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Hairy roots were initiated from Ipomoea batata through the mediation of agropine strain of Agrobacterium rhizogenes 15834 (Chandran and Potty, 2008) and
co-cultivated Arbuscular Mycorrhizal Fungi (AMF) Glomus microcarpum var. microcarpum in them
and was grown in laboratory scale in a simple bioreactor. The obligate biotrophic nature of
AMF made it difficult to culture them in synthetic media. To overcome this difficulty,
transgenic hairy roots were used to grow this fungus. Hairy roots have a lot of advantages over
normal roots, as they can grow much faster than normal roots and are capable of
unlimited propagation in culture media and show genetic and biochemical stability (Hamill et al., 1986). Hairy roots can be cultivated in a simple medium without the addition
of phytohormones and can grow from low inocula to high final biomass densities, with
only minimal lag phase.
Mugnier and Mosse (1987), Becard and Fortin (1988) and Declerck et al. (1996) used transformed carrot roots, in the place of whole plants, to provide a simple in vitro system, which allows reproducible observation of all stages of Vesicular-Arbuscular
Mycorrhizal (VAM) development under aseptic conditions (Chabot et al., 1992). Jolicoeur et al. (1999)
used two submerged culture systems, petri dish and airlift bioreactor, for the production
of mycorrhizal propagules of Glomus
intraradices using Daucus carota hairy roots
transformed by Agrobacterium rhizogenes. Chandran and Potty (2002) observed that Hairy
Root Technology (HRT) is the best alternative tool to study AMF symbiosis, and it can also
be used for the production of monoxenic inoculum of AMF. The present study reports
the cultivation of mycorrhized transgenic hairy roots of Ipomoea batata in a newly designed simple bioreactor.
Materials and Methods. |