• Plant Biotechnology Reports
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• 제3권3호
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• pp.243-250
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• 2009

In the present study, a simple one medium formulation protocol for callus culture, somatic embryogenesis and in vitro production of ${\beta}-carboline$ alkaloids and diosgenin in Tribulus terrestris L. was developed. Extensive callus induction and proliferation was obtained in leaf explant on Murashige and Skoog (MS) medium supplemented with $5.0{\mu}M$ 6 benzyl adenine (BA) and $2.5{\mu}M$ ${\alpha}-naphthaleneacetic$ acid (NAA). The embryogenic callus was maintained on subculture to fresh parental medium at 4-week intervals over a period of 28 months. The frequency of embryo formation was at a maximum ($18.1{\pm}0.9$ per g of callus) on MS medium containing $5.0{\mu}M$ BA and $2.5{\mu}M$ NAA together with $75mg\;1^{-1}$ casein hydrolysate. Globular embryo developed into torpedo stage embryo under the influence of starvation. The accumulation of ${\beta}-carboline$ alkaloids (harmaline and harmine) and steroidal saponin (diosgenin) in non-embryogenic and embryogenic callus culture derived from leaf explant was compared with root, leaf, stem, and fruit of the mother plant. The embryogenic callus accumulated equivalent amounts of harmaline ($66.4{\pm}0.5{\mu}g/g$ dry weight), harmine ($82.7{\pm}0.6{\mu}g/g$ dry weight), and diosgenin ($170.7{\pm}1.0{\mu}g/g$ dry weight) to that of the fruit of T. terrestris. The embryogenic callus culture of this species might offer a potential source for production of important pharmaceuticals.

• 식물조직배양학회지
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• 제22권5호
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• pp.283-290
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• 1995

미나리의 체세포 배발생 조건 및 기작을 구명하고자 배발생 캘러스의 획득에 적합한 시료와 배지를 구명하고 배발달의 과정을 관찰하여 본 결과, 기내 식물체 확보를 위한 미나리의 경정배양은 발생한 줄기 수와 생육상태로 보아 BA가 0.1 - 0.5 mg/L 첨가된 MS배지가 적합하였으며 배발생 캘러스의 발생은 배유와 함께 채취ㆍ배양한 유배를 2,4- D가 1 mg/L 첨가된 배지에서 2 개월간 배양하였을 때 발생하였다. 기내에서 생장한 줄기와 엽병을 배양하였을 경우는 치상후 2과에 엽병의 절단 부위에서 발생한 캘러스는 모두 배발생 캘러스가 아니였으나 치상 후 6 - 8주에 줄기와 엽병의 표피부위에서 발생한 캘러스는 배발생 캘러스이었다. 배발생 캘러스는 계대배양에 의하여 대양 증식이 가능하며 이들은 배발생 캘러스와 비배발생 캘러스를 동시에 형성하였다. 비배발생 캘러스는 다양한 생장조절제를 첨가한 액체 및 고체배지에 반복 및 지체배양하여도 배발생 캘러스로의 분화는 일어나지 않았다. 비배발생 캘러스는 고체배지에 배양하면 쉽게 증식되어 뿌리를 분화하며, 액체배지 에 현탁배양할 경우에는 단세포로 단리되고, 다시 이들은 작은 원형세포괴를 형성한 후 단지 뿌리만을 발생하였다.

• 식물조직배양학회지
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• 제27권2호
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• pp.137-142
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• 2000

천궁 (Cnidium officinale)의 잎, 엽병 및 화기 외식편을 재료로 하여 2,4-D가 첨가된 배지에 배양하였을때 캘러스 형성은 어느 외식편에서나 비슷한 수준으로 유기되었지만 배형성능 캘러스는 화기유래 캘러스에서만 형성되었다. 체세포배발생의 유도는 2mg/L 2,4-D를 첨가한 MS배지에서 잘 일어났으며 2,4-D제거배지에서 계대배양하면 외식편당 78개의 체세포배가 형성되었다. 체세포배의 자엽수에 있어서 변이가 빈번하게 관찰되었으나 배지에 1% 활성탄을 첨가하면 비정상적인 자엽수를 갖는 체세포배의 발생률이 감소되는 효과를 얻을 수 있었다. 자엽기 체세포배는 MS 기본배지에서 저조한 발아율을 보이는 반면에 활성탄 첨가배지에서는 현저한 발아 향상을 보였다.

