Abstract
A method based on PCR amplification of the 16S rRNA gene (rDNA)-23S rDNA intergenic spacer regions (ISR) was developed for the identification of species within the novel group hydrogen-producing anaerobes. The sizes of the PCR products varied from 1264 to 398 bp. Strain of isolate Rennanqilyf 3 was characterized as having products of 1262, 398, 638, 437 and 436 bp. The isolate Rennanqilyf 1 had product of 1264 bp. The isolate Rennanqilyf 13 had products of 1261, 579 and 485 bp. Of the 3 species of the novel group hydrogen-producing anaerobes examined, no one was indistinguishable. Two environmental isolates were identified as hydrogen-producing bacteria, which were new species in present taxon. Rennanqilyf 3 could not be associated with any Clostridium sp. studied. Rennanqilyf 1 could be classified into Clostridium genus. The combination between 16S rDNA equencing and length polymorphisms of IRS in 16S-23S rDNA is a better method for determining species of the hydrogen-producing bacteria.
| Original language | English |
|---|---|
| Pages (from-to) | 691-694 |
| Number of pages | 4 |
| Journal | Journal of Harbin Institute of Technology (New Series) |
| Volume | 14 |
| Issue number | 5 |
| State | Published - Oct 2007 |
Keywords
- Biohydrogen production
- Hydrogen-producing Anaerobes
- ISR of 16S-23S rDNA
- Length polymorphisms
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