2017
DOI: 10.1371/journal.pone.0173813
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Lignin-degrading peroxidases in white-rot fungus Trametes hirsuta 072. Absolute expression quantification of full multigene family

Abstract: Ligninolytic heme peroxidases comprise an extensive family of enzymes, which production is characteristic for white-rot Basidiomycota. The majority of fungal heme peroxidases are encoded by multigene families that differentially express closely related proteins. Currently, there were very few attempts to characterize the complete multigene family of heme peroxidases in a single fungus. Here we are focusing on identification and characterization of peroxidase genes, which are transcribed and secreted by basidio… Show more

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Cited by 40 publications
(17 citation statements)
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“…B). The ‘brown rot’ fungus Postia and the ‘white rot’ fungus Trametes (Vasina et al ., ) also exhibited a relatively higher gene expression in the lignocellulose treatments – suggesting that their activity was stimulated by this substrate. Most of the genes expressed encode hypothetical proteins with as‐of‐yet no biochemically determined function (Fig.…”
Section: Resultsmentioning
confidence: 94%
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“…B). The ‘brown rot’ fungus Postia and the ‘white rot’ fungus Trametes (Vasina et al ., ) also exhibited a relatively higher gene expression in the lignocellulose treatments – suggesting that their activity was stimulated by this substrate. Most of the genes expressed encode hypothetical proteins with as‐of‐yet no biochemically determined function (Fig.…”
Section: Resultsmentioning
confidence: 94%
“…6B). High relative expression genes encoding hypothetical proteins from the basidiomycete genera Wallemia, the 'brown rot' fungus Postia, and the 'white rot' fungus Trametes (Vasina et al, 2017) were detected ( Fig. 6B).…”
Section: Metatranscriptomicsmentioning
confidence: 99%
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“…In contrast, during cultivation of T . hirsuta on various media, secretion of peroxidases was shown to precede laccase secretion [ 22 , 48 ]. Such a difference in the secretion profiles of ligninolytic enzymes may be due to the fact that J .…”
Section: Discussionmentioning
confidence: 99%
“…Increasingly, however, it is becoming an indispensable tool in transcript abundance analysis as it exhibits greater sensitivity than qPCR when examining subtle fold-differences and has bene ts when mRNA is in low abundance (7). Additionally, ddPCR allows for reliable and reproducible measurements when anticipating closely related gene sequences or in the examination of highly similar mRNAs, such as those in multigene families (8). Due to the capacity of ddPCR to absolutely quantify the number of copies of the target in a given sample, normalization, such as the use of a reference gene, is not considered obligatory.…”
Section: Introductionmentioning
confidence: 99%