• 제목/요약/키워드: shoot clumps

검색결과 14건 처리시간 0.021초

라울리아 신초 추출물의 항산화 및 항염 효능에 관한 연구 (Study on Anti-oxidant and Anti-inflammatory Activity of the Tissue-cultured Shoot Clumps from Raoulia australis)

  • 박창민;한나경;정민석;백기엽;최종완
    • 대한화장품학회지
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    • 제40권4호
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    • pp.349-357
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    • 2014
  • 본 연구에서는 생물반응장치를 이용하여 조직 배양된 라울리아 신초에 대하여 화장품 성분으로써 응용가치를 평가하였다. 조직 배양한 라울리아 신초에 대한 항산화 및 항염 활성 효과를 연구하였다. 라울리아는 뉴질랜드나 호주에서 자생하는 국화과의 야생초본식물이다. 이미 몇몇 보고 된 논문에서 라울리아는 기관지염, 수막염 그리고 호흡기 질병 등을 유발하는 바이러스에 대한 증식 억제 활성이 있다고 보고되었다. 실험 결과 조직배양된 라울리아 신초 추출물은 자연 상태의 라울리아 추출물과 비교하여 항산화 활성 및 항염 활성 효과가 우수하였다. 조직 배양된 라울리아 신초 추출물은 자연에서 자란 라울리아 추출물보다 $50{\mu}L/mL$ 농도에서 10~25% 항산화 활성을 증가시켰다. 또한 조직 배양된 라울리아 신초 추출물은 LPS로 유도된 대식세포에서 iNOS와 COX-2의 단백질 발현이 자연에서 자란 라울리아 추출물보다 억제되었다. 본 연구의 결과들로, 조직배양 한 라울리아 신초 추출물은 피부 보호를 위한 천연 화장품 성분으로써 우수한 가능성을 제공할 수 있을 것으로 사료된다.

Development of Plant Regeneration and Genetic Transformation System from Shoot Apices of Sorghum bicolor (L.) Moench

  • Syamala, D.;Devi, Prathibha
    • 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.

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 제9차 국제심포지움 및 추계정기학술발표회
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    • pp.6-7
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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.(중략)

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In vitro shoot proliferation of Alnus japonica (Thunberg) Steudel

  • Kang, Ho-duck;Lee, Min-Soon
    • Plant Resources
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    • 제7권1호
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    • pp.1-6
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    • 2004
  • In vitro proliferation system was achieved by using nodal segment excised from greenhouse grown juvenile stock plants of Alnus japonica. Stem explants were cultured on MS medium supplemented with different plant growth regulators of cytokinin and/or their combinations. The most effective cytokinin source was the combination of zeatin 2.0 mg/L and TDZ 0.05 mg/L producing the average number of shoots (16.8 $\pm$ 3.6). In addition, healthy roots were formed after small clumps of shoots were transferred to half strength of MS medium containing IBA 0.02 mg/L with optimal rooting capacity. Soil acclimatization was successfully conducted in cell tray containing artificially mixed soil with 92 % survival rate.

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In vitro propagation of Bambusa nutans Wall. ex Munro through axillary shoot proliferation

  • Negi, Divya;Saxena, Sanjay
    • Plant Biotechnology Reports
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    • 제5권1호
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    • pp.35-43
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    • 2011
  • This communication describes for the first time an efficient and reproducible protocol for large-scale multiplication of Bambusa nutans. Nodal segments collected from field-grown clumps and cultured on Murashige and Skoog (MS) medium supplemented with $4.4{\mu}M$ benzylaminopurine (BA) and $2.32{\mu}M$ kinetin (Kin) gelled with 0.2% gelrite yielded 80% aseptic cultures with 100% bud-break. The in vitro-formed shoots obtained after bud-break were successfully multiplied in MS liquid medium supplemented with $13.2{\mu}M$ BA, $2.32{\mu}M$ Kin, and $0.98{\mu}M$ indole-3-butyric acid (IBA). Sub-culturing of shoots every 3 weeks on fresh multiplication medium yielded a consistent proliferation rate of 3.5-fold. Shoot clusters containing three to five shoots were successfully rooted with 100% success on half-strength MS liquid medium supplemented with $9.8{\mu}M$ IBA, $2.85{\mu}M$ indole-3-acetic acid (IAA), $2.68{\mu}M$ naphthaleneacetic acid (NAA), and 3% sucrose. Plantlets grown in vitro were acclimatized and subsequently transferred to the field. Inter-simple sequence repeat analysis has confirmed the genetic uniformity of the tissue-cultured plants up to 27 passages.

An Efficient Plant Regeneration System for Sorghum bicolor - a Valuable Major Cereal Crop

  • Baskaran P.;Jayabalan N.
    • Journal of Plant Biotechnology
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    • 제7권4호
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    • pp.247-257
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    • 2005
  • An efficient, rapid and large-scale in vitro clonal propagation of agronomically important Indian cereal crop genotypes (NSH27 & K5) of Sorghum bicolor (L.) Moench. by enhanced shoot proliferation in shoot tip segments was designed. MS medium fortified with plant growth regulators and coconut water markedly influenced in vitro propagation of Sorghum bicolor. In vitro plantlet production system has been investigated on Murashige and Skoog (MS) medium with the synergistic combination of 6-benzyladenine ($22.2\;{\mu}M$), kinetin ($4.6\;{\mu}M$), adenine sulphate ($2.8\;{\mu}M$), 5% coconut water and 3% sucrose which promoted the maximum number of shoots as well as beneficial shoot length. Subculturing of shoot tip segments on a similar medium enabled continuous production of more than 100 healthy shoots with similar frequency. When the healthy shoot clumps were cultured on MS medium fortified with 6-benzyladenine ($22.2\;{\mu}M$), kinetin ($4.6\;{\mu}M$), adenine sulphate ($2.8\;{\mu}M$), ${\alpha}$-naphthaleneacetic acid ($2.7\;{\mu}M$), ascorbic acid ($30.0\;{\mu}M$) and 5% coconut water, a rapid production of axillary and adventitious buds was developed after 8 wk culture. More than 300 shoots were produced 10 wk after culture. Rooting was highest (100%) on half strength MS medium containing 22.8 mM IAA. Micropropagated plants established in garden soil, farmyard soil and sand (2:1:1) were uniform and identical to the donor plant with respect to growth characteristics. These plants grew normally without showing any traits.

