File Download
  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Dominance of Candidatus Scalindua species in anammox community revealed in soils with different duration of rice paddy cultivation in Northeast China

TitleDominance of Candidatus Scalindua species in anammox community revealed in soils with different duration of rice paddy cultivation in Northeast China
Authors
Keywords16S rRNA gene
Anammox bacteria
Hydrazine oxidoreductase gene
Rice paddy soil
Issue Date2013
PublisherSpringer. The Journal's web site is located at http://link.springer.de/link/service/journals/00253/index.htm
Citation
Applied Microbiology And Biotechnology, 2013, v. 97 n. 4, p. 1785-1798 How to Cite?
AbstractThe anaerobic ammonium-oxidizing (anammox) bacteria play an important role in the oxygen-limited zone for nitrogen cycling, but their roles in agricultural ecosystems are still poorly understood. In this study, soil samples were taken from the rhizosphere and non-rhizosphere and from surface (0-5 cm) and subsurface (20-25 cm) layers with 1, 4, and 9 years of rice cultivation history on the typical albic soil of Northeast China to examine the diversity and distribution of anammox bacteria based on 16S rRNA gene and hydrazine oxidoreductase encoding gene (hzo). By comparing these soil samples, no obvious difference was observed in community composition between the rhizosphere and non-rhizosphere or the surface and subsurface layers. Surprisingly, anammox bacterial communities of these rice paddy soils were consisted of mainly Candidatus Scalindua species, which are best known to be dominant in marine and pristine environments. The highest diversity was revealed in the 4-year paddy soil based on clone library analysis. Phylogenetic analysis of 16S rRNA gene and deduced HZO from the corresponding encoding gene showed that most of the obtained clones are grouped together with Candidatus Scalindua sorokinii, Candidatus Scalindua brodae, and Candidatus Scalindua spp. of seawater. The obtained clone sequences from all samples are distributed in two subclusters that contain sequences from environmental samples only. Tentative new species were also discovered in this paddy soil. This study provides the first evidence on the existence of anammox bacteria with limited diversity in agricultural ecosystems in Northern China. © 2012 The Author(s).
Persistent Identifierhttp://hdl.handle.net/10722/147125
ISSN
2021 Impact Factor: 5.560
2020 SCImago Journal Rankings: 1.074
ISI Accession Number ID
References

Amano T, Yoshinaga I, Okada K, Yamagishi T, Ueda S, Obuchi A, Sakoand Y, Suwa Y (2007) Detection of anammox activity and diversity of anammox bacteria-related 16S rRNA genes in coastal marine sediment in Japan. Microbes Environ 22:232–242 doi: 10.1264/jsme2.22.232

Cao H, Hong Y, Li M, Gu J-D (2011a) Diversity and abundance of ammonia-oxidizing prokaryotes in sediments from the coastal Pearl River Estuary to the South China Sea. Anton Leeuw Int J G 100:545–556 doi: 10.1007/s10482-011-9610-1

Cao H, Hong Y, Li M, Gu J-D (2011b) Phylogenetic diversity and ecological pattern of ammonia-oxidizing archaea in the surface sediments of the Western Pacific. Microb Ecol 62:813–823 doi: 10.1007/s00248-011-9901-0

Cao H, Li M, Dang H, Gu J-D (2011c) Responses of aerobic and anaerobic ammonia/ammonium-oxidizing microorganisms to anthropogenic pollution in coastal marine environments. Method Enzymol 496:35–62 doi: 10.1016/B978-0-12-386489-5.00002-6

Cao H, Li M, Hong Y, Gu J-D (2011d) Diversity and abundance of ammonia-oxidizing archaea and bacteria in polluted mangrove sediment. Syst Appl Microbiol 34:513–523 doi: 10.1016/j.syapm.2010.11.023

Jetten MSM (2008) The microbial nitrogen cycle. Environ Microbiol 10:2903–2909 doi: 10.1111/j.1462-2920.2008.01786.x

Jetten MSM, de Bruijn P, Kuenen JG (1997) Hydroxylamine metabolism in Pseudomonas PB16: involvement of a novel hydroxylamine oxidoreductase. Antonie Van Leeuwenhoek 71:69–74 doi: 10.1023/A:1000145617904

