2020
DOI: 10.1016/j.talanta.2020.121238
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New method for rapid identification and quantification of fungal biomass using ergosterol autofluorescence

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Cited by 14 publications
(7 citation statements)
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“…Similar procedures have opened also valuable perspective for the autofluorescence-based assessment of the fungal biomass in solid or semisolid fermentation processes, for example to monitor the consumption of nutrients, CO 2 generation in the production of compounds of industrial and commercial interest. Only a simple extraction procedure is required, making particularly easy and fast to assay filamentous fungi from solid or semisolid mass, with a technique potentially extendable to the analysis of fungal food contamination [160].…”
Section: Fungimentioning
confidence: 99%
“…Similar procedures have opened also valuable perspective for the autofluorescence-based assessment of the fungal biomass in solid or semisolid fermentation processes, for example to monitor the consumption of nutrients, CO 2 generation in the production of compounds of industrial and commercial interest. Only a simple extraction procedure is required, making particularly easy and fast to assay filamentous fungi from solid or semisolid mass, with a technique potentially extendable to the analysis of fungal food contamination [160].…”
Section: Fungimentioning
confidence: 99%
“…It is also a target of many azole antifungal drugs ( Michael and Galina, 2005 ; Galina and Michael, 2006 ). The lack or complete absence of ergosterol biosynthesis will alter the fluidity of the fungal cell membrane and might change the activities of related enzymes on the fungal cell membrane, affecting the function of the fungal cell membrane and inhibiting the growth of fungi ( Daum et al, 1998 ; Lees et al, 1999 ; Minnebruggen et al, 2010 ; Felipe et al, 2020 ). In the study of antifungal mechanism of cinnamaldehyde, under the action of cinnamaldehyde, the expression of the ERG11 gene encoding sterol 14 α-demethylase in Fusarium sambucinum was downregulated, and the ergosterol content in this fungus was decreased by 67.94%, which resulted in cell membrane damage, a slow spore growth rate, and a decrease in pathogenicity ( Wei et al, 2020 ).…”
Section: Introductionmentioning
confidence: 99%
“…As shown in Fig. 6 a, P. ostreatus could not colonization when directly using mixed raw DGW as the substrates because no ergosterol, which is commonly used as a marker to characterize fungal growth [ 59 ], was detected in the DGW substrate. By comparison, after 48 h of composting, DGW was the favorable substrate for P. ostreatus growth.…”
Section: Resultsmentioning
confidence: 99%