• 한국약용작물학회지
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• 제8권1호
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• pp.41-48
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• 2000

큰용담을 대상으로 실시한 체세포배의 형성, 재분화 체계의 확립 및 multiple shoot의 형성 등의 대량증식에 관한 일련의 실험의 결과는 다음 몇 가지로 요약된다. 큰용담의 잎절편을 2, 4-D 2 mg/ l 에 배양한 경우 callus 형성율이 90%, embrogenic callus 형성율이 70% 로 높은 형성율을 나타내었으나 실제 형성되는 체세포배의 발생 숫자를 조사하였을 때 2,4-D 단독처리시 보다 2, 4-D 0.5 mg/ l 와 BAP 0.5 mg/ l이 조합처리 시 잎절편체 당 18.8 개의 높은 체세포배가 형성되었다. 큰용담의 줄기와 마디를 배양한 결과 캘러스의 형성은 단독처리시 $20{\sim}30%$의 캘러스 형성율을 보인 반면 고농도의 2,4-D에 TDZ를 조합처리 하여 줄기마디를 배양한 경우 50% 이상의 우수한 캘러스 형성이 이루어지는 것으로 나타났으며 재분화식물체는 단독처리에서 MS medium 에 BAP 2 mg/ l 처리한 줄기마디 배양에서 7개의 재분화 식물체를 얻음으로 해서 가장 높은 shoot 분화율을 나타내었다. 큰용담에서는 TDZ, BAP를 조합처리한 결과 TDZ 1 mg/ l 와 BAP 1 mg/ l 조합처리하였을 경우 multiple shoot를 형성하였으며 explant 당 $70{\sim}80$개의 식물체가 분화되었다. 식물체의 각 치상조직을 배양한 결과 정아 마디 줄기 순으로 식물체 많이 유도되는 것으로 나타났으며 잎조직에서는 새로운 신초는 유도되지 않았다. 배양기간에서 대한 차이는 배양한지 30일 경과한것 보다 60 일이 경과한것에서 거의 모든 조직에서 2배 이상의 신초형성을 보였다.

• Journal of Plant Biotechnology
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• 제30권4호
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• pp.375-380
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• 2003

줄기기저부절편조직을 이용한 호접란 조직배양묘 생산 체계를 확립하기 위하여 원괴체 유도와 원괴체 증식의 조건을 구명하고자 하였다. 치상조직별 원괴체 유도 성공률을 비교한 결과 줄기기저부절편조직에서 약 45％의 높은 성공률을 나타내었고 다음은 화경액아 배양으로 약 30％ 정도의 성공률을 나타낸 반면 근단, 화경절간절편, 화경엽, 성숙엽의 경우에는 성공률이 1％ 미만으로 매우 낮았다. 품종별 원괴체의 유도능력에서의 차이를 알아보기 위하여 11개 품종에서 줄기기저부 절편배양을 한 결과 백색계 와 핑크계품종 모두에서 30％이상의 높은 원괴체 성공률을 나타내었다. 줄기기저부배양에서 줄기기저부를 절단하지 않고 천체조직을 치상하였을 경우 거대 원괴체가 유도되었는데 이 거대 원괴체는 진한 녹색으로 보통 원괴체의 3∼5배 정도 이상 큰 것으로 나타났다. 이 거대 원괴체를 증식하기 위해 절단하여 증식배지에 치상하였으나 새로 나온 원괴체는 정상적인 크기의 PLB로 유도되었다. 줄기저부배양에서 얻어낸 원괴체들은 증식과정을 거쳐 정상적인 조직배양묘를 형성하였다 그러므로 이 방법은 호접란 클론묘생산에 쓰일 수 있는 효율적이고 실용적인 방법의 하나라고 판단되었다. 그리고 줄기기저부 절편배양을 이용하여 원괴체를 유도 증식하고 플라스크묘를 만든 뒤 다시 그 묘의 줄기기저부절편을 이용하여 원괴체를 유도 증식하고 플라스크묘를 만들어내는 시스템에 응용함으로써 무한수의 조직배양묘를 연속적으로 생산할 수 있다는 체계가 제시되었다.

• 한국자원식물학회지
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• 제27권5호
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• pp.540-545
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• 2014

