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作 者:纪明山[1] 李博强[1] 陈捷[1] 谷祖敏[1] 王英姿[1]
出 处:《中国生物防治》2005年第2期104-108,共5页Chinese Journal of Biological Control
基 金:辽宁省自然科学基金项目(002043)
摘 要:对绿色木霉TR 8菌株抑制尖镰孢的拮抗机制进行了研究。平板对峙培养结果表明,绿色木霉生长快于尖镰孢FO G1,接触后FO G1生长停止,TR 8继续生长,覆盖FO G1的菌落并大量产孢,但不形成抑菌圈。观察了TR 8对FO G1的重寄生现象,TR 8菌丝首先向FO G1趋性生长,然后紧贴FO G1菌丝平行生长或穿入菌丝生长,最后FO G1菌丝瓦解。在扫描电镜下可以看到FO G1菌丝原生质凝结,菌丝上有孔洞出现。发酵7d,TR 8发酵液中β1,3 葡聚糖酶的活性为20 15U/ml,几丁质酶的活性为11 67U。发酵原液对FO G1菌丝生长和孢子萌发均无抑制作用,但TR 8的挥发性分泌物对病菌孢子萌发具有一定的抑制作用。含有TR 8分泌物的培养基对病菌孢子萌发有很强的抑制作用,抑制率高达75 06%。The antifungal mechanism of Trichoderma viride strain TR-8 against Fusarium oxysporum was studied. When TR-8 and F. oxysporum strain FO-G1 were dual-cultured on PDA plate, TR-8 grew faster than FO-G1. After the two kinds of mycelia contacted, mycelial growth of FO-G1 stopped. Later, TR-8 continued to grow, covered FO-G1 colony and produced large number of conidia. Inhibition ring was not found. The mycoparastism of TR-8 against FO-G1 was observed. It was revealed microscopically that at first TR-8 mycelia grew to FO-G1, then developed in parallel or penetrated FO-G1 mycelia, eventually FO-G1 mycelia collapsed. After TR-8 was fermented 7 d, the activities of 1,3-β-glucosidase and chitinase were 20.15U/ml and 11.67U respectively. Low antibiosis of TR-8 was detected. In vitro, fermentative liquid, even which was not diluted, couldn't inhibit both the mycelial growth and spore germination of FO-G1. The volatile substances secreted by TR-8 could inhibit spore germination, with inhibition rate reached 75.06%.
关 键 词:绿色木霉 拮抗机制 尖镰孢 菌株 3-葡聚糖酶 抑制作用 孢子萌发 菌丝生长 重寄生现象 对峙培养 扫描电镜 几丁质酶 分泌物 抑菌圈 原生质 β-1 发酵液 挥发性 培养基 抑制率 活性 病菌 趋性
分 类 号:S435.72[农业科学—农业昆虫与害虫防治] TQ925.9[农业科学—植物保护]
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