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Identification of fungal microorganisms by MALDI-TOF mass spectrometry

期刊

BIOTECHNOLOGY ADVANCES
卷 32, 期 1, 页码 230-241

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.biotechadv.2013.11.002

关键词

Biotyping; Fungi; Identification; Intact cell/spore mass spectrometry; MALDI; Mildew; Peptide; Protein; Taxonomy; Yeasts

资金

  1. OP RDI [ED0007/01/01]
  2. student and academic staff mobilities within the Austria-Czech Republic exchange program AKTION [7AMB12AT018]
  3. OP EC [CZ.1.07/2.4.00/31.0130]
  4. Ministry of Education Youth and Sports, Czech Republic

向作者/读者索取更多资源

Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) has emerged as a reliable tool for fast identification and classification of microorganisms. In this regard, it represents a strong challenge to microscopic and molecular biology methods. Nowadays, commercial MALDI systems are accessible for biological research work as well as for diagnostic applications in clinical medicine, biotechnology and industry. They are employed namely in bacterial biotyping but numerous experimental strategies have also been developed for the analysis of fungi, which is the topic of the present review. Members of many fungal genera such as Aspergillus, Fusarium, Penicillium or Trichoderma and also various yeasts from clinical samples (e.g. Candida albicans) have been successfully identified by MALDI-TOF MS. However, there is no versatile method for fungi currently available even though the use of only a limited number of matrix compounds has been reported. Either intact cell/spore MALDI-TOF MS is chosen or an extraction of surface proteins is performed and then the resulting extract is measured. Biotrophic fungal phytopathogens can be identified via a direct acquisition of MALDI-TOF mass spectra e.g. from infected plant organs contaminated by fungal spores. Mass spectrometric peptide/protein profiles of fungi display peaks in the m/z region of 1000-20000, where a unique set of biomarker ions may appear facilitating a differentiation of samples at the level of genus, species or strain. This is done with the help of a processing software and spectral database of reference strains, which should preferably be constructed under the same standardized experimental conditions. (C) 2013 Elsevier Inc. All rights reserved.

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