Research Article
Desorption electrospray ionization mass spectrometry of intact bacteria
Article first published online: 13 JUL 2007
DOI: 10.1002/jms.1250
Copyright © 2007 John Wiley & Sons, Ltd.
Additional Information
How to Cite
Meetani, M. A., Shin, Y.-S., Zhang, S., Mayer, R. and Basile, F. (2007), Desorption electrospray ionization mass spectrometry of intact bacteria. J. Mass Spectrom., 42: 1186–1193. doi: 10.1002/jms.1250
Publication History
- Issue published online: 22 AUG 2007
- Article first published online: 13 JUL 2007
- Manuscript Accepted: 8 MAY 2007
- Manuscript Received: 5 FEB 2007
Funded by
- National Institutes of Health-National Center for Research Resources. Grant Number: R15-RR020354-01A1
- Agricultural Research Service of the United States Department of Agriculture. Grant Number: 448800
- Individual Research Grant. Grant Number: 06-03-2-11/06
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Keywords:
- desorption electrospray ionization;
- bacteria;
- biodetection;
- principal components analysis;
- biomarkers
Abstract
Desorption electrospray ionization (DESI) mass spectrometry (MS) was used to differentiate seven bacteria species on the basis of their measured DESI-mass spectral profile. Both gram-positive and gram-negative bacteria were tested and included Escherichia coli, Staphyloccocus aureus, Enterococcus sp., Bordetella bronchiseptica, Bacillus thuringiensis, Bacillus subtilis and Salmonella typhimurium. Distinct DESI-mass spectra, in the mass range of 50–500 u, were obtained from whole bacteria in either positive or negative ion modes in less than 2 mins analysis time. Positive ion DESI-mass spectral fingerprints were compared using principal components analysis (PCA) to investigate reproducibility for the intraday and the day-to-day measurements and the method selectivity to differentiate the bacteria studied. Detailed study of variances in the assay revealed that a large contribution to the DESI-mass spectral fingerprint variation was the growth media preparation procedure. Specifically, experiments conducted with the growth media prepared using the same batch yielded highly reproducible DESI-mass spectra, both in intraday and in day-to-day analyses (i.e. one batch of growth media used over a 3-day period versus a new batch every day over the same 3-day period). Conclusions are drawn from our findings in terms of strategies for rapid biodetection with DESI-MS. Copyright © 2007 John Wiley & Sons, Ltd.

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