Istiana Prihatini, Farah Aulya Faradilla, S. Suranto
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引用次数: 0
摘要
需要对BCA候选物进行体内控制活性试验来评价其有效性。该试验包括在接种BCA和病原菌后鉴定寄生在实验植物上的真菌种类。BCA防治活性试验中寄生真菌的鉴定可通过在人工培养基上培养真菌进行。真菌种类可以根据真菌培养物的形态特征或遗传特征进行鉴定。本研究旨在确定PCR ITS-RFLP分子标记在真菌分离物DNA序列鉴定前的初始选择过程中的潜力,并选择产生多态性PCR ITS-RFLP模式的酶。3种酶(DraI、EcoRI和HinfI)根据PCR ITS DNA的模式成功地将8个真菌培养物分成3组,而另外5种酶(BamHI、BclI、HaeII、HpaI和HindIII)除1株分离物外,均未能切割DNA ITS片段。
TEKNIK PCR ITS-RFLP UNTUK SELEKSI ISOLAT JAMUR PADA PENGUJIAN AGEN PENGENDALI HAYATI PADA SERANGAN GANODERMA TANAMAN Acacia mangium
In vivo control activities test of BCA candidate is required to evaluate its effectiveness. This test involved identification of the fungal species that inhabited the experimental plant after inoculation of BCA and pathogen. Identification of inhabitant fungi in the BCA control activity test can be conducted by culturing the fungi on artificial media. Fungal species can be identified based on morphological characters or genetic characters of fungal culture. This study was conducted to determine the potential of PCR ITS-RFLP molecular markers in the initial selection process of fungal isolates before identification based on DNA sequences and to select the enzyme that produce polymorphic PCR ITS RFLP pattern. Three enzymes (DraI, EcoRI and HinfI) were successfully separated 8 fungal cultures used in this study into three groups based on the pattern of PCR ITS DNA, while five other enzymes (BamHI, BclI HaeII, HpaI, and HindIII) were failed to cut the DNA ITS fragments, except for one isolate.