• Journal of Plant Biotechnology
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• 제41권4호
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• pp.223-228
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• 2014

팔레놉시스 PLB (protocorm-like bodies) 조직을 이용하여 대량증식 및 신초재분화 체계 확립을 위하여 다양한 증식배지, 액체배지와 고체배지의 효과, sucrose 농도 등이 PLB 증식과 신초 재분화에 효과가 있는지 그리고 활성탄소, citric acid 및 ascorbic acid 등이 팔레놉시스 PLB 배양시 갈변화 현상을 감소하는데 효과가 있는지 알아 보고자 본 연구를 수행하였다. 그 결과, 난과 식물에서 증식배지로 널리 사용되는 VW, HCa, Orchimax 및 Kudson C 배지 중 VW 배지가 PLB 증식에서 타 배지와 비교해서 최소 1.3배에서 최대 2배의 증식효율 그리고 신초 재분화에서도 50% 이상 높은 효율을 보여 주었다. 최적 배지로 선정된 VW배지에 apple powder 및 banana powder를 첨가한 VWAB 배지를 기반으로 액체 및 고체배양에서 PLB 증식효율과 신초재분화율을 비교한 결과, 통계적으로 유의한 차이는 발견되지 않았다. Sucrose 농도를 0 ~ 50 g 처리한 실험에서는 PLB 증식과 재분화 효율 둘 다 10 g 처리구에서 가장 좋은 결과를 보여 주었다. 마지막으로 팔레놉시스 PLB 증식 및 재분화 과정에서 자주 발생하는 갈변화를 감소시키기 위하여 활성탄소, citric acid와 ascorbic acid를 처리한 실험에서는 활성탄소 1 g이 1.5%의 가장 낮은 갈변율을 나타내었다. 이러한 실험결과는 향후 팔레놉시스 PLB를 이용한 대량증식 및 재분화 체계 확립에 크게 기여하리라 판단된다.

• Journal of Plant Biotechnology
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• 제5권3호
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• pp.169-172
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• 2003

Somatic embryogenesis was initiated from in vitro grown leaf explants of rose following an induction period of four weeks on MS basal medium supplemented with auxin and several subcultures on MS medium with cytokinin. '4th of July' showed the highest regeneration frequencies on 1 mg/L NAA followed by culture on medium with 4 mg/L zeatin. The embryogenic callus was propagated on MS medium with NAA, zeatin and $GA_3$. Germination of somatic embryos was achieved on MS medium with 1 mg/L BA. Somatic embryo derived plantlets were hardened and successfully transferred to the greenhouse.

• 한국산림과학회지
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• 제84권2호
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• pp.145-150
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• 1995

기내배양된 아까시나무(Robinia pseudoacacia L.)의 줄기기부에서 발생된 callus로부터 기관발생을 통하여 식물체재분화 시스템을 확립하였다. Callus는 줄기를 BA 또는 NAA가 함유된 MS배지에 배양하였을 때 유도되었으며, BA처리구가 NAA처리구보다 유도율이 높았다. BA가 첨가된 배지에 줄기를 배양하였을 때 기부 callus의 생장은 광조건 및 암조건에서도 잘 증식되었다. 줄기기부에서 발생된 callus는 녹색과 희면서 노란색을 띠는 callus로 분리되어 2.0mg/l BA와 0.5mg/l NAA가 함유된 mMS배지에 배양하였을 때 녹색의 callus로부터 줄기가 재분화되었다. 재분화된 줄기는 생장조절제가 함유되지 않은 ${\frac{1}{2}}MS$배지에서 발근되었다.

• 식물조직배양학회지
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• 제27권6호
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• pp.447-451
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• 2000

나리‘Gelria’의 인편에서 캘러스를 유도, 증식시키고, 증식된 캘러스에서 식물체를 재분화하여 캘러스를 통한 재분화 기술체계를 확립하고자 실험한 결과, 인편에서 캘러스의 유도는 생장조절제가 전혀 첨가되지 않은 배지에서도 유도되었고, kinetin 0.5 ∼ l.0 mg/L와 NAA 0.1 ∼ l.0 mg/L가 첨가된 배지에서는 유연성이 높은 캘러스가 100%유도되었다. 생장조절제가 첨가되지 않은 배지에서도 캘러스의 증식이 양호하였으며, 생장조절제가 첨가된 배지에서는 증식률이 높아 캘러스가 왕성하게 증식되었다. 또한 캘러스로부터 신초가 발생하여 캘러스의 증식과 신초의 재분화가 동시에 발생하였다. 캘러스는 암배양보다는 명배양에서, 액체배양보다는 고체배양에서 더 잘 증식하였다. 생장조절제가 첨가된 배지에서는 캘러스가 왕성하게 증식하였고 신초의 재생은 생장조절제가 첨가되지 않은 배지에서 높았고, 다음으로 1.0mg.L의 BA와 NAA가 첨가된 배지에서 높았다.

