Towards a detailed understanding of bacterial metabolism -: Spectroscopic characterization of Staphylococcus epidermidis

被引:177
作者
Neugebauer, Ute
Schmid, Ulrike
Baumann, Knut
Ziebuhr, Wilma
Kozitskaya, Svetlana
Deckert, Volker
Schmitt, Michael
Popp, Juergen [1 ]
机构
[1] Univ Jena, Inst Phys Chem, D-6900 Jena, Germany
[2] Inst Phys Hochtechnol eV, D-07745 Jena, Germany
[3] Univ Wurzburg, Inst Pharm & Lebensmittelchem, D-97074 Wurzburg, Germany
[4] Inst Mol Infekt Biol, D-97070 Wurzburg, Germany
[5] Inst Analyt Sci, ISAS, D-44139 Dortmund, Germany
关键词
D O I
10.1002/cphc.200600507
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Bacteria are a major cause of infection. To fight disease and growing resistance, research interest is focused on understanding bacterial metabolism. For a detailed evaluation of the involved mechanisms, a precise knowledge of the molecular composition of the bacteria is required. In this article, various vibrational spectroscopic techniques are applied to comprehensively characterize, on a molecular level, bacteria of the strain Staphylococcus epidermidis, an opportunistic pathogen which has evolved to become a major cause of nosocomial infections. IR absorption spectroscopy reflects the overall chemical composition of the cells, with major focus on the protein vibrations. Smaller sample volumes-down to a single cell-are sufficient to probe the overall chemical composition by means of micro-Roman spectroscopy. The nucleic-acid and aromatic amino-acid moieties are almost exclusively explored by UV resonance Raman spectroscopy. In combination with statistical evaluation methods [hierarchical cluster analysis (HCA), principal component analysis (PCA), linear discriminant analysis (LDA)], the protein and nucleic-acid components that change during the different bacterial growth phases can be identified from the in vivo vibrational spectra. Furthermore, tip-enhanced Raman spectroscopy (TERS) provides insight into the surface structures and follows the dynamics of the polysaccharide and peptide components on the bacterial cells with a spatial resolution below the diffraction limit. This might open new ways for the elucidation of host-bacteria and drug-bacteria interactions.
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页码:124 / 137
页数:14
相关论文
共 56 条
[1]   Cell biology: Hopping fences [J].
Abbott, A .
NATURE, 2005, 433 (7027) :680-682
[2]   A systematic evaluation of the benefits and hazards of variable selection in latent variable regression. Part I. Search algorithm, theory and simulations [J].
Baumann, K ;
Albert, H ;
von Korff, M .
JOURNAL OF CHEMOMETRICS, 2002, 16 (07) :339-350
[3]   Chance correlation in variable subset regression: Influence of the objective function, the selection mechanism, and ensemble averaging [J].
Baumann, K .
QSAR & COMBINATORIAL SCIENCE, 2005, 24 (09) :1033-1046
[4]   Identification and preliminary characterization of cell-wall-anchored proteins of Staphylococcus epidermidis [J].
Bowden, MG ;
Chen, W ;
Singvall, J ;
Xu, Y ;
Peacock, SJ ;
Valtulina, V ;
Speziale, P ;
Höök, M .
MICROBIOLOGY-SGM, 2005, 151 :1453-1464
[5]   Bagging predictors [J].
Breiman, L .
MACHINE LEARNING, 1996, 24 (02) :123-140
[6]   Investigating microbial (micro)colony heterogeneity by vibrational spectroscopy [J].
Choo-Smith, LP ;
Maquelin, K ;
van Vreeswijk, T ;
Bruining, HA ;
Puppels, GJ ;
Thi, NAG ;
Kirschner, C ;
Naumann, D ;
Ami, D ;
Villa, AM ;
Orsini, F ;
Doglia, SM ;
Lamfarraj, H ;
Sockalingum, GD ;
Manfait, M ;
Allouch, P ;
Endtz, HP .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2001, 67 (04) :1461-1469
[7]   Raman spectroscopic study of Lactarius spores (Russulales, Fungi) [J].
De Gussem, K ;
Vandenabeele, P ;
Verbeken, A ;
Moens, L .
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 2005, 61 (13-14) :2896-2908
[8]  
DIERINGER JA, 2005, FARADAY DISCUSS, P1
[9]  
DIETTERICH TG, 2001, ENSEMBLE METHODS MAC
[10]   FOURIER-TRANSFORM RAMAN-SPECTROSCOPIC STUDY OF FUNGI [J].
EDWARDS, HGM ;
RUSSELL, NC ;
WEINSTEIN, R ;
WYNNWILLIAMS, DD .
JOURNAL OF RAMAN SPECTROSCOPY, 1995, 26 (8-9) :911-916