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Membrane cytoplasmic

The term protoplasm is used to indicate the thick viscous semifluid or almost jelly-like colorless, transparent material which makes up the essential substance of both the cell body and the nucleus, including the cytoplasmic membrane but not the cell wall. It contains a high percentage of water and holds fine granules in suspension. [Pg.87]

This membrane appears in young cells as an interfacial fluid film, [Pg.87]


Fig. 4. Comparison of the three types of tetracycline resistance where T represents the tetracycline molecule O, a tetracycline transporter and aaa/, the ribosome A shows the effect of tetracycline exposure on a sensitive cell B, the efflux of resistance where a cytoplasmic membrane protein ( D) pumps tetracycline out of the cell as fast as the tetracycline transporter takes it up C, the ribosomal protection type of resistance where the ribosome is modified by ( ) to block productive binding and D, the tetracycline modification type of resistance where t is an inactive form of tetracycline. Reproduced with... Fig. 4. Comparison of the three types of tetracycline resistance where T represents the tetracycline molecule O, a tetracycline transporter and aaa/, the ribosome A shows the effect of tetracycline exposure on a sensitive cell B, the efflux of resistance where a cytoplasmic membrane protein ( D) pumps tetracycline out of the cell as fast as the tetracycline transporter takes it up C, the ribosomal protection type of resistance where the ribosome is modified by ( ) to block productive binding and D, the tetracycline modification type of resistance where t is an inactive form of tetracycline. Reproduced with...
Considerable work has been done to try to explain why quats are antimicrobial. The following sequence of steps is beheved to occur in the attack by the quat on the microbial cell (/) adsorption of the compound on the bacterial cell surface (2) diffusion through the cell wall (J) binding to the cytoplasmic membrane (4) dismption of the cytoplasmic membrane (5) release of cations and other cytoplasmic cell constituents (6) precipitation of cell contents and death of the cell. [Pg.130]

Cells make use of many different types of membranes. All cells have a cytoplasmic membrane, or plasma membrane, that functions (in part) to separate the cytoplasm from the surroundings. In the early days of biochemistry, the plasma membrane was not accorded many functions other than this one of partition. We now know that the plasma membrane is also responsible for (1) the exclusion of certain toxic ions and molecules from the cell, (2) the accumulation of cell nutrients, and (3) energy transduction. It functions in (4) cell locomotion, (5) reproduction, (6) signal transduction processes, and (7) interactions with molecules or other cells in the vicinity. [Pg.260]

Polymyxins Polyene antifungals Inhibition of synthesis or damage to cytoplasmic membrane... [Pg.151]

Currently, five different molecular classes of mdr efflux pumps are known [5], While pumps of the the ATP-binding cassette (ABC) transporter superfamily are driven by ATP hydrolysis, the other four superfamilies called resistance-nodulation-division (RND), major facilitator superfamily (MFS), multidrug and toxic compound extrusion (MATE), and small multidrag resistance transporter (SMR) are driven by the proton-motive force across the cytoplasmic membrane. Usually a single pump protein is located within the cytoplasmic membrane. However, the RND-type pumps which are restricted to Gram-negative bacteria consist of two additional components, a periplasmic membrane fusion protein (MFP) which connects the efflux pump to an outer... [Pg.105]

Furthermore, if the antibiotic passes membranes through a specific port of entry, its mutational loss leads to resistance. The lack of the outer membrane protein OprD in P. aeruginosa causes resistance to the (3-lactam antibiotic imipenem. Fosfomycin passes the cytoplasmic membrane via an L-a-glycerol phosphate permease. This transport system is not essential for bacterial growth and therefore mutants with a reduced expression are frequently selected under therapy. [Pg.772]

Proteins identified by their ability to bind labelled (3-lactam antibiotics in vivo and in vitro. The intrinsic activities of PBPs include transglycosylase/transpepti-dase, carboxypeptidase and endopeptidase activities required for the formation of the bacterial murein sacculus forming the bacterial cell wall. The enzymes are located in the cytoplasmic membrane. [Pg.936]

The current understanding on activation of Tec kinases fits into a two-step model. In the first step an intramolecular interaction between the SH3 domain and aproline-rich region in the TH domain is disrupted by binding ofthe PH domain to phosphoinositides, G protein subunits, or the FERM domain of Fak. These interactions lead to conformational changes of Tec and translocation to the cytoplasmic membrane where, in a second step, Src kinases phosphorylate a conserved tyrosine residue in the catalytic domain thereby increasing Tec kinase activity. Autophosphorylation of a tyrosine residue in the SH3 domain further prevents the inhibitory intramolecular interaction resulting in a robust Tec kinase activation. [Pg.1261]

