2015
DOI: 10.5941/myco.2015.43.1.1
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Current Technologies and Related Issues for Mushroom Transformation

Abstract: Mushroom transformation requires a series of experimental steps, including generation of host strains with a desirable selective marker, design of vector DNA, removal of host cell wall, introduction of foreign DNA across the cell membrane, and integration into host genomic DNA or maintenance of an autonomous vector DNA inside the host cell. This review introduces limitations and obstacles related to transformation technologies along with possible solutions. Current methods for cell wall removal and cell membra… Show more

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Cited by 22 publications
(16 citation statements)
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References 88 publications
(114 reference statements)
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“…4). Binary vector pBHg-BCA1, the promoter of glyceraldehyde-3-phosphate dehydrogenase with the first exon and intron (Pgpd) (33) and the terminator of trpC (TtrpC) (34,35) were used to construct pdd1-OE and pdd1-RNAi. The pdd1 overexpression vector was completed by introducing a copy of pdd1 flanked by Pgpd and TtrpC (Fig.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…4). Binary vector pBHg-BCA1, the promoter of glyceraldehyde-3-phosphate dehydrogenase with the first exon and intron (Pgpd) (33) and the terminator of trpC (TtrpC) (34,35) were used to construct pdd1-OE and pdd1-RNAi. The pdd1 overexpression vector was completed by introducing a copy of pdd1 flanked by Pgpd and TtrpC (Fig.…”
Section: Resultsmentioning
confidence: 99%
“…4A and B, respectively. In both plasmids, the promoter of glyceraldehyde-3-phosphate dehydrogenase-encoding gene gpd (Pgpd) and the terminator of indole-3-glycerol phosphate synthase-encoding gene trpC (TtrpC) were used to control expression of pdd1 or the sense and antisense sequences of pdd1 (33)(34)(35).…”
Section: Methodsmentioning
confidence: 99%
“…The binary vector pBHg-BCA1 containing the resistance gene of hygromycin was used in the construction of the Fvcpc2 overexpression plasmid and RNAi plasmid as previously described (Wu et al, 2019). The promoter of glyceraldehyde-3-phosphate dehydrogenase Pgpd and terminator of trpC (TtrpC) were used to control the expression of Fvcpc2 or the sense and antisense sequence of Fvcpc2 in both plasmids (Kuo et al, 2004;Sekiya et al, 2013;Kim et al, 2015).…”
Section: Plasmid Construction and Transformation In F Velutipesmentioning
confidence: 99%
“…To understand the function of Fvcpc2 in F. velutipes, the Fvcpc2 overexpression vector Fvcpc2-OE and the Fvcpc2 knockdown vector Fvcpc2-RNAi were constructed, respectively. The binary vector pBHg-BCA1, the promoter of glyceraldehyde-3-phosphate dehydrogenase (Pgpd) (Kuo et al, 2004) and the terminator of trpC (TtrpC) (Sekiya et al, 2013;Kim et al, 2015) were used to construct these plasmids as previously described (Wu et al, 2019).…”
Section: Generation Of Mutants For Fvcpc2 Overexpression and Knockdowmentioning
confidence: 99%
“…Because of the high regeneration efficiency and easy preparation, mycelia were used in this study. Successful ATMT of filamentous fungi relies on several factors, such as acetosyringone (AS) concentration, strains of A. tumefaciens , cultivation conditions, recipient tissue, and so on [30].…”
Section: Introductionmentioning
confidence: 99%