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Eukaryotes defined

Eukaryotes, defined, 3 757t Eukaryotic cell biology, study of, 26 446 Eukaryotic chromosomes, 17 610 Euler equations, 11 742 Eulerian model, 11 822 Euler integration method, 20 688 Euler number, 11 745 23 190 Euphococcinine, 2 73 Euphorbiaceae, alkaloids in, 2 75 Eurasian Patent Convention, 18 198 Europe... [Pg.338]

Eig. 5. Restriction map of the yeast artificial chromosome (YAC) vector used for cloning very large fragments of eukaryotic DNA. Terms defined in text... [Pg.233]

The native form of chromatin in cells assumes a higher order stmcture called the 30-nm filament, which adopts a solenoidal stmcture where the 10-nm filament is arranged in a left-handed cod (Fig. 5). The negative supercoiling of the DNA is manifested by writhing the hehcal axis around the nucleosomes. Chromatin stmcture is an example of toroidal winding whereas eukaryotic chromosomes are linear, the chromatin stmctures, attached to a nuclear matrix, define separate closed-circular topological domains. [Pg.253]

The eukaryotic somatic cell cycle is defined by a sequential order of tasks a dividing cell has to complete it must replicate its DNA, segregate its chromosomes, grow, and divide. The cell cycle can be divided into four discrete phases. DNA replication is restricted to S phase (DNA synthesis phase), which is preceded by a gap phase called G1 and followed by a gap phase called G2. During mitosis (M phase) the sister chromatids are segregated into two new daughter nuclei and mitosis is completed by the division of the cytoplasm termed cytokinesis (Fig. 1). [Pg.340]

Ribosomes are ancient ribonucleoprotein complexes that are the sites of protein synthesis in living cells. Their core structures and fundamental functional mechanisms have been conserved throughout the three domains of life bacteria, archaea and eukaryotes. All ribosomes are organized into two subunits that are defined by their apparent sedimentation coefficient, measured in Svedberg units (S). There is a general... [Pg.1085]

A three-dimensional meshwork of proteinaceous filaments of various sizes fills the space between the organelles of all eukaryotic cell types. This material is known collectively as the cytoskeleton, but despite the static property implied by this name, the cytoskeleton is plastic and dynamic. Not only must the cytoplasm move and modify its shape when a cell changes its position or shape, but the cytoskeleton itself causes these movements. In addition to motility, the cytoskeleton plays a role in metabolism. Several glycolytic enzymes are known to be associated with actin filaments, possibly to concentrate substrate and enzymes locally. Many mRNA species appear to be bound by filaments, especially in egg cells where they may be immobilized in distinct regions thereby becoming concentrated in defined tissues upon subsequent cell divisions. [Pg.85]

The multiple sites that serve as origins for DNA replication in eukaryotes are poorly defined except in a few animal viruses and in yeast. However, it is clear that initiation is regulated both spatially and temporaUy, since clusters of adjacent sites initiate rephcation synchronously. There are suggestions that functional domains of chromatin replicate as intact units, implying that the origins of rephcation are specificaUy located with respect to transcription units. [Pg.331]

It is clear that the signals in DNA which control transcription in eukaryotic cells are of several types. Two types of sequence elements are promoter-proximal. One of these defines where transcription is to commence... [Pg.346]

The possibility of customization is the principal scientific advantage of the system. The microarray design, layout, and format are specific for each scientist s needs and objectives. The Design-on-Demand service offer by CombiMatrix try to cover this versatility. The researcher, though would define his experimental strategy with CombiMatrix support. Available libraries include eukaryotic, microbial, and viral genomes. Direct customer services are also offered. [Pg.257]

The distribution of elements in single-cell non-photosynthetic eukaryotes is probably best seen in terms of the well-defined compartments of yeast. The central cytoplasmic compartment containing the nucleus has many free element concentrations, only somewhat different from those in all known aerobic prokaryotes (Figure 7.7). (The nuclear membrane is a poor barrier to small molecules and ions and so we include the nucleus with the cytoplasm.) We do not believe in fact that the free cytoplasmic values of Mg2+, Mn2+, Fe2+, Ca2+, and possibly Zn2+, have changed greatly throughout evolution. As stressed already there are limitations since free Mg2+ and Fe2+ are essential for the maintenance of the primary synthetic routes of all cells, and changes in other free metal ions could well have imposed... [Pg.294]

The biosphere includes ecological niches where microbes peacefully co-exist with their eukaryotic host in the human this includes the concept of the micro-biome [14], which is defined as the totality of microbial organisms that co-habit with human beings. On the other hand, microbial colonization of human mucosal surfaces or prosthetic devices, often results in the development of biofilms, with significant deleterious effects on human health [15]. These are some of the challenges in infectious diseases that reflect the need to maximally utilize genomic sequence information and related sciences to better control microbial disease in human populations, and to develop anti-microbial agents with a better therapeutic index. [Pg.14]

The cytoskeleton is one of several biological elements that define eukaryotic cells 124... [Pg.123]

Vesicular proteins and lipids that are destined for the plasma membrane leave the TGN sorting station continuously. Incorporation into the plasma membrane is typically targeted to a particular membrane domain (dendrite, axon, presynaptic, postsynaptic membrane, etc.) but may or may not be triggered by extracellular stimuli. Exocytosis is the eukaryotic cellular process defined as the fusion of the vesicular membrane with the plasma membrane, leading to continuity between the intravesicular space and the extracellular space. Exocytosis carries out two main functions it provides membrane proteins and lipids from the vesicle membrane to the plasma membrane and releases the soluble contents of the lumen (proteins, peptides, etc.) to the extracellular milieu. Historically, exocytosis has been subdivided into constitutive and regulated (Fig. 9-6), where release of classical neurotransmitters at the synaptic terminal is a special case of regulated secretion [54]. [Pg.151]

Chemical transmission between nerve cells involves multiple steps 167 Neurotransmitter release is a highly specialized form of the secretory process that occurs in virtually all eukaryotic cells 168 A variety of methods have been developed to study exocytosis 169 The neuromuscular junction is a well defined structure that mediates the presynaptic release and postsynaptic effects of acetylcholine 170 Quantal analysis defines the mechanism of release as exocytosis 172 Ca2+ is necessary for transmission at the neuromuscular junction and other synapses and plays a special role in exocytosis 174 Presynaptic events during synaptic transmission are rapid, dynamic and interconnected 175... [Pg.167]

A number of synthetic methods to prepare all the three main classes of AHLs have appeared in the literature. Initially the methods were developed to prepare the authentic AHLs with defined stereochemistry to confirm the identity of the natural signal molecule. Subsequently, when some of these molecules, e.g. AT-(3-oxododecanoyl)-L-homoserine lactone were found to impact on eukaryotic signalling systems [ 16,50-52], detailed studies not only of their preparation but also of their structural analogues were undertaken by many laboratories. [Pg.304]


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