• 제목/요약/키워드: transformed root cultures

검색결과 19건 처리시간 0.021초

미치광이풀(Scopolia parviflora)의 모상근 배양에 의한 Tropane Alkaloid 생산 (Production of Tropane Alkaloids by Hairy Root Cultures of Scopolia parviflora)

  • 안준철
    • Journal of Plant Biology
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    • 제36권3호
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    • pp.225-231
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    • 1993
  • Transformed hairy roots of Scopolia parviflora, producing tropane alkaloids and native to Korea, were obtained following infection of rhizome segments with Agrobacterium rhizogenes A4. Each root tip induced from inoculum sites excised and cultured in MS agar or liquid medium. About seventy of hairy root clones were established. Among them, several fast growing hairy root clones were examined for alkaliod content. Two dimensional TLC analysis showed that the tropane alkaloid pattern of hairy root was more complicated than that in the rhizome of mother plant. On the other hand, some hairy root clones did not produce scopolamine and hyoscyamine. In HPLC analysis, some hairy root clones yield higher levels of scopolamine and hyoscyamine than those of mother plant rhizome which used for infection. Scopolamine and hyoscyamine were identified by comparison of their retention times and of their spectra data with those of authentic compounds.

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Characteristics of Transformed Panax ginseng C.A. Meyer Hairy Roots: Growth and Nutrient Profile

  • Jeong Gwi-Taek;Park Don-Hee
    • Biotechnology and Bioprocess Engineering:BBE
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    • 제11권1호
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    • pp.43-47
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    • 2006
  • Ginseng (Panax ginseng CA. Meyer) hairy root cultures, which are established via the infection of ginseng root discs with Rhizobium rhizogenes, have been used to construct profiles of both biomass growth and nutrient consumption in flask cultures. In a 250 mL shake flask culture, the maximum biomass was observed on the 59th day of the culture period, at 216.8 g (fresh wt) per liter or 11.4 g (dry wt) per liter. The hairy roots were determined to have a growth rate of 0.355 g-DW/g cells/day during the exponential growth phase and a maximum specific growth rate on day 7. Total ginseng saponin and phenolic compound contents were noted to have increased within the latter portion of the culture period. Linear correlations between increases in biomass weight and nutrient uptake were used to imply the conductivity yield $2.60g-DW/(L{\cdot}mS)$ and carbon yield 0.45 g-DW/(g sugar) in the 250 mL flask cultures. The biomass yield when two different nitrogen sources were used (ammonia and nitrate) was shown to remain approximately constant. at $0.47g-DW/(L{\cdot}mM\;NH_4$) and $0.33g-DW/(L{\cdot}mM\;NO_3$); it remained at these levels for 16 days with the ammonia. and for 24 days with the nitrate. The biomass yield when a phosphate source was used was also shown to remain approximately constant for 9 days, at $3.17g-DW/(L{\cdot}mM\;PO_4$), with an $R^2$ of 0.99.

Optimization of ginseng hairy roots culture and its ginsenoside analysis

  • Ji, Joong Gu;Yoo, Sun Kyun
    • 한국응용과학기술학회지
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    • 제35권4호
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    • pp.995-1002
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    • 2018
  • Hairy root culture of ginseng is industrially prospected because the cultivation period of ginseng is relatively long. In this study, the effect of medium concentration and sucrose concentration on hairy root culture of ginseng was evaluated. The optimization of ginseng hairy roots transformed by Agrobacterium rhizogene were performed liquid medium. The MS(Murashinge & Skoog basal medium) concentration was selected with 1/2 strength MS and the optimal sucrose concentration was determined at 2-3%(w/v). At the optimum culture condition, The yield (the ratio of weight of grown hairy root cultures to weight of fresh ginseng hairy roots) and production rate of ginseng root were 19.42 times and 5.73 g/l-day. The major ginsenosides were Rb group, Re and Rg1. The produced total ginsenoside content in the solid medium was 9.87 (mg/g) and increased 1.34 times in the liquid medium (13.23 mg/g). In solid culture, the contents of ginsenosides Rb, Re and Rg1 were 2.14, 3.65 and 1.87 mg/g, respectively. In liquid culture, the contents of ginsenosides Rb, Re and Rg1 were 3.54, 4.12 and 2.63 mg/g, respectively.

