• Title/Summary/Keyword: NaaS

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In vitro Propagation and Protocorm-like Body Formation of Endangered Species, Dendrobium moniliforme (멸종위기 수종 석곡(Dendrobium moniliforme)의 Protocorm-like Body 형성 및 기내증식)

  • Bae, Kee Hwa;Kim, Nam Young;Song, Jae Mo;Song, Gwanpil
    • Journal of Forest and Environmental Science
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    • v.30 no.1
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    • pp.126-132
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    • 2014
  • This experiment was conducted to establish the in vitro propagation of Dendrobium moniliforme through protocorm like body (PLB) induction from the culture of leaf, stem and root explants. Frequency of PLB formation from root explants was higher than those of leaf and stem explants. PLB's proliferation in MS medium including 1.0 mg/L NAA was better than 1.0 mg/L IBA. Frequency of PLB's proliferation on medium with various concentrations of BA, Kinetin, Tidiazuron (0. 1.0, 3.0 mg/L) and NAA (0, 1.0 mg/L) was tested. The maximun proliferation of PLB's was obtained on MS medium supplemented with 3.0 mg/L BA and 1.0 mg/L NAA after 6 weeks of culture. Addition of 200 mg/L activated charcoal (AC) and 30 g/L sucrose was effective on PLB proliferation for D. moniliforme.

Determination of k0 factors of short-lived nuclides 46mSc and 110Ag for the k0-NAA

  • Truong Son Truong;Van Doanh Ho;Manh Dung Ho
    • Nuclear Engineering and Technology
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    • v.55 no.9
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    • pp.3202-3205
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    • 2023
  • The k0-standardization neutron activation analysis method has successfully determined the mass fraction of elements of interest using around a hundred analytical radionuclides. However, several very short-lived nuclides with half-life less than 100 s have not been used at Dalat research reactor. One of the reasons is that the values of k0-factors of these nuclides are significantly different. Therefore, this work focused on re-determination and evaluation of k0-factors of very short-lived nuclides 110Ag (T1/2 = 24 s) and 46mSc (T1/2 = 18.75 s). The results of determination of the short-lived nuclides revealed that k0-factor of 110Ag is significantly difference between the existing data and the obtained results in this work. The evaluation of the k0-factors was done by using the obtained results for application of k0-NAA for NIST-1566b and NIST-2711A standard reference materials.

Production of Phytol, an ACAT Inhibitor, from Callus Culture of Lettuce (Lactuca sativa L.) (상추 (Lactuca sativa L.) callus로부터 ACAT 억제 활성물질, phytol의 생산)

  • An, Kwang-Hee;Jang, Tae-O;Baek, Nam-In;Kim, Se-Young
    • Journal of Plant Biotechnology
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    • v.29 no.1
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    • pp.63-68
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    • 2002
  • The possibility for mass production of phytol, inhibitory diterpene against ACAT (Acyl-CoA: Cholesterol acyltransferase) was investigated by using callus culture of lettuce. The callus were induced from lettuce cotyledon explants on MS medium containing 0.5 mg.L$^{-1}$ NAA after 4 week's culture. Adventitious roots were formed from the explants on MS medium containing 0.5 mg.L$^{-1}$ IBA or 1.0 mg.L$^{-1}$ NAA. Adventitious shoots and roots were emerged from the callus when the callus was transferred to MS medium containing auxin alone, or with cytokinin. The plant growth regulators and their concentrations for the organogenesis were 1.0 mg.L$^{-1}$ NAA, 0.1 mg.L$^{-1}$ BA, 0.5 mg.L$^{-1}$ NAA with 0.1 mg.L$^{-1}$ kinetin, or 0.5 g.L$^{-1}$ 2.4-D with 1.0 mg.L$^{-1}$ kinetin. Analyses of chlorophyll contents showed that chlorophyll contents were higher in morphogenic calli than in non-morphogenic calli. However, the chemical analyses of gas chromatography indicated that phytol contents were not proportionate to the chlorophyll contents of callus. The content of phytol was higher in callus than in lettuce cotyledon.ledon.

Anthraquinone Productivity by the Cultures of Adventitious Roots and Hairy Roots from Curled Dock (Rumex crispus) (소리쟁이 (Rumex crispus)의 부정근과 모상근 배양에 의한 Anthraquinone 생산성)

  • 장석원;김인현;한태진
    • Korean Journal of Plant Tissue Culture
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    • v.26 no.1
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    • pp.7-14
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    • 1999
  • In order to survey anthraquinone productivity from in vitro root culture, transformed hairy roots of Rumex crispus were induced from leaf segments by infection with Agrobacterium rhizogenes strain $A_4$ and compared with adventitious roots. The optimum condition of adventitious root formation from leaf segments was 5 $\mu$M NAA added to MS medium. Mannopine was detected in the extract of hairy roots by paper electrophoresis, but not in adventitious roots. Secondary root tips of both adventitious roots and hairy roots elongated without lateral root branching in hormone free MS medium, but primary root tips showed more rapid growth with extensive lateral root branching. MS basal medium was the best for growth of the adventious roots and hairy roots for anthraquinone content. Adventitious root tips and hairy root tips cultured in liquid MS medium supplemented with 0.05 $\mu$M NAA and 0.1 $\mu$M kinetin (contained 5% sucrose) showed the maximal growth and anthraquinone content. Anthraquinone content of hairy roots was increased by the culture periods, but was reduced after 25 days of culture.