• 한국약용작물학회지
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• 제1권2호
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• pp.184-190
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• 1993

1. 지황의 잎 조직에서 캘러스 유도는 옥신류와 사이토키닌류의 단독처리보다는 BA와 NAA를 혼합처리하는 경우에 캘러스 유도가 잘 되었다. 2. 옥신류의 embryogenic 캘러스 유도는 5% 정도로 극히 낮았으나 사이토키닌류를 처리한 경우는 $40{\sim}55%$로 높아졌다. 3. BA 4mg/1 NAA 0.5mg/1 처리에서 embryogenic 캘러스 유도가 가장 양호하였다. 4. 배지 종류별로는 Linsmaier-Skoog배지가 embryogenic 캘러스 유도와 유도량이 가장 많았다. 5. Embryogenic 캘러스 유지도 BA 4mg/1과 NAA 0.5mg /1 처리 에서 가장 효과적 이었다. 6. 계대배양 회수가 증가할수록 캘러스 생장량은 증가하였지만 embryogenic 캘러스 빈도는 감소되는 경향을 보였다. 7. 현탁배양시 체세포배 생산은 BA 1mg/1처리 에서 가장 많았다 8. 체세포배에서 식물체 분화는 식물 생장조절제가 처리되지 않은 1/2 LS기본배지에서 가장 잘 되었으며 토양활착율은 75% 정도이었다.

• Journal of Plant Biotechnology
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• 제7권4호
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• pp.211-218
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• 2005

Genetic transformation was carried out by using biolistic gun method. The hypocotyl derived embryogenic calli (explants) of cotton (Gossypium hirsutum L.) cv. Cocker-312 were transformed with a recombinant pGreen II plasmid, in which both, bar (selection marker) and GUS (${\beta}$-glucuronidase) reporter genes were incorporated. Explants were arranged on osmoticum-containing medium (0.5M mannitol) 4 hours prior to and 16 hours after bombardment that was resulted into an increase about >80% for GUS stable expression. 3 days after bombardment, GUS assay was performed, which exhibited, $18.36{\pm}1.00$ calli showed blue spots. The transformed embryogenic calli were cultured on selection medium (@ 6 mg/L basta) for 3 months. The putative transgenic plants were developed via selective somatic embryogenesis (@1.50 mg/L basta); maximum $27.58{\pm}1.25$ somatic embryos were obtained while $17.47{\pm}1.00$ embryos developed into plantlets (@ 0.75mg/L basta). In five independent experiments, up to 7.24% transformation efficiency was recorded. The presence of the transgenes was analyzed by using PCR and southern hybridization analysis. The transgenic plants were developed with in 6-7 months, but mostly transformants were abnormal in morphology.

• 식물조직배양학회지
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• 제21권4호
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• pp.233-237
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• 1994

용담의 잎 절편 배양을 통하여 유도된 배발생 캘러스로 부터 식물체의 재분화 체계를 확립하였다. 캘러스는 0.5 mg/L2,4-D, 2 mg/L BAP가 첨가된 MS 배지에서 유도되었으며, 이 캘러스를 2 mg/L P-CPA, 0.5 mg/L 2,4-D 및 0.5mg/L kinetin이 첨가된 SH 배지에 옮겼을 때 배발생 캘러스의 유도가 가능하였다. 배발생 캘러스는 SH 기본 배지에 옮겨 슈트의 증식 및 뿌리 발생을 유도하였다. 재분화 식물체는 피트모스, 펄라이트, 버미클라이트가 2:1:1의 비율로 혼합된 인공 토양에서 순화시킨 후 토양에 활착시켰다. 토양에 활착된 재분화 식물체는 키, 줄기의 모양과 수, 개화기등에서 표현형적 변이를 나타냈다. 세포유전적 분석에서 모식물체와 재분화 식물체의 염색체는 2n=26으로 안정성을 보였는데, 이는 본 연구에서 적용된 재분화 체계가 안정하다는 것을 시사한다.