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

  • 장석원;김인현;한태진
    • 식물조직배양학회지
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    • 제26권1호
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    • pp.7-14
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    • 1999
  • 형질전환된 소리쟁이 모상근의 기내 배양시 그 생장 특성과 anthraquinone생산성을 조사하기 위하여 소리쟁이의 모상근을 Agrobacterium rhirogenes strain $A_4$ 접종에 의하여 잎 절편으로부터 유기하여 부정근과 비교하였다. 잎 절편에서의 부정근 형성은 5 $\mu$M NAA를 첨가한 MS배지에서 가장 양호하였다. Paper electrophoresis를 통한 opine분석 결과 모상근에서만 mannopine이 검출되고 부정근에서는 검출되지 않았다. 부정근과 모상근 모두에서 2차근인 측근 근단은 호르몬을 첨가하지 않은 배지에서 신장만 할 뿐 분지하지 않았으나, 1차근인 주근의 근단은 많은 측지를 내며 빠르게 생장하였다. Anthraquinone 함량 증대에 따른 부정근과 모상근의 생장에는 MS기본 배지가 가장 양호하였다. 부정근과 모상근 배양시 생장량과 anthraquinone함량은 5% sucrose를 포함한 0.05 $\mu$M NAA와 0.1 $\mu$M kinetin으로 조성된 MS 액체 배지에서 가장 높은 것으로 나타났으며, 모상근의 anthraquinone함량은 배양 일수에 따라 증가하다가 배양 25일 이후에는 감소하였다.

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In Vitro Germination and Propagation by Embryo Culture of Taxus cuspidata for the Taxol Production

  • Park, Myung-Suk
    • Journal of Plant Biotechnology
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    • 제2권1호
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    • pp.29-33
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    • 2000
  • To develop an efficient propagation method for yew tree, zygotic embryos were cultured under various conditions. When dissected embryos were cultured on GA$_3$ containing media, the highest germination frequency was observed on WPM medium contaning 1.0 mg/L GA$_3$. For germination of the embryos, two different conditions were compared; culturing embryos with endosperm (Method I), and 2) culturing embryos only (Method II). Maximum germination was achieved in 0.5 mg/L GA$_3$ when embryos with endosperm were cultured on the media. Of the media tested, White and WPM medium were the most suitable on germination of embryos. The abnormality of yew embryos found was observed when it cultured on GA$_3$ or culture media. About 40% of the precociously germinated embryos could be developed into full seedlings. Seedlings contained taxol in high quantity (535 $\mu\textrm{g}$/g dry weight). In vitro techniques will be sewed as a useful tool for the development of transformed root cultures and biosynthesis studies.

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An easy and efficient protocol in the production of pflp transgenic banana against Fusarium wilt

  • Yip, Mei-Kuen;Lee, Sin-Wan;Su, Kuei-Ching;Lin, Yi-Hsien;Chen, Tai-Yang;Feng, Teng-Yung
    • Plant Biotechnology Reports
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    • 제5권3호
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    • pp.245-254
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    • 2011
  • This study describes an efficient protocol for Agrobacterium tumefaciens-mediated transformation of two subgroups of genotype AAA bananas (Musa acuminata cv. Pei Chiao and Musa acuminata cv. Gros Michel). Instead of using suspension cells, cauliflower-like bud clumps, also known as multiple bud clumps (MBC), were induced from sucker buds on MS medium containing $N^6$-Benzylaminopurine (BA), Thidiazuron (TDZ), and Paclobutrazol (PP333). Bud slices were co-cultivated with A. tumefaciens C58C1 or EHA105 that carry a plasmid containing Arabidopsis root-type ferredoxin gene (Atfd3) and a plant ferredoxin-like protein (pflp) gene, respectively. These two strains showed differences in transformation efficiency. The EHA105 strain was more sensitive in Pei Chiao, 51.3% bud slices were pflp-transformed, and 12.6% slices were Atfd3-transformed. Gros Michel was susceptible to C58C1 and the transformation efficiency is 4.4% for pflp and 13.1% for Atfd3. Additionally, gene integration of the putative pflp was confirmed by Southern blot. Resulting from the pathogen inoculation assay, we found that the pflp transgenic banana exhibited resistance to Fusarium oxysporum f. sp. cubense tropical race 4. This protocol is highly advantageous to banana cultivars that have difficulties in setting up suspension cultures for the purpose of quality improvement through genetic transformation. In addition, this protocol would save at least 6 months in obtaining explants for transformation and reduce labor for weekly subculture in embryogenic cell suspension culture systems.

