국내 딸기 재배품종의 잎절편 배양으로부터 고빈도 식물체 재생

To develop a high efficiency plant regeneration system from in vitro cultures of strawberry, cv. Yeobong, petiole and leaf explants were cultured on MS basal medium containing a combination of 0.5 mg/L IBA and 3.2 mg/L kinetin or zeatin or benzyl amino purine (BAP) for 6 weeks, and leaf explants wit...

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Published inJournal of plant biotechnology Vol. 32; no. 3; pp. 175 - 179
Main Authors 조미애(Mi Ae Cho), 최규명(Kyu Myeong Choi), 고석민(Suck Min Ko), 민성란(Sung Ran Min), 정화지(Hwa Ji Chung), 유장렬(Jang Ry
Format Journal Article
LanguageKorean
Published Korean Society for Plant Biotechnology 2005
(사)한국식물생명공학회
한국식물생명공학회
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ISSN1229-2818
1598-6365
2384-1397

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Summary:To develop a high efficiency plant regeneration system from in vitro cultures of strawberry, cv. Yeobong, petiole and leaf explants were cultured on MS basal medium containing a combination of 0.5 mg/L IBA and 3.2 mg/L kinetin or zeatin or benzyl amino purine (BAP) for 6 weeks, and leaf explants with dark pretreatment for a week ($T_1$), 2 weeks ($T_2$), and 4 weeks ($T_3$) were cultured on medium supplemented with 0.5 mg/L IBA and 3.2 mg/L zeatin under 16 hr photoperiod for 6 weeks. Shoot organogenesis was observed from the greenish calli containing minimal anthocyanin formed at proximal cutting edges of the leaf explant (57%) when cultured adaxial side on the medium, whereas was directly formed from a cutting edges of petiole explant (6.3%). Frequency of callus formation and shoot organogenesis at large size of leaf explant ($1.0{\sim}1.5\;cm^2$) was higher than small size ($0.5{\sim}1.0\;cm^2$), and dark pretreatment significantly improved the frequency of leaf explants that produced calli and shoots. The maximum frequency (87%) for shoot organogenesis was obtained from the leaf explants that transferred to a 16 hr photoperiod condition after the initial 4 weeks dark period. The improved frequency (87%) in comparision with control without dark pretreatment (27%). When the shoots were transferred to 1/2 MS basal medium, formed roots with 20 d of culture. The rooted plants were subsequently transferred to the pots and to the field. 딸기 기내배양으로부터 고빈도 식물체재생 방법을 개발하기 위하여 여봉딸기의 잎과 엽병절편을 0.5 mg/L IBA와 3.2 mg/L kinetin, BAP, zeatin을 각각 조합 첨가한 MS배지에서, 그리고 1주, 2주, 4주동안 암 전처리한 잎 절편을 0.5 mg/L IBA와 3.2 mg/L zeatin이 첨가된 배지에서 6주동안 16시간 광주기 조건으로 배양하였다. 신초 발생은 잎을 adaxial상태로 치상하였을때 절단부위로부터 안토시아닌 색소를 함유한 녹색 캘러스로부터 유도되었고 (57.0%), 엽병의 경우 절단부위로부터 직접 발생되었다(6.3%). 캘러스와 신초발생율은 잎 절편 크기가 클수록 ($1.0{\sim}1.5\;cm^2$) 높았으며, 암 전처리는 그 발생율을 점차 증가시켜 4주동안 암 전처리한 후 16시간 광조건으로 옮겼을 때 가장 높은 발생율 (87.0%)을 얻을 수 있었다. 이러한 shoot발생율 (87%)은 암 전처리를 하지 않은 대조군 (27%) 에 비하여 현저하게 증가된 것이다. 신초를 분리하여 1/2 MS기본배지에 옮겨20동안 배양하였을 때 뿌리가 발생되었으며, 이때 소식물체를 토양에 옮겨 순화시켰다.
Bibliography:KISTI1.1003/JNL.JAKO200517033423343
G704-000847.2005.32.3.007
ISSN:1229-2818
1598-6365
2384-1397