About: Enzymatic and Nonenzymatic Dehalogenation of 1,2-chloroethane and 1,2-dibromoethane     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : http://linked.opendata.cz/ontology/domain/vavai/Vysledek, within Data Space : linked.opendata.cz associated with source document(s)

AttributesValues
rdf:type
Description
  • 1,2-Dichloroethane (DCE) and 1,2-dibromoethane (DBE) are toxic and mutagenic halogenated compounds. As many other synthetic halogenated aliphatic compounds, both are rather resistant to biodegradation and persist in the environment1. Nevertheless, several bacterial cultures that are able to use DCE as the only carbon and halogen source have been isolated. The most efficient catalysis has been observed with the haloalkane dehalogenase DhlA from Xanthobacter autotrophicus GJ10 and substantially low activity with haloalkane dehalogenase LinB from Sphingomonas paucimobilis UT262. A crystallographic analysis of LinB-DCE complex showed non-productive binding of DCE to the enzyme active site, while molecular docking suggested that DCE molecule can possibly bind to the active site but is prevented by chloride ion and/or water molecules3. The different reactivity of DCE and DBE was examined by quantum mechanical calculations as well as by molecular dynamics simulations of enzyme-substrate complexes The calcula
  • 1,2-Dichloroethane (DCE) and 1,2-dibromoethane (DBE) are toxic and mutagenic halogenated compounds. As many other synthetic halogenated aliphatic compounds, both are rather resistant to biodegradation and persist in the environment1. Nevertheless, several bacterial cultures that are able to use DCE as the only carbon and halogen source have been isolated. The most efficient catalysis has been observed with the haloalkane dehalogenase DhlA from Xanthobacter autotrophicus GJ10 and substantially low activity with haloalkane dehalogenase LinB from Sphingomonas paucimobilis UT262. A crystallographic analysis of LinB-DCE complex showed non-productive binding of DCE to the enzyme active site, while molecular docking suggested that DCE molecule can possibly bind to the active site but is prevented by chloride ion and/or water molecules3. The different reactivity of DCE and DBE was examined by quantum mechanical calculations as well as by molecular dynamics simulations of enzyme-substrate complexes The calcula (en)
  • Byla studována enzymatická a neenzymatická dehalogenace 1,2-chloroethanu a 1,2-dibromoethanu. (cs)
Title
  • Enzymatic and Nonenzymatic Dehalogenation of 1,2-chloroethane and 1,2-dibromoethane
  • Enzymatic and Nonenzymatic Dehalogenation of 1,2-chloroethane and 1,2-dibromoethane (en)
  • Enzymatická a neenzymatická dehalogenace 1,2-chloroethanu a 1,2-dibromoethanu (cs)
skos:prefLabel
  • Enzymatic and Nonenzymatic Dehalogenation of 1,2-chloroethane and 1,2-dibromoethane
  • Enzymatic and Nonenzymatic Dehalogenation of 1,2-chloroethane and 1,2-dibromoethane (en)
  • Enzymatická a neenzymatická dehalogenace 1,2-chloroethanu a 1,2-dibromoethanu (cs)
skos:notation
  • RIV/61989592:15310/04:00002220!RIV/2005/MSM/153105/N
http://linked.open.../vavai/riv/strany
  • 261-262
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • Z(MSM 153100007)
http://linked.open...iv/cisloPeriodika
  • Suppl.
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 563008
http://linked.open...ai/riv/idVysledku
  • RIV/61989592:15310/04:00002220
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • Dehalogenation;1,2-chloroethane;1,2-dibromoethane (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • CZ - Česká republika
http://linked.open...ontrolniKodProRIV
  • [605ADBE56065]
http://linked.open...i/riv/nazevZdroje
  • Acta Universitatis Palackianae Olomucensis, Facultas Rerum Naturalium, Chemica
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 43
http://linked.open...iv/tvurceVysledku
  • Damborský, Jiří
  • Otyepka, Michal
  • Otyepková, Eva
  • Prokop, Zdeněk
  • Boháč, Michal
http://linked.open...n/vavai/riv/zamer
issn
  • 0232-0061
number of pages
http://localhost/t...ganizacniJednotka
  • 15310
Faceted Search & Find service v1.16.118 as of Jun 21 2024


Alternative Linked Data Documents: ODE     Content Formats:   [cxml] [csv]     RDF   [text] [turtle] [ld+json] [rdf+json] [rdf+xml]     ODATA   [atom+xml] [odata+json]     Microdata   [microdata+json] [html]    About   
This material is Open Knowledge   W3C Semantic Web Technology [RDF Data] Valid XHTML + RDFa
OpenLink Virtuoso version 07.20.3240 as of Jun 21 2024, on Linux (x86_64-pc-linux-gnu), Single-Server Edition (126 GB total memory, 58 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software