• 제목/요약/키워드: Shoots proliferation

검색결과 102건 처리시간 0.027초

희귀(稀貴) 수종(樹種) 산개나리의 기내(器內) 번식(繁殖) (Micropropagation of a Rare Species, Forsythia saxatilis N. through Tissue Culture)

  • 문흥규;석진영;김선창
    • 한국산림과학회지
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    • 제86권4호
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    • pp.430-434
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    • 1997
  • 희귀 수종인 산개나리(3년생)의 산초지 액아를 배양하여 식물체를 유도하였다. 효과적인 증식법 구명을 위해 MS 배지에서 세 가지 싸이토키닌(BAP, kinetin, zeatin)의 농도별 효과를 조사하였다. 증식은 식물 생장조절 물질이나 농도별 효과가 뚜렷하지 않았으나 zeatin 처리시 줄기 및 잎의 발달에 효과가 있었다. kinetin 처리는 줄기 생장과 더불어 모두 발근되는 특징을 보였고, BAP와 zeatin은 발근은 가능하나 고농도로 갈수록 발근율이 감소하였다. 황화처리는 줄기의 생장을 촉진하였다. 줄기는 3년 이상의 계대배양 후에도 정상적인 증식이 가능했다. 발근된 식물체는 인공 배양토에서 100% 활착되었으며 산지에 이식하여 정상 생장하였다. 이상의 결과는 희귀 수종인 산개나리의 기내 번식으로 자생지의 복원이 가능함을 시사한다.

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희귀 수종 시로미의 액아줄기 유도 미세번식 (Micropropagation of a Rare Tree Species, Empetrum nigrum var. japonicum K. Koch via Axillary Bud Culture)

  • 한무석;박소영;문흥규;강영제
    • 한국산림과학회지
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    • 제99권4호
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    • pp.568-572
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    • 2010
  • 희귀수종 시로미(Empetrum nigrum var. japonicum K. Koch.)의 기내증식 방법을 구명하기 위해 당년생 신초를 재료로 증식에 미치는 배지염류, 싸이토키닌 효과와 기내발근에 미치는 배지 및 오옥신의 효과를 시험하였다. 액아 마디로부터의 줄기 유도는 WPM 배지가 MS 배지보다 양호한 반응을 나타냈다. WPM 배지의 염류농도에 따른 줄기유도는 뚜렷한 차이가 없었으나 기본배지에서 비교적 건전한 줄기가 유도되었다. 다경 유도에는 zeatin이 BA보다 효과적인 반면에 줄기 생장은 BA가 더 양호한 것으로 나타났다. 증식된 줄기로부터 기내 발근은 1/2MS 배지보다는 WPM 배지가 효과적인 것으로 나타났으며 5.0 mg/L IBA 처리 시 가장 높은 발근율을 보였다. 발근묘는 인공 배양토에서 4 주후 93% 이상이 활착되었다. 이상의 결과는 희귀종 시로미의 기내배양을 통한 증식 가능성을 보여주었다.

Mixed Infection of 16S rDNA I and V Groups of Phytoplasma in a Single Jujube Tree

  • Lee, Sang-Hun;Han, Sang-Sub;Cha, Byeong-Jin
    • The Plant Pathology Journal
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    • 제25권1호
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    • pp.21-25
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    • 2009
  • Jujube trees infected with phytoplasma exhibit symptoms of typical witches' broom, such as yellowing, abnormally small leaves, short internodes and proliferation of shoots. A 1.2 kb fragment of the 16S rDNA from jujube phytoplasma was generated by R16F2n/R16R2 primer pair from earlier amplified P1/P7 PCR products of cloned jujube witches' broom phytoplasmas. Enzymatic restriction fragment length polymorphism (RFLP) and sequence analysis of 16S rDNA revealed that the jujube tree was infected with 16S rDNA I and V groups of phytoplasmas. Extensive comparative analyses of restriction enzyme profiles from Alu I, Hha I, Msp I, and Rsa I clearly classified the two into different phytoplasma groups. The phylogenie analyses based on 16S rDNA showed that the similarity of the two different clones was 87.5%. This is the first report of a mixed phytoplasmal infection in a single jujube tree.

