

Molecular Interactions of LLCs with Proteins and Nucleotides

Nucleosides and Nucleotides in the Presence of Growth Inhibitors

Nucleotide excision-repair of DNA

Nucleotide handles and specificity of metabolism

Nucleotide handles of coenzymes

Nucleotide sequence of DNA and RNA chains

Nucleotide sequence of M13mp7 7238 residues

Nucleotide sequence of aspartate aminotransferse

Nucleotide sequence of gene

Nucleotide sequence of genes and genomes

Nucleotide sequence of viruses

Nucleotides Constituents of Nucleic Acids

Of nucleosides and nucleotides

Oligonucleotides with Modifications of the Nucleotide-Linkage

Overview of Nucleotide Metabolism

Oxidation-reduction potentials of pyridine nucleotide system

Phosphate groups of nucleotides

Physiological Roles of Nicotinamide Nucleotide Transhydrogenases

Platination of Nucleotides and DNA

Polymerization of nucleotides

Reactions of Sugar-Derived Radicals in Nucleosides and Nucleotides

Recognition and Removal of Bulky DNA Lesions by the Nucleotide Excision Repair System

Recycling of Sugar Nucleotides in Enzymatic Glycosylation

Redox State of Mitochondrial Nicotinamide Nucleotides

Reducing Power —the Synthesis and Utilization of Pyridine Nucleotides

Reduction of nucleotides

Release of nucleotides and their derivatives

Roles of nucleotides

SATA Modification of Amines on Nucleotides

SPDP Modification of Amines on Nucleotides

Saccharides esters of nucleotides

Salvage synthesis of nucleotides

Separation of Nucleotides on Dowex Formate Columns

Separation of nucleotides

Signalling Functions of Pyridine Nucleotides

Sources of MSG and 5-Nucleotides

Structure of enzyme-bound nucleotides

Structures and Functions of Nucleotides

Structures of Nucleotides and Oligonucleotides

Synthesis of Cytidine Nucleotides

Synthesis of High-Energy Nucleotides

Synthesis of Nucleotides

Synthesis of Pyrimidine Nucleotides

Synthesis of Sugar Nucleotides

Synthesis of Thymidine Nucleotides

Synthesis of the Nicotinamide Nucleotide Coenzymes

Tautomers of nucleotide bases

Technologies for the Analysis of Single Nucleotide Polymorphisms—An Overview

The Anabolism of Pyrimidine Nucleotides

The Detection, Analysis and Chemistry of Sugar Nucleotides

The Determination of Nucleotide Sequences in DNA and RNA

The Determination of Nucleotide in DNA and RNA

The Discovery of Sugar Nucleotides

The Synthesis of Nicotinamide Nucleotides from Tryptophan

The existence of a purine nucleotide binding site on brown fat mitochondria

Tissue and Whole Blood Concentrations of Nicotinamide Nucleotides

Transfer of Energy Stored in Nucleotides

Transport of Adenine Nucleotides to and from Mitochondria

Triplets of nucleotides

Utilization of Energy Stored in Nucleotides

© 2024 chempedia.info