棘孢木霉TCS007菌株固态发酵条件优化及粗提产物的抑菌活性

    Optimization of solid-state fermentation conditions for Trichoderma asperellum strain TCS007 and antibacterial activity of crude extracts

    • 摘要: 前期研究表明,棘孢木霉TCS007 (Trichoderma asperellum TCS007) 菌株具有抑菌、促进植物生长和诱导植物抗逆的能力,而其发酵代谢产物对油菜菌核病菌 (Sclerotinia sclerotiorum) 具有较高的抑菌活性。为提高TCS007菌株固态粗提发酵产物产量,通过单因素试验结合响应曲面法,对TCS007菌株固态发酵培养基组分和发酵培养条件进行了优化,并以油菜菌核病菌为靶标,测定了其粗提发酵产物的抑菌活性。结果表明:影响TCS007菌株固态粗提发酵产物产量的3个关键因素为培养时间、黄豆粉添加量和加水量。优化后的发酵培养基配方及发酵条件为:大米72 g,黄豆粉添加量为大米质量的 3.5%、加水量47 mL、接种量1 mL (1 × 107个孢子/mL)、培养时间29 d、光照周期为12 h/12 h、温度28 ℃、初始pH为7.0。在此条件下,TCS007菌株粗提发酵产物产量为1.21 g,与响应面模型预测的发酵产物产量1.22 g拟合性较好,比初始发酵条件的产物产量提高了1.34倍;进一步采用浅盘法扩大培养,粗提发酵产物产量可达1.45 g。此外,在50 μg/mL质量浓度下,TCS007菌株优化培养所得的粗提发酵产物对油菜菌核病菌、苹果褐斑病菌 (Marssonina coronaria)、黄瓜灰霉病菌 (Botrytis cinerea) 及水稻纹枯病菌 (Rhizoctonia solani) 的抑制率分别为96.87%、77.42%、71.07%和62.50%。以油菜菌核病菌为靶标进行毒力测定,结果表明,优化培养所得粗提发酵产物的EC50值为0.51 μg/mL,而初始条件培养所得粗提发酵产物的EC50值为17.91 μg/mL,抑菌活性提高了35 倍;且优化培养所得粗提发酵产物能抑制菌核的形成和萌发,对菌核形成的抑制率为63.93%。该研究结果可为棘孢木霉TCS007后续生防微生物农药产品发酵工艺研究提供理论依据。

       

      Abstract: The previous research indicates that Trichoderma asperellum TCS007 possesses the abilities of antifungal activity, plant growth promotion, and induction of plant stress resistance, while its metabolites exhibit stronger antifungal activity against Sclerotinia sclerotiorum. To improve the yield of crude solid-state fermentation extracts of TCS007, the medium composition and fermentation conditions were optimized using single-factor experiments in combination with response surface methodology (RSM), with S. sclerotiorum as the target pathogen. The results showed that the three major factors influencing the yield of crude solid-state fermentation extracts were fermentation time, soybean powder addition, and water addition. The optimized fermentation medium and conditions were as follows: 72 g of rice, soybean flour at 3.5% (m/m) of the rice, 47 mL of water, 1 mL of inoculum (1 × 107 spores/mL), a 29 days of fermentation period, a 12 h light/12 h dark photoperiod, a 28 °C incubation temperature, and an initial pH of 7.0. Under these conditions, the yield of crude fermentation extracts reached 1.21 g, which was in good agreement with the predicted yield of 1.22 g using response surface methodology, representing a 1.34-fold increase compared with the initial fermentation conditions. Furthermore, shallow-pan cultivation further increased the yield to 1.45 g. At a concentration of 50 μg/mL, the optimized crude fermentation extracts inhibited the growth of S. sclerotiorum, Marssonina coronaria, Botrytis cinerea, and Rhizoctonia solani by 96.87%, 77.42%, 71.07%, and 62.50%, respectively. The antifungal activity test targeting S. sclerotiorum showed that the EC50 value of the crude extracts obtained under the initial fermentation conditions was 17.91 μg/mL, whereas that decreased to 0.51 μg/mL after optimization, indicating a 35-fold enhancement in antifungal activity. In addition, the optimized extracts significantly inhibited sclerotial formation by 63.93% and suppressed sclerotial germination. These findings provide a theoretical basis for further development of fermentation processes for biocontrol microbial pesticide products by T. spinosum TCS007.

       

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