𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A microcolorimetric assay of inorganic pyrophosphatase

✍ Scribed by Jennie B. Shatton; Cynthia Ward; Albert Williams; Sidney Weinhouse


Publisher
Elsevier Science
Year
1983
Tongue
English
Weight
473 KB
Volume
130
Category
Article
ISSN
0003-2697

No coin nor oath required. For personal study only.

✦ Synopsis


A procedure is described for the assay of inorganic pyrophosphatase in tissues by a microcolorimetric procedure, taking advantage of the marked color intensification of phosphomolybdate by malachite green. Conditions are described for optimum enzyme activity, color stability, and sensitivity. With 1-cm cuvettes the AM660 is 100,000, allowing accurate measurement of Pi in the 1-nmol range. Reaction is conducted at 25 degrees C for 10 min in 0.5 ml of a 50 mM histidine buffer, pH 7.2, containing 0.2 mM inorganic pyrophosphate and 4 mM Mg2+, terminated by addition of 0.05 ml 2.4 M HClO4, cooled in ice, and 0.45 ml of color reagent is added. After standing 10 min at 0 degrees C, the contents are transferred to 1-cm cuvettes and the absorbance is read at 660 nm. Blanks are low, nonenzymatic hydrolysis of PPi is negligible, and color is stable without addition of detergents. The high sensitivity makes this procedure well-adapted to measurement of optimal activities in crude tissue preparations.


πŸ“œ SIMILAR VOLUMES


A new and convenient colorimetric determ
✍ Jukka K. Heinonen; Reijo J. Lahti πŸ“‚ Article πŸ“… 1981 πŸ› Elsevier Science 🌐 English βš– 408 KB

A new and convenient method for the determination of P, was developed. Phosphomolybdate is measured calorimetrically, without reduction to molybdenum blue, by dissolving the whole assay mixture in acetone, where phosphomolybdate is bright yellow. The hydrolysis of acidlabile phosphates (e.g., creati

Inorganic pyrophosphatase as a label in
✍ A.A. Baykov; V.N. Kasho; S.M. Avaeva πŸ“‚ Article πŸ“… 1988 πŸ› Elsevier Science 🌐 English βš– 475 KB

Inorganic pyrophosphatase from Escherichia coli has been employed as a label in heterogeneous enzyme immunoassays. Enzyme-antibody conjugates were prepared with the use of glutaraldehyde and purified by gel permeation chromatography. Enzyme activity was measured by means of a sensitive one-step colo