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PCR-RFLP and Sequencing of TrnS/trnfM Fragment of Enhalus Acoriodes From Sanur Coastal Waters, Bali, Indonesia: a Preliminary Study

机译:印度尼西亚巴厘岛沙努尔近岸水域中食性回肠En虫的PCR-RFLP和TrnS / trnfM片段测序:初步研究

摘要

This study aimed to evaluate the resolution of PCR-RFLP and sequencing of trnS/trnfM in detecting genetic diversity of seagrass Enhalus acoroides at Sanur Beach, Sindhu Beach and Semawang Beach. This research used six samples E. acoroides from each location. DNA extraction method followed Doyle and Doyle. PCR amplifications were done using primers P672/P673, P674/P675 and ITS4/ITS5 followed by digestion using restriction enzymes EcoRI, PstI, HindIII, BamHI, Rsa, Mva and HinfI. Sequencing analysis used PCR products of primers trnS/trnfM. Testing of DNA sequences of E. acoroides were conducted using BLAST (Basic Local Alignment Search Tool). DNA sequences were further analyzed using MEGA 5.2 software (Molecular Evolutionary Genetic Analysis) to evaluate variations of DNA. The sequence alignments were done using ClustalW software to determine the homology between the DNA sequences. The results showed that 18 samples of E. acoroides from Sanur, Sindhu and Semawang Beach have no polymorphism based on restriction enzyme analyses. Furthermore, sequencing of trnS/trnfM region of 18 samples E. acoroides showed that the sequences were identical.
机译:这项研究旨在评估PCR-RFLP的分辨率和trnS / trnfM的测序,以检测沙努尔海滩,信德海滩和三马旺海滩的海草Enhalus蚁类的遗传多样性。这项研究从每个位置使用了六个样本的大肠杆菌。 DNA提取方法遵循Doyle和Doyle。使用引物P672 / P673,P674 / P675和ITS4 / ITS5进行PCR扩增,然后使用限制酶EcoRI,PstI,HindIII,BamHI,Rsa,Mva和HinfI进行消化。测序分析使用引物trnS / trnfM的PCR产物。使用BLAST(基本局部比对搜索工具)进行了对大肠杆菌的DNA序列的测试。使用MEGA 5.2软件(分子进化遗传分析)进一步分析DNA序列,以评估DNA的变异。使用ClustalW软件进行序列比对以确定DNA序列之间的同源性。结果表明,基于限制性内切酶分析,沙努尔,信德湖和三马旺海滩的大肠埃希菌18个样品没有多态性。此外,对18个样品大肠杆菌的trnS / trnfM区域进行测序表明,这些序列是相同的。

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