• 제목/요약/키워드: friable embryogenic callus (FEC)

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Lilium longiflorum 'Nellie White'의 인편으로부터 Friable 배발생 캘러스를 통한 소자구 분화 (Bulblet Differentiation through the Formation of Friable Embryogenic Callus from Bulb Scales of Lilium longiflorum 'Nellie White')

  • 한봉희;이수영;서은정;우종규
    • Journal of Plant Biotechnology
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    • 제32권2호
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    • pp.123-128
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    • 2005
  • Lilium longiflorum 'Nellie White'에서 부서지기 쉬운 배발생 캘러스 (FEC)를 유도하여 FEC를 통한 소자구 재분화 체계를 확립하고자 실시하였다. FEC를 통한 나리 소자구 분화는 2.0 mg/L dicamba가 첨가된 MS 기본배지에 나리 인편을 배양하여 단단한 캘러스를 유도하고, 유도된 단단한 캘러스를 동일배지에서 3번 이상 계대배양하여 단단한 일반 캘러스를 증식하였다. 증식된 단단한 캘러스는 $1{\sim}2mm$ 정도의 크기로 절단하여 2.0 mg/L dicamba와 90 g/L sucrose가 첨가된 MS배지에서 배양하여 FEC를 유도하였다. 2개월 간격으로 계대배양하면서 FEC를 유도하였으며, FEC 유도율은 단단한 캘러스를 동일 배지에 계대배양 하였을 때 증가하였다. 유도된 FEC는 $1.0{\sim}2.0\;mg/L$ dicamba와 90 g/L sucrose가 첨가된 MS배지에서 5배 이상의 증식율을 보였다. 증식된 FEC에서 소자구 분화는 0.1 mg/L BA, 1.0 g/L NAA, 30 g/L maltose가 첨가된 1/2 MS 배지에서 양호하였다. 그러나 많은 재분화된 소자구가 투명화 되었다. 건전한 소자구의 재분화는 30 g/L sucrose와 $0.5{\sim}1.0%$ 활성탄이 첨가된 MS 배지가 가장 효과적이었다.

Picloram을 이용한 효율적인 백합 캘러스 유도 체계 확립 (Establishment of Efficient Callus Induction System with Picloram Hormone in Lily Plants)

  • 김종보
    • 문화기술의 융합
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    • 제7권3호
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    • pp.605-608
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    • 2021
  • 나리는 세계 5대 절화에 속하는 주요 절화 중의 하나이며, 아시아, 유라시아 및 북아메리카 등 다양한 지역에 서식한다. 나리 신품종개발을 위해서는 교배, 돌연변이 및 선발육종 기술 외에 조직배양 기술을 포함하는 생명공학기술 도입을 통한 신품종 육성이 필요한데 조직배양 체계확립은 나리 육종체계에 있어서 필수적인 요소 중 하나이다. 조직배양의 많은 분야 중 배발생캘러스를 이용하여 식물체 재분화 증식 체계확립이 많은 작물에서 연구 중인데 본 연구에서도 배발생캘러스 유도에 사용되는 오옥신 중 picloram을 다양한 농도로 처리하여 최적의 배발생캘러스 유도 농도를 선정하고자 실험을 수행하였다. 실험 결과, 3-4주 후부터 CEC (compact embryogenic callus), FEC (friable embryogenic callus) 및 백색캘러스 이렇게 3가지 형태 캘러스가 발생했는데 1.0 mg/l 처리구에서 CEC와 FEC 모두 높은 효율을 나타내었으나 갈변율이 높은 관계로 0.75 mg/l를 나리 배발생캘러스 유도에 적합한 최적 농도로 선정하였다. 이러한 연구결과는 향후 배발생캘러스를 이용한 나리 식물체 재분화 체계 확립 그리고 우량품종 증식체계 확립에 기여할 것이다.

Production of transgenic Alstroemeria plants containing virus resistance genes via particle bombardment

  • Kim, Jong Bo
    • Journal of Plant Biotechnology
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    • 제47권2호
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    • pp.164-171
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    • 2020
  • Transgenic Alstroemeria plants resistant to Alstroemeria mosaic virus (AlMV) were generated through RNA-mediated resistance. To this end, the friable embryogenic callus (FEC) of Alstroemeria was induced from the leaf axil tissue and transformed with a DNA fragment containing the coat protein gene and 3'-nontranslated region of AlMV through an improved particle bombardment system. The bar gene was used as a selection marker. More than 300 independent transgenic FEC lines were obtained. Among these, 155 lines resistant to phosphinothricin (PPT) were selected under low stringent conditions. After increasing the stringency of PPT selection, 44 transgenic lines remained, and 710 somatic embryos from these lines germinated and developed into shoots. These transgenic shoots were then transferred to the greenhouse and challenged with AlMV. In total, 25 of the 44 lines showed some degree of resistance. PCR analysis confirmed the presence of the viral sequence. Virus resistance was observed at various levels. Establishment of an efficient transformation system for Alstroemeria will allow inserting transgenes into this plant to confer resistance to viral and fungal pathogens. Accordingly, this is the first report on the production of a transgenic virus-resistant Alstroemeria and lays the foundation for alternative management of viral diseases in this plant.

