Biological Nitrogen Removal Database

A manually curated data resource for microbial nitrogen removal


Detailed information

Microorganism

Uncultured crenarchaeote

Taxonomy

  • Phylum : Crenarchaeota
  • Class : nan
  • Order : nan
  • Family : nan
  • Genus : nan

Isolation Source

San Francisco Bay, North Bay station 1, sediment

Enzyme Name

putative ammonia monooxygenase subunit A

  • Encoding Gene:amoA
  • DNA Size:606 bp
  • Nucleotide FASTA sequence: Link

  • UniProt I.D: Q3I2T0

Protein Information

  • Pro_GenBank I.D: AAZ81164.1

  • Length:202 aa
  • Protein FASTA_sequence: Link

Information about Article

  • Reference:Francis et al., 2005
  • Title:Ubiquity and diversity of ammonia-oxidizing archaea in water columns and sediments of the ocean
  • Pubmed ID:16186488.0
  • Pubmed link: Link

  • Full research link: Link

  • Abstract:Nitrification, the microbial oxidation of ammonia to nitrite and nitrate, occurs in a wide variety of environments and plays a central role in the global nitrogen cycle. Catalyzed by the enzyme ammonia monooxygenase, the ability to oxidize ammonia was previously thought to be restricted to a few groups within the β- and γ-Proteobacteria. However, recent metagenomic studies have revealed the existence of unique ammonia monooxygenase α-subunit (amoA) genes derived from uncultivated, nonextremophilic Crenarchaeota. Here, we report molecular evidence for the widespread presence of ammonia-oxidizing archaea (AOA) in marine water columns and sediments. Using PCR primers designed to specifically target archaeal amoA, we find AOA to be pervasive in areas of the ocean that are critical for the global nitrogen cycle, including the base of the euphotic zone, suboxic water columns, and estuarine and coastal sediments. Diverse and distinct AOA communities are associated with each of these habitats, with little overlap between water columns and sediments. Within marine sediments, most AOA sequences are unique to individual sampling locations, whereas a small number of sequences are evidently cosmopolitan in distribution. Considering the abundance of nonextremophilic archaea in the ocean, our results suggest that AOA may play a significant, but previously unrecognized, role in the global nitrogen cycle.