인삼 모상근의 캘러스를 이용한 ginsenoside 생산 (Production of Ginsenoside in Callus of Ginseng Hairy Roots)

  • 권정희;천현준;양덕조
    • Journal of Ginseng Research
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    • 제27권2호
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    • pp.78-85
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    • 2003
  • Agrobacterium rhizognes $A_4$ Ti-plasmid를 인삼 뿌리에 도입하여 유전적으로 안정하며 반영구적으로 이용할 수 있는 형질전환된 인삼모상근 캘러스(GHC-T78)를 유도하였다. 특정 ginsenoside를 대량으로 생산할 수 있는 최적배양조건을 확립하기 위해서 먼저 모상근으로부터 캘러스의 유도하는 과정에서 BA의 단독 처리구는 auxin과 cytokinin의 혼합 처리구보다 캘러스 형성이 더 우수하였다. 인삼 캘러스 형성율은 Benzyladenine(BA)를 1 mg-3 mg/L 까지 첨가한 배지에서 가장 높게 나타났으며, ginsenoside 함량 역시 bezyladenine 단독처리구는 가장 우수하였다. 캘러스 세포의 액체배양 기간을 4주로 설정할 때 BA의 농도 역시 BA 2 mg/L로 첨가한 배지에서 가장 우수한 캘러스 생장률을 보였다. 실제로 인삼 모상근 캘러스의 생장율은 암상태에서 배양하는 것이 광상태에서 보다 다소 양호하였으나, ginsenoside의 생성에는 연속광상태에서 더 효과적임이 확인되었다. 모상근 캘러스에서 얻은 이러한 결과는 국내외 처음으로 보고되는 내용이며, 액체배양의 캘러스 세포에서 분화된 무수히 많은 단일 모상근 근모의 형성은 액체배양을 통한 특정 ginsenosid의 새로운 생산방법을 개발할 수 있도록 하고 있다.

형질전환(形質轉換)된 포플러의 딱정벌레에 대한 저항성(抵抗性) 유전자(遺傳子)(Proteinase Inhibitor II) 발현(發現) (Gene Manipulation of Pin 2(Proteinase Inhibitor II) to the Cottonwood Leaf Beetle(Coleoptera : Chrysomelidae) in Transgenic Poplar(Populus deltodies × P. nigra))

  • 강호덕
    • 한국산림과학회지
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    • 제86권4호
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    • pp.407-414
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    • 1997
  • 외래 저항성 유전자, Proteinase inhibitor II가 형질전환된 3계통의 벨기에 포플러를 대상으로 딱정벌레에 대한 유전자 발현정도가 기내에서 조사되었다. 포플러 계통은 선발 유전자로서 Nos-promoter와 Neomycin phosphotransferase gene에 의하여 조절되고 곤충에 대한 저항성 유전자로서 CaMV-35S와 Pin2(Proteinase inhibitor II)에 의한 형질전환체이다. 특히, 형질전환된 포플러의 내충성 저항력을 조기검정하기 위하여, 조직배양을 응용한 새로운 방법으로서 곤충의 알을 표면 살균하여 기내의 조직배양묘와 배양하는 동시배양 방법이 이용되었다. 형질전환된 포플러의 저항성은 기내에서 유충에 의해 섭취된 잎면적, 잎 섭취에 의한 유충의 무게 증감, 유충의 성장단계 등에 의하여 조사되었다. 특히, 잎면적은 각각의 LPI(Leaf plastochron index)별로 측정되었고, 잎면적, 유충의 무게, 곤충의 성장 속도는 형질전환체와 비형질전환체 간에 큰 차이를 보였다. 기내에서 무병상태로 배양된 알들이 부화된 후, 유충의 잎 섭취도는 LPI 4와 5사이에서 가장 높았다. 본 실험의 기내 배양법은 외래유전자를 삽입한 이후에 곧바로 발현을 빠른 시간내에 조기검정 할 수 있는 새로운 방법의 개발이라 할 수 있다.

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