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1.
Mycobiology ; : 1-6, 2016.
Artículo en Inglés | WPRIM | ID: wpr-729460

RESUMEN

Ganoderma lucidum has a long history of use as a traditional medicine in Asian countries. However, the taxonomy of Ganoderma species remains controversial, since they were initially classified on the basis of their morphological characteristics. Recently, it was proposed that G. lucidum from China be renamed as G. sichuanense or G. lingzhi. In the present study, phylogenetic analysis using the internal transcribed spacer region rDNA sequences of the Ganoderma species indicated that all strains of the Korean 'G. lucidum' clustered into one group together with G. sichuanense and G. lingzhi from China. However, strains from Europe and North American, which were regarded as true G. lucidum, were positioned in a clearly different group. In addition, the average size of the basidiospores from the Korean cultivated Yeongji strains was similar to that of G. lingzhi. Based on these results, we propose that the Korean cultivated Yeongji strains of 'G. lucidum' should be renamed as G. lingzhi.


Asunto(s)
Humanos , Pueblo Asiatico , China , Clasificación , ADN Ribosómico , Europa (Continente) , Ganoderma , Corea (Geográfico) , Medicina Tradicional , Filogenia , Reishi
2.
Mycobiology ; : 327-332, 2015.
Artículo en Inglés | WPRIM | ID: wpr-729629

RESUMEN

Phenylalanine ammonia-lyase (PAL) gene is known to be expressed in plants, and is involved in the differentiation, growth and synthesis of secondary metabolites. However, its expression in fungi remains to be explored. To understand its expression in mushroom fungi, the PAL gene of the edible mushroom Flammulina velutipes (Fvpal) was cloned and characterized. The cloned Fvpal consists of 2,175 bp, coding for a polypeptide containing 724 amino acids and having 11 introns. The translated amino acid sequence of Fvpal shares a high identity (66%) with that of ectomycorrhizal fungus Tricholoma matsutake. Distinctively, the Fvpal expression in the mycelium was higher in minimal medium supplemented with L-tyrosine than with other aromatic amino acids. During cultivation of the mushroom on sawdust medium, Fvpal expression in the fruit body correspondingly increased as the mushroom grew. In the fruiting body, Fvpal was expressed more in the stipe than in the pileus. These results suggest that F. velutipes PAL activity differs in the different organs of the mushroom. Overall, this is first report to show that the PAL gene expression is associated with mushroom growth in fungi.


Asunto(s)
Agaricales , Secuencia de Aminoácidos , Aminoácidos , Aminoácidos Aromáticos , Codificación Clínica , Células Clonales , Clonación de Organismos , Flammulina , Frutas , Hongos , Expresión Génica , Intrones , Micelio , Fenilanina Amoníaco-Liasa , Fenilalanina , Tricholoma , Tirosina
3.
Mycobiology ; : 322-330, 2014.
Artículo en Inglés | WPRIM | ID: wpr-729866

RESUMEN

The aim of this study was to identify and characterize new Flammulina velutipes laccases from its whole-genome sequence. Of the 15 putative laccase genes detected in the F. velutipes genome, four new laccase genes (fvLac-1, fvLac-2, fvLac3, and fvLac-4) were found to contain four complete copper-binding regions (ten histidine residues and one cysteine residue) and four cysteine residues involved in forming disulfide bridges, fvLac-1, fvLac-2, fvLac3, and fvLac-4, encoding proteins consisting of 516, 518, 515, and 533 amino acid residues, respectively. Potential N-glycosylation sites (Asn-Xaa-Ser/Thr) were identified in the cDNA sequence of fvLac-1 (Asn-454), fvLac-2 (Asn-437 and Asn-455), fvLac-3 (Asn-111 and Asn-237), and fvLac4 (Asn-402 and Asn-457). In addition, the first 19~20 amino acid residues of these proteins were predicted to comprise signal peptides. Laccase activity assays and reverse transcription polymerase chain reaction analyses clearly reveal that CuSO4 affects the induction and the transcription level of these laccase genes.


Asunto(s)
Sulfato de Cobre , Cisteína , ADN Complementario , Flammulina , Hongos , Genoma , Histidina , Lacasa , Reacción en Cadena de la Polimerasa , Señales de Clasificación de Proteína , Transcripción Reversa
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