- 영문명
- Protoplast culture and fusion in cruciferae Ⅰ. Plant regeneration from mesophyll protoplast of rape(brassica napus L.)
- 발행기관
- 한국육종학회
- 저자명
- Byung Jun Park(朴炳俊) Bong Ho Lee(李奉鎬) Jae Kyun Shon(孫再根) Hyung Soo Suh(徐亨洙) Gun Sik Chung(鄭根植)
- 간행물 정보
- 『한국육종학회지』Vol.18 No.3, 42~49쪽, 전체 8쪽
- 주제분류
- 농수해양 > 기타농수해양
- 파일형태
- 발행일자
- 1986.09.30

국문 초록
영문 초록
The experiments were conducted to identify several factors influencing mesophyll protoplast isolation, culture and plant regeneration of rape(Brassica napus cv. ‘Hanrayuchae’) The results obtained were summarized as follows ;
It was required to preplasmolyse the mesophyll tissue before enzyme treatment to increase yield and stability of protoplasts.
The most healthy protoplasts could be obtained when the tissue was treated with enzymes containing macerozyme 1.0% and cellulase 2.0% for 4 hours.
Sustained cell division was obtained after culturing the protoplasts in liquid 8P-KM medium supplemented with 2.4-D 0.2mg/ℓ, NAA 1.0mg/ℓ, BAP 0.5mg/ℓ, glucose 0.4M, and mannitol 0.1M.
First cell division was observed 5 days after plating and was sustained to eventually produce cell colonies after another 16 days. When micro-calli 4-5 weeks after plating were transferred to B₅ basal medium with NAA 1.0mg/ℓ, BAP 0.5mg/ℓ, sucrose 30g/ℓ and agarose 6g/ℓ, green calli were proliferated to be at least 0.5-1.0cm in diameter 8 weeks after initial plating.
Multiple shoots were induced on MS medium supplemented with BAP 1.0mg/ℓ and NAA 0.01mg/ℓ. After transferring differentiated shoots onto MS medium without hormones, intact plants were eventually produced.
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