Mycobiology.  2003 Mar;31(1):32-35. 10.4489/MYCO.2003.31.1.032.

The Efficient Transformation of Pleurotus ostreatus using REMI Method

Affiliations
  • 1Department of Biochemistry, Kon-kuk University, Chung-Ju 380-701, Korea.
  • 2Molecular physiology division, National Institute of Agricultural Biotechnology, Suwon 441-707, Korea. bgkimyes@rda.go.kr
  • 3Applied microbiology division, National Institute of Agricultural Sciences and Technologies, Suwon 441-707, Korea.

Abstract

Restriction enzyme-mediated integration (REMI) was used to transform uracil auxotrophs of Pleurotus ostreatus to prototrophy. When protoplasts of Pleurotus ostreatus were treated by the reaction mixture containing 10 units of BamHI, the frequency of REMI was about 64 transformants per 1 microg of DNA. This efficiency was increased by 14.2 times compared with that of the conventional PEG transformation. The optimal condition for REMI of P. ostreatus was achieved when 1 microg of linearized pTRura3-2 DNA was added into 1x10(7) protoplasts along with 10 units BamHI. Southern blot analysis revealed that about 50% of transformants examined were caused by REMI event and 30% carried single copy insertion at the genome. This suggested that the REMI method might be a useful tool for efficient transformation and tagging mutagenesis of P. ostreatus.

Keyword

Pleurotus ostreatus; Restriction enzyme-mediated integration (REMI); Uracil auxotrophic marker

MeSH Terms

Blotting, Southern
DNA
Genome
Mutagenesis
Pleurotus*
Protoplasts
Uracil
DNA
Uracil
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