Publications by authors named "Claudia Banchini"

Arbuscular mycorrhizal (AM) fungi are difficult to manipulate and observe due to their permanent association with plant roots and propagation in the rhizosphere. Typically, AM fungi are cultured under in vivo conditions in pot culture with an autotrophic host or under in vitro conditions with Ri Transfer-DNA transformed roots (heterotrophic host) in a Petri dish. Additionally, the cultivation of AM fungi in pot culture occurs in an opaque and non-sterile environment.

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Article Synopsis
  • Three strains, MHB01, MHB02, and MHB03, were extracted from superabsorbent polymer and associated with an arbuscular mycorrhizal fungus.
  • The whole-genome sequencing showed that MHB01 has a genome size of 4.57 Mb, MHB02 has 7.13 Mb, and MHB03 has 5.49 Mb.
  • The G + C content for these strains varied significantly, with MHB01 at 36.9%, MHB02 at 62.5%, and MHB03 at 58.2%.
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Rhizophagus irregularis is the model species for arbuscular mycorrhizal fungi (AMF) research and the most widely propagated species for commercial plant biostimulants. Using asymbiotic and symbiotic cultivation systems initiated from single spores, advanced microscopy, Sanger sequencing of the glomalin gene, and PacBio sequencing of the partial 45S rRNA gene, we show that four strains of R. irregularis produce spores of two distinct morphotypes, one corresponding to the morphotype described in the R.

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Over the past three decades, root organ cultures (ROCs) have been the gold standard method for studying arbuscular mycorrhizal fungi (AMF) under conditions, and ROCs derived from various plant species have been used as hosts for AM monoxenic cultures. While there is compelling evidence that host identity can significantly modify AMF fitness, there is currently no standardized methodology to assess the performance of ROCs in the propagation of their fungal symbionts. We describe , a robust methodological approach that models the propagation of AMF in symbiosis with ROCs.

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