조직배양에 의한 씨마늘의 상업적 생산 (Commercial Production of Seed Garlic by Tissue Culture Technique)

  • 남상일;박주현;최종인;권기석;엄정식
    • 한국식물생명공학회:학술대회논문집
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    • 한국식물생명공학회 2002년도 추계학술대회
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    • pp.33-40
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    • 2002
  • We, Tong Yang Moolsan Co. Ltd. (TYM) set up the mass-production system for virus-free seed garlic via tissue culture technique. TYM's tissue culture technique is called as 'Multiple shoot propagation technique'. This technique can lead mass propagation of genetically homogeneous seed garlic in a short period because of its highly proliferation rate of in vitro shoots ($15^{10}$ /year). TYM researchers applied the technique to some selected garlic cultivars with superior characteristics and carried out field test of productivity in the inside and outside of the country for several years. According to the yearly results of field test with virus-free seed garlic, we ascertained that virus-free seed garlic can produce the highly yield increase (max. above $50\%$) and also can enhance the product quality. Consequently, we estimated that TYM's seed garlic will contribute to farmers with increase of income and can elevate the national position of garlic market in the world for its competitive power of technical and production cost.

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액아유도에 의한 Eucalyptus pellita의 기내번식 (Micropropagation via Axillary Bud Induction of Eucalyptus pellita)

  • 문홍규;김지아;이현신;강호덕
    • 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.

Micro-propagation Factors Essential for Mass Production of Synthetic Seeds in Banana

  • Hassanein A. M.;Ibrahiem I. A.;Galal A. A.;Salem J. M. M.
    • Journal of Plant Biotechnology
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    • 제7권3호
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    • pp.175-181
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    • 2005
  • This work described some essential factors necessary for micro-propagation of banana for mass production of synthetic seeds for germ plasm conservation, and how peroxides activity of conserved tissue was influenced. Shoot tips of field grown plants were used to obtain shoot clusters on shoot proliferation medium (MS medium supplemented with 5 mg/l BAP). Using longitudinally-split shoot tip technique, 18720, 8640, 7488, 2016 plantlets were obtained from one shoot tip of Maghraby, Grand Naine, Balady, and Williams, respectively, in six subculture, one month each, on solid medium. Shoot tips excised from in vitro grown plantlets were encapsulated in calcium-alginate beads and stored at $4^{\circ}C$ for one month on half-strength MS basal medium without growth regulators or sugars. After one month all the viable-conserved synseeds formed shoots when they were transferred to MS basal medium, some of them showed synchronous formation of shoot and root systems in one week. Plants retrieved from encapsulated shoot tips were hardened off and transferred to soil.

주야 온도차[DIF]와 시토키닌이 '캠벨얼리' 포도의 기내생장에 미치는 영향 (Effect of DIF and Cytokinins on In Vitro Growth of 'Campbell Early' Crapes (Vitis spp.))

  • 김승희;김선규
    • Journal of Plant Biotechnology
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    • 제29권2호
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    • pp.105-110
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    • 2002
  • 포도 Campbell Early을 공시하여 기내 배양에 의한 대량 증식과 건전묘의 생산시 영향을 미치는 DIF조건과 cytokinin의 종류 (BA, TDZ, zeatin, 2iP, kinetin)및 농도의 최적 조건을 구명 하고자 수행한 실험의 결과는 다음과 같다. 신초생장은 0(25/2$^{\circ}C$)및 +7DIF(25/18$^{\circ}C$) 처리에서 좋았고. -7DIF(25/18$^{\circ}C$)에서는 생장이 전반적으로 나빴다. DIF 처리와 관계없이 BA와 TDZ 처리에서는 생장이 나빴으며 -7DIF 처리는 생육이 억제되었다. 분지수와 총절편체수도 모든 DIF 처리에서 신초 생장이 적었던 BA와 TDZ 처리에서 분지가 많았고, 총절편체수도 BA와 TDZ 처리에서 많은 것으로 나타났다. DIF와 상관없이 모든 zeatin과 kinetin 처리는 신초형성 효과는 없었고 오히려 억제적으로 작용하였다. 모든 DIF 처리구에서 주온과 야온에 상관없이 대조구와 같거나 약간 낮았다. 0DIF 처리에서 절간수가 증가하였으며 - 및 +7DIF 처리에서는 모든 시토키닌 처리구에서 0DIF 처리보다 낮은 결과를 보였다. 생체중은 0DIF 처리에서만 효과가 좋았으며 모든 DIF 처리의 대조구도 생체중이 상당히 낮았다. DIF 처리는 포도 기내배양의 생체중에 영향을 미쳤는데, 이는 신초 생장과 관계가 깊은 것으로 추정된다.

