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Expression of hygromycin B resistance in oyster culinary-medicinal mushroom, Pleurotus ostreatus (Jacq.:Fr.)P. Kumm. (higher Basidiomycetes) using three gene expression systems
- Source :
- International journal of medicinal mushrooms. 14(1)
- Publication Year :
- 2012
-
Abstract
- Three hygromycin B phosphotransferase (hph) gene expression systems for culinary-medicinal Oyster mushroom, Pleurotus ostreatus, plasmid pSHC, pAN7-1, and pBHt1 were evaluated through PEG/CaCl(2)-mediated protoplast transformation. Plasmid pSHC is a newly constructed hph gene expression system, composed of Escherichia coli hph gene, the P. ostreatus sdi promoter, and the CaMV35S terminator. The vector pAN7-1 was commonly used for integrative transformation in filamentous fungi. Plasmid pBHtl is a T-DNA binary vector, usually introduced into fungi by Agrobacterium-mediated transformation. The results showed that plasmids pSHC, pAN7-1, and pBHt1 were all integrated into the host chromosomes and expressed hygromycin B resistance in P. ostreatus. pAN7-1 had the highest transformation efficiency and hph gene expression level, pSHC the second, and pBHt1 the lowest. Growth rates of the transformants on plates containing hygromycin B were in correspondence with their hph gene expression levels. To our knowledge, this is the first report on integrated transformation of plasmid pAN7-1 and pBHt1 in P. ostreatus.
- Subjects :
- Pharmacology
Regulation of gene expression
Mushroom
biology
Protoplast
biology.organism_classification
Pleurotus
Applied Microbiology and Biotechnology
Gene Expression Regulation, Enzymologic
Microbiology
chemistry.chemical_compound
Phosphotransferases (Alcohol Group Acceptor)
Plasmid
chemistry
Gene Expression Regulation, Fungal
Drug Discovery
Gene expression
Pleurotus ostreatus
Hygromycin B
Promoter Regions, Genetic
Transformation efficiency
Plasmids
Subjects
Details
- ISSN :
- 15219437
- Volume :
- 14
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- International journal of medicinal mushrooms
- Accession number :
- edsair.doi.dedup.....f0e9b7df92556661abf7e83d00b06a8f