• Plant Biotechnology Reports
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• 제3권3호
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• pp.175-182
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• 2009

Simple, reproducible, high frequency, improved plant regeneration protocol in Eastern Cottonwood (Populus deltoides) clones, WIMCO199 and L34, has been reported. Initially, aseptic cultures established from axillary buds of nodal segments from mature plus trees on MS liquid medium supplemented with $0.25mg\;1^{-1}$ KIN and $0.25mg\;1^{-1}$ IAA. Nodal and internodal segments were found to be extra-prolific over shoot apices during course of aseptic culture establishment, while $0.25mg\;1^{-1}$ KIN concentration played a stimulatory role in high frequency plant regeneration. Diverse explants, such as various leaf segments, internodes, and roots from in vitro raised cultures, were employed. Direct plant regeneration was at high frequency of 92% in internodes, 88% in leaf segments, and 43% in root segments. This led to the formation of multiple shoot clusters on established culture media with rapid proliferation rates. Many-fold enhanced shoot elongation and growth of the clusters could be achieved on liquid MS medium supplemented with borosilicate glass beads, which offer physical support for proliferating shoots leading to faster growth in comparison to semi-solid agar or direct liquid medium. SEM examination of initial cultures confirmed direct plant regeneration events without intervening calli. In vitro regenerated plants induced roots on half-strength MS medium with $0.15mg\;1^{-1}$ IAA. Rooted 5- to 6-week-old in vitro regenerated plants were transferred into a transgenic greenhouse in pots containing 1:1 mixture of vermicompost and soil at $27{\pm}2^{\circ}C$ for hardening and acclimatization. 14- to 15-week-old well-established hardened plants were transplanted to the field and grown to maturity. The mature in vitro raised poplar trees exhibited a high survival rate of 85%; 4-year-old healthy trees attained an average height of 8 m and an average trunk diameter of 25 cm and have performed well under field conditions. The regeneration protocol presented here will be very useful for undertaking genetic manipulation, providing a value addition to Eastern Cottonwood propagation in future.

• Plant Biotechnology Reports
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• 제4권2호
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• pp.125-128
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• 2010

Culture conditions were established for high frequency plant regeneration via somatic embryogenesis from cell suspension cultures of Nymphoides coreana. Zygotic embryos formed pale-yellow globular structures and calluses at a frequency of 85.6% when cultured on half-strength Murashige and Skoog (MS) medium supplemented with 0.3 $mg\;l^{-1}$ of 2,4-D. However, the frequency of pale-yellow globular structures and white callus formation decreased slightly with an increasing concentration of 2,4-D up to 10 $mg\;l^{-1}$ with the frequency rate falling to 16.7%. Cell suspension cultures were established from zygotic embryo-derived calluses using half-strength MS medium supplemented with 0.3 $mg\;l^{-1}$ of 2,4-D. Upon plating onto half-strength MS basal medium, over 92.3% of cell aggregates gave rise to numerous somatic embryos and developed into plantlets. Regenerated plantlets were successfully transplanted into potting soil and achieved full growth to an adult plant in a growth chamber. The high frequency plant regeneration system for Nymphoides coreana established in this study will be useful for genetic manipulation and cryopreservation of this species.

• Plant Resources
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• 제1권1호
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• pp.22-25
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• 1998

To establish direct multipropagation through organogenesis from nodal explants of Anoectochilus formosanus Hayata, the nodes were cultured on LS medium containing various concentrations of 6-benzyladenine(BA). High plant regeneration and adventitious bud formation were obtained from supplemented with 4.0mg/l of BA. Plant height was promoted by adding 0.3% activated charcoal. Plantlet regeneration capacity from nodes was depended on nodal parts on the stem, upper position was the best comparing with intermediate and lower.

• 식물조직배양학회지
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• 제21권2호
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• pp.69-76
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• 1994

일반적으로 캘러스상태로 오랫동안 계대배양시 식물체분화능력 이 상실되거나 감소한다. 캘러스배양이나 현탁배양을 이용하여 제초제 및 각종 저항성 식물체를 선발하고저 할 때 장시간이 소요되므로 장기간 계대배양된 세포나 캘러스로 부터 식물체를 분화시키는 체계를 확립하는 것이 중요하다. 따라서 본 실험은 2년 이상 캘러스상태로 기내에서 장기간 계대배양한 수종의 Solanum과 Lycopenicon종으로 부터 캘러스 생장 및 식물체분화에 미치는 무기염류, 생장 조절물질 및 타이아민의 효과를 조사하였다. 캘러스 생장 및 식물체분화에는 MG배지가 다른 MS, Gamborg, White배지보다 더 효과적이었으며 낮은 농도의 IAA와 높은 농도의 BA가 조합처리 되었을때 높은 식물체분화율을 보였다. 타이아민이 첨가되었을때가 무처리보다 식물체분화와 생장을 증가시켰으며 타이아민의 농도가 증가함에 따라 식물체분화와 생장을 증가시켰으며 그 농도는 10 mg/L에서 30mg/L까지가 적합한 것으로 보였다.