Jetten MSM, Sliekers O, Kuypers M, Dalsgaard T, van Niftrik L, Cirpus I, van de Pas-Schoonen K, Lavik G, Thamdrup B, Le Paslier D, Op den Camp HJM, Hulth S, Nielsen LP, Abma W, Third K, Engström P, Kuenen JG, Jorgensen BB, Canfield DE, Damsté JSS, Revsbech NP, Fuerst J, Weissenbach J, Wagner M, Schmidt I, Schmid M, Strous M (2003) Anaerobic ammonium oxidation by marine and freshwater planctomycete-like bacteria. Appl Microbiol Biotechnol 63:107–114 doi: 10.1007/s00253-003-1422-4

Kartal B, Geerts W, Jetten MS (2011) Cultivation, detection, and ecophysiology of anaerobic ammonium-oxidizing bacteria. Methods Enzymol 486:89–108 doi: 10.1016/B978-0-12-381294-0.00004-3

Klotz MG, Stein LY (2008) Nitrifier genomics and evolution of the nitrogen cycle. FEMS Microbiol Lett 278:146–156 doi: 10.1111/j.1574-6968.2007.00970.x

Klotz MG, Schmid MC, Strous M, Op den Camp HJ, Jetten MS, Hooper AB (2008) Evolution of an octahaem cytochrome c protein family that is key to aerobic and anaerobic ammonia oxidation by bacteria. Environ Microbiol 10:3150–3163 doi: 10.1111/j.1462-2920.2008.01733.x

Konneke M, Bernhard AE, de la Torre JR, Walker CB, Waterbury JB, Stahl DA (2005) Isolation of an autotrophic ammonia-oxidizing marine archaeon. Nature 437:543–546 doi: 10.1038/nature03911

Koop-Jakobsen K, Giblin A (2009) Anammox in tidal marsh sediments: The role of salinity, nitrogen loading, and marsh vegetation. Estuar Coasts 32:238–245 doi: 10.1007/s12237-008-9131-y

Kumar S, Dudley J, Nei M, Tamura K (2008) MEGA: A biologist-centric software for evolutionary analysis of DNA and protein sequences. Brief Bioinform 9:299–306 doi: 10.1093/bib/bbn017

Kuypers MM, Lavik G, Woebken D, Schmid M, Fuchs BM, Amann R, Jorgensen BB, Jetten MS (2005) Massive nitrogen loss from the Benguela upwelling system through anaerobic ammonium oxidation. Proc Natl Acad Sci USA 102:6478–6483 doi: 10.1073/pnas.0502088102

Lam P, Jensen MM, Lavik G, McGinnis DF, Muller B, Schubert CJ, Amann R, Thamdrup B, Kuypers MM (2007) Linking crenarchaeal and bacterial nitrification to anammox in the Black Sea. Proc Natl Acad Sci USA 104:7104–7109 doi: 10.1073/pnas.0611081104

Li H, Chen S, Mu BZ, Gu J-D (2010a) Molecular detection of anaerobic ammonium-oxidizing (anammox) bacteria in high-temperature petroleum reservoirs. Microb Ecol 60:771–783 doi: 10.1007/s00248-010-9733-3

Li M, Hong Y, Klotz MG, Gu J-D (2010b) A comparison of primer sets for detecting 16S rRNA and hydrazine oxidoreductase genes of anaerobic ammonium-oxidizing bacteria in marine sediments. Appl Microbiol Biotechnol 86:781–790 doi: 10.1007/s00253-009-2361-5

Li M, Cao H, Hong Y, Gu J-D (2011a) Seasonal dynamics of anammox bacteria in estuarial sediments of Mai Po Nature Reserve revealed by 16S rRNA and hzo genes analysis. Microbes Environ 26:15–22 doi: 10.1264/jsme2.ME10131

Li M, Ford T, Li X-Y, Gu J-D (2011b) Cytochrome cd1-containing nitrite reductase encoding gene nirS as a new functional biomarker for detection of anaerobic ammonium oxidizing (Anammox) bacteria. Environ Sci Technol 45:3547–3553 doi: 10.1111/j.1574-6941.1995.tb00281.x

Li M, Hong Y, Cao H, Gu J-D (2011c) Mangrove trees affect the community structure and distribution of anammox bacteria at an anthropogenic-polluted mangrove in the Pearl River Delta reflected by 16S rRNA and hydrazine oxidoreductase (HZO) encoding gene analyses. Ecotoxicology 20(8):1780–1790 doi: 10.1007/s10646-011-0711-4

