Subcellular localization of an ATPase in anammox bacteria using proteomics and immunogold electron microscopy. Issue 1 (7th April 2014)

• Record Type: Journal Article
• Authors: Karlsson, Roger; Karlsson, Anders; Bäckman, Ola; Johansson, Bengt R.; Hulth, Stefan
• Is Part Of: FEMS microbiology letters. Volume 354:Issue 1(2014:May)
• Page Start: 10
• Page End: 18
• Publication Date: 2014-04-07
• Subjects: Microbiology -- Periodicals; 579
• DOI: 10.1111/1574-6968.12425
• Languages: English
• ISSNs: 0378-1097

Abstract

<abstract abstract-type="main" id="fml12425-abs-0001"> <title>Abstract</title> <p>Anaerobic ammonium oxidation (anammox) has received significant attention during optimization of waste‐water treatment and constitutes an important pathway for the removal of bioavailable nitrogen from natural environments. Studies of key catabolic enzymes indicate that the anammox reaction takes place inside the anammoxosome, an organelle‐like membranous compartment of anammox bacteria. The anammoxosome has also been suggested as a site for ATP synthesis. A lipid‐based protein immobilization technique, previously used to identify proteins essential for the anammox reaction, was in this study used to select linear epitopes for antibodies specifically targeted against an identified ATPase. The approach of using proteomics and bioinformatics as tools for selecting antibody targets for immunolocalization provides an important alternative to traditional methods for selection of specific antibodies. Immunogold electron microscopy and statistical evaluations indicated that the antibodies against the ATPase were exclusively found associated with the anammoxosome membrane. This provides strong evidence for ATP synthesis by an intracellular proton motive force in anammox bacteria. Within prokaryotes, an ATP synthase associated with an intracellular compartment is a feature unique for anammox bacteria.</p> </abstract>