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Negative lipids

DOPC with Negative Lipids without Sink... [Pg.181]

With the noted exceptions above, the other negative-lipid combinations (Table 7.8) show consistently lower permeabilities compared to neutral DOPC. Surprisingly, the retentions are not concomitantly higher than in the neutral DOPC lipid. [Pg.181]

A. P. Winiski, A. C. McLaughlin, R. V. McDaniel, M. Eisenberg, and S. McLaughlin, An experimental test of the discreteness-of-charge effect in positive and negative lipid bilayers,... [Pg.270]

Phospholipid Lecithin o/w oral, parenteral Emulsifying properties dependent on number of negative lipids... [Pg.1553]

The binding site for blood clotting factors can be enriched in negative lipids but, if domains of different composition compared to the bulk are formed, they must be very small in size and/or their composition must be very close to that of the initial mixture. [Pg.190]

Some polymyxins are sold for second-line systemic therapy. Polymyxin B sulfate and colistimethate sodium can be used for intravenous, intramuscular, or intrathecal administration, especially for Pseudomonas aerupinosa mP QXiosis, but also for most other gram-negative organisms, such as those resistant to first-line antibiotics. Nephrotoxicity and various neurotoxicities are common in parenteral, but not in topical, use. Resistance to polymyxins develops slowly, involves mutation and, at least in some bacteria, adaptation, a poorly understood type of resistance that is rapidly lost on transfer to a medium free of polymyxin. Resistance can involve changes in the proteins, the lipopolysaccharides, and lipids of the outer membrane of the cell (52). Polymyxin and colistin show complete cross-resistance. [Pg.149]

Lipids in model systems are often found in asymmetric clusters (see Figure 9.8). Such behavior is referred to as a phase separation, which arises either spontaneously or as the result of some extraneous influence. Phase separations can be induced in model membranes by divalent cations, which interact with negatively charged moieties on the surface of the bilayer. For example, Ca induces phase separations in membranes formed from phosphatidylserine (PS)... [Pg.265]

As shown in Figure 9.24, the outer membrane of Gram-negative bacteria is coated with a highly complex lipopolysaccharide, which consists of a lipid group (anchored in the outer membrane) joined to a polysaccharide made up of long chains with many different and characteristic repeating structures... [Pg.281]

Gram-negative (whole organisms peptidoglycans lipopolysaccharides [lipid A])... [Pg.501]

A lipopolysaccharide (LPS) is any compound consisting of covalently linked lipids and polysaccharides. The term is used more frequently to denote a cell wall component from Gram-negative bacteria. LPS has endotoxin activities and is a polyclonal stimulator of B-lymphocytes. [Pg.696]

FIGURE 6-15 Schematic representation of the ion permeability modulation for cation-responsive voltammetric sensors based on negatively charged lipid membranes. Complexation of the guest cation to the phospholipid receptors causes an increase of the permeability for the anionic marker ion. (Reproduced with permission from reference 49.)... [Pg.187]

A monoaminopentose, 4-amino-4-deoxy-L-arabinose, is known as a component of some Gram-negative bacteria. It is linked, as the )5-pyranosyl phosphate (18), to a 2-amino-2-deoxy-y -D-glucopyranosyI residue in the lipid A part of the LPS. ... [Pg.290]

A number of amide- and ester-linked fatty acids and (/ )-3-hydroxy acids are components of the lipid A part in the LPS from Gram-negative bacteria. The acids have been tabulatedand the chemistry of lipid A summarized. The most common acids in lipid A from Enterobacteriaceae are the saturated 12 0,14 0, and 16 0, and the (/ )-3-hydroxy-14 0, The last is linked to N-2 and 0-3 of the 2-amino-2-deoxy-D-glucopyranosyl residues, and the others are ester-linked to the hydroxy acid, as in the lipid A (44) of Salmonella minnesota. Other linear and branched fatty acids, unsaturated acids, S)-2- and (/ )-3-hydroxy acids, and 3-oxotetradecanoic acid are components of lipid A from certain different species. In the lipid A from Rhizobium trifolii, 2,7-dihydroxyoctanoic acid is linked as amide to a 2-amino-2-deoxy-D-gl ucopy ranosy 1 residue. ... [Pg.308]


See other pages where Negative lipids is mentioned: [Pg.475]    [Pg.132]    [Pg.157]    [Pg.171]    [Pg.4127]    [Pg.182]    [Pg.277]    [Pg.438]    [Pg.123]    [Pg.475]    [Pg.132]    [Pg.157]    [Pg.171]    [Pg.4127]    [Pg.182]    [Pg.277]    [Pg.438]    [Pg.123]    [Pg.2609]    [Pg.1078]    [Pg.113]    [Pg.473]    [Pg.475]    [Pg.475]    [Pg.259]    [Pg.1078]    [Pg.250]    [Pg.266]    [Pg.279]    [Pg.315]    [Pg.179]    [Pg.38]    [Pg.105]    [Pg.257]    [Pg.1211]    [Pg.67]    [Pg.81]    [Pg.181]    [Pg.54]    [Pg.55]    [Pg.56]    [Pg.367]    [Pg.377]    [Pg.378]    [Pg.432]    [Pg.454]   
See also in sourсe #XX -- [ Pg.295 ]




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DOPC with Negative Lipids without Sink

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