Cell envelopes of prokaryotic organisms (archaea and bacteria) are characterized by the presence of two distinct components the cytoplasmic membrane, which constitutes the inner layer, and an outer supramolecular layered cell wall (for reviews see Ref. 4), which pre-... [Pg.333]

In this context it is interesting to note that archaea, which possess S-layers as exclusive cell wall components outside the cytoplasmic membrane (Fig. 14), exist under extreme environmental conditions (e.g., high temperatures, hydrostatic pressure, and salt concentrations, low pH values). Thus, it is obvious one should study the effect of proteinaceous S-layer lattices on the fluidity, integrity, structure, and stability of lipid membranes. This section focuses on the generation and characterization of composite structures that mimic the supramolecular assembly of archaeal cell envelope structures composed of a cytoplasmic membrane and a closely associated S-layer. In this biomimetic structure, either a tetraether... [Pg.362]

FIG. 14 Schematic illustration of an archaeal cell envelope structure (a) composed of the cytoplasmic membrane with associated and integral membrane proteins and an S-layer lattice, integrated into the cytoplasmic membrane, (b) Using this supramolecular construction principle, biomimetic membranes can be generated. The cytoplasmic membrane is replaced by a phospholipid or tetraether hpid monolayer, and bacterial S-layer proteins are crystallized to form a coherent lattice on the lipid film. Subsequently, integral model membrane proteins can be reconstituted in the composite S-layer-supported lipid membrane. (Modified from Ref. 124.)... [Pg.363]

Three fundamental divisions of the bacterial cell occur in all species cell wall, cell or cytoplasmic membrane, and cytoplasm. [Pg.4]

Flagella are threads of protein often 2fim. long which start as small basal organs just beneath the cytoplasmic membrane. They are responsible for the movement of motile bacteria. Their number and distribution varies. Some species bear a single flagellum, others are flagellate over their whole surface. [Pg.10]

In addition to the protein coat, many animal vims particles are surrounded by a hpoprotein envelope which has generally been derived fiom the cytoplasmic membrane of their last host cell. [Pg.55]

All enveloped human vimses acquire their phospholipid coating by budding through cellular membranes. The maturation and release of enveloped influenza particles is illustrated in Fig. 3.8. The capsid protein subunits are transported flom the ribosomes to the nucleus, where they combine with new viral RNA molecules and are assembled into the helical capsids. The haemagglutinin and neuraminidase proteins that project fiom the envelope of the normal particles migrate to the cytoplasmic membrane where they displace the normal cell membrane proteins. The assembled nucleocapsids finally pass out from the nucleus, and as they impinge on the altered cytoplasmic membrane they cause it to bulge and bud off completed enveloped particles flxm the cell. Vims particles are released in this way over a period of hours before the cell eventually dies. [Pg.70]

Cytoplasmic membrane Polymyxins Polyenes Imidazoles and triazoles Naftidine Disrupt bacterial membranes Disrupt fungal membranes Inhibit ergosterol synthesis Inhibits ergosterol synthesis Bind to LPS and phospholipids Bind preferentially to ergosterol Pathway not in mammalian cells Pathway not in mammalian cells... [Pg.163]


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Antimicrobial cytoplasmic membrane

Cytoplasm

Cytoplasmic membrane active transport system

Cytoplasmic membrane activity

Cytoplasmic membrane bacteria

Cytoplasmic membrane disruption

Cytoplasmic membrane fluidity

Cytoplasmic membrane fungal

Cytoplasmic membrane oligosaccharides

Cytoplasmic membrane pathways

Cytoplasmic membrane permeability

Cytoplasmic membrane porins

Cytoplasmic membrane vesicles

Cytoplasmic membrane, bacterial

Cytoplasmic membrane, bacterial channels

Cytoplasmic membrane, bacterial functions

Cytoplasmic membrane, bacterial group translocators

Cytoplasmic membrane, bacterial transport across

FhuB protein cytoplasmic membrane

Fungi cytoplasmic membrane

Gram-negative bacteria cytoplasmic membrane

Gram-positive bacteria cytoplasmic membrane

Inhibition of Cytoplasmic Membranes

Membranes cytoplasmic membrane

Membranous cytoplasmic bodies

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