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Plant regeneration and soil acclimatization through photoautotrophic culture from leaf explant of a rare species in Sedum tosaense Makino (희귀수종인 주걱비름(Sedum tosaense Makino)의 잎절편으로부터 기내 식물체 재분화 및 광독립배양을 통한 토양순화)

  • Ko, Myoung-Suk;Bae, Kee Hwa;Song, Gwanpil;So, In Sup
    • Journal of Plant Biotechnology
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    • v.40 no.2
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    • pp.79-87
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    • 2013
  • The aim of this study was to establish plant regeneration from leaf explants of Sedum tosaense Makino, which is globally rare and endangered species. The leaf explants of S. tosaense were cultured on the MS medium supplemented with different concentration of BA and NAA for callus induction. Callus induction was showed the highest (100%) on MS medium containing $2.0mg{\cdot}L^{-1}$ BA and $1.0mg{\cdot}L^{-1}$ NAA. The highest number of shoots were regenerated when callus were cultured on MS medium containing $2.0mg{\cdot}L^{-1}$ BA and $1.0mg{\cdot}L^{-1}$ NAA for 5 weeks. The axillary bud were cultured on the MS media supplemented with combination of BA and NAA for in vitro propagation. The highest number of adventitious shoot (7.9 per explants) formed at $1.0mg{\cdot}L^{-1}$ NAA and $2.0mg{\cdot}L^{-1}$ BA. For rooting, MS medium supplemented with or without $2.0g{\cdot}L^{-1}$ activated charcoal was tested. The optimal results were observed using MS medium supplemented with $2.0g{\cdot}L^{-1}$ activated charcoal, on which 85.7 (No. of root), 4.6 cm (length of root). 1,200 ppm $CO_2$ and 350 ppm $CO_2$ were supplied for make certain the effects of $CO_2$ on pre-acclimatization by photoautotrophic culture. 1,200 ppm $CO_2$ treatment was established higher than 350 ppm $CO_2$ treatment. Soil acclimatization of in vitro plantlets was the best in mixture soil consisted of peat moss and perlite with 100% survival rate and they showed the maximum growth.

In Vitro Flowering Response of Ocimum basilicum L.

  • Sudhakaran, S.;Sivasankari, V.
    • Journal of Plant Biotechnology
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    • v.4 no.4
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    • pp.179-181
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    • 2002
  • Nodal explants of Ocimum basilicum L. (Sweet basil, Lamiaceae), showed shoot proliferation after 7-10 days on MS media containing 1.5 mg/L kinetin. In vitro flowering was achieved from 90% of the shootlets which were sub cultured on a half strength MS media fortified with 5 mg/L BAP and 1 mg/L IAA. Cytokinin alone or in combination with $CA_3$and NAA resulted in shoot proliferation only. For rooting the plantlets were subcultured on MS basal medium supplemented with 3 mg/L NAA and rootlets emerged after 10 days of incubation. The survival percentage of transplanted plantlets was 70%.

Effect of growth regulators on shoot regeneration and root formation during in vitro culture of bulb segments from Narcissus (cv. Dutck Master) (수선화 구근의 기내배양시 성장조절제의 조직별 재분화와 뿌리 형성에 미치는 효과)

  • Kim Younghee
    • Proceedings of the KAIS Fall Conference
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    • 2005.05a
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    • pp.269-271
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    • 2005
  • 본 연구는 수선화 구근의 각 조직으로부터 기내배양시 캘러스형성과 신초재분화를 위한 성장조절제의 효과를 측정하기 써하여 시행되었다. 신초형성과 callus의 형성은 기저부를 포함하는 floral axis에서 $50\%$의 신초발아율을 관찰하였고 scale 에서는 신초형성이 거의 관찰되지 않았다. 그리고 floral axis만을 치상한 경우는 아주 저조한 신초형성율이 관찰되었다. 지저부를 포함한 floral axis의 신초형성은 callus의 형성과 같은 NAA 0.5 mg/L과 BA 1.0 mg/L을 포함하는 MS 배지에서 만족할만한 결과를 얻었다. 신초형성으로부터 모든 신초가 형성되기까지는 약 140일이 소요되었다. 신초가 형성된 구근조직을 NAA 5.0 mg/L과 TDZ 0.02 mg/L을 포함하는 뿌리유도 MS배지에서 뿌리가 유도되는 결과를 얻었다. 본 실험에서는 수선화의 재 분화에 있어서 구근의 조직에 따라 신초형성이 다르게 나타남을 발견 할 수 있었다.