산마늘 다신초 증식과 인경형성에 효율적인 생물반응기 배양방식 (High Efficiency Bioreactor Culture System for Mass Proliferation and Bulblet Formation of Allium victorialis var. platyphyllum Makino)

  • 박소영;이위영;안진권;권영진;박혜진
    • Journal of Plant Biotechnology
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    • 제31권2호
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    • pp.127-132
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    • 2004
  • 본 실험은 산마늘의 산초 증식과 인경 형성에 적합한 생물반응기 배양방식과 인경 형성시 배양방식에 따른 당 대사를 구명하고자 실시되었다. 다신초 증식에는 생물반응기에 망을 걸고 배지에 절편체를 접하게 배양한 RC와 MRC (13-15개)에서 가장 좋은 결과를 얻었다. 인경형성과 비대에는 간헐적으로 배지를 공급해준 E&FS에서 93.4%의 인경형성이 이루어졌고 크기에 있어서도 균일하였다. RC와 MRC에서 형성된 인경은 뿌리가 무성하였으며 인경의 크기도 균일하지 않았다. 배양방식별로 수확한 인경내 유리당 함량은 전반적으로 E&FS.에서 낮았던데 반해 전분 함량은 높았다. 배지내 sucrose, glucose와 fructose는 인경 비대 시기에 감사되었는데 이는 첨가한 sucrose가 가수분해 되기도 전에 glucose나 fructose와 함께 식물체로 바로 이용됨을 보여주는 것이었다.

High-frequency Plant Regeneration from Cultured Flower Bud Receptacles of Allium hookeri L.

  • Koo, Ja Choon
    • 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.

산마늘 다신초 덩어리로부터 인경 형성과 비대에 미치는 methy jjasmonate의 영향 (Effect of Methyl Jasmonate on in vitro Bulblet Formation and Enlargement from Shoot Clump of Allium victorialis)

  • 박소영;안진권;이위영;박혜진
    • Journal of Plant Biotechnology
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    • 제31권1호
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    • pp.79-82
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    • 2004
  • 산마늘의 다신초 덩어리로부터 인경형성을 위해 ABA와 MeJA가 첨가된 MS 배지에서 배양하였다. 저농도 (0.01mg/L)의 ABA처리구는 인경 형성보다 오히려 신초의 증식을 유도하였다. 인경은 MeJA처리구에서 배양 4∼6주 후 형성되기 시작하여 1.0mg/L MeJA 처리구에서 다신초 덩어리로부터 100% 인경형성이 이루어졌다. 조직학적 관찰 결과 생장조절제가 첨가되지 않은 배지의 인경과는 달리 MeJA처리구에서 비대된 인경의 외피세포는 크고 둥글며 단백질 등의 물질로 가득 차 있었다. 산마늘의 다신초 덩어리로부터 인경형성에 MeJA가 촉진적임을 알 수 있었다.

미나리의 體細胞 胚 생산 硏究 (Production of Somatic Embryos in Oenanthe javanica (BL.) DC.)

  • KOH, Gab Cheon;AHN, Chang Soon
    • 식물조직배양학회지
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    • 제24권2호
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    • pp.107-112
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    • 1997
  • 본 연구는 미나리의 배발생 캘러스를 배양하여 정상적이고 균일한 형태의 체세포 배를 대량 생산할 수 있는 조건을 구명하고, 생산된 체세포배를 종묘로 이용하기 위한 기초연구로 실시하였다. 배발생 캘러스를 생장조절제, 당, 질소원등을 농도별로 첨가한 MS배지에 현탁배양한 결과는 아래와 같다. 배발생 캘러스를 생장조절제가 첨가되지 않은 액체배지에 현탁배양하면 배발생 세포괴 및 체세포 배가 왕성하게 증식되었다. 구형단계의 배를 IBA와 NAA를 첨가한 배지에 현탁배양하면 배발생 세포괴의 증식과 함께 배의 발달도 진행됐으나, 2,4-D가 첨가된 배지에서 배양하면 배발생 세포괴 및 세포만 증식하고 배의 발달은 진행되지 많았다. 질소원의 종류에 따른 배발생 세포괴의 생장 발육상태에서 $\textrm{KNO}_3$$\textrm{NH}_4\textrm{NO}_3$가 각각 20mM 첨가되었을 때 가장 좋았다. 유아 발달에는 $\textrm{NH}_4\textrm{NO}_3$가, 유근발달에는 $\textrm{KNO}_3$가 효과적이었다. 구형단계의 배를 sucrose가 3-6 % 첨가된 배지에 배양하면 발육이 좋았다. 구형단계의 배를 ABA가 첨가되지 않은 배지에 배양하면 하배축의 이상신장 및 다배현상이 일어나지만 ABA가 $10\mu\textrm{M}$ 첨가된 배지에 배양하면 하배축의 길이가 단축되고 이차배 발생도 현저히 감소하였다. 고체배지에 배발생캘러스를 계속 배양하여 다양의 구형배를 얻을 수 있고 이들을 생장조절제가 첨가되지 않은 배지에서 배양하면 종자 유내 식물체와 유사한 유식물을 얻을 수 있었다.

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