Details zur Publikation

Kategorie Textpublikation
Referenztyp Zeitschriften
DOI 10.1016/j.copbio.2016.06.002
Titel (primär) Stable isotope fractionation concepts for characterizing biotransformation of organohalides
Autor Nijenhuis, I.; Richnow, H.H.
Quelle Current Opinion in Biotechnology
Erscheinungsjahr 2016
Department ISOBIO
Band/Volume 41
Seite von 108
Seite bis 113
Sprache englisch
UFZ Querschnittsthemen RU3;
Abstract Recent development allows multi-element compound-specific isotope analysis of D, 13C, 37Cl and 81Br for characterizing the degradation pathways of halogenated organic substances in the environment. The apparent kinetic isotope effect (AKIE) obtained in (bio)degradation experiments yields information on the chemical mechanism of the bond cleavage. In biochemical reactions, rate limitation such as uptake into cells, substrate transport in cells and binding to enzymes as well as equilibrium isotope effects (EIE) are modifying the observed isotope fractionation associated with the bond cleavage reactions, thus, complicating mechanistic interpretation of isotope effect. One way for improved analysis of bond cleavage reactions by isotope effects reactions is the combination of isotope effects from two or more elements forming the reactive organic moieties where bond change reaction takes place as indicator. A further option is the combination of enantiomeric with isotope fractionation as complementary indicator for enzymatic bond cleavage reaction governing biodegradation. Finally an interesting concept with large potential for elucidation of the biochemical reaction mechanisms of biological dehalogenation may be quantum mechanical/molecular mechanical (QM/MM) modelling in combination with experimental multi-element isotope analysis, thus merging quantum chemical theory with experimental observation.
dauerhafte UFZ-Verlinkung
Nijenhuis, I., Richnow, H.H. (2016):
Stable isotope fractionation concepts for characterizing biotransformation of organohalides
Curr. Opin. Biotechnol. 41 , 108 - 113 10.1016/j.copbio.2016.06.002