首页> 外文会议>International Conference on Biological Science >Molecular species identification of red shrimp (Crustacea: Decapoda: Barbouriidae) from Tanjung Sanjangan (Tolitoli, Central Sulawesi) through 16S rRNA mitochondrial gene
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Molecular species identification of red shrimp (Crustacea: Decapoda: Barbouriidae) from Tanjung Sanjangan (Tolitoli, Central Sulawesi) through 16S rRNA mitochondrial gene

机译:红虾(甲壳状:甲板:Barbouriidae)的分子种类鉴定来自Tanjung Sanjangan(Tolitoli,Centrawesi)到16S rRNA线粒体基因

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Red shrimp is one of the endemic aquatic animals inhabited at Tanjung Sanjangan, Tolitoli, Central Sulawesi. However, the molecular identification of red shrimp has not been investigated. Accurate identification of the red shrimp is important for conservation in its habitat. Therefore, the objective of this study was to identify the red shrimp in Tanjung Sanjangan, Tolitoli, Central Sulawesi based on the 16S mitochondrial gene. The method applied in this study was a PCR method with universal primers 16Sar and 16Sbr. The species identification was analyzed using Nucleotide BLAST. Intraspecific and interspecific analysis was done using DnaSP. The Neighbor-Joining method with Kimura 2 Parameter model was used to reconstruct phylogenetic tree. Additional 16S rRNA sequences taken from GenBank was used for a comparative purpose and outgroup. Nucleotide BLAST analysis revealed that all of the 10 samples of red shrimps collected from Tanjung Sanjangan were verified as Parhippolyte uveae. The NJ tree was also supported the 10 samples of red shrimp clustered with Parhippolyte uveae (accession number KF178886). For the 533 bp sequence examined in the red shrimp, two haplotypes were detected with one variable site which was considered as parsimony informative. Haplotype diversity and nucleotide diversity were 0.556 and 0.001 respectively. This occurrence indicated low genetic variation of the red shrimps collected from Tanjung Sanjangan, Tolitoli, Central Sulawesi.
机译:红虾是居住在劳拉威西中部托里托利托利托利的地方性水生动物之一。然而,尚未研究红虾的分子鉴定。准确的红虾鉴定对于栖息地的保护是重要的。因此,本研究的目的是鉴定基于16S线粒体基因的苏拉威西中央劳拉维的Tanjung Sanjangan的红虾。本研究中应用的方法是具有通用引物16SAR和16SBR的PCR方法。使用核苷酸爆炸分析物种鉴定。使用DNASP进行了内部和特异性分析。使用Kimura 2参数模型的邻近方法用于重建系统发育树。从Genbank取出的另外16S rRNA序列用于比较目的和小组。核苷酸爆炸分析显示,从坦正三南收集的10种红色虾样品被验证为普雷希聚酯uveae。 NJ树也得到了10个红色虾的样本,与普利普洛特UVEAE聚集(加入号码KF178886)。对于在红色虾中检查的533bp序列,用一个可变部位检测到两个单倍型,被认为是副划症信息。单倍型多样性和核苷酸多样性分别为0.556和0.001。这种发生表明,从劳拉威西中部托利托利吐露山脉收集的红色虾的低遗传变异。

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