筛选有机基质,开发有效的生物杀菌剂防治腰果枯萎病。

Journal of biological methods Pub Date : 2025-02-21 eCollection Date: 2025-01-01 DOI:10.14440/jbm.2025.0089
Stanslaus A Lilai, Juma Hussein, Fortunus A Kapinga, Wilson A Nene, Stela G Temu, Donatha D Tibuhwa
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引用次数: 0

摘要

背景:生物技术行业通常使用合成培养基来培养生物防治剂(BCA);然而,这些培养基往往被认为不切实际,尤其是在发展中国家:本研究旨在确定最适合培养用于防治腰果镰刀菌枯萎病的生物防治剂的当地有机基质:在 2022 年和 2023 年对五种基质(即稻壳(RH)、米糠(RB)、去壳小米、煮熟的大米及其组合)进行了实验,作为芽孢杆菌菌株和毛霉的生长培养基。基质中的碳水化合物和蛋白质含量用比色法定量:蛋白质和碳水化合物含量分别为 13.4 - 19.8% 到 76.3 - 82.7%。BCA在所有测试基质上的定殖率都很高,其中复合基质的定殖率最高,其次是RH和RB。不同基质和培养温度下的内生孢子形成和分生孢子水平随时间变化很大(p ≤ 0.05)。在冷藏、室温和培养箱条件下,除混合基质、相对湿度和相对湿度外,两季中大多数基质的种群密度随着时间的推移而下降。最终种群数量如下2.1 × 107 ± 4.9 × 105 和 1.0 × 107 ± 0.3 × 105 菌落总数(CFU)/毫升(组合基质)、2.3 × 107 ± 5.4 × 105 和 5.7 × 107 ± 1.1 × 106 CFUs/毫升(RH)、3.6 × 105 ± 2.1 × 104 和 3.3 × 105 ± 1.6 × 104 CFUs/毫升(RB),而在冷藏条件下,种群密度在整个研究期间保持相对不变:根据研究结果,建议使用混合基质、单用 RH 或单用 RB 作为大规模生产所研究生物杀真菌剂的适当培养基。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Screening of organic substrates for the development of effective biofungicides to manage cashew fusarium wilt disease.

Background: The biotechnology industry commonly utilizes synthetic media to grow biological control agents (BCAs); however, these media are often considered impractical, particularly in developing countries.

Objective: This study aimed to identify the most suitable locally available organic substrates for the cultivation of BCAs used against cashew fusarium wilt disease.

Materials and methods: Experiments were conducted in 2022 and 2023 on five substrates, namely rice husk (RH), rice bran (RB), hulled millet, parboiled rice, and their combinations, as growth media for combined Bacillus strains and Trichoderma asperellum. The carbohydrate and protein content of the substrates were quantified colorimetrically.

Results: Protein and carbohydrate contents ranged from 13.4 - 19.8% to 76.3 - 82.7%, respectively. The BCAs exhibited high colonization rates on all tested substrates, with combined substrates supporting the highest colonization, followed by RH and RB. Endospore formation and conidiation levels varied significantly over time across substrates and incubation temperatures (p ≤ 0.05). Population densities decreased over time under refrigerated, room temperature, and incubator conditions for most substrates in both seasons, except for combined substrates, RH, and RB. Final population counts were as follows: 2.1 × 107 ± 4.9 × 105 and 1.0 × 107 ± 0.3 × 105 colony-forming units (CFUs)/mL (combined substrates), 2.3 × 107 ± 5.4 × 105 and 5.7 × 107 ± 1.1 × 106 CFUs/mL (RH), 3.6 × 105 ± 2.1 × 104 and 3.3 × 105 ± 1.6 × 104 CFUs/mL (RB), while under refrigerated conditions, population densities remained relatively unchanged throughout the study period.

Conclusion: Based on the findings, it is recommended to use a mixture of substrates, RH alone, or RB alone as appropriate media for the large-scale production of the studied biofungicides.

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