VYTISKOVÁ, Soňa, Sigrid VAN DYCK, Ann VAN SCHEPDAEL, Jos HOOGMARTENS and Zdeněk GLATZ. Study of enzyme kinetics of phenol sulfotransferase by electrophoretically mediated microanalysis. Journal of Chromatography A. Netherlands: Elsevier, 2004, vol. 1032, (1+2), p. 319-326. ISSN 0021-9606.
Other formats:   BibTeX LaTeX RIS
Basic information
Original name Study of enzyme kinetics of phenol sulfotransferase by electrophoretically mediated microanalysis
Name in Czech Studium enzymove kinetiky enzymu fenolsulfotranferasy metodou EMMA
Authors VYTISKOVÁ, Soňa (203 Czech Republic, guarantor), Sigrid VAN DYCK (56 Belgium), Ann VAN SCHEPDAEL (56 Belgium), Jos HOOGMARTENS (56 Belgium) and Zdeněk GLATZ (203 Czech Republic).
Edition Journal of Chromatography A, Netherlands, Elsevier, 2004, 0021-9606.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10600 1.6 Biological sciences
Country of publisher Netherlands
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 3.105
RIV identification code RIV/00216224:14310/04:00009928
Organization unit Faculty of Science
UT WoS 000220121200043
Keywords in English Capillary electrophoresis; enzymes; EMMA; sulfotranferase
Tags Capillary electrophoresis, EMMA, enzymes, sulfotranferase
Changed by Changed by: prof. RNDr. Zdeněk Glatz, CSc., učo 1865. Changed: 19/5/2009 18:44.
Abstract
Electrophoretically mediated microanalysis (EMMA) was applied for the study of the kinetic parameters of the enzymatic reaction of phenol sulfotransferase SULT1A1 isoenzyme with 4-nitrophenol as a substrate. The SULT1A1 activity was determined by the quantitation of the product, 4-nitrophenyl sulfate, at 274 nm by using different injection and separation steps. This new approach solved the problem of the presence of the very strong inhibitor, adenosine 3',5'-bisphosphate (PAP), in the co-substrate solution (adenosine 3'-phosphate 5'-phosphosulfate, PAPS) which is unstable at room temperature. The inhibitor PAP was electrophoretically separated from the co-substrate PAPS before the injection of enzyme and substrate inside the capillary (and thus before their in-capillary encountering). With the developed in-capillary SULT1A1 activity assay an average Michaelis constant (Km) for 4-nitrophenol was calculated to be 0.84 M, a value which is consistent with a previously reported value. Strong substrate inhibition (above a 4-nitrophenol concentration of 2.5 M) was observed, and this is also in accordance with literature values.
Abstract (in Czech)
Metoda EMMA byla využita pro studium enzymove kinetiky enzymu fenolsulfotranferasy.
Links
GA203/03/1125, research and development projectName: Využití kapilární zónové elektroforézy pro studium enzymů
Investor: Czech Science Foundation, Application of capillary zone electrophoresis for the study of enzymes
MSM 143100005, plan (intention)Name: Strukturně-funkční vztahy biomolekul a jejich role v metabolismu
Investor: Ministry of Education, Youth and Sports of the CR, Biomolecular Structure-function Relationships and their role in the Metabolism
PrintDisplayed: 29/7/2024 22:20