Microprogation And Environment Conditions Affecting On Growth Of In Vitro And Ex Vitro Of A. Formosanus Hay

  • Ket, Nguyen-Van;Paek, Kee-Yoeup
    • 한국자원식물학회:학술대회논문집
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    • 한국자원식물학회 2002년도 심포지엄
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    • pp.29-30
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    • 2002
  • The goal of this research was to develop the effectiveness of in vitro culture method for A. formosanus and study the environment in vitro conditions affecting on growth. The first series of experiments were examined to investigate the response of three different basal media, MS (Murashige and Skoog, 1962), Knudson (KC; Knudson, 1946) and modified hyponex on growth and multiplication during in vitro culture. Multiple shoot proliferation was induced in shoot tip explants on Hyponex (H3) media supplemented with BA (1 mg1$\^$-1/) or TDZ (1-2 mg1$\^$-1/). Addition of activated charcoal (1%) to the TDZ containing medium promoted rapid shoot tip proliferation (11.1 shoots per explant) but the same medium had an opposite effect resulting in poor proliferation in the nodal explants. However, the regenerated shoots had slow growth rate and failed to elongate. This problem was overcome by transferring the shoot clumps to a hormone free H3 media supplemented with 2% sucrose and 0.5% activated charcoal. Using bioreactor culture for scaling up was also shown the best way for multiple shoot induction and growth of this plant. The second series of experiments was studied to investigate the effect of physical environment factors on growth of in vitro plantlets. The Anoectochilus formosanus plantlets were cultured under different air exchange rate (0.1, 0.9, 1.2h$\^$-1/), without sucrose or supplement 20g.1$\^$-1/ (photoautotrophic or photomixotrophic, respectively), and different photosynthesis photon flux (40, 80, 120 ,${\mu}$mol.m$^2$.s$\^$-1/- PPF). Under non-enrichment CO$_2$ treatment, slow growth was observed in photoautotrophical condition as compared with photomixotrophical condition on shoot height, fresh weigh and dry weight parameters; High air exchange (1.2.h-l) was found to be inadequate for plant growth in photomixotrophical condition. On the contrary, under CO$_2$, enrichment treatment, the plant growth parameters were sharply (visibly) improved on photoautotrophic treatments, especially on the treatment with air exchange rate of 0.9.h-1. The growth of plant in photoautotrophic condition was not inferior compared with photomixotrophic, and the best growth of plantlet was observed in treatment with low air exchange rate (0.9.h-1). Raising the PPF level from 80 to 120${\mu}$mol.m$\^$-2/.s$\^$-1/ decreased the plant height, particularly at 120${\mu}$mol.m$\^$-2/.s$\^$-1/ in photoautotrophic condition, fresh weight and dry weight declined noticeably. At the PPF of 120${\mu}$mol.m$\^$-2/,s$\^$-1/, chlorophyll contents lowed compared to those grown under low PPF but time courses of net photosynthesis rate was decreased noticeably. Light quality mainly affected morphological variables, changes of light quality also positively affected biomass production via changes in leaf area, stem elongation, chlorophyll content. Plant biomass was reduced when A. formosanus were grown under red LEDs in the absence of blue wavelengths compare to plants grown under supplemental blue light or under fluorescent light. Stem elongation was observed under red and blue light in the present experiment. Smaller leaf area has found under blue light than with other lighting treatments. Chlorophyll degradation was more pronounced in red and blue light compared with white light or red plus blue light which consequent affected the photosynthetic capacity of the plant. The third series of experiment were studied to investigate the effect of physical environment factors on growth of ex vitro plants including photosynthesis photon flux (PPF), light quality, growing substrates, electrical conductivity (EC) and humidity conditions. In the present experiments, response of plant on PPF and light quality was similar in vitro plants under photosynthesis photon flux 40${\mu}$mol.m,$\^$-2/.s$\^$-1/ and white light or blue plus red lights were the best growth. Substrates testing results were indicated cocopeat or peat moss were good substrates for A. formosanus growth under the greenhouse conditions. In case of A. formosanus plants, EC is generally maintained in the range 0.7 to 1.5 dS.m-1 was shown best results in growth of this plant. Keeping high humidity over 70% under low radiation enhanced growth rate and mass production.

