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dc.creatorZhang,Yuejin
dc.creatorQin,Yali
dc.creatorGuo,Lijun
dc.creatorZhou,Zili
dc.creatorLiang,Zongsuo
dc.creatorZhang,Chenlu
dc.creatorGuo,Hongbo
dc.date2012-09-01
dc.date.accessioned2019-05-03T12:44:59Z
dc.date.available2019-05-03T12:44:59Z
dc.identifierhttps://scielo.conicyt.cl/scielo.php?script=sci_arttext&pid=S0717-34582012000500010
dc.identifier.urihttp://revistaschilenas.uchile.cl/handle/2250/85296
dc.descriptionBackground: The dried sclerotium of medicinal fungus Polyporus umbellatus (Pers.) Fries has many pharmacological functions such as diuretic and anticancer activity, in which high-content polysaccharides may play an important role. However, RNA isolation is difficult in filamentous fungi and lacking in P. umbellatus. Results: Five methods for RNA extraction from five strains collected from four provinces were assessed for their ability to recover a high-quality RNA applicable for sequence-related amplification polymorphism (SRAP) PCR and GDP-D-mannose pyrophosphorylase (GMP) gene expression profiles. Both A260/A280 and A260/A230 ratios of the best Trizol Plus + RNAiso-mate for Plant Tissue method are around 2 with a yield of 1122.00 ± 0.21 ng μl-1. The Trizol method also showed good quality with the yield 469.60 ng μl-1. The SRAP PCR amplified clear and polymorphic bands in all five cDNA samples transcribed from RNA by using primer Me4-Em4. GMP gene fragment (1251 bp) was successfully amplified by RT-PCR, suggesting the integrity of isolated RNA. Conclusion: All these results showed that the total RNA isolated by this protocol is of sufficient quality for subsequent molecular applications.
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dc.languageen
dc.publisherPontificia Universidad Católica de Valparaíso
dc.rightsinfo:eu-repo/semantics/openAccess
dc.sourceElectronic Journal of Biotechnology v.15 n.5 2012
dc.subjectChuling
dc.subjectmedicinal fungus
dc.subjectPolyporus umbellatus
dc.subjectRNA isolation
dc.titleIsolation of high quality RNA from Polyporus umbellatus (Pers.) Fries


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