경상남도 농업기술원에서 육성된 둥굴레 '건강백세(Polygonatum odoratum cv. Gungangbeaksea)'를 분양받아 배양하였다. 둥굴레 지하경 절편체를 MS 배지에 BA 3.0 mg/L가 첨가된 배지에서 배양하면서 증식된 부정신초괴를 실험재료로 사용하였다. 배양 8주후, 신초의 증식은 TDZ 3.0 mg/L 첨가배지에서 2.8개로 가장 많았으며 생체중도 절편체당 2.32 g으로 가장 높게 나타났다. TDZ와 NAA가 첨가된 배지에서는 신초 및 부정신초괴의 증식이 다소 증가하였다. TDZ 3.0 mg/L와 NAA 5.0 mg/L 첨가배지, TDZ 5.0 mg/L와 NAA 3.0 mg/L 첨가배지에서 신초수 3.7개, 생체중 2.9 g으로 다소 증가하였다. MS 염류농도가 높아질수록 신초 및 부정신초괴의 증식은 저조하였다. 그러나 sucrose 농도가 3%에서 7%로 증가함에 따라 신초수, 생체중 및 부정신초괴의 형성이 증가하였다. 뿐 만 아니라 둥굴레 부정신초절편체에서 신초 및 부정신초괴의 증식은 MS 배지에 TDZ와 NAA 3.0~5.0 mg/L와 sucrose 7%가 첨가된 배지가 적합하였다. 발근율은 IBA 3.0 mg/L 또는 NAA 2.0 mg/L 첨가배지에서 80% 이상으로 높았으며, 발근된 식물체의 순화는 vermiculite 단용 또는 perlite, vermiculite 1:1 혼용처리에서 순화율 100%로 적합하였다.

• 한국약용작물학회지
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• 제5권3호
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• pp.186-190
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• 1997

This study was carried out to investigate the effect of polyamines, salt strength. sucrose and gelling agents on the regeneration of plantlets by meristem culture of Aloe arborescens Mill. and Aloe vera L.. Shoot multiplication was more effective when 10mg/ l spermine in Aloe arborescens and 1mg/ l spermidine in Aloe vera added into MS medium than when other polyamines were treated into media. A quarter strength of MS medium was effective for rooting of shoots regenerated. Higher concentration of sucrose (45g/ l) was more effective for shoot regeneration. Addition of 4g/ l gelrite into the medium was effective for induction of multiple shoots from Aloe than that of agar or other concentrations of gelrite. When plantlets regenerated from meristem culture were transferred to pot. survival rate of plantlets was 80% on perlite and was 95% on vermiculite. respectively.

• 한국산림과학회지
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• 제95권2호
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• pp.155-159
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• 2006

An efficient method for in vitro propagation of the medicinal plant Hovenia duleis, was established. Plantlets for micropropagation of H. dulcis were obtained from in vitro germinated seeds. The effectiveness of various levels of cytokinins (BAP, Kinetin and TDZ) on multiple shoot formation from stem nodes was tested. BAP (1.0 mg/L) treatment induced highest number of multiple shoots. The growth pattern of plantlet on various culture media was undertaken. The shoot elongation was optimal on 2MS basal medium without growth regulators. The in vitro rooting ability of H. dulcis shoots was examined with two-auxins IAA and IBA. The IAA (1.0 mg/L) treatments induced earliest rooting with maximum number of roots and root growth. Rooted shoots were transferred directly to small pots with artificial soil and such established plant exhibited a normal growth pattern similar to wild plantlet.

• Journal of Plant Biotechnology
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• 제30권3호
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• pp.269-273
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• 2003

In order to develop an efficient micropropagation protocal for Eucalyptus pellita, on in vitro culture system has been was established by inducing axillary buds from greenhouse stock materials. Among 6different media tested, DKW medium was the best ot induce bast induce both shoot proliferation and growth. Average number of proliferated shoots of 403per explant was obtained at the concentration of 0.1mg/LBA. Most of the stem materials excreted phenolic compounds at the proximal part of the explant and caused darking of the media. Therefore, it was necessary to transfer frequently to a fresh medium and/or to add activated charcoal at the concentration of 0.02％(w/v). Generally on vitro roots were formed easily on 1/2DKW medium with NAA treatment. All the explants rooted at the medium containing 0.2mg/L NAA and displayed vigorous root growth in vitro culture conditions. After transferred to an artificial soil mixture (peatmoss: vermiculrite: perlite, 1:1:1, v/v/v) in the greenhouse, most rooted plantlets survived well without any morphological abnormalities. The results show that the species can be micropropagated effectively by the application of axillary bud culture system.

• Journal of Plant Biotechnology
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• 제33권4호
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• pp.249-255
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• 2006

Effects of ethylene inhibitors like silver nitrate $(AgNO_3)$, cobalt chloride $(CoCl_2)$ and Salicylic acid (SA) on multiple shoot induction and their impact on ethylene production using embryonal cotyledon cultures of Cucumis sativus L. were examined. The optimum concentration of $AgNO_3\;(40{\mu}M),\;CoCl_2\;(20{\mu}M)\;and\;SA\;(20{\mu}M)$, separately, induced maximum number of shoots on Murashige and Skoog's (MS) medium supplemented optimally with $4.44{\mu}M$ BA and $0.25{\mu}M$ NAA. Among the three ethylene inhibitors tested, $AgNO_3$ produced maximum number of shoots when compared to $CoCl_2$ and SA Ethylene production was monitored in all the treatments with $AgNO_3/CoCl_2/SA$ and it was observed that the treatment with $AgNO_3$ alone showed increase in ethylene production when compared to $CoCl_2$ and SA Even though ethylene concentration was the highest in $AgNO_3$ treated explants, maximum number of shoots was obtained.