• 한국자원식물학회지
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• 제19권3호
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• pp.427-431
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• 2006

In vitro high-frequency plant regeneration of Muscari comosum var. plumosum through somatic embryogenesis was obtained via two developmental pathways: direct embryos and multiple shoots regenerated from embryogenic callus. Flower bud with pedicel, receptacle, petal and ovary wall, floral stalk and leaf as explants were cultured in MS medium supplemented with various plant growth regulators. Embryos formed directly from pedicel, receptacle and floral stalk. Depending on explant sources, the optimal medium was MS medium supplemented with 0.2 mg/L IBA and 0.3 mg/L BA, 3.0 mg/L IBA and 3.0 mg/L BA, and MS-free medium for pedicel, receptacle, and floral stalk, respectively. Multiple shoots regenerated from embryogenic cal]i which was initiated from petal, ovary and leaf were observed in MS medium with different concentrations and combinations of hormone. The most suitable medium for each type of explant was 3.0 mg/L IBA and 3.0 mg/L BA(petal and ovary) and 5.0 mg/L IBA and 5.0 mg/L BA (leaf) Furthermore, the combination of 0.1 mg/L 2,4-D and 1.0 mg/L BA was also good for all sources of explants not only for direct embryo formation, but also, for embryogenic callus induction.

• Plant Biotechnology Reports
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• 제3권4호
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• pp.333-340
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• 2009

Developmental anomalies in the plumule meristem of peanut (Arachis hypogaea L.) somatic embryos resulted in poor shoot differentiation and reduced plant recovery. Existing meristems with caulogenic potential have never been tested for embryogenesis in peanut. The present experiment was designed to test the mature zygotic embryo axis derived plumule with three meristems for somatic embryogenesis. Embryogenic masses and embryos developed from the caulogenic meristems in the axils. Exposure of 2 weeks in primary medium with $90.5{\mu}M$ 2,4-D suppressed the shoot tip differentiation temporarily which then regained the ability to form the shoot on withdrawal of 2,4-D. Exposure of 4 weeks in primary medium with $90.5{\mu}M$ 2,4-D suppressed the shoot tip differentiation irreversibly. No shoot formation was noted from the tips in any of the cultures which were in secondary medium with $13.6{\mu}M$ 2,4-D. Development of somatic embryos directly from axillary meristems was confirmed histologically. Conversion frequency of these embryos was 11%. Thus, in this report, we describe a method to obtain somatic embryos from the determined organogenic buds of the axillary meristem, by culturing the nodal explant vertically on embryo induction medium. It also displays the possibility of obtaining both embryogenic and organogenic potential in two parts of the same explant simultaneously. The possibility of extending this approach for genetic transformation in in vivo system through direct DNA delivery or Agrobacterium injection in meristems can also be explored. Using Agrobacterium rhizogenes, we have demonstrated the possibility of gene transfer in the axillary meristems of seed-derived plumule explant.

• Plant Resources
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• 제7권1호
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• pp.60-64
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• 2004

The establishment of an efficient protocol for plant regeneration and micropropagation from leaf explant cultures of Chicory, Cichorium intybus L. var. sativus. is reported. Callus formation rate appeared 100% from explant in all growth regulators, but calli formed in the prensence of naphthaleneacetic acid (NAA) were appeared very compact and non-embryogenic state. The regenerated shoots were obtained from leaf explant cultures on solid MS medium containing different concentrations of cytokinins and auxin. The highest number of shoots (5.7) per explant and shoot growth (2.8cm) was obtained on MS medium containing 0.1 mg BAP L$^{-1}$ and 0.1 mg NAA L$^{-1}$ . Indole acetic acid was the most suitable auxin for root formation among three auxins tested. 2,4-D had no effect on shoot and root formation.

• Plant Biotechnology Reports
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• 제3권3호
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• pp.199-203
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• 2009

Rugosa rose (Rosa rugosa) is cultivated as a garden flower and an important genetic resource for the breeding of roses (R. hybrida). This study describes culture conditions for high frequency plant regeneration from zygotic embryo explants via somatic embryogenesis in rugosa rose. Mature zygotic embryo, cotyledon, and radicle explants formed embryogenic calluses at frequencies of 38, 6.7, and 8.8% when cultured on half-strength Murashige and Skoog medium (${\frac{1}{2}}MS$) supplemented with 2.26, 9.05, and $9.05{\mu}M$ 2,4-dichlorophenoxyacetic acid, respectively. Embryogenic calluses produced numerous somatic embryos, which then developed into plantlets on ${\frac{1}{2}}MS$ without growth regulators. Regenerated plantlets were grown to whole plants in a growth chamber.