Energized outer membrane and spatial separation of metabolic processes in the hyperthermophilic Archaeon "Ignicoccus hospitalis"

Küper, Ulf and Meyer, Carolin and Müller, Volker and Rachel, Reinhard and Huber, Harald (2010) Energized outer membrane and spatial separation of metabolic processes in the hyperthermophilic Archaeon "Ignicoccus hospitalis". Proceedings of the National Academy of Sciences of the United States of America (PNAS) 107 (7), pp. 3152-3156.

[img]
PDF - Repository staff only - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader
818Kb

Abstract

ATP synthase catalyzes ATP synthesis at the expense of an electrochemical ion gradient across a membrane that can be generated by different exergonic reactions. Sulfur reduction is the main energy-yielding reaction in the hyperthermophilic strictly anaerobic Crenarchaeon Ignicoccus hospitalis. This organism is unusual in having an inner and an outer membrane that are separated by a huge intermembrane compartment. Here we show, on the basis of immuno-EM analyses of ultrathin sections and immunofluorescence experiments with whole I. hospitalis cells, that the ATP synthase and H2:sulfur oxidoreductase complexes of this organism are located in the outer membrane. These two enzyme complexes are mandatory for the generation of an electrochemical gradient and for ATP synthesis. Thus, among all prokaryotes possessing two membranes in their cell envelope (including Planctomycetes, Gram-negative bacteria), I. hospitalis is a unique organism, with an energized outer membrane and ATP synthesis within the periplasmic space. In addition, DAPI staining and EM analyses showed that DNA and ribosomes are localized in the cytoplasm, leading to the conclusion that in I. hospitalis energy conservation is separated from information processing and protein biosynthesis. This raises questions regarding the function of the two membranes, the interaction between these compartments, and the general definition of a cytoplasmic membrane.

Item Type:Article
Institutions: Biology, Preclinical Medicine > Institut für Biochemie, Genetik und Mikrobiologie > Lehrstuhl für Mikrobiologie > Prof. Dr. Michael Thomm
Identification Number:
ValueType
10.1073/pnas.0911711107DOI
Keywords:Archaea, ATP synthase, ATPase, immunolabeling, sulfur reductase
Subjects:500 Science > 570 Life sciences
Status:Published
Refereed:Unknown
Created at the University of Regensburg:Unknown
Owner:Petra Gürster
Deposited On:11 Jul 2011 12:50
Last Modified:21 Jul 2011 04:15
Item ID:21394
Owner Only: item control page