首页> 外文会议>International conference on environmental biotechnology and materials engineering;EBME 2011 >Sequence length variation of internal genic space of 16S rDNA-23S rDNA in bacterium with high yield of hydrogen production
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Sequence length variation of internal genic space of 16S rDNA-23S rDNA in bacterium with high yield of hydrogen production

机译:高产氢细菌中16S rDNA-23S rDNA内部基因空间的序列长度变异

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To develop the identification of species for fermentative biohydrogen-producing bacterium, scholars have found a method which is based on PCR amplification of the 16S rRNA gene (rDNA)-23S rDNA intergenic regions. In the study, a large fragment of the rDNA operon, including the 16S rDNA, the intergenic spacer region (ISR) and approximately 2000 bases of the 23S rDNA, were polymerasechain reaction (PCR) amplified. The PCR amplification of the genomic DNA of Leptonema ilk strain 3055 using primers directed against conserved regions of the rRNA operon provided evidence that the 16S and 23S rRNA genes were linked via an intergenic spacer region. The sequencing of the intergenic spacer region indicated that it was 435 nucleotides in length and sequence similarity searches revealed that it bore no homology to any known sequences including tRNA available in databases.
机译:为了开发用于鉴定发酵性生物产氢细菌的物种,学者们发现了一种基于PCR扩增16S rRNA基因(rDNA)-23S rDNA基因间区域的方法。在这项研究中,rDNA操纵子的大片段,包括16S rDNA,基因间隔区(ISR)和23S rDNA的大约2000个碱基,被聚合酶链反应(PCR)扩增了。使用针对rRNA操纵子保守区域的引物对Leptonema ilk菌株3055的基因组DNA进行PCR扩增,提供了16S和23S rRNA基因通过基因间隔区连接的证据。基因间隔区的测序表明,它的长度为435个核苷酸,序列相似性搜索显示,它与数据库中已知的任何已知序列(包括tRNA)没有同源性。

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