TELNAROVÁ, Magdaléna, Kateřina PAPEŽOVÁ, Soňa VYTISKOVÁ and Zdeněk GLATZ. Complex Study of Haloalkane Dehalogenase by Means of Electrophoretically Mediated Microanalysis (Complex Study of Haloalkane Dehalogenase by Means of Electrophoretlcally Mediated Microanalysis). In Book of abstract 14 th International Symposium on Capillary Electroseparation Techniques ITP 2004. ím: Consiglio Nazionale delle Ricerche, 2004, p. 103.
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Basic information
Original name Complex Study of Haloalkane Dehalogenase by Means of Electrophoretically Mediated Microanalysis
Name in Czech Komplexní studie enzymu haloalkandehalogeansy metodou EMMA
Authors TELNAROVÁ, Magdaléna (203 Czech Republic), Kateřina PAPEŽOVÁ (203 Czech Republic), Soňa VYTISKOVÁ (203 Czech Republic) and Zdeněk GLATZ (203 Czech Republic, guarantor).
Edition ím, Book of abstract 14 th International Symposium on Capillary Electroseparation Techniques ITP 2004, p. 103-103, 2004.
Publisher Consiglio Nazionale delle Ricerche
Other information
Original language English
Type of outcome Proceedings paper
Field of Study 10600 1.6 Biological sciences
Country of publisher Italy
Confidentiality degree is not subject to a state or trade secret
RIV identification code RIV/00216224:14310/04:00010517
Organization unit Faculty of Science
Keywords in English microcystins; capillary electrochromatography
Tags Capillary electrochromatography, microcystins
Changed by Changed by: prof. RNDr. Zdeněk Glatz, CSc., učo 1865. Changed: 19/5/2009 18:44.
Abstract
Halogenated aliphatic hydrocarbons constitute one of the largest groups of environmental pollutants. Haloalkane dehalogenases are a group of enzymes involved in the biodegradation of these compounds by catalysing cleavage of the carbon-halogen bond. The study of the biochemistry of dehalogenation processes may help to understand and evaluate the potential for their degradation in nature. This work aims to develop Electrophoretically Mediated MicroAnalysis (EMMA)-based assays for the complex study of haloalkane dehalogenase. EMMA utilizes the different electrophoretic mobilities of enzyme, substrate and product to initiate reaction inside the capillary and to separate components from each other for final in-capillary quantitation. The Michaelis constants for different substrates, the inhibition constant for inhibitor 1,2-dichloroethane, substrate inhibition of 1,2-dibromoethane and the effect of temperature on enzymatic reaction of haloalkane dehalogenase from Sphingomonas paucimobilis UT26 were evaluated by means of the combination of the EMMA methodology with partial filling technique. In this set-up part of the capillary is filled with the buffer best for the enzymatic reaction whereas the rest of the capillary is filled with the background electrolyte optimal for separation of substrates and products. The direct and the indirect detection methods have been used in this study. EMMA combines all advantages of capillary electrophoresis in the assay of enzyme kinetics. The minimal sample and reagent requirements as well as high separation efficiency of capillary zone electrophoresis are fully utilized. The absence of manual procedures and complete automation minimize the risk of cross contamination and strongly reduce the assay cost.
Abstract (in Czech)
Jedná se o komplexní studii enzymu haloalkandehalogeansy metodou EMMA.
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
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