• Journal of Plant Biotechnology
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• 제39권3호
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• pp.182-188
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• 2012

Iris dichotoma Pall. is an important endangered plant belonging to the family Iridaceae. A method was developed for the rapid micropropagation of I. dichotoma through plant regeneration from leaf, rhizome, and root explant-derived calli. Leaf, rhizome, and root segments were cultured on Murashige and Skoog (MS) medium supplemented with 2,4-dichlorophenoxy acetic acid (2,4-D; $0-3.0mg{\cdot}L^{-1}$) for callus induction. Callus production was highest at $1.0mg{\cdot}L^{-1}$ 2,4-D, where 73.8% and 45.5% of cultured rhizome and root cuttings, respectively, produced calli. The viable calli were maintained at an induced concentration of 2,4-D ($3.0mg{\cdot}L^{-1}$). They were then transferred to MS medium supplemented with various concentrations of 2,4-D ($0-3.0mg{\cdot}L^{-1}$) in combination with 6-benzyladenine (BA: 0, 1.0 and $3.0mg{\cdot}L^{-1}$) for adventitious shoot regeneration. The addition of a low concentration of 2,4-D into BA-containing medium significantly increased the frequency of shoot regeneration in leaf, rhizome, and root-derived calli. The highest number of adventitious shoots (26.4 per callus) formed at $0.5mg{\cdot}L^{-1}$ 2,4-D and 1.0 mg/l BA. For rooting of the shoots, half- strength MS medium supplemented with different concentrations of indole 3-butyric acid (IBA) $0-3.0mg{\cdot}L^{-1}$ was tested. The optimal results were observed using half-strength MS medium supplemented with $1.0mg{\cdot}L^{-1}$ IBA, on which 98% of the regenerated shoots developed roots with an average of 3.5 roots per shoot within 45 days. The plantlets raised in vitro were acclimatized and transferred to soil with 95% success. This in vitro propagation protocol will be useful for conservation and mass propagation of this endangered plant.

• 식물조직배양학회지
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• 제27권3호
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• pp.191-195
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• 2000

사과나무 교배잡종 (P.16 $\times$ M. prunifolia)의 자엽과 배축 조직을 배양하여 신초의 재분화에 미치는 2,4-D, NAA 키네틴, BA, thidiazuron의 처리효과를 조사하였다. 자엽조직은 1.0 mg/L＋ NAA +2.0 mg/L BA 처리구에서, 배축조직은 0.5 mg/L NAA+0.5mg/L BA처리구에서 가장 많은 수의 신초가 분화하였으며, BA 무첨가구에서는 신초의 재분화가 전혀 이루어지지 않았다. 자엽조직보다는 배축조직을 배양하는 것이 더 효과적이었으며 특히, 배축의 상위부분을 치상하였을때 신초 재분화가 더 양호하였다. 재분화된 신초를 1/2 MS에 1.0mg/L NAA를 첨가한 발근배지에 계대배양한 결과 발근이 양호하였으며 정상적인 식물체로 생장하였다.

• 한국약용작물학회지
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• 제15권2호
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• pp.73-81
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• 2007

An efficient regeneration system was developed using leaf, petiole, and internode explants. Highly embryogenic callus was obtained following cultivation on MS basal nutrient supplemented with 2 $mg/{\ell}$ 2,4-D. Globular, heart, torpedo and cotyledon shaped somatic embryo were produced from the surface of embryogenic callus. Direct shoot regeneration without intermediate callus formation has been achieved on MS medium supplemented NAA and BAP. The percentage of response varies with different concentration of auxin and cytokinin treated individually or in combination. The best shoot regeneration response (54.28%) and number of shoot per explant (12.67) were achieved on the medium supplemented with 0.1 $mg/{\ell}$ NAA and 1 $mg/{\ell}$ BAP. The regenerated shoot transformed into young plant when cultured into elongation and root induction medium. More than 90% of in vitro propagated plants could survive when transferred to the greenhouse for acclimation. This optimized regeneration system can be used for rapid shoot proliferation and genetic transformation.

