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Giannone, Richard J. ; Huber, Harald ; Karpinets, Tatiana ; Heimerl, Thomas ; Kueper, Ulf ; Rachel, Reinhard ; Keller, Martin ; Hettich, Robert L. ; Podar, Mircea

Proteomic Characterization of Cellular and Molecular Processes that Enable the Nanoarchaeum equitans-Ignicoccus hospitalis Relationship

Giannone, Richard J., Huber, Harald, Karpinets, Tatiana, Heimerl, Thomas, Kueper, Ulf, Rachel, Reinhard, Keller, Martin, Hettich, Robert L. and Podar, Mircea (2011) Proteomic Characterization of Cellular and Molecular Processes that Enable the Nanoarchaeum equitans-Ignicoccus hospitalis Relationship. PLOS ONE 6 (8), e22942.

Date of publication of this fulltext: 17 Feb 2012 08:43
Article
DOI to cite this document: 10.5283/epub.23459


Abstract

Nanoarchaeum equitans, the only cultured representative of the Nanoarchaeota, is dependent on direct physical contact with its host, the hyperthermophile Ignicoccus hospitalis. The molecular mechanisms that enable this relationship are unknown. Using whole-cell proteomics, differences in the relative abundance of >75% of predicted protein-coding genes from both Archaea were measured to identify ...

Nanoarchaeum equitans, the only cultured representative of the Nanoarchaeota, is dependent on direct physical contact with its host, the hyperthermophile Ignicoccus hospitalis. The molecular mechanisms that enable this relationship are unknown. Using whole-cell proteomics, differences in the relative abundance of >75% of predicted protein-coding genes from both Archaea were measured to identify the specific response of I. hospitalis to the presence of N. equitans on its surface. A purified N. equitans sample was also analyzed for evidence of interspecies protein transfer. The depth of cellular proteome coverage achieved here is amongst the highest reported for any organism. Based on changes in the proteome under the specific conditions of this study, I. hospitalis reacts to N. equitans by curtailing genetic information processing (replication, transcription) in lieu of intensifying its energetic, protein processing and cellular membrane functions. We found no evidence of significant Ignicoccus biosynthetic enzymes being transported to N. equitans. These results suggest that, under laboratory conditions, N. equitans diverts some of its host's metabolism and cell cycle control to compensate for its own metabolic shortcomings, thus appearing to be entirely dependent on small, transferable metabolites and energetic precursors from I. hospitalis.



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Details

Item typeArticle
Journal or Publication TitlePLOS ONE
Publisher:PUBLIC LIBRARY SCIENCE
Place of Publication:SAN FRANCISCO
Volume:6
Number of Issue or Book Chapter:8
Page Range:e22942
DateAugust 2011
InstitutionsBiology, Preclinical Medicine > Institut für Biochemie, Genetik und Mikrobiologie > Lehrstuhl für Mikrobiologie (Archaeenzentrum)
Biology, Preclinical Medicine > Institut für Biochemie, Genetik und Mikrobiologie > Lehrstuhl für Mikrobiologie (Archaeenzentrum) > Prof. Dr. Reinhard Rachel
Identification Number
ValueType
10.1371/journal.pone.0022942DOI
KeywordsSET ENRICHMENT ANALYSIS; QUANTITATIVE PROTEOMICS; SHOTGUN PROTEOMICS; MASS-SPECTROMETRY; OUTER-MEMBRANE; PROTEIN; ARCHAEA; INSIGHTS; GENOME; DATABASE;
Dewey Decimal Classification500 Science > 570 Life sciences
StatusPublished
RefereedYes, this version has been refereed
Created at the University of RegensburgUnknown
URN of the UB Regensburgurn:nbn:de:bvb:355-epub-234596
Item ID23459

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