Abstract

In matrix-assisted laser-desorption and ionization mass spectrometry, spectral differences are frequently observed using different growth media on agar plates and/or different growth times in culture, which add undesirable analytical variance. In this article, we explore an approach to the above problem based upon the rationale that, while protein expression in fungal mycelium may well vary under different growth conditions, this might not apply to the same extent in fungal spores. To this end, we have exploited the fact that while mycelium is generally anchored to the fungal-growth substrate, some fungi produce physically-isolated spores which, as such, are amenable to manipulation using dielectrophoresis (the translational motion of charged or uncharged matter caused by polarization effects in a non-uniform electrical field). Such fields can be conveniently generated through the charging of an insulator using the triboelectric effect (the transfer of charge between two objects through friction when they are rubbed together). In this study, polystyrene microbiological inoculating loops were used in combination with nylon-fabric rubbing to harvest fungal spores from five species from within the genus Penicillium, which were grown on agar plates containing two different media over an extended time course. In terms of average Bruker spectral-comparison scores, our method generated higher scores in 80% of cases tested and, in terms of average coefficients of variation, our method generated lower spectral variability in 93% of cases tested. Harvesting of spores using a rapid, inexpensive and simple dielectrophoretic method, therefore, facilitates improved fungal identification for the Penicillium species tested.

Highlights

  • Characterization and/or identification of biological samples can be achieved through analysis of the mass spectra of their constituent proteins [1, 2]

  • We explore an approach to the above problem based upon the rationale that, while protein expression in fungal mycelium may well vary under different growth conditions, this might not apply to the same extent in fungal spores

  • The spectra obtained by both methods are visibly similar, though noticeably more peaks are obtained from P. corylophilum IMI 273248 grown on Malt-extract agar (MEA) for biomass scraped from the agar

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Summary

Introduction

Characterization and/or identification of biological samples can be achieved through analysis of the mass spectra of their constituent proteins [1, 2] To this end, one rapid and inexpensive technique is matrix-assisted laser-desorption and ionization mass spectrometry (MALDI-TOF MS) [1, 3]. After an initial acceleration in this manner, their times-of-flight along an evacuated tube are proportional to the square root of their mass-over-charge (m/z) ratios [1]. Using this simple mathematical relationship, a mass spectrum can readily be generated for the protein components in a particular biological sample

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