Details zur Publikation

Kategorie Textpublikation
Referenztyp Zeitschriften
DOI 10.1007/s00253-008-1755-0
Volltext Shareable Link
Titel (primär) Impact of cell density on microbially induced stable isotope fractionation
Autor Kampara, M.; Thullner, M.; Harms, H.; Wick, L.Y.
Quelle Applied Microbiology and Biotechnology
Erscheinungsjahr 2009
Department UMB
Band/Volume 81
Heft 5
Seite von 977
Seite bis 985
Sprache englisch
Keywords Bioavailability; Cell density; Biodegradation; Fractionation factor; Stable isotope fractionation analysis; Toluene
Abstract Quantification of microbial contaminant biodegradation based on stable isotope fractionation analysis (SIFA) relies on known, invariable isotope fractionation factors. The microbially induced isotope fractionation is caused by the preferential cleavage of bonds containing light rather than heavy isotopes. However, a number of non-isotopically sensitive steps preceding the isotopically sensitive bond cleavage may affect the reaction kinetics of a degradation process and reduce the observed (i.e., the macroscopically detectable) isotope fractionation. This introduces uncertainty to the use of isotope fractionation for the quantification of microbial degradation processes. Here, we report on the influence of bacterial cell density on observed stable isotope fractionation. Batch biodegradation experiments were performed under non-growth conditions to quantify the toluene hydrogen isotope fractionation by exposing Pseudomonas putida mt-2(pWWO) at varying cell densities to different concentrations of toluene. Observed isotope fractionation depended significantly on the cell density. When the cell density rose from 5 × 105 to 5 × 108cells/mL, the observed isotope fractionation declined by 70% and went along with a 55% decrease of the degradation rates of individual cells. Theoretical estimates showed that uptake-driven diffusion to individual cells depended on cell density via the overlap of the cells' diffusion-controlled boundary layers. Our data suggest that biomass effects on SIFA have to be considered even in well-mixed systems such as the cell suspensions used in this study.
dauerhafte UFZ-Verlinkung https://www.ufz.de/index.php?en=20939&ufzPublicationIdentifier=306
Kampara, M., Thullner, M., Harms, H., Wick, L.Y. (2009):
Impact of cell density on microbially induced stable isotope fractionation
Appl. Microbiol. Biotechnol. 81 (5), 977 - 985 10.1007/s00253-008-1755-0