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Genome Analysis and Identification of Gelatinase Encoded Gene in Enterobacter aerogenes

机译:肠杆菌空气发生器中明胶酶编码基因的基因组分析及鉴定

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In this study, bioinformatic analysis towards genome sequence of E. aerogenes was done to determine gene encoded for gelatinase. Enterobacter aerogenes was isolated from hot spring water and gelatinase species-specific bacterium to porcine and fish gelatin. This bacterium offers the possibility of enzymes production which is specific to both species gelatine, respectively. Enterobacter aerogenes was partially genome sequenced resulting in 5.0 mega basepair (Mbp) total size of sequence. From pre-process pipeline, 87.6 Mbp of total reads, 68.8 Mbp of total high quality reads and 78.58 percent of high quality percentage was determined. Genome assembly produced 120 contigs with 67.5% of contigs over 1 kilo base pair (kbp), 124856 bp of N50 contig length and 55.17 % of GC base content percentage. About 4705 protein gene was identified from protein prediction analysis. Two candidate genes selected have highest similarity identity percentage against gelatinase enzyme available in Swiss-Prot and NCBI online database. They were NODE_9_length_26866_cov_148.013245_12 containing 1029 base pair (bp) sequence with 342 amino acid sequence and NODE_24_length_155103_cov_177.082458_62 which containing 717 bp sequence with 238 amino acid sequence, respectively. Thus, two paired of primers (forward and reverse) were designed, based on the open reading frame (ORF) of selected genes. Genome analysis of E. aerogenes resulting genes encoded gelatinase were identified.
机译:在该研究中,对E. Aimogenes的基因组序列进行生物信息分析以确定编码Gelatinase的基因。从温泉水和明胶酶物种特异性细菌中分离出肠杆菌空气到猪和鱼明胶。该细菌能够分别提供酶产生的可能性,其特异于含有含有的凝胶。肠杆菌空气是部分基因组测序,导致5.0兆底座(MBP)总序列。从预处理管道,总读数的87.6 MBP,68.8 MBP总高质量读数和78.58%的高质量百分比确定。基因组组件产生120个葡萄片,67.5%以上超过1千吨碱基对(KBP),124856 BP的N50葡萄球菌长度和55.17%的GC基础含量百分比。从蛋白质预测分析中鉴定了大约4705个蛋白质基因。选择的两种候选基因具有最高的相似性对瑞士 - PROT和NCBI在线数据库提供的明胶酶的百分比。它们是Node_9_Length_26866_Cov_148.013245_Cov_148.013245_12,其含有342个氨基酸序列和Node_24_Length_155103_Cov_177.082458_Cov_177.082458_62,其分别包含具有238个氨基酸序列的717bp序列。因此,基于所选基因的开放阅读框(ORF)设计了两个引物(前向和反向)。鉴定了E. E. evemoges含有基因编码明胶酶的环境分析。

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