<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>4(1)</volume><submitter>Reeve MA</submitter><funding>Crop Health and Protection Limited</funding><pubmed_abstract>Matrix-assisted laser-desorption and ionization time-of-flight mass spectrometry can be used for the characterization and identification of filamentous fungi, for which it is desirable to have a means of growth in which the resulting spectra remain as consistent as possible over time. To this end, we initially opted for growth in oil-overlaid small-volume liquid culture, using a medium (Czapek Dox) not containing significant amount of proteins or peptides, and with protein extraction from the entire culture volume. For both 3-week and 10-day time courses, however, we observed marked spectral changes over growth time, along with lower peak richness compared to agar-plate controls. Guided by the above, we next employed a more nutrient-rich MALDI-TOF MS-compatible liquid-culture medium, now u</pubmed_abstract><journal>Biology methods &amp; protocols</journal><pagination>bpz003</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7200990</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A method for filamentous fungal growth and sample preparation aimed at more consistent MALDI-TOF MS spectra despite variations in growth rates and/or incubation times.</pubmed_title><pmcid>PMC7200990</pmcid><pubmed_authors>Bachmann D</pubmed_authors><pubmed_authors>Reeve MA</pubmed_authors></additional><is_claimable>false</is_claimable><name>A method for filamentous fungal growth and sample preparation aimed at more consistent MALDI-TOF MS spectra despite variations in growth rates and/or incubation times.</name><description>Matrix-assisted laser-desorption and ionization time-of-flight mass spectrometry can be used for the characterization and identification of filamentous fungi, for which it is desirable to have a means of growth in which the resulting spectra remain as consistent as possible over time. To this end, we initially opted for growth in oil-overlaid small-volume liquid culture, using a medium (Czapek Dox) not containing significant amount of proteins or peptides, and with protein extraction from the entire culture volume. For both 3-week and 10-day time courses, however, we observed marked spectral changes over growth time, along with lower peak richness compared to agar-plate controls. Guided by the above, we next employed a more nutrient-rich MALDI-TOF MS-compatible liquid-culture medium, now u</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019</publication><modification>2025-04-07T12:26:17.67Z</modification><creation>2020-05-22T19:58:35Z</creation></dates><accession>S-EPMC7200990</accession><cross_references><pubmed>32395622</pubmed><doi>10.1093/biomethods/bpz003</doi></cross_references></HashMap>