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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:PCR-RFLP和Trns / Trnfm of Anhalus acoriodes的Trns / Trnfm片段来自Sanur沿海水域,巴厘岛,印度尼西亚(Andonesia):初步研究

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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:这项研究的目的是评估在沙努尔海滩,娜斯迪胡海滩和海滩前往Semawang检测海草海菖蒲属acoroides的遗传多样性TRNS / trnfM的PCR-RFLP和测序的分辨率。本研究采用六个样本E. acoroides从每个位置。 DNA提取方法随后道尔和Doyle。 / ITS5接着消化用限制性酶EcoRI,PstI位,HindIII位,的BamHI,RSA,MVA和的HinfⅠPCR扩增使用引物P672 / P673,P674 / P675和ITS4完成。测序分析的引物TRNS / trnfM的PCR产物。 E. acoroides的DNA序列的检测使用BLAST进行(基本局部比对搜索工具)。使用MEGA 5.2软件(Molecular进化遗传分析)来评估DNA的变体的DNA序列进行进一步分析。所述序列比对使用ClustalW比软件以确定的DNA序列之间的同源性进行。结果表明,从沙努尔,娜斯迪胡和海滩前往Semawang E. acoroides的18个样品具有基于限制性内切酶分析没有多态性。此外,18个样品TRNS / trnfM区域的测序E. acoroides表明,序列是相同的。

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