DNA-based identification of Lentinula edodes strains with species-specific primers
Author(s) -
L George Pheba,
R Sripathi Venkateswara,
T Nyaku Seloame,
Chandra Govind,
V Kantety Ramesh
Publication year - 2016
Publication title -
african journal of biotechnology
Language(s) - English
Resource type - Journals
ISSN - 1684-5315
DOI - 10.5897/ajb2015.15089
Subject(s) - lentinula , biology , flammulina , primer (cosmetics) , grifola frondosa , agaricus bisporus , basidiomycota , mushroom , boletus , polymerase chain reaction , fungus , lentinus , agaricales , edible mushroom , microbiology and biotechnology , botany , gene , genetics , chemistry , taxonomy (biology) , organic chemistry
Lentinula edodes is among the five globally cultivated edible mushrooms, which are wood decaying spore bearing Basidiomycetes possessing separate hyphae. Specific identification of this fungus from others in the division Basidiomycota using specific primers enables a fast and accurate detection through polymerase chain reaction (PCR). As a prelude to additional nutritional and sequence characterization research, we have developed a species-specific PCR assay for this fungus after screening four primer-pairs and two universal primer pairs. The primer-pair LE1F/R was specific in amplifications of ATCC-defined L. edodes strains and did not amplify DNA from six medicinally and nutritionally important fungal reference strains, Oyster (Pleurotus ostreatus), Maitake (Grifola frondosa), Enoki (Flammulina velutipes), Baby bella (Agaricus bisporus), Porcini (Boletus edulis), and Chanterelle (Cantharellus cibarius). However, amplifications using the universal primers were positive for all six strains. This assay will therefore serve to validate morphology-based-identifications of L. edodes strains. Key words: Lentinula edodes, LE1F/R, species-specific primers.
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