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Metagenomic analysis of anammox communities in three different microbial aggregates

Jianhua Guo; Yongzhen Peng; Lu Fan; Liang Zhang; Bing‐Jie Ni; Boran Kartal; Xin Feng; Mike S. M. Jetten; Zhiguo Yuan
Environmental Microbiology · Vol. 18, Issue 9 · pp. 2979-2993 · 2016

Abstract

Summary There is great potential to understand the functional diversity of microorganisms that are involved in waste water treatment through metagenomic analyses. This study presents the first metagenomic comparison of taxonomic and functional profiles of the microbial communities occurring in different aggregates from anaerobic ammonium‐oxidizing (anammox) bioreactors. The anammox bacterial communities in both biofilm and granule sludge samples showed relatively high abundance and diversity compared with floccular sludge. Four of the five known genera of anammox bacteria were detected in the three cultures except Candidatus Jettenia, which was absent in the granules. C andidatus K uenenia comprised the major population of anammox bacteria in these three sludges, independent of their growth morphologies. The genome assembled for the C andidatus K uenenia in the granule was very similar to the published reference genome of C andidatus K . stuttgartiensis. Genes involved in the metabolism of the anammox process were highly detected in the biofilm and granule sludges. In particular, the abundance of hydrazine synthase gene ( hzs ) in the biofilm was around 486 times more pronounced than that in the granules. The knowledge gained in this study highlights an important role of sludge aggregate in affecting community structure and metabolic potential of anammox systems.

Bibliographic Information

JournalEnvironmental Microbiology
PublisherWiley
Publication Date2016-09-01
Publication Year2016
Volume18
Issue9
Pages2979-2993
Document TypeJournal Article
Print ISSN1462-2912
eISSN1462-2920
DOI10.1111/1462-2920.13132
SubjectMicrobial Ecology

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NARA Access Coverage1999-01-01~Current
Journal Homepagehttps://onlinelibrary.wiley.com/loi/14622920
Publisher PageOpen Publisher Page
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