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Cellular genetic material

Moreover, the morpholino backbone s immunity to enzymatic attack avoids the potential for nonspecific interactions associated with degradation by-products. In contrast, modified nucleosides or nucleotides resulting from degradation of other antisense compounds might be toxic or might be incorporated into cellular genetic material and thereby lead to mutations or other undesired biologic effects. [Pg.373]

The results of the Ames test for mutagenesis Indicate that many ruthenium compounds Introduce serious lesions into cellular genetic material so that an error-prone DNA repair mechanism is Induced. These results are similar to those obtained for clsplatln (M) and suggest that these complexes probably bind directly to nuclear DNA. In concert with this, many of the ruthenium complexes also Inhibit cellular DNA synthesis (H, ), another property also noted for the cls-platlnum drugs. Unfortunately, however, there Is no correlation between either of these studies and the antitumor activity of ruthenium compounds tested In animal systems. [Pg.174]

Numerous cellular changes occur in the genetic material of the cancer cell so that programmed cell death, or apoptosis, does not occur. Proliferation of cancer cells goes unregulated. [Pg.1277]

The law of the minimum is easy to understand on a cellular, molecular, and atomic level and is applicable to all organisms. Organisms cannot grow by producing partial cells and to produce a whole cell they must have all the constituents in the correct proportion, ft is not possible to have a functioning cell that does not have a complete cell membrane, complete genetic material, functional mitochondria, and all the other parts of a functioning cell. [Pg.23]

The last term in equation 5.245 represents the dilution of active component /, by the expansion of the biomass. Esener et al.m also present a two-compartment model which takes this effect into account and they emphasise the need to devise the theory so that it can be tested by experiment. In their model they identify a K compartment of the biomass which comprised the RNA and other small cellular molecules. The other compartment contained the larger genetic material, enzymes, and structural material. The model assumes that the substrate is absorbed by the cell to produce, in the first instance, K material, and thence it is transformed into G material. Additionally, the G material can be reconverted to K material, a feature intended to account for the maintenance requirement of the micro-organism. A series of material balances for the cellular components during growth in a CSTF produced the following differential equations ... [Pg.401]

Cells are able to synthesize genetic material (DNA, RNA) from endogenous metabolites known as purine and pyrimidine nucleotides (Fig. 36-3). Certain anticancer drugs are structurally similar to these endogenous metabolites and compete with these compounds during DNA/RNA biosynthesis. These drugs are therefore called antimetabolites because they interfere with the normal metabolites during cellular biosynthesis.16,80... [Pg.569]

Eukaryotic cell Advanced cell type with a nuclear membrane surrounding genetic material and numerous membrane-bound organelles dispersed in a complex cellular structure see Eukaryotes. Volume 1(8). [Pg.389]

The synthesis of secondary metabolites requires materials in the form of atoms that compose the secondary metabolites, energy to form covalent bonds between the atoms, the enzymes that carry out the formation reactions, the genetic material that codes and synthesizes the enzymes, and the cellular machinery that maintains pH, ionic strength, and redox potentials within a range that allow enzymes to function properly.85 Some materials such as hydrogen and oxygen are readily available and cheap, and contribute little to the material cost of synthesis. Other materials such as phosphorus and nitrogen are of limited supply in many marine habitats.86 The use of these rare materials in secondary metabolites is probably costly as they limit many primary metabolic pathways, which helps explain the rarity of secondary metabolites that contain N or P.2 Fixed carbon... [Pg.331]


See other pages where Cellular genetic material is mentioned: [Pg.926]    [Pg.927]    [Pg.38]    [Pg.309]    [Pg.1375]    [Pg.5]    [Pg.597]    [Pg.926]    [Pg.927]    [Pg.38]    [Pg.309]    [Pg.1375]    [Pg.5]    [Pg.597]    [Pg.129]    [Pg.25]    [Pg.206]    [Pg.1284]    [Pg.31]    [Pg.943]    [Pg.1278]    [Pg.23]    [Pg.439]    [Pg.132]    [Pg.421]    [Pg.428]    [Pg.38]    [Pg.105]    [Pg.451]    [Pg.151]    [Pg.19]    [Pg.55]    [Pg.465]    [Pg.472]    [Pg.667]    [Pg.337]    [Pg.29]    [Pg.29]    [Pg.628]    [Pg.176]    [Pg.126]    [Pg.143]    [Pg.226]    [Pg.500]    [Pg.52]    [Pg.306]    [Pg.236]    [Pg.144]    [Pg.122]    [Pg.4]   
See also in sourсe #XX -- [ Pg.597 ]




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