acid-phosphatase and 2-2-4-trimethylpentane

acid-phosphatase has been researched along with 2-2-4-trimethylpentane* in 2 studies

Other Studies

2 other study(ies) available for acid-phosphatase and 2-2-4-trimethylpentane

ArticleYear
Superactivity and phase-sensitivity of potato acid phosphatase entrapped in reverse micelles.
    Biochemistry and molecular biology international, 1996, Volume: 40, Issue:3

    Potato acid phosphatase, AcPase (E.C. 3.1.3.2) was entrapped in reverse micelles of cationic surfactant cetyltrimethylammonium bromide (CTAB) in isooctane and chloroform (1:1). The activity was studied at different values of Wo = ([water]/[surfactant]). AcPase exhibited superactivity in the reverse micellar system. At very low Wo value, activity was found to be less than that of in buffer and further increase in Wo value enhanced the activity thousand fold. At Wo = 50, the activity was enhanced more than twenty fold. The effect of second surfactant, TritonX-100, on superactivity was studied. There was a slight decrease in overall activity, when 3.33 mM TritonX-100 was added to the above reverse micellar system.

    Topics: Acid Phosphatase; Cetrimonium; Cetrimonium Compounds; Chloroform; Micelles; Octanes; Octoxynol; Solanum tuberosum; Surface-Active Agents

1996
Continuous assay for acid phosphatase using phenyl phosphate.
    Analytical biochemistry, 1996, Oct-15, Volume: 241, Issue:2

    A continuous spectrophotometric assay for the determination of the initial rate of an acid phosphatase-catalyzed reaction in an acidic environment, using phenyl phosphate as a substrate, is presented. The method is based on the continuous determination of phenol, a product of the enzymatic hydrolysis, by the kinetic measurement of its absorbance. The method allows for the direct estimation of acid phosphatase activity in an acidic solution. This is possible without interrupting the reaction by alkalization or precipitation required for commonly used end-point colorimetric detection procedures for phosphate or phenol, and without the use of any coupled assays. The method has been developed for acid phosphatase activity determination in an aqueous solution and in sodium bis(2-ethylhexyl)sulfosuccinate (AOT)-isooctane-water reverse micelles in a broad pH range (pH 3.8 to 8.8). The proposed procedure has been used for the determination of kinetic constants (K(m) and kcat) for human prostatic acid phosphatase in aqueous solutions, and in AOT-isooctane-water reverse micelles, at pH 3.8, 4.5, and 5.7.

    Topics: Acid Phosphatase; Dioctyl Sulfosuccinic Acid; Humans; Hydrogen-Ion Concentration; Kinetics; Male; Micelles; Octanes; Organophosphates; Prostate; Spectrophotometry, Ultraviolet; Water

1996