Details zur Publikation

Referenztyp Zeitschriften
DOI / URL Link
Titel (primär) Development of a fatty acid and RNA stable isotope probing-based method for tracking protist grazing on bacteria in wastewater
Autor Kuppardt, S.; Chatzinotas, A.; Kästner, M.;
Journal / Serie Applied and Environmental Microbiology
Erscheinungsjahr 2010
Department UMB; UBT;
Band/Volume 76
Heft 24
Sprache englisch;
Abstract Removal of potential pathogenic bacteria, for example, during wastewater treatment, is effected by sorption, filtration, natural die-off, lysis by viruses, and grazing by protists, but the actual contribution of grazing has never been assessed quantitatively. A methodical approach for analyzing the grazing of protists on 13C-labeled prey bacteria was developed which enables mass balances of the carbon turnover to be drawn, including yield estimation. Model experiments for validating the approach were performed in closed microcosms with the ciliate Uronema sp. and 13C-labeled Escherichia coli as model prey. The transfer of bacterial 13C into grazing protist biomass was investigated by fatty acid (FA) and RNA stable isotope probing (SIP). Uronema sp. showed ingestion rates of 390 bacteria protist-1 h-1, and the temporal patterns of 13C assimilation from the prey bacteria to the protist FA were identified. Nine fatty acids specific for Uronema sp. were found (20:0, i20:0, 22:0, 24:0, 20:19c, 20:19t, 22:19c, 22:19t, and 24:1). Four of these fatty acids (22:0, 20:19t, 22:19c, and 22:19t) were enriched very rapidly after 3 h, indicating grazing on bacteria without concomitant cell division. Other fatty acids (20:0, i20:0, and 20:19c) were found to be indicative of growth with cell division. The fatty acids were found to be labeled with a percentage of labeled carbon (atoms percent [atom%]) up to 50. Eighteen percent of the E. coli-derived 13C was incorporated into Uronema biomass, whereas 11% was mineralized. Around 5 mol bacterial carbon was necessary in order to produce 1 mol protist carbon (y/ 0.2), and the temporal pattern of 13C labeling of protist rRNA was also shown. A consumption of around 1,000 prey bacteria (98 atom% 13C) per protist cell appears to be sufficient to provide detectable amounts of label in the protist RNA. The large shift in the buoyant density fraction of 13C-labeled protist RNA demonstrated a high incorporation of 13C, and reverse transcription-real-time PCR (RT-qPCR) confirmed that protist rRNA increasingly dominated in the heavy RNA fraction.
ID 10222
dauerhafte UFZ-Verlinkung http://www.ufz.de/index.php?en=20939&ufzPublicationIdentifier=10222
Kuppardt, S., Chatzinotas, A., Kästner, M. (2010):
Development of a fatty acid and RNA stable isotope probing-based method for tracking protist grazing on bacteria in wastewater
Appl. Environ. Microb. 76 (24), 8222 - 8230