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首页> 外文期刊>Plant Cell Reports >Genetic transformation of Gentiana macrophylla with Agrobacterium rhizogenes: growth and production of secoiridoid glucoside gentiopicroside in transformed hairy root cultures
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Genetic transformation of Gentiana macrophylla with Agrobacterium rhizogenes: growth and production of secoiridoid glucoside gentiopicroside in transformed hairy root cultures

机译:发根农杆菌对大庆龙胆的遗传转化:经转化的毛状根培养物中土生龙脑苷的生长和产量

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Hairy root cultures of Gentiana macrophylla were established by infecting the different explants four Agrobacterium rhizogenes strains namely A(4)GUS, R1000, LBA 9402 and ATCC11325, and hairy root lines were established with A. rhizogenes strain R1000 in 1/2 MS + B(5) medium. Initially, 42 independent hairy root clones were maintained and seven clones belongs to different category were evaluated for growth, morphology, integration and expression of Ri T-DNA genes, and alkaloid contents in dry root samples. On the basis of total root elongation, lateral root density and biomass accumulation on solid media, hairy root clones were separated into three categories. PCR and Southern hybridization analysis revealed both left and right T-DNA integration in the root clones and RT-PCR analysis confirmed the expression of hairy root inducible gene. GUS assay was also performed to confirm the integration of left T-DNA. The accumulation of considerable amounts of the root-specific secoiridoid glucosides gentiopicroside was observed in GM1 (T +/L and T +/R) and the GM2 (T +/L and T -/R DNA) type clones in considerably higher amount whether as two T -/L but T +/R callus-type clones (GM3) accumulated much less or only very negligible amounts of gentiopicroside. Out of four media composition the 1/2 MS + B(5) vitamin media was found most suitable. We found that initial establishment of root cultures largely depends on root:media ratio. Maximum growth rate was recorded in 1:50 root:media ratio. The maximum biomass in terms of fresh weight (33-fold) was achieved in 1/2 MS + B(5) media composition after 35 days in comparison to sixfold increase in control. The biomass increase was most abundant maximum from 15 to 30 days. Influence of A. rhizogenes strains and Ri plasmid of hairy root induction, the possible role of the T(L)-DNA and T(R)-DNA genes on growth pattern of hairy root, initial root inoculum:media ratio and effect of media composition is discussed.
机译:通过感染不同外植体4个发根农杆菌菌株A(4)GUS,R1000,LBA 9402和ATCC11325来建立大秦ent的毛根培养物,并用1/2 MS + B的发根根霉R1000建立毛状根系。 (5)中等。最初,维护了42个独立的毛状根克隆,并评估了7个属于不同类别的克隆的Ri T-DNA基因的生长,形态,整合和表达,以及干燥根样品中生物碱的含量。根据固体培养基上的总根伸长,侧根密度和生物量积累,将毛状根克隆分为三类。 PCR和Southern杂交分析揭示了根克隆中左右T-DNA的整合,RT-PCR分析证实了毛状根诱导基因的表达。还进行了GUS分析,以确认左T-DNA的整合。在GM1(T + / L和T + / R)和GM2(T + / L和T-/ R DNA)型克隆中观察到大量的根特异类芥子苷苷龙胆苦苷的积累量是否较高。因为两个T-/ L但T + / R愈伤组织型克隆(GM3)积聚的龙胆苦味苦苷少得多或仅可忽略不计。在四种培养基成分中,发现最适合使用1/2 MS + B(5)维生素培养基。我们发现,根文化的初步建立很大程度上取决于根与培养基的比例。以1:50的根:培养基比例记录最大生长速率。 35天后,在1/2 MS + B(5)培养基成分中实现了以鲜重计的最大生物量(33倍),而对照则增加了六倍。从15天到30天,生物量增加最为丰富。发根农杆菌菌株和毛状根诱导的Ri质粒的影响,T(L)-DNA和T(R)-DNA基因对毛状根生长方式,初始根接种物:培养基比例和培养基作用的可能作用组成进行了讨论。

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