Somatic embryogenesis induction in four cassava landraces in East Java, Indonesia

  • Slameto;Indri Fariroh;Budi Kriswanto;Didik Pudji Restanto;Kacung Hariyono
    • Journal of Plant Biotechnology
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    • 제50권
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    • pp.11-18
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    • 2023
  • Manihot esculenta Crantz, commonly known as cassava, is a staple aliment that is a significant source of revenue for farmers. The embryogenic callus is crucial in the genetic engineering of various crop species, including cassava. Four cultivar cassava landraces from East Java were assessed for their ability to produce friable embryogenic callus (FEC) for protoplast isolation. In this study, four cassava cultivars; (Kaspro, Kuning, Gajah, and Gendruwo); were used to obtain FEC, which involved the culture of immature leaf lobes (ILLs) and apical buds (ABs) media containing MS supplemented with 33 μM picloram and 2 μM of CuSO4 (M1) or MS supplemented with 50 μM 2,4-D and 2 μM CuSO4 (M2). The highest FEC induction efficiency ranged from 72% to 57%, and the highest FEC number ranged from 4.7 to 3.7 with AB explants in media containing MS + 33 μM pilocram and 2 μM CuSO4 (M1). On the other hand, the efficiency of somatic embryogenesis induction ranged from 67% to 53%, and the number ranged from 4.4 to 3.4. The efficiencies of FEC induction ranged from 48% to 42%, and the number ranged from 3.1 to 2.6 with AB explants in media containing MS + 50 μM 2,4-D and 2 μM CuSO4 (M2); the efficiency of FEC induction ranged from 56% to 50%, and the value ranged from 3.6 to 2.4 with ILL explants. The FEC induction of the Gendruwo cultivar, which was examined using AB and ILL explants, demonstrated the lowest efficiency. Nevertheless, all four cultivars showed the ability to generate FEC, even though their effectiveness differed depending on the explant genotype and the applied media.

An efficient protocol for the production of transgenic Alstroemeria plants via particle bombardment

  • Kim, Jong Bo
    • Journal of Plant Biotechnology
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    • 제47권1호
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    • pp.66-72
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    • 2020
  • Alstroemeria plants were transformed by using an improved particle-gun-mediated transformation system. Friable embryogenic callus (FEC) induced from the leaves with axil tissues of Alstroemeria plant was used as the target tissue. Also, FEC was transformed with the bar gene was used as a selectable marker. In the case of plasmid pAHC25, 7.5% of the twice-bombarded FEC clumps showed blue foci, whereas the clumps with single bombardment showed only 2.3%. Additionally, a 90° rotation with double bombardment led to a higher frequency (6 times) of luciferase gene expression in PBL9780 than the control treatment. After 8 weeks of bombardment, more than 60 independent transgenic lines were obtained for pAHC25 and nearly 150 independent transgenic lines were obtained for PBL9780, all of which were resistant to PPT and demonstrated either GUS or luciferase activity. Regarding effect of osmotic treatment (0.2 M mannitol) with 7 different periods, the highest transient gene expression was obtained in 8 h before and 16 h after transformation in both pAHC25 and PBL9780. Compared with the control, at least three times more GUS foci and photons were observed in this treatment. With respect to different combinations of mannitol and sorbitol with 8 h before and 16 h after transformation, high numbers of transient and stable transgene expressions were observed in both 0.2 M mannitol and 0.2 M sorbitol used in the osmotic pre-culture. This combination showed the highest transformation efficiency in both pAHC25 (8.5%) and PBL9780 (14.5%). In the control treatment, only 10% of the FEC clumps produced somatic embryos. However, by using 0.2 M mannitol and 0.2 M sorbitol, the frequency of somatic embryos increased to 36.5% (pAHC25) and 22.9% (PBL9780). Of the somatic embryos produced, at least 60% germinated. Approximately 100 somatic embryos from these 210 independent transgenic lines from 2 plasmids developed into shoots, which were then transferred to the greenhouse. PCR analysis confirmed the presence of the bar gene. This is the report on the production of transgenic Alstroemeria plants by using particle bombardment with a high efficiency, thereby providing a new alternative for the transferring of gene of interests in Alstroemeria in the breeding program in the future.

유전자총과 아그로박테리움을 이용한 여러 가지 한국 잔디류의 형질전환체계 확립 (Establishment of a transformation protocol combination particle bombardment with Agrobacterium tumefaciens in different zoysiagrass cultivars)

  • 김종보;김경덕;박대섭
    • 아시안잔디학회지
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    • 제18권3호
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    • pp.141-148
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    • 2004
  • 다양한 Zoysiagrass 4가지 품종들을 식물재료로 사용하여 Agrobacterium만 이용한 방법 그리고 particle bombardment로 배발생캘러스에 상처를 낸 후, Agrobacterium으로 공동배양 시키는 2가지 다른 형질전환 방법을 비교하였다. 예비실험에서 일반적으로 형질전환에 널리 사용되는 kanamycin과 PPT(phospinitricin)의 적적선발농도에 대해서 실험하였는데, kanamycin의 경우 300mg/l 그리고 PPT의 경위 50mg/l의 농도에서 가장 효과적인 선발 효율을 나타내었다. Agrobacterium을 이용한 형질전환은 Agrobacterium을 2일간 배양시킨 다음, 박테리아 농도를 O.D 600nm=1.0-1.2로 맞추고, 배발생캘러스를 30분간 간염 시키는 방법이 효과적이었는데, particle bombardment를 이용하여 캘러스에 상처를 유발시킨 후, Agrobacterium으로 감염시키면 3배 이상 높은 형질전환 수율을 획득할 수 있었다. 이상의 결과는 한국잔디 형질전환에 있어서 particle bombardment과 Agrobacterium을 병행하여 실시한 최초의 보고이고, 이러한 시스템을 기반으로 하여 향후 한국잔디를 포함하여 다른 난지형 및 한지형 잔디의 품종개량에 널리 이용되리라 생각된다.