RESUMO
The study had the objective of examining the aspects involved in the cultivation of ectomycorrhizal fungi for the production of commercially sustainable inoculant to attend the demands of the seedling nursery industry. It focused on certain parameters, such as the oxygen consumption levels, during the cultivation of the ectomycorrhizal fungus Rhizopogon nigrescens CBMAI 1472, which was performed in a 5-L airlift bioreactor. The dynamic method was employed to determine the volumetric coefficient for the oxygen transfer (k L a) and the specific oxygen uptake rate (Q O2 ). The results indicate that specific growth rates (µ X ) and oxygen consumption decline rapidly with time, affected mainly by increases in biomass concentration (X). Increases in X are obtained primarily by increases in the size of pellets that are formed, altering, consequently, the cultivation dynamics. This is the result of natural increases in transferring resistance that are observed in these environments. Therefore, to avoid critical conditions that affect viability and the productivity of the process, particular settings are discussed.
Assuntos
Basidiomycota/crescimento & desenvolvimento , Basidiomycota/metabolismo , Reatores Biológicos , Consumo de Oxigênio , Oxigênio/metabolismo , Basidiomycota/isolamento & purificação , Biomassa , Micorrizas/crescimento & desenvolvimento , Micorrizas/metabolismoRESUMO
The viability and infectivity of an ectomycorrhizal inoculum (isolate UFSC-Rh90, Rhizopogon nigrescens), produced by submerged cultivation in an airlift bioreactor and immobilized in beads of calcium alginate gel, was studied. Inoculum remained 100% viable after 18 months in a 0.85% NaCl solution at 8 ± 1ºC. Mycelium grew from the beads after 48 h when they were placed on a solid culture medium at 25 ± 1ºC. Viability of pellets of non-immobilized mycelium stored under the same conditions decreased gradually after the third month of storage, reaching 0% by the 12th month. These pellets presented a gradual darkening, which was more intense in those located near the surface of the NaCl solution. In culture medium, these dark pellets showed no viability. Gel immobilization helps to maintain mycelium viability during storage and offers a physical protection when the inoculum is applied to the planting substrate. After eight months refrigeration, the immobilized inoculum was still able to infect Pinus taeda seedlings, colonizing an average of 37% of the root tips when inoculated in the plant growth substrate under greenhouse conditions. This inoculum presents a commercial potential to be produced and applied in forest nurseries.
Estudou-se a viabilidade e a infectividade de inoculante fúngico ectomicorrízico (isolado UFSC-Rh90, Rhizopogon nigrescens), produzido através de cultivo submerso em biorreator airlift e encapsulado em gel de alginato de cálcio. O inoculante permaneceu viável após 18 meses em solução de NaCl (0,85%) a 8 ± 1ºC. O micélio emergiu dessas cápsulas após 48 h de incubação a 25 ± 1ºC em meio de cultura sólido. A viabilidade dos pellets de micélio não imobilizado, armazenados sob as mesmas condições, reduziu-se gradualmente após três meses de armazenamento e atingiu 0% aos 12 meses. Esses pellets apresentaram um escurecimento gradual que foi mais intenso naqueles localizados próximos à superfície da solução de NaCl. Em meio de cultura, os pellets escurecidos mostraram-se inviáveis. A imobilização em gel mantém a viabilidade do micélio durante o armazenamento, além de oferecer uma barreira física quando aplicado ao substrato de plantio. Após oito meses de armazenamento sob refrigeração, o inoculante imobilizado colonizou uma média de 37% das raízes curtas de mudas de Pinustaeda, quando aplicado ao substrato de plantio sob condições de casa-de-vegetação. Esse inoculante apresenta potencial para produção comercial e aplicação nos viveiros florestais.