• Journal of Plant Biotechnology
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• 제6권2호
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• pp.77-85
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• 2004

Development of efficient plant regeneration and genetic transformation protocols (using the Particle Inflow micro-projectile Gun and the shoot-tips as target tissue) of Sorghum bicolor (L.) Moench in terms of expression of the reporter gene, $\beta$-glucuronidase(uidA) is reported here. Two Indian cultivars of sorghum were used in the study, viz. M-35-1 and CSV-15. Plant regeneration was achieved from one-week-old seedling shoot-tip explants via multiple-shoot-clumps and also somatic embryos. The multiple-shoot-clumps were produced on MS medium containing BA (0.5, 1.0 or 2.0 mg/$L^{-1}$), with biweekly subculture. Somatic embryos were directly produced on the enlarged dome shaped expansive structures that developed from shoot-tip explants (without any callus formation) when cultured on MS medium supplemented both with BA (0.5, 1.0 or 2.0 mg/$L^{-1}$) and 2,4-D (0.5 mg/$L^{-1}$). Whereas each multiple-shoot-clump was capable of regenerating more than 80 shoots via an intensive differentiation of both axillary and adventitious shoot buds, the somatic embryos were capable of 90% germination, plant conversion and regeneration. The regenerated shoots could be efficiently rooted on MS medium containing 1.0mg/$L^{-1}$ IBA and successfully transplanted to the glasshouse and grown to maturity with a survival rate of 92%. The plant regeneration efficiency of both the genotypes were similar. After the micro-projectile bombardment, expression of uidA gene was determined by scoring blue transformed cell sectors in the bombarded tissue by an in situ enzyme assay. The optimal conditions comprising a helium pressure of 2200 K Pa, the target distance of 11 cm with helium inlet fully opened and the use of osmoticum have been defined to aid our future strategies of genetic engineering in sorghum with genes for tolerance to biotic and abiotic stresses.

• Journal of Plant Biology
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• 제36권3호
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• pp.211-218
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• 1993

Plant regeneration was accomplished from protoplast culture of rice (Oryza sativa L. cv. Taebaeg). Embryogenic callus was induced from mature seed on MS medium containing 5 mM proline, 2.5 mg/L 2,4-D, 30 g/L sucrose in the dark at 28$^{\circ}C$ and used to establish embryogenic cell suspension culture. Suspension cells were subcultured every one week in N6 medium supplemented with 5 mM proline, 200 mg/L casein hydrolysate, 2.5 mg/L 2,4-D and amino acids of AA medium. Suspension cultures were composed of cells that were densely cytoplasmic, potentially embryogenic and were at least maintained for more than 6 months in liquid medium. Protoplasts were isolated from fast-growing suspension culture cells and cultured in a slightly modified KpR medium by mixed nurse culture. Isolated protoplasts began to divide within 5~7 days and thereafter, protoplast-derived calli were sequentially transferred to callus proliferating medium that soft agar MS medium contained 2 mg/L 2,4-D and produced distinct embryogenic cells. Microcolonies were then transferred to solid medium which consisted of MS medium containing 5 mg/L kinetin, 1 mg/L NAA, 1 mg/L ABA, 30 g/L sucrose and 10 g/L sorbitol under fluorescent light. Mulitple shoots of 4~5 per callus emerged and were transferred to hormone-free MS medium for root initiation. Thereafter, The plantlets were transferred to pots of soil to mature in the culture room.

• 한국한의학연구원논문집
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• 제14권1호
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• pp.113-116
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• 2008

Petiole explant of Glehnia littoralis Fr. Schmidt was in vitro cultured MS plant medium(DUCHEFA co.) supplemented with various plant growth regulators and examined to find out their optimum combination and concentration for plantlet regeneration. We investigated optimal condition for efficient plant regeneration through adventitious shoot formation on MS plant medium with various kinds of plant growth regulators. Embryogenic calli and adventitious shoot formation were greatly influenced by plant growth regulators. Embryogenic calli induction showed a good response on MS medium supplemented with NAA and BA than others. Especially, combination of 1.0 mg/L NAA and 0.5 mg/L BA on MS medium led to the greatest frequency in adventitious shoot. The results suggest that plant regulator selection be important factor to achieve an efficient regeneration.