Skoči na glavni sadržaj

Izvorni znanstveni članak

https://doi.org/10.2478/10004-1254-60-2009-1915

Rat Serum Carboxylesterase Partly Hydrolyses Gamma-Butyrobetaine Esters

Lida Bagdoniené ; Department of Biochemistry and Biophysics, Vilnius University, Vilnius, Lithuania
Danutė Labeikytė ; Department of Biochemistry and Biophysics, Vilnius University, Vilnius, Lithuania
Ivars Kalviņš ; Latvian Institute of Organic Synthesis, Riga, Latvia
Veronika Borutinskaitė ; Department of Developmental Biology, Institute of Biochemistry, Vilnius, Lithuania
Aleksandrs Prokofjevs ; Latvian Institute of Organic Synthesis, Riga, Latvia
Pēteris Trapencieris ; Latvian Institute of Organic Synthesis, Riga, Latvia
Benediktas Juodka ; Department of Biochemistry and Biophysics, Vilnius University, Vilnius, Lithuania
Nikolajs Sjakste ; Latvian Institute of Organic Synthesis, Riga, Latvia


Puni tekst: engleski pdf 168 Kb

str. 147-156

preuzimanja: 1.118

citiraj


Sažetak

Although described some time ago, gamma-butyrobetaine esters and related compounds have not gained much attention from researchers, and their physiological function remains obscure. Formerly we detected GBB-esterase enzymatic activity in rat blood serum using phenylated gamma-butyrobetaine as an artificial substrate of the enzyme and HPLC. The aim of the present work was to develop an assay that would enable spectrophotometric or colorimetric determination of the reaction products of GBB-esterase activity and to reveal individual proteins performing GBB-esterase activity in rat blood serum. For this purpose gammabutyrobetaine 1-naphthyl ester was synthesised. Hydrolysis of this ester releases 1-naphthol, which increases the optical absorbance at 322 nm. We have shown that the enzymatic hydrolysis of GBB 1-naphthyl ester to 1-naphthol in rat blood serum is due to GBB-esterase activity. An attempt was done to purify the enzyme from rat blood serum. By combining DEAE Sepharose at pH 4.2 and affinity chromatography with procainamide we achieved a 68-fold enrichment of GBB-esterase activity in our preparations. Separation of fraction proteins in 2D protein electrophoresis with following mass-spectrometry indicated that GBB esterase activity in rat blood serum is performed in part by carboxylesterase.

Ključne riječi

1-naphtol; 2D electrophoresis; colorimetry; HPLC; spectrophotometry

Hrčak ID:

38386

URI

https://hrcak.srce.hr/38386

Datum izdavanja:

12.6.2009.

Podaci na drugim jezicima: hrvatski

Posjeta: 2.456 *