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Mycelial biomass estimation and metabolic quotient of Lentinula edodes using species-specific qPCR
Lentinula edodes, commonly known as shiitake, is an edible mushroom that is cultivated and consumed around the globe, especially in Asia. Monitoring mycelial growth inside a woody substrate is difficult, but it is essential for effective management of mushroom cultivation. Mycelial biomass also affe...
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Published in: | PloS one 2020-05, Vol.15 (5), p.e0232049-e0232049 |
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description | Lentinula edodes, commonly known as shiitake, is an edible mushroom that is cultivated and consumed around the globe, especially in Asia. Monitoring mycelial growth inside a woody substrate is difficult, but it is essential for effective management of mushroom cultivation. Mycelial biomass also affects the rate of wood decomposition under natural conditions and must be known to determine the metabolic quotient, an important ecophysiological parameter of fungal growth. Therefore, developing a method to measure it inside a substrate would be very useful. In this study, as the first step in understanding species-specific rates of fungal decomposition of wood, we developed species-specific primers and qPCR procedures for L. edodes. We tested primer specificity using strains of L. edodes from Japan and Southeast Asia, as well as related species of fungi and plant species for cultivation of L. edodes, and generated a calibration curve for quantification of mycelial biomass in wood dust inoculated with L. edodes. The qPCR procedure we developed can specifically detect L. edodes and allowed us to quantify the increase in L. edodes biomass in wood dust substrate and calculate the metabolic quotient based on the mycelial biomass and respiration rate. Development of a species-specific method for biomass quantification will be useful for both estimation of mycelial biomass and determining the kinetics of fungal growth in decomposition processes. |
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Monitoring mycelial growth inside a woody substrate is difficult, but it is essential for effective management of mushroom cultivation. Mycelial biomass also affects the rate of wood decomposition under natural conditions and must be known to determine the metabolic quotient, an important ecophysiological parameter of fungal growth. Therefore, developing a method to measure it inside a substrate would be very useful. In this study, as the first step in understanding species-specific rates of fungal decomposition of wood, we developed species-specific primers and qPCR procedures for L. edodes. We tested primer specificity using strains of L. edodes from Japan and Southeast Asia, as well as related species of fungi and plant species for cultivation of L. edodes, and generated a calibration curve for quantification of mycelial biomass in wood dust inoculated with L. edodes. The qPCR procedure we developed can specifically detect L. edodes and allowed us to quantify the increase in L. edodes biomass in wood dust substrate and calculate the metabolic quotient based on the mycelial biomass and respiration rate. Development of a species-specific method for biomass quantification will be useful for both estimation of mycelial biomass and determining the kinetics of fungal growth in decomposition processes.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0232049</identifier><identifier>PMID: 32421692</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Basidiocarps ; Biology and Life Sciences ; Biomass ; Calibration ; Cultivation ; Decomposition ; Deoxyribonucleic acid ; DNA ; Dust ; Ecology and Environmental Sciences ; EDTA ; Environmental conditions ; Forest products ; Fungi ; Fungiculture ; Genetic testing ; Growth ; Lentinula edodes ; Measurement ; Metabolism ; Mushrooms ; Mycelia ; Mycelium ; Plant biomass ; Plant species ; Quotients ; Research and Analysis Methods ; Shiitake ; Species ; Substrates ; Wood</subject><ispartof>PloS one, 2020-05, Vol.15 (5), p.e0232049-e0232049</ispartof><rights>COPYRIGHT 2020 Public Library of Science</rights><rights>2020 Jomura et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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Monitoring mycelial growth inside a woody substrate is difficult, but it is essential for effective management of mushroom cultivation. Mycelial biomass also affects the rate of wood decomposition under natural conditions and must be known to determine the metabolic quotient, an important ecophysiological parameter of fungal growth. Therefore, developing a method to measure it inside a substrate would be very useful. In this study, as the first step in