Medical Journals

Real-time Pcr Quantification of Nitrite Reductase (Nirs) Genes in a Nitrogen Removing Fluidized Bed Reactor.

Authors:
  • Araki N
  • Tsukamoto Y
  • Nagano A
  • Yamaguchi T
  • Harada H

From: Department of Civil Engineering, Nagaoka National College of Technology, Nishi-Katakai 888, Nagaoka 940-8532, Japan. araki@nagaoka-ct.ac.jp

Water science and technology : a journal of the International Association on Water Pollution Research

  • Publish Date: 2006
  • ISSN: 0273-1223
  • Volume: 53
  • Issue: 6
  • Pages: 59-65
  • Medium: Print
  • Language: English
  • Citation (JAMA): Araki N, Tsukamoto Y, Nagano A, et al. Real-time Pcr Quantification of Nitrite Reductase (Nirs) Genes in a Nitrogen Removing Fluidized Bed Reactor.. Water Sci. Technol. 2006;53:59-65

Abstract

Molecular approaches were applied to identify and enumerate denitrifying bacteria subsisting in a fluidized bed reactor (FBR). The FBR was continuously operated as a unit for the removal of nitrogen from the effluents of domestic sewage treatment plant, with an additional supply of methanol as a carbon source. By denaturing gradient gel electrophoresis (DGGE) and sequence analysis of 16S ribosomal RNA genes, Thauera group was found to be dominant among the denitrifying bacteria in the FBR sludge. Oligonucleotide probe THA155 for fluorescence in situ hybridization (FISH) was newly designed for specifically targeting the Thauera group. However, the THA155 signal obtained from the sludge was only 0.9-5.7% of the DAPI-stained total cells. The real-time polymerase chain reaction (PCR) targeting the sequences of nitrite reductase (NIR) gene, a key enzyme of denitrification processes, was performed to quantify the cells of denitrifying bacteria cells including the Thauera group in FBR sludge. An excellent correlation was obtained between the numbers of nirS genes and the activity of denitrifiers in the FBR sludge.

Mesh Headings (Keywords): Bacteria, Biodegradation, Environmental, Bioreactors, DNA Primers, Electrophoresis, Polyacrylamide Gel, Genes, Bacterial, In Situ Hybridization, Fluorescence, Nitrite Reductases, Nitrogen, RNA, Ribosomal, 16S, Reverse Transcriptase Polymerase Chain Reaction, Sewage, Thauera, Waste Disposal, Fluid


Check for Full Text / PubMed Unique Identifier (PMID): 16749440


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

Linked medical terms appearing on this page are added by Healia to help readers find more information and are not part of the original PubMed document.

The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


Advertisements

About | Privacy Policy | Business Solutions | Advertise | Contact | Add Healia to your site

©2012. Healia / Meredith Corporation  

Use of this site constitutes acceptance of our Terms of Service and Privacy Policy. All content on this Web site, including medical opinion and any other health-related information, is for informational purposes only and should not be used for a specific diagnosis or individual treatment plan for any situation. Use of this site and the information contained herein does not create a doctor-patient relationship. Always seek the direct advice of your doctor in connection with any questions or issues you may have regarding your own health or the health of others.