首页> 外文期刊>African Journal of Microbiology Research >A novel method to optimize culture conditions for biomass and sporulation of the nematophagous fungus Metarhizium anisopliae SQZ-1-21 and the entomopathogenic fungus Metarhizium anisopliae RS-4-1
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A novel method to optimize culture conditions for biomass and sporulation of the nematophagous fungus Metarhizium anisopliae SQZ-1-21 and the entomopathogenic fungus Metarhizium anisopliae RS-4-1

机译:一种优化培养条件的新方法,该方法可用于食肉线虫厌食菌SQZ-1-21和昆虫致病性真菌厌食菌RS-4-1的生物量和孢子形成

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Metarhizium anisopliae is a fungus that offers great potential for the biocontrol of a wide range of host species. In this study, we developed a novel two-stage cultivation method to optimize nutrition and environmental conditions for M. anisopliae SQZ-1-21 and M. anisopliae RS-4-1. Both species were cultured on basal medium (19.00 g sucrose, 4.06 g soy peptone, 1.00 g K2HPO4, 0.50 g KCl, 0.50 g MgSO4, 0.01 g FeSO4 and 17.00 g Bactor) during the first four days at room temperature, and then one of them was transferred to sporulation medium (38.09 g sucrose, 0.43 g urea, 0.05 gL-1 ZnSO4?7H2O, 0.05 gL-1 CuSO4?5H2O, 0.005 gL-1 H3BO4, 0.01 gL-1 MnSO4?H2O, and 17.00 g Bactor), and the other was transferred to a distinct sporulation medium (9.52 g sucrose, 10.00 g soy peptone, 0.05 g/L ZnSO4?7H2O, 0.05 gL-1 H3BO4 and 17.00 g Bactor) for an additional four days. Basal and sporulation medium of M. anisopliae SQZ-1-21 was cultured under the following environmental conditions separately: -1.2 MPa, pH 9, 12 h light, and 29°C and -1.2 MPa, pH 9, 0 h light and 29°C. Basal and sporulation medium of M. anisopliae RS-4-1 was cultured under the following conditions separately: -0.3 MPa, pH 8, 24 h light, and 29°C and -3.9 MPa, pH 5, 12 h light and 26°C. These results provide important information on the mass production of this potential biocontrol fungus.
机译:拟南芥(Antrahizium anisopliae)是一种真菌,可为多种宿主物种的生物防治提供巨大潜力。在这项研究中,我们开发了一种新颖的两阶段栽培方法,以优化对虾M. anisopliae SQZ-1-21和对虾M. anisopliae RS-4-1的营养和环境条件。在室温下的前四天中,在基础培养基(19.00 g蔗糖,4.06 g大豆蛋白ept,1.00 g K2HPO4、0.50 g KCl,0.50 g MgSO4、0.01 g FeSO4和17.00 g Bactor)上培养这两种物种,然后在室温下进行培养。将它们转移到孢子形成培养基(38.09 g蔗糖,0.43 g尿素,0.05 gL-1 ZnSO4?7H2O,0.05 gL-1 CuSO4?5H2O,0.005 gL-1 H3BO4、0.01 gL-1 MnSO4?H2O和17.00 g细菌)再将另一种转移至独特的孢子形成培养基(9.52 g蔗糖,10.00 g大豆蛋白ept,0.05 g / L ZnSO4?7H2O,0.05 gL-1 H3BO4和17.00 g Bactor)中再培养4天。分别在以下环境条件下培养沙门氏菌SQZ-1-21的基础和孢子形成培养基:-1.2 MPa,pH 9,12 h光照,29°C和-1.2 MPa,pH 9,0 h光照和29 ℃。分别在以下条件下培养无芒分枝杆菌RS-4-1的基础和孢子培养基:-0.3 MPa,pH 8,24 h,29°C和-3.9 MPa,pH 5,12 h,26°C C。这些结果提供了有关这种潜在的生物防治真菌的大量生产的重要信息。

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