Tiwari Rajesh Kumar, Trivedi Mala, Guang Zhang Chun, Guo Guang-Qin, Zheng Guo-Chang
Institute of Cell Biology, School of Life Sciences, Lanzhou University, Lanzhou, 73000, Gansu, PR China.
Plant Cell Rep. 2007 Feb;26(2):199-210. doi: 10.1007/s00299-006-0236-0. Epub 2006 Sep 14.
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.
通过用4种发根农杆菌菌株,即A(4)GUS、R1000、LBA 9402和ATCC11325感染不同外植体,建立了秦艽的毛状根培养物,并在1/2 MS + B(5)培养基中用发根农杆菌菌株R1000建立了毛状根系。最初,维持了42个独立的毛状根克隆,并对属于不同类别的7个克隆进行了生长、形态、Ri T-DNA基因的整合和表达以及干根样品中生物碱含量的评估。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检测以确认左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根特异性裂环烯醚萜苷龙胆苦苷的积累,其含量相当高,而作为两个T -/L但T +/R愈伤组织型克隆(GM3)积累的龙胆苦苷要少得多或仅为极少量。在四种培养基组成中,发现1/2 MS + B(5)维生素培养基最合适。我们发现根培养物的初始建立很大程度上取决于根与培养基的比例。在根与培养基比例为1:50时记录到最大生长速率。与对照中六倍的增加相比,在1/2 MS + B(5)培养基组成中35天后实现了最大鲜重生物量(33倍)。生物量增加在第15至30天最为丰富。讨论了发根农杆菌菌株和Ri质粒对毛状根诱导的影响、T(L)-DNA和T(R)-DNA基因对毛状根生长模式的可能作用、初始根接种物与培养基的比例以及培养基组成的影响。