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Colonization of Glomus microcarpum in RiT-DNA transformed roots of Ipomoea batatas (SI 010) in synthetic medium

机译:小球果在合成培养基中的RiT-DNA转化的番薯(SI 010)根中定植

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摘要

Arbuscular mycorrhizal (AM) fungi are obligate biotrophs and they cannot complete their life cycle in the absence of a host plant root. AM fungus, Glomus microcarpum was successfully co-cultivated in transgenic hairy roots of J. batatas (variety SI010) initiated through the mediation of Agrobacterium rhizogenes ATCC15834. Murashige and Skoog (MS) medium composition was modified to support maximum hairy root growth and MS vitamins were replaced with B5 vitamins for better growth of hairy roots. Temperature, pH and light regimens were standardized for optimum hairy root growth and AM colonization. Eighty percent mycorrhizal colonization was observed after 20 days of co-cultivation in modified MS medium in petri dish. Various stages of mycorrhizal infection, pre-infection, penetration, vesicle/arbuscule formation were observed and viability of fungal structures was also studied.This technique can be used for the large scale production of monospecific culture of AM fungi.
机译:丛枝菌根(AM)真菌是专性生物营养菌,在没有寄主植物根的情况下它们无法完成其生命周期。通过发根土壤杆菌ATCC15834的介导,成功地在AM真菌真菌Glomus microcarpum中共培养了转基因J. batatas毛状根(品种SI010)。修改了Murashige和Skoog(MS)培养基的组成,以支持最大的毛根生长,并用B5维生素代替了MS维生素,以更好地促进毛根生长。对温度,pH和光照方案进行了标准化,以实现最佳的毛状根生长和AM定植。在培养皿中的改良MS培养基中共培养20天后,观察到80%的菌根定植。观察了菌根感染,感染前,渗透,囊泡/丛枝形成的各个阶段,并研究了真菌结构的活力。该技术可用于大规模生产AM真菌的单特异性培养。

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