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희귀 및 멸종위기 수종 개느삼의 액아배양을 통한 기내번식 (In vitro propagation of a rare and endangered species, Echinosophora koreensis Nakai, by axillary bud culture)

  • 문흥규;김용욱
    • Journal of Plant Biotechnology
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    • 제35권3호
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    • pp.229-234
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    • 2008
  • 희귀 및 멸종위기 수종 개느삼의 액아배양을 통한 기내증식을 시험하였다. 2년생 개느삼의 액아 줄기를 절편으로 MS, WPM 및 DKW 배지에 배양결과 DKW 배지에서 양호한 생장을 보였다. DKW 배지를 기본으로 BA 단독처리 혹은 BA+TDZ 혼용 처리로 증식시험을 실시하였다. 액아로부터 줄기의 증식은 BA 단독처리보다 BA 및 TDZ의 혼용처리가 효과적이었으며, 절편당 $6{\sim}10$개의 줄기가 유도되었다. 배양과정에서 비정상적인 줄기나 잎은 나타나지 않았으나 TDZ를 0.05 mg/L 이상 처리시에는 잎이 작고, 전개되지 않았으며 과수화 현상이 나타났다. 증식된 줄기의 기내 발근은 대체로 저조하였다. 1/2DKW 배지에 $0.2{\sim}1.0$ mg/L IBA 처리시 전혀 발근되지 않았으며, 0.5 mg/L 및 1.0 mg/L NAA 처리시 각각 9.1% 및 19.2%의 발근을 보였고, 1개의 뿌리만 내렸다 반면 개느삼의 발근유도는 기외 micro-cutting의 방법으로 발근율 향상이 가능하였다. 기내증식된 줄기를 재료로 멸균된 인공 상토(버미큘라이트)에 기외 삽목을 실시한 결과 IBA 100 mg/L 처리시 58.6%까지 발근되었고, 뿌리수도 식물체 당 평균 3개가 유도되었다. 이러한 발근묘는 온실에서 90% 이상 순화되었고, 포지에 이식하여 2년까지 정상 생장이 가능하였다. 본 실험결과는 액아 배양을 통한 개느삼의 기내 줄기증식이 가능하며 micro-cutting의 방법을 좀더 개선하면 효율적인 묘목생산이 가능함을 보여주었다.

현사시나무 기내배양(器內培養) 엽육조직(葉肉組織)에서 분리(分離)된 원형질체(原形質体) 배양(培養) 및 식물체(植物体) 재분화(再分化) (Culture and Regeneration of Populus alba × glandulosa Leaf Protoplasts Isolated from in vitro Cultured Explant)

  • 박용구;손성호
    • 한국산림과학회지
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    • 제77권2호
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    • pp.208-215
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    • 1988
  • 현사시(Populus alba ${\times}$ glandulosa) 기내배양(器內培養)한 엽육조직(葉肉組織)에서 원형질체(原形質體)를 분리(分離), 배양(培養)하여 식물체(植物體) 재분화(再分化) 과정(過程)에 관(關)해 조사(調査) 검토(檢討)하였다. $NH_4NO_3$를 뺀 MS배지(培地)에 BAP 0.5mg/l와 2.4-D 2.0mg/l를 첨가(添加)하여 liquid plating 법(法)으로 원형질체(原形質體)를 배양(培養)하였을때 비교적(比較的) 높은 세포분열(細胞分裂)이 일어났다. colony 형성율(形成率)은 gauze를 넣은 semi-solid agar plating 법(法)에서 가장 높게 일어나서 배양(培養) 5주후(週後)에는 micro-callus가 형성(形成)되었다. gauze를 제거(除去)한 후(後)에는 원형질체(原形質體) 분리배양후(分離培養後) 8주(週)가 되었을때 mini-callus가 형성(形成)되었으며 이들 callus는 2, 4-D 0.5mg/l와 BAP 0.1mg/l를 첨가(添加)한 MS배지에서 증식되었다. shoot 형성(形成)은 zeatin 1.0mg/l를 첨가(添加)한 배지에서 이식한지 3주(週)만에 일어나기 시작했으며 6주후(週後)에 뿌리발달을 도모하고져 생장조절물질(生長調節物質)이 첨가(添加)되지 않은 1/2MS배지로 이식하였다. 이식한지 4주후(週後)에 많은 뿌리가 형성(形成)되었다. 발근(發根)이 된 개체(個體)는 온실(温室)에 이식(移植)하였는데 원형질체(原形質體)를 분리(分離)하여 완전식물체(完全植物體)로 분화(分化)시켜 온실(温室)에 이식(移植)하기 까지는 22주(週)가 걸렸다.

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