understanding species-specific rates of fungal decomposition of wood, we developed species-specific primers and qPCR procedures for L. edodes. We tested primer specificity using strains of L. edodes from Japan and Southeast Asia, as well as related species of fungi and plant species for cultivation of L. edodes, and generated a calibration curve for quantification of mycelial biomass in wood dust inoculated with L. edodes. The qPCR procedure we developed can specifically detect L. edodes and allowed us to quantify the increase in L. edodes biomass in wood dust substrate and calculate the metabolic quotient based on the mycelial biomass and respiration rate. Development of a species-specific method for biomass quantification will be useful for both estimation of mycelial biomass and determining the kinetics of fungal growth in decomposition processes.</description><subject>Basidiocarps</subject><subject>Biology and Life Sciences</subject><subject>Biomass</subject><subject>Calibration</subject><subject>Cultivation</subject><subject>Decomposition</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Dust</subject><subject>Ecology and Environmental Sciences</subject><subject>EDTA</subject><subject>Environmental conditions</subject><subject>Forest products</subject><subject>Fungi</subject><subject>Fungiculture</subject><subject>Genetic testing</subject><subject>Growth</subject><subject>Lentinula edodes</subject><subject>Measurement</subject><subject>Metabolism</subject><subject>Mushrooms</subject><subject>Mycelia</subject><subject>Mycelium</subject><subject>Plant biomass</subject><subject>Plant 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biomass estimation and metabolic quotient of Lentinula edodes using species-specific qPCR</title><author>Jomura, Mayuko ; Kuwayama, Tomoko ; Soma, Yuto ; Yamaguchi, Muneyoshi ; Komatsu, Masabumi ; Maruyama, Yutaka</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c688t-22a221f39ab665c5c81fd27533dde93964edf52d2ccbd0c311ce88030b9ccf493</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Basidiocarps</topic><topic>Biology and Life Sciences</topic><topic>Biomass</topic><topic>Calibration</topic><topic>Cultivation</topic><topic>Decomposition</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>Dust</topic><topic>Ecology and Environmental Sciences</topic><topic>EDTA</topic><topic>Environmental conditions</topic><topic>Forest products</topic><topic>Fungi</topic><topic>Fungiculture</topic><topic>Genetic testing</topic><topic>Growth</topic><topic>Lentinula 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shiitake, is an edible mushroom that is cultivated and consumed around the globe, especially in Asia. Monitoring mycelial growth inside a woody substrate is difficult, but it is essential for effective management of mushroom cultivation. Mycelial biomass also affects the rate of wood decomposition under natural conditions and must be known to determine the metabolic quotient, an important ecophysiological parameter of fungal growth. Therefore, developing a method to measure it inside a substrate would be very useful. In this study, as the first step in understanding species-specific rates of fungal decomposition of wood, we developed species-specific primers and qPCR procedures for L. edodes. We tested primer specificity using strains of L. edodes from Japan and Southeast Asia, as well as related species of fungi and plant species for cultivation of L. edodes, and generated a calibration curve for quantification of mycelial biomass in wood dust inoculated with L. edodes. The qPCR procedure we developed can specifically detect L. edodes and allowed us to quantify the increase in L. edodes biomass in wood dust substrate and calculate the metabolic quotient based on the mycelial biomass and respiration rate. Development of a species-specific method for biomass quantification will be useful for both estimation of mycelial biomass and determining the kinetics of fungal growth in decomposition processes.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>32421692</pmid><doi>10.1371/journal.pone.0232049</doi><tpages>e0232049</tpages><orcidid>https://orcid.org/0000-0002-9858-3771</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Basidiocarps Biology and Life Sciences Biomass Calibration Cultivation Decomposition Deoxyribonucleic acid DNA Dust Ecology and Environmental Sciences EDTA Environmental conditions Forest products Fungi Fungiculture Genetic testing Growth Lentinula edodes Measurement Metabolism Mushrooms Mycelia Mycelium Plant biomass Plant species Quotients Research and Analysis Methods Shiitake Species Substrates Wood |
title | Mycelial biomass estimation and metabolic quotient of Lentinula edodes using species-specific qPCR |
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