• 원예과학기술지
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• 제32권5호
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• pp.694-701
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• 2014

Allium hookeri L. (Alliaceae family) is an important ethnomedicinal plant native to the Himalayan region of Asia. The aim of this research was to establish a high-frequency plant regeneration system for in vitro propagation of A. hookeri. Among the tissue types examined, receptacle explants derived from immature flower buds showed the highest regeneration rate of shoots ($93.33{\pm}4.63%$), roots ($76.67{\pm}7.85%$), and calli ($80.00{\pm}7.43%$) when cultured on Gamborg B5 (B5) medium containing $10{\mu}M$ 6-benzylaminopurine (BA) + $1{\mu}M$ naphthalene acetic acid (NAA), $0.5{\mu}M$ BA + $5{\mu}M$ NAA, and $1{\mu}M$ BA + $10{\mu}M$ NAA, respectively. Shoot multiplication was superior when cultured in liquid rather than on solid medium and relatively high concentrations of BA, ranging from 5 to $10{\mu}M$. Efficient bulblet formation following root induction from shoot clumps was achieved with culture in liquid B5 medium containing 7% (w/v) sucrose. Regenerated bulblets were successfully acclimatized to ex vitro conditions with a greater than 95% survival rate. By this method, a maximum of 62 plantlets per receptacle could be propagated within 9 weeks of initial culture. The in vitro propagation system established in this study will promote A. hookeri biotechnology, including large-scale production of healthy and aseptic clones, preserving parental genotypes with desirable traits, and genetic manipulation to enhance medicinal value.

• Journal of Plant Biotechnology
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• 제47권1호
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• pp.53-65
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• 2020

Here, we describe an efficient and rapid protocol for the micropropagation of Thymus pallidus Cosson ex Batt., a very rare medicinal and aromatic plant in Morocco. After seed germination, we tested the effect of different macronutrients, cytokinins alone or in combination with gibberellic acid (GA₃) or auxins, on T. pallidus plantlet growth. We found that Margara macronutrients (N₃₀K) had the best effect on the in vitro development of the plantlets. The addition of 0.93 μM/L 1,3-diphenylurea (DPU), 0.46 μM/L adenine (Ad), and 0.46 and 0.93 μM/L kinetin (Kin) resulted in the best shoot multiplication and elongation. In addition, the combination of 0.46 μM/L Kin, DPU, or Ad with gibberellic acid, in particular, 0.46 μM/L Ad + 0.58 μM/L GA₃ and 0.46 μM/L Kin + 1.15 μM/L GA₃, led to better bud and shoot multiplication. Moreover, the integration of the combinations of 0.46 μM/L Kin and auxins, namely 0.46 μM/L Kin + 2.85 μM/L indole-3-acetic acid (IAA), 0.46 μM/L Kin + 2.85 or 5.71 μM/L indole-3-butyric acid (IBA), and 0.46 μM/L Kin + 0.3 or 0.57 μM/L 1-naphthaleneacetic acid (NAA), in the culture medium led to better root development and optimized aerial growth. Finally, the in vitro plants from the medium containing N₃₀K + 0.46 μM/L Kin + 2.85 μM/L IAA were successfully acclimatized; these plants served as a source for repeating in vitro culture.

• 한국자원식물학회:학술대회논문집
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• 한국자원식물학회 2021년도 춘계학술대회
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• pp.24-24
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• 2021

The Cassava (Manihot esculenta Crantz) is one of the major food crops in the tropical or subtropical regions. Recently, clean planting materials of improved cassava cultivars are in high demand. Problems in the propagation of cassava are virus vulnerable and low rates of seed germination. Thus, the study was undertaken to develop an efficient in vitro mass propagation protocol of Manihot esculenta Crantz. So we tried to optimize protocols for mass production from axillary buds of Cassava. Young and actively growing stem segments were excised from adult plants of cassava. Samples were cut into a 3~4 cm nodal segments with axillary buds, and cultivated in the different medium supplemented with various plant growth regulators for 4 weeks. For shoot multiplication, axillary buds approximately 1 cm in length were taken from in vitro derived shoots and subcultured. After 4~6 weeks, the shoot generation rate showed 55.6%. The shoot number and its length was 1.0/explant and 2.3 cm in the most favorable medium composition. The auxin β-indolebutyric acid(IBA) 0~2.0 mg/L was proved to be effective on root development. Plantlets with fibrous roots easily generated tuberous roots in vitro. The tuberous roots were induced only when both kinetin and IBA were used in combination. after 8 weeks, the root generation rate showed 100%. The root number and its length was 17.2/explant and 2.2 cm in the most promising medium composition. Our experiments confirmed that in vitro growth and multiplication of plantlets could depend on its reaction to the different medium composition, and this micropropagation techniques could be a useful system for healthy and vigorous plant production.