• 한국식물병리학회지
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• 제3권2호
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• pp.124-130
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• 1987

수도 도열병균(Pyricularia oryzae)의 균사체로부터 다량의 원형질체의 분리 및 세포벽 재생을 하기 위하여 필요한 몇가지 조건을 선발하였다. 나출을 위하여 기본용액으로 0.02M potassium phosphate buffer와 pH 5.2, 0.6M KCl로 삼투압을 조절하였고 분해효소는 ml당 각각 20mg Cellulase R-10, 5mg Macerozyme $-10, 10mg Driselase를 사용하였는데 각각의 단독처리구보다 3가지 효소의 복합처리구에서 원형질체 나출 정도가 우수하였다. 또한 선발된 복합효소액에 2일간 액체배양된 어린 균사체를 3시간, $30^{\circ}C$ 항온기에서 진탕했을 때 가장 많은 원형질체가 분리되었다. 원형질체로부터 세포벽의 재생은 순수 정제한 원형질체를 0.2M potassium phosphate와 0.6M KCl을 삼투압을 조절한 감자한철배지에 접종시켜 가장 높은 재생율을 얻을 수 있었다.

• Journal of Plant Biotechnology
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• 제33권2호
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• pp.99-104
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• 2006

L. longifilorum Georgia $\times$ L. elegans Kakutanohikari 잡종 배로부터 유식물체를 분화시키고, 이때 유도된 캘러스의 증식과 이 캘러스로부터 유식물체 분화과정을 조직학적으로 관찰하였다. 잡종 배는 배양한 60개 절편 중 48개 절편에서 86개체의 배주가 발아되었으며, 1 mg/L NAA가 캘러스로부터 식물체의 재분화에 가장 효과적이었으며, 재분화를 억제한 캘러스만을 증식시키기 위해서는 0.1 mg/L NAA + 1 mg/L BA가 가장 양호하였다. 또한 Pyridoxin-HCI을 첨가하지 않은 경우에는 유식물체의 재분화가 거의 보이지 않았으며 50 mg/L의 Pyridoxin-HCI을 첨가한 배지에서 유식물체의 재분화가 가장 효과적이었다. 배에서 발생된 캘러스의 원형성층 지역으로부터 체세포배가 형성되었으며, NAA가 전형성층 부분에서 배발생적 세포 또는 전배 발생의 증식을 자극하는 것으로 생각되었다.

• 아시안잔디학회지
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• 제12권4호
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• pp.195-202
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• 1998

The development of a protocol for high efficiency of embryogenic callus separation, maintenance and plant regeneration from the seeds of zoysiagrass cv. Zenith was studied. Embryogenic callus ratio is absolutely determined by genotype, but by adding high concentration of copper into medium, changing light condition and maintaining callus on initial induction medium for 8∼10 weeks, embryogenic callus can be easily distinguished and its growth can be promoted. There were significant differences among selected callus lines (each from one seed) according to their growth rates and regeneration percentages. Callus pre-treatment with activated charcoal inhibited callus growth, increased the level of precocious germination during culture and promoted shoot cluster formation after transfer to regeneration medium. For long-term callus maintenance, N6AA medium was better than MS medium, because the former inhibited non-embryogenic callus formation and kept vigor of embryogenic callus. The best callus lines Z-(5) has been successfully used for transformation and somaclonal variation selection in our laboratory.

• Journal of Plant Biology
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• 제36권1호
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• pp.1-8
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• 1993

Polyamine contents and the activities of their main biosynthetic enzymes, arginine decarboxylase (ADC) and ornithine decarboxylase(ODC), were investigated in Populus leaf segments during adventitious shoot regeneration with the addition of 1 millimolar polyamine synthesis inhibitors. From the study of polyamine synthesis inhibitors, ODC was found to be the principal route of polyamine biosynthesis in adventitious shoot regeneration of Populus leaf segments. The ADC inhibitor difluoromethyl arginine(DFMA) and ODC inhibitor difluoromethyl ornithine(DFMO) strongly reduced the putrescine content. On the contarary, DCHA, an inhibitor of spermidine synthase, increased it. Spermidine content was decreased with the treatment of each polyamine synthesis inhibitor, but the inhibitory effect of DCHA was stronger than any other polyamine inhibitor. The decreased polyamine level by polyamine synthesis inhibitors was restored with the exogenously applied polyamine. Comparing the polyamine contents with the adventitious shoot regeneration rate, were observed a close correlation between spermidine content and adventitious shoot regeneration of Populus leaf segments.

• 한국식물학회:학술대회논문집
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• 한국식물학회 2001년도 춘계학술발표대회:발표눈문요지록
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• pp.21-21
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• 2001

• 식물조직배양학회지
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• 제25권6호
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• pp.501-505
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• 1998

오이의 국내 F1 품종인 조생낙합의 하배축 유래 배발생 현탁배양 세포의 초저온 보존 시스템을 개발하였다. 액체질소 저장 후 캘러스 재생률은 2M DMNSO와 0.4 M sucrose를 혼용 처리하였을 때 캘러스 재생률이 85%로 가장 높았다. 그러나 glycerol 처리구에서는 처리농도에 상관없이 모든 처리구에서 캘러스 재생이 이루어지지 않았다. 또한 고농도의 삼투용액에서 배양세포의 전처리 과정은 필요하지 않았다. 재생된 캘러스를 1 mg/L 2,4-D가 첨가된 MS 배지로 이식하여 배양하였을 때 다수의 체세포배가 발달하였으며, 체세포배를 MS 기본배지로 옮겨 명배양한 결과 다수의 소식물체가 발달하였다.