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Influence of Hormones and Selection of Stable Cell Lines of Plumbago rosea for Accumulation of Plumbagin

  • Komaraiah P.;Jogeswar G.;Naga Amrutha R.;Sri Laxmi P.;Lavanya B.;Rama Krishna S.V.;Kavi Kishor P.B.
    • Journal of Plant Biotechnology
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    • v.5 no.3
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    • pp.181-185
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    • 2003
  • Callus and suspension cultures derived from leaf explants of Plumbago rosea were established on Murashige and Skoog's medium containing 1 mg/L IAA, 0.5 mg/L NAA and 0.3 mg/L BAP. Callus cultures were tested for their growth and accumulation of plumbagin, a naphthoquinone and was identified by $^1H$ NMR and electron ionization mass spectroscopy. While auxins (not 2,4-D) influenced growth and plumbagin accumulation, cytokinins did not influence them much. Increasing concentrations of IAA in presence of NAA and BAP increased plumbagin in suspensions only up to 1 mg/L. Growth of callus was optimum (8.3 g DCW/I) at a hormonal combination of 1.5 mg/L IAA, 0.5 mg/L NAA and 0.3 mg/L BAP, but high plumbagin accumulation (4.9 mg/g DCW) was recorded at 1.0 mg/L IAA plus 0.3 mg/L BAP. Since instability in growth and secondary metabolite accumulation was noticed, several cell lines/clumps of callus were screened for plumbagin accumulation by visual and analytical methods. Biomass and accumulation of plumbagin showed a negative correlation in several cell lines. But one cell line showed stability both in terms of biomass and plumbagin accumulation over a period of 6 months.

Studies on Production of Alkaloid by Plant Cell Culture of Corydalis remota (세포 현탁배양에 의한 현호색 알칼로이드의 생산)

  • Chang, Jung-In;Chi, Hyung-Joon;Shin, Seung-Won
    • Korean Journal of Pharmacognosy
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    • v.27 no.4
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    • pp.289-294
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    • 1996
  • In previous paper, we described the induced callus of Corydalis remota contains a significant amount of alkaloids. This study describes an optimal condition to maximize alkaloid production. The suspension cultures maintained alkaloid production ability after fifth subculture and a small amount of alkaloid seemed to be released out of cells. The yields of alkaloid by cultured cells was varied depending on the concentrations of NAA, carbon sources and phosphate ion and depending on the vitamin combinations and concentrations. Biosynthetic precursor and an elicitor treatment also affected the total alkaloid yield of the cultures. The optimal conditions for alkaloid production were as follows: 1) MS basal salt containing 30 g/l of glucose, 1.0 mg/l of NAA, and vitamins of LS medium should be used. 2) The culture should be treated with tyrosine 20 mg/l, and yeast extract 1.5 ml/l after the culture reached a stationary phase of growth. Five alkaloids were isolated from the cultures and they were characterized. The spectral data unambiguously revealed that the isolated compounds were dihydrosanguinarine, protopine. tetrahydropalmatine, allocyptopine and ambinine, respectively.

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Design and optimization of thermal neutron activation device based on 5 MeV electron linear accelerator

  • Mahnoush Masoumi;S. Farhad Masoudi;Faezeh Rahmani
    • Nuclear Engineering and Technology
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    • v.55 no.11
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    • pp.4246-4251
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    • 2023
  • The optimized design of a Neutron Activation Analysis (NAA) system, including Delayed Gamma NAA (DGNAA) and Prompt Gamma NAA (PGNAA), has been proposed in this research based on Mevex Linac with 5 MeV electron energy and 50 kW power as a neutron source. Based on the MCNPX 2.6 simulation, the optimized configuration contains; tungsten as an electron-photon converter, BeO as a photoneutron target, BeD2 and plexiglass as moderators, and graphite as a reflector and collimator, as well as lead as a gamma shield. The obtained thermal neutron flux at the beam port is equal to 2.06 × 109 (# /cm2.s). In addition, using the optimized neutron beam, the detection limit has been calculated for some elements such as H-1, B-10, Na-23, Al-27, and Ti-48. The HPGe Coaxial detector has been used to measure gamma rays emitted by nuclides in the sample. By the results, the proposed system can be an appropriate solution to measure the concentration and toxicity of elements in different samples such as food, soil, and plant samples.