Li M, Cao H, Hong Y, Gu J-D (2011d) Spatial distribution and abundances of ammonia-oxidizing archaea (AOA) and ammonia–oxidizing bacteria (AOB) in mangrove sediments. Appl Microbiol Biotechnol 89:1243–1254 doi: 10.1007/s00253-010-2929-0

Liesack W, Schnell S, Revsbec NP (2000) Microbiology of flooded rice paddies. FEMS Microbiol Rev 24(5):625–664 doi: 10.1111/j.1574-6976.2000.tb00563.x

Lozupone C, Hamady M, Knight R (2006) UniFrac—an online tool for comparing microbial community diversity in a phylogenetic context. BMC Bioinform 7:371 doi: 10.1186/1471-2105-7-371

Neef A, Amann R, Schlesner H, Schleifer KH (1998) Monitoring a widespread bacterial group: in situ detection of planctomycetes with 16S rRNA-targeted probes. Microbiology 144:3257–3266 doi: 10.1128/AEM.66.2.754-762.2000

Mandel M, Higa A (1970) Calcium-dependent bacteriophage DNA infection. J Mol Biol 53:159–162 doi: 10.1016/0022-2836(70)90051-3

Mulder A, van de Graaf AA, Robertson LA, Kuenen JG (1995) Anaerobic ammonium oxidation discovered in a denitrifying fluidized bed reactor. FEMS Microbiol Ecol 16:177–184 doi: 10.1099/00221287-144-12-3257

Noll M, Matthies D, Frenzel P, Derakshani M, Liesack W (2005) Succession of bacterial community structure and diversity in a paddy soil oxygen gradient. Environ Microbiol 7:382–395 doi: 10.1111/j.1462-2920.2005.00700.x

Rich JJ, Dale OR, Song B, Ward BB (2008) Anaerobic ammonium oxidation (anammox) in Chesapeake Bay sediments. Microb Ecol 55(2):311–320 doi: 10.1007/s00248-007-9277-3

Rysgaard S, Glud RN, Risgaard-Petersen N, Dalsgaard T (2004) Denitrification and anammox activity in Arctic marine sediments. Limnol Oceanogr 49:1493–1502 doi: 10.4319/lo.2004.49.5.1493

Schalk J, de Vries S, Kuenen JG, Jetten MS (2000) Involvement of a novel hydroxylamine oxidoreductase in anaerobic ammonium oxidation. Biochemistry 39:5405–5412 doi: 10.1128/AEM.01978-06

Schloss PD, Handelsman J (2005) Introducing DOTUR, a computer program for defining operational taxonomic units and estimating species richness. Appl Environ Microbiol 71:1501–1506 doi: 10.1128/AEM.71.3.1501-1506.2005

Schmid M, Schmitz-Esser S, Jetten M, Wagner M (2001) 16S-23S rDNA intergenic spacer and 23S rDNA of anaerobic ammonium-oxidizing bacteria: implications for phylogeny and in situ detection. Environ Microbiol 3:450–459 doi: 10.1046/j.1462-2920.2001.00211.x

Schmid M, Walsh K, Webb R, Rijpstra WIC, van de Pas-Schoonen K, Verbruggen MJ, Hill T, Moffett B, Fuerst J, Schouten S, Damste JSS, Harris J, Shaw P, Jetten M, Strous M (2003) Candidatus “Scalindua brodae”, sp. nov., Candidatus “Scalindua wagneri”, sp. nov., two new species of anaerobic ammonium oxidizing bacteria. Syst Appl Microbiol 26:529–538 doi: 10.1078/072320203770865837

Schmid MC, Risgaard-Petersen N, van de Vossenberg J, Kuypers MMM, Lavik G, Petersen J, Hulth S, Thamdrup B, Canfield D (2007) Anaerobic ammonium-oxidizing bacteria in marine environments: widespread occurrence but low diversity. Environ Microbiol 9:1476–1484 doi: 10.1111/j.1462-2920.2007.01266.x

Shimamura M, Nishiyama T, Shinya K, Kawahara Y, Furukawa K, Fujii T (2008) Another multiheme protein, hydroxylamine oxidoreductase, abundantly produced in an anammox bacterium besides the hydrazine-oxidizing enzyme. J Biosci Bioeng 105:243–248 doi: 10.1111/j.1462-2920.2008.01732.x

Schubert CJ, Durisch-Kaiser E, Wehrli B, Thamdrup B, Lam P, Kuypers MM (2006) Anaerobic ammonium oxidation in a tropical freshwater system (Lake Tanganyika). Environ Microbiol 8:1857–1863 doi: 10.1111/j.1462-2920.2006.01074.x

Shimamura M, Nishiyama T, Shigetomo H, Toyomoto T, Kawahara Y, Furukawa K, Fujii T (2007) Isolation of a multiheme protein with features of a hydrazine-oxidizing enzyme from an anaerobic ammoniumoxidizing enrichment culture. Appl Environ Microbiol 73:1065–1072 doi: 10.1263/jbb.105.243

Strous M, Jetten MSM (2004) Anaerobic oxidation of methane and ammonium. Ann Rev Microbiol 58:99–117 doi: 10.1146/annurev.micro.58.030603.123605

Trimmer M, Nicholls JC, Deflandre B (2003) Anaerobic ammonium oxidation measured in sediments along the Thames estuary, United Kingdom. Appl Environ Microbiol 69:6447–6454 doi: 10.1128/AEM.69.11.6447-6454.2003

van de Vossenberg J, Rattray JE, Geerts W, Kartal B, van Niftrik L, van Donselaar EG, Sinninghe Damsté JS, Strous M, Jetten MSM (2008) Enrichment and characterization of marine anammox bacteria associated with global nitrogen gas production. Environ Microbiol 10:3120–3129 doi: 10.1111/j.1462-2920.2008.01643.x

Zhu G, Jetten MS, Kuschk P, Ettwig KF, Yin C (2010) Potential roles of anaerobic ammonium and methane oxidation in the nitrogen cycle of wetland ecosystems. Appl Microbiol Biotechnol 86:1043–1055 doi: 10.1007/s00253-010-2451-4

Zhu G, Wang S, Wang Y, Wang C, Risgaard-Petersen N, Jetten MSM, Yin C (2011) Anaerobic ammonia oxidation in a fertilized paddy soil. ISME J 5:1905–1912 doi: 10.1038/ismej.2011.63

Schmid M, Twachtmann U, Klein M, Strous M, Juretschko S, Jetten M, Metzger JW, Schleifer KH, Wagner M (2000) Molecular evidence for genus level diversity of bacteria capable of catalyzing anaerobic ammonium oxidation. Syst Appl Microbiol 23:93–106 doi: 10.1080/01490451.2011.559304

Dale OR, Tobias CR, Song B (2009) Biogeographical distribution of diverse anaerobic ammonium oxidizing (anammox) bacteria in Cape Fear River estuary. Environ Microbiol 11:1194–1207 doi: 10.1111/j.1462-2920.2008.01850.x

Dalsgaard T, Canfield DE, Petersen J, Thamdrup B, Acuna-Gonzalez J (2003) N2 production by the anammox reaction in the anoxic water column of Golfo Dulce, Costa Rica. Nature 422:606–608 doi: 10.1038/nature01526

Dalsgaard T, Donald BT, Canfield E (2005) Anaerobic ammonium oxidation (anammox) in the marine environment. Res Microbiol 156:457–464 doi: 10.1016/j.resmic.2005.01.011

Francis CA, Beman JM, Kuypers MM (2007) New processes and players in the nitrogen cycle: the microbial ecology of anaerobic and archaeal ammonia oxidation. ISME J 1:19–27 doi: 10.1038/ismej.2007.8

Hofstra N, Bouwman AF (2005) Denitrification in agricultural soils: summarizing published data and estimating global annual rates. Nutr Cycl Agroecosys 72:267–278 doi: 10.1007/s10705-005-3109-y

Hong Y, Li M, Cao H, Gu J-D Hong (2011a) Residence of habitat-specific anammox bacteria in the deep-sea subsurface sediments of the South China Sea: analyses of marker gene abundance with physical chemical parameters. Microb Ecol 62:36–47 doi: 10.1007/s00248-011-9849-0

Hong Y, Yin B, Zheng TL (2011b) Diversity and abundance of anammox bacterial community in the deep-ocean surface sediment from equatorial Pacific. Appl Microbiol Biotechnol 89:1233–1241 doi: 10.1007/s00253-010-2925-4

 

DC FieldValueLanguage
dc.contributor.authorWang, Jen_HK
dc.contributor.authorGu, JDen_HK
dc.date.accessioned2012-05-28T08:19:23Z-
dc.date.available2012-05-28T08:19:23Z-
dc.date.issued2013en_HK
dc.identifier.citationApplied Microbiology And Biotechnology, 2013, v. 97 n. 4, p. 1785-1798en_HK
dc.identifier.issn0175-7598en_HK
dc.identifier.urihttp://hdl.handle.net/10722/147125-
dc.description.abstractThe anaerobic ammonium-oxidizing (anammox) bacteria play an important role in the oxygen-limited zone for nitrogen cycling, but their roles in agricultural ecosystems are still poorly understood. In this study, soil samples were taken from the rhizosphere and non-rhizosphere and from surface (0-5 cm) and subsurface (20-25 cm) layers with 1, 4, and 9 years of rice cultivation history on the typical albic soil of Northeast China to examine the diversity and distribution of anammox bacteria based on 16S rRNA gene and hydrazine oxidoreductase encoding gene (hzo). By comparing these soil samples, no obvious difference was observed in community composition between the rhizosphere and non-rhizosphere or the surface and subsurface layers. Surprisingly, anammox bacterial communities of these rice paddy soils were consisted of mainly Candidatus Scalindua species, which are best known to be dominant in marine and pristine environments. The highest diversity was revealed in the 4-year paddy soil based on clone library analysis. Phylogenetic analysis of 16S rRNA gene and deduced HZO from the corresponding encoding gene showed that most of the obtained clones are grouped together with Candidatus Scalindua sorokinii, Candidatus Scalindua brodae, and Candidatus Scalindua spp. of seawater. The obtained clone sequences from all samples are distributed in two subclusters that contain sequences from environmental samples only. Tentative new species were also discovered in this paddy soil. This study provides the first evidence on the existence of anammox bacteria with limited diversity in agricultural ecosystems in Northern China. © 2012 The Author(s).en_HK
dc.languageengen_US
dc.publisherSpringer. The Journal's web site is located at http://link.springer.de/link/service/journals/00253/index.htmen_HK
dc.relation.ispartofApplied Microbiology and Biotechnologyen_HK
dc.rightsThe Author(s)en_US
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.en_US
dc.subject16S rRNA geneen_HK
dc.subjectAnammox bacteriaen_HK
dc.subjectHydrazine oxidoreductase geneen_HK
dc.subjectRice paddy soilen_HK
dc.titleDominance of Candidatus Scalindua species in anammox community revealed in soils with different duration of rice paddy cultivation in Northeast Chinaen_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://www.springerlink.com/link-out/?id=2104&code=P0897G11P8L691V5&MUD=MPen_US
dc.identifier.emailGu, JD: jdgu@hkucc.hku.hken_HK
dc.identifier.authorityGu, JD=rp00701en_HK
dc.description.naturepublished_or_final_versionen_US
dc.identifier.doi10.1007/s00253-012-4036-xen_HK
dc.identifier.pmid22526793-
dc.identifier.scopuseid_2-s2.0-84874354885en_HK
dc.identifier.hkuros224973-
dc.relation.referencesAmano T, Yoshinaga I, Okada K, Yamagishi T, Ueda S, Obuchi A, Sakoand Y, Suwa Y (2007) Detection of anammox activity and diversity of anammox bacteria-related 16S rRNA genes in coastal marine sediment in Japan. Microbes Environ 22:232–242en_US
dc.relation.referencesdoi: 10.1264/jsme2.22.232en_US
dc.relation.referencesBothe H, Jost G, Schloter M, Ward B, Witzel KP (2000) Molecular analysis of ammonia oxidation and denitrification in natural environments. FEMS Microbiol Ecol 24:673–690en_US
dc.relation.referencesCao H, Hong Y, Li M, Gu J-D (2011a) Diversity and abundance of ammonia-oxidizing prokaryotes in sediments from the coastal Pearl River Estuary to the South China Sea. Anton Leeuw Int J G 100:545–556en_US
dc.relation.referencesdoi: 10.1007/s10482-011-9610-1en_US
dc.relation.referencesCao H, Hong Y, Li M, Gu J-D (2011b) Phylogenetic diversity and ecological pattern of ammonia-oxidizing archaea in the surface sediments of the Western Pacific. Microb Ecol 62:813–823en_US
dc.relation.referencesdoi: 10.1007/s00248-011-9901-0en_US
dc.relation.referencesCao H, Li M, Dang H, Gu J-D (2011c) Responses of aerobic and anaerobic ammonia/ammonium-oxidizing microorganisms to anthropogenic pollution in coastal marine environments. Method Enzymol 496:35–62en_US
dc.relation.referencesdoi: 10.1016/B978-0-12-386489-5.00002-6en_US
dc.relation.referencesCao H, Li M, Hong Y, Gu J-D (2011d) Diversity and abundance of ammonia-oxidizing archaea and bacteria in polluted mangrove sediment. Syst Appl Microbiol 34:513–523en_US
dc.relation.referencesdoi: 10.1016/j.syapm.2010.11.023en_US
dc.relation.referencesdoi: 10.1038/ismej.2009.125en_US
dc.relation.referencesJetten MSM (2008) The microbial nitrogen cycle. Environ Microbiol 10:2903–2909en_US
dc.relation.referencesdoi: 10.1111/j.1462-2920.2008.01786.xen_US
dc.relation.referencesJetten MSM, de Bruijn P, Kuenen JG (1997) Hydroxylamine metabolism in Pseudomonas PB16: involvement of a novel hydroxylamine oxidoreductase. Antonie Van Leeuwenhoek 71:69–74en_US
dc.relation.referencesdoi: 10.1023/A:1000145617904en_US
dc.relation.referencesJetten MSM, Sliekers O, Kuypers M, Dalsgaard T, van Niftrik L, Cirpus I, van de Pas-Schoonen K, Lavik G, Thamdrup B, Le Paslier D, Op den Camp HJM, Hulth S, Nielsen LP, Abma W, Third K, Engström P, Kuenen JG, Jorgensen BB, Canfield DE, Damsté JSS, Revsbech NP, Fuerst J, Weissenbach J, Wagner M, Schmidt I, Schmid M, Strous M (2003) Anaerobic ammonium oxidation by marine and freshwater planctomycete-like bacteria. Appl Microbiol Biotechnol 63:107–114en_US
dc.relation.referencesdoi: 10.1007/s00253-003-1422-4en_US
dc.relation.referencesJetten MSM, van Niftrik L, Strous M, Kartal B, Keltjens JT, Op den Camp HJ (2009) Biochemistry and molecular biology of anammox bacteria. Crit Rev Biochem Mol Biol 44:65–84en_US
dc.relation.referencesKartal B, Geerts W, Jetten MS (2011) Cultivation, detection, and ecophysiology of anaerobic ammonium-oxidizing bacteria. Methods Enzymol 486:89–108en_US
dc.relation.referencesdoi: 10.1016/B978-0-12-381294-0.00004-3en_US
dc.relation.referencesLi M, Gu J-D (2011) Advances in methods for detection of anaerobic ammonium oxidizing (anammox) bacteria. Appl Microbiol Biotechnol 90:1241–1252en_US
dc.relation.referencesKlotz MG, Stein LY (2008) Nitrifier genomics and evolution of the nitrogen cycle. FEMS Microbiol Lett 278:146–156en_US
dc.relation.referencesdoi: 10.1111/j.1574-6968.2007.00970.xen_US
dc.relation.referencesKlotz MG, Schmid MC, Strous M, Op den Camp HJ, Jetten MS, Hooper AB (2008) Evolution of an octahaem cytochrome c protein family that is key to aerobic and anaerobic ammonia oxidation by bacteria. Environ Microbiol 10:3150–3163en_US
dc.relation.referencesdoi: 10.1111/j.1462-2920.2008.01733.xen_US
dc.relation.referencesKonneke M, Bernhard AE, de la Torre JR, Walker CB, Waterbury JB, Stahl DA (2005) Isolation of an autotrophic ammonia-oxidizing marine archaeon. Nature 437:543–546en_US
dc.relation.referencesdoi: 10.1038/nature03911en_US
dc.relation.referencesKoop-Jakobsen K, Giblin A (2009) Anammox in tidal marsh sediments: The role of salinity, nitrogen loading, and marsh vegetation. Estuar Coasts 32:238–245en_US
dc.relation.referencesdoi: 10.1007/s12237-008-9131-yen_US
dc.relation.referencesKumar S, Dudley J, Nei M, Tamura K (2008) MEGA: A biologist-centric software for evolutionary analysis of DNA and protein sequences. Brief Bioinform 9:299–306en_US
dc.relation.referencesdoi: 10.1093/bib/bbn017en_US
dc.relation.referencesdoi: 10.1007/s00253-011-3230-6en_US
dc.relation.referencesKuypers MM, Lavik G, Woebken D, Schmid M, Fuchs BM, Amann R, Jorgensen BB, Jetten MS (2005) Massive nitrogen loss from the Benguela upwelling system through anaerobic ammonium oxidation. Proc Natl Acad Sci USA 102:6478–6483en_US
dc.relation.referencesdoi: 10.1073/pnas.0502088102en_US
dc.relation.referencesLam P, Jensen MM, Lavik G, McGinnis DF, Muller B, Schubert CJ, Amann R, Thamdrup B, Kuypers MM (2007) Linking crenarchaeal and bacterial nitrification to anammox in the Black Sea. Proc Natl Acad Sci USA 104:7104–7109en_US
dc.relation.referencesdoi: 10.1073/pnas.0611081104en_US
dc.relation.referencesLi J, Zhong S, Wang M, Yang J, Xu W (2009) Dynamic simulation of ammonia- and nitrate N leakage from paddy field under different N supply. Chin J Appl Ecol 20:1369–1374en_US
dc.relation.referencesLi H, Chen S, Mu BZ, Gu J-D (2010a) Molecular detection of anaerobic ammonium-oxidizing (anammox) bacteria in high-temperature petroleum reservoirs. Microb Ecol 60:771–783en_US
dc.relation.referencesdoi: 10.1007/s00248-010-9733-3en_US
dc.relation.referencesLi M, Hong Y, Klotz MG, Gu J-D (2010b) A comparison of primer sets for detecting 16S rRNA and hydrazine oxidoreductase genes of anaerobic ammonium-oxidizing bacteria in marine sediments. Appl Microbiol Biotechnol 86:781–790en_US
dc.relation.referencesdoi: 10.1007/s00253-009-2361-5en_US
dc.relation.referencesLi M, Cao H, Hong Y, Gu J-D (2011a) Seasonal dynamics of anammox bacteria in estuarial sediments of Mai Po Nature Reserve revealed by 16S rRNA and hzo genes analysis. Microbes Environ 26:15–22en_US
dc.relation.referencesdoi: 10.1264/jsme2.ME10131en_US
dc.relation.referencesLi M, Ford T, Li X-Y, Gu J-D (2011b) Cytochrome cd1-containing nitrite reductase encoding gene nirS as a new functional biomarker for detection of anaerobic ammonium oxidizing (Anammox) bacteria. Environ Sci Technol 45:3547–3553en_US
dc.relation.referencesdoi: 10.1111/j.1574-6941.1995.tb00281.xen_US
dc.relation.referencesdoi: 10.1021/es103826wen_US
dc.relation.referencesLi M, Hong Y, Cao H, Gu J-D (2011c) Mangrove trees affect the community structure and distribution of anammox bacteria at an anthropogenic-polluted mangrove in the Pearl River Delta reflected by 16S rRNA and hydrazine oxidoreductase (HZO) encoding gene analyses. Ecotoxicology 20(8):1780–1790en_US
dc.relation.referencesdoi: 10.1007/s10646-011-0711-4en_US
dc.relation.referencesLi M, Cao H, Hong Y, Gu J-D (2011d) Spatial distribution and abundances of ammonia-oxidizing archaea (AOA) and ammonia–oxidizing bacteria (AOB) in mangrove sediments. Appl Microbiol Biotechnol 89:1243–1254en_US
dc.relation.referencesdoi: 10.1007/s00253-010-2929-0en_US
dc.relation.referencesLiesack W, Schnell S, Revsbec NP (2000) Microbiology of flooded rice paddies. FEMS Microbiol Rev 24(5):625–664en_US
dc.relation.referencesdoi: 10.1111/j.1574-6976.2000.tb00563.xen_US
dc.relation.referencesLozupone C, Hamady M, Knight R (2006) UniFrac—an online tool for comparing microbial community diversity in a phylogenetic context. BMC Bioinform 7:371en_US
dc.relation.referencesdoi: 10.1186/1471-2105-7-371en_US
dc.relation.referencesLüdemann H, Arth I, Liesack W (2000) Spatial changes in the bacterial community structure along a vertical oxygen gradient in flooded paddy soil cores. Appl Environ Microbiol 66:754–762en_US
dc.relation.referencesNeef A, Amann R, Schlesner H, Schleifer KH (1998) Monitoring a widespread bacterial group: in situ detection of planctomycetes with 16S rRNA-targeted probes. Microbiology 144:3257–3266en_US
dc.relation.referencesdoi: 10.1128/AEM.66.2.754-762.2000en_US
dc.relation.referencesMandel M, Higa A (1970) Calcium-dependent bacteriophage DNA infection. J Mol Biol 53:159–162en_US
dc.relation.referencesdoi: 10.1016/0022-2836(70)90051-3en_US
dc.relation.referencesMulder A, van de Graaf AA, Robertson LA, Kuenen JG (1995) Anaerobic ammonium oxidation discovered in a denitrifying fluidized bed reactor. FEMS Microbiol Ecol 16:177–184en_US
dc.relation.referencesdoi: 10.1099/00221287-144-12-3257en_US
dc.relation.referencesNoll M, Matthies D, Frenzel P, Derakshani M, Liesack W (2005) Succession of bacterial community structure and diversity in a paddy soil oxygen gradient. Environ Microbiol 7:382–395en_US
dc.relation.referencesdoi: 10.1111/j.1462-2920.2005.00700.xen_US
dc.relation.referencesRich JJ, Dale OR, Song B, Ward BB (2008) Anaerobic ammonium oxidation (anammox) in Chesapeake Bay sediments. Microb Ecol 55(2):311–320en_US
dc.relation.referencesdoi: 10.1007/s00248-007-9277-3en_US
dc.relation.referencesRysgaard S, Glud RN, Risgaard-Petersen N, Dalsgaard T (2004) Denitrification and anammox activity in Arctic marine sediments. Limnol Oceanogr 49:1493–1502en_US
dc.relation.referencesdoi: 10.4319/lo.2004.49.5.1493en_US
dc.relation.referencesSchalk J, de Vries S, Kuenen JG, Jetten MS (2000) Involvement of a novel hydroxylamine oxidoreductase in anaerobic ammonium oxidation. Biochemistry 39:5405–5412en_US
dc.relation.referencesdoi: 10.1128/AEM.01978-06en_US
dc.relation.referencesdoi: 10.1021/bi992721ken_US
dc.relation.referencesSchloss PD, Handelsman J (2005) Introducing DOTUR, a computer program for defining operational taxonomic units and estimating species richness. Appl Environ Microbiol 71:1501–1506en_US
dc.relation.referencesdoi: 10.1128/AEM.71.3.1501-1506.2005en_US
dc.relation.referencesSchmid M, Schmitz-Esser S, Jetten M, Wagner M (2001) 16S-23S rDNA intergenic spacer and 23S rDNA of anaerobic ammonium-oxidizing bacteria: implications for phylogeny and in situ detection. Environ Microbiol 3:450–459en_US
dc.relation.referencesdoi: 10.1046/j.1462-2920.2001.00211.xen_US
dc.relation.referencesSchmid M, Walsh K, Webb R, Rijpstra WIC, van de Pas-Schoonen K, Verbruggen MJ, Hill T, Moffett B, Fuerst J, Schouten S, Damste JSS, Harris J, Shaw P, Jetten M, Strous M (2003) Candidatus “Scalindua brodae”, sp. nov., Candidatus “Scalindua wagneri”, sp. nov., two new species of anaerobic ammonium oxidizing bacteria. Syst Appl Microbiol 26:529–538en_US
dc.relation.referencesdoi: 10.1078/072320203770865837en_US
dc.relation.referencesSchmid MC, Risgaard-Petersen N, van de Vossenberg J, Kuypers MMM, Lavik G, Petersen J, Hulth S, Thamdrup B, Canfield D (2007) Anaerobic ammonium-oxidizing bacteria in marine environments: widespread occurrence but low diversity. Environ Microbiol 9:1476–1484en_US
dc.relation.referencesdoi: 10.1111/j.1462-2920.2007.01266.xen_US
dc.relation.referencesSchmid MC, Hooper AB, Klotz MG, