Antagonistic effects of actinomycetes towards plant pathogen Phellinus noxius

Y. Yanti, M. N. Zainon, A. H. U. Marshida
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引用次数: 1

Abstract

Several strains of actinomycetes have been found to protect plant from plant pathogens because the capacity to produce a wide variety of antibiotics, extracellular enzymes and also show their antagonistic effects towards plant pathogen. Actinomycetes play an important role in degradation of chitin which is a component of cell wall of fungi. Application of selected Actinomycetes as biocontrol can decrease the environmental pollution and an alternative to fungicides. Brown root disease caused by Phellinus noxius was observed in teak plantations of Sabak Bernam in Selangor, Kuala Kangsar in Perak, Sik in Kedah and Lendu in Malacca. It will affect the plantations industry if no measures are taken to control or manage it. This pathogen grew faster on the Potato Dextrose Agar and also on selective media such as Malt Yeast Extract Agar. Analysis of the 16S rDNA begins by extracting the Actinomycetes DNA and amplifying the gene coding for 16S rDNA using the polymerase chain reaction. The purified DNA fragments are directly sequenced and identification of the actinomycetes was done using phylogenetic analysis procedures. However, analysis of 16S rDNA generally allows us to identify the organisms up to the genus level only. Three selected actinomycetes isolated from the soil were found to control this plant pathogen. These actinomycetes controlled the plant pathogen by hyperparasiting it and colonizing its hyphae. The chitinase production of actinomycetes was determined by inoculating culture strains on chitin-yeast-extract agar and its chitinolytic activity was determined by formation of clear zones around the actinomycetes colonies.
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放线菌对植物病原菌黑松菌的拮抗作用
由于放线菌能够产生多种抗生素和胞外酶,并对植物病原体表现出拮抗作用,因此已发现几种放线菌具有保护植物免受植物病原体侵害的作用。放线菌在真菌细胞壁成分甲壳素的降解中起着重要作用。选择放线菌进行生物防治,可以减少对环境的污染,是杀菌剂的替代选择。在雪兰莪州的沙巴伯南、霹雳州的瓜拉甘沙、吉打州的锡和马六甲的伦都等柚木人工林中发现了由褐根病引起的褐根病。如果不采取控制或管理措施,它将影响人工林工业。这种病原菌在马铃薯葡萄糖琼脂和麦芽酵母膏琼脂等选择性培养基上生长更快。对16S rDNA的分析首先提取放线菌DNA,用聚合酶链反应扩增16S rDNA编码基因。对纯化的DNA片段进行直接测序,并利用系统发育分析程序对放线菌进行鉴定。然而,对16S rDNA的分析通常只允许我们识别到属水平的生物。从土壤中分离出3种放线菌,对该植物病原菌具有控制作用。这些放线菌通过寄生和定植菌丝来控制植物病原体。通过在几丁质酵母提取物琼脂上接种培养菌来测定放线菌的几丁质酶产量,并通过在放线菌菌落周围形成清晰的区域来测定放线菌的几丁质酶降解活性。
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