Abstract
This chapter describes the production of conidia by Metarhizium anisopliae using solid-state fermentation. Before production of conidia, procedures for strains conservation, reactivation, and propagation are essential in order to provide genetic stability of the strains. The strain is conserved in freeze-dried vials and then reactivated through insect inoculation. Rice is used as a substrate for the conidia production in two different bioreactors: plastic bags and tubular bioreactor. The CO2 production in the tubular bioreactors is measured with a respirometer; this system allows calculating indirect growth parameters as lag time (tlag) (25–35 h), maximum rate of CO2 production (rCO2 max) (0.5–0.7 mg/gdm h), specific rate of CO2 production (μ) (0.10–0.15 1/h), and final CO2 production (CO2) (100–120 mg/gdm). Conidial yield per gram of dry substrate (gdm) should be above 1 × 109 conidia/gdm after 10 days of incubation. Germination and viability of conidia obtained after 10 days of incubation should be above 80 % and 75 %, respectively. Bioassays using of Tenebrio molitor as a host insect should yield a final mortality above 80 %.
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Acknowledgement
This work was supported by Universidad Autónoma Metropolitana-Iztapalapa, the Secretaría de Ciencia, Tecnología e Innovación (SECITI), D.F. and the Centro Nacional de Referencia de Control Biológico, Tecomán, Colima, México.
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Loera-Corral, O., Porcayo-Loza, J., Montesinos-Matias, R., Favela-Torres, E. (2016). Production of Conidia by the Fungus Metarhizium anisopliae Using Solid-State Fermentation. In: Glare, T., Moran-Diez, M. (eds) Microbial-Based Biopesticides. Methods in Molecular Biology, vol 1477. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-6367-6_6
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DOI: https://doi.org/10.1007/978-1-4939-6367-6_6
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