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1.
J Colloid Interface Sci ; 346(1): 100-6, 2010 Jun 01.
Article in English | MEDLINE | ID: mdl-20227084

ABSTRACT

Formation and properties of viscoelastic wormlike aqueous micellar solutions of the zwitterionic surfactant p-dodecyloxybenzyldimethylamine oxide (pDoAO) were studied. Semi-dilute aqueous solutions of pDoAO show a sharp increase in viscosity, which exceeds 160 cST for concentrations >50 mM, leading to viscoelastic solutions. Viscoelasticity relates to the surfactant charge type. In fact this viscoelastic system reverses to fluid when acid is added (pH<2), which changes the system to cationic. Under acidic conditions the system resembles solutions of the similar cationic surfactant p-dodecyloxybenzyltrimethylammonium bromide, (pDoTABr) in terms of viscosity. Properties of aqueous solutions of pDoAO were investigated by dynamic light scattering (DLS), rheology and small angle neutron scattering (SANS). Data support the idea that small micelles grow in length (wormlike or threadlike micelles) as surfactant concentration increases and viscoelastic solutions form as micelles become entangled. The micellar diameter as calculated by different techniques is about 5 nm.


Subject(s)
Amines/chemistry , Oxides/chemistry , Surface-Active Agents/chemistry , Viscoelastic Substances/chemical synthesis , Micelles , Molecular Structure , Rheology , Surface Properties , Viscoelastic Substances/chemistry
2.
Eur J Biochem ; 268(24): 6491-7, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11737204

ABSTRACT

alpha-Chymotrypsin activity was tested with N-glutaryl-l-phenylalanine p-nitroanilide (GPNA) in aqueous media in the presence of synthetic surfactants, which differ in the flexibility of their bulky head groups. Superactivity can be ascribed to the presence of the tributylammonium residue on the surfactant head group, as in p-octyloxybenzyltributylammonium bromide (pOOTBABr), while in the presence of a more rigid moiety, i.e. a cyclic one, no activation was found. A nonmicellizable quaternary ammonium salt, the tetrabutylammonium bromide (TBABr), which has a head group structure very similar to pOOTBABr, not only induces a remarkable superactivation, at a concentration 80-fold higher than pOOTBABr, but also allows the enzyme to retain a high residual activity for long periods of time. The presence of a lipophilic chain, which by interacting with apolar residues on the enzyme surface, probably penetrates into hydrophobic pockets of the protein and causes a rapid inactivation. In 0.4 m TBABr, a 20-fold increase both in kcat and Km values, with respect to buffer alone, was found. The increase of Km could be attributed either to a true decrease in affinity between enzyme and substrate or alternatively to the presence of TBA+ ions near the catalytic region. They could interact with protein residues around the active site and bind to negatively charged GPNA molecules, lowering the local substrate concentration. Spectroscopic experiments (CD and fluorescence) show minor changes of protein conformation in 0.4 m TBABr, while at 1 m a strong modification of both spectra was observed.


Subject(s)
Chymotrypsin/metabolism , Animals , Cations , Cattle , Circular Dichroism , Enzyme Stability , Kinetics , Spectrometry, Fluorescence , Surface-Active Agents/pharmacology
3.
J Colloid Interface Sci ; 211(2): 179-184, 1999 Mar 15.
Article in English | MEDLINE | ID: mdl-10049533

ABSTRACT

The SN2 reaction of Br- with methylnaphthalene-2-sulfonate (MeONs) in water is accelerated by micelles of tetradecyldialkyl amine oxide (alkyl = methyl, n-propyl) and rates increase sharply in HBr due to increased binding of Br- to the protonated amine oxide. Second-order rate constants at the micellar surface are similar to those at surfaces of trialkylammonium and sulfobetaine micelles. The reaction of OH- with MeONs is weakly inhibited by amine oxide micelles, showing that dispersive, as well as coulombic and charge-dipole, forces play a major role in the association of ions with surfaces of micellar aggregates. Copyright 1999 Academic Press.

4.
Biol Reprod ; 59(2): 309-13, 1998 Aug.
Article in English | MEDLINE | ID: mdl-9687300

ABSTRACT

Human semen contains membranous vesicles called prostasomes. They are secreted by the prostate gland and contain large amounts of cholesterol, sphingomyelin, and Ca2+. Prostasomes enhance the motility of ejaculated spermatozoa and are involved in a number of additional biological functions. No prostasome-like vesicles have been described in horse semen up to now. We have demonstrated the presence of prostasome-like vesicles in the equine semen and characterized them as to size, morphology, and lipid composition; we have found that they are similar to human prostasomes in many respects. We propose that these vesicles might be important for the fecundity of horse semen. This is of interest since the success of artificial insemination is limited by the fact that stallion sperm barely survive cryopreservation.


Subject(s)
Horses/physiology , Semen/physiology , Seminal Vesicles/physiology , Subcellular Fractions/physiology , Animals , Humans , In Vitro Techniques , Lipid Metabolism , Male , Microscopy, Electron , Seminal Vesicles/metabolism , Seminal Vesicles/ultrastructure , Subcellular Fractions/ultrastructure
5.
Biotechnol Prog ; 11(1): 107-11, 1995.
Article in English | MEDLINE | ID: mdl-7765984

ABSTRACT

The activity and stability of beef liver catalase have been investigated in the presence of different ionic and zwitterionic surfactants. All cationic and zwitterionic surfactants used in this work have no effect on the initial activity of catalase, but several of them allow the enzyme to retain a high residual activity for longer periods of time than those observed in the absence of any additives. However, the interactions between surfactants and catalase appear to be very peculiar, and certain zwitterionic surfactants have been found to remarkably slow down enzyme degradation, with the enzyme completely preserving its activity after several weeks at temperatures of up to 30 degrees C. This effect is probably due to an interaction between the surfactant and the intersubunit region of the protein; this interaction could stabilize the quaternary structure of the enzyme.


Subject(s)
Catalase/metabolism , Surface-Active Agents/pharmacology , Animals , Buffers , Cattle , Enzyme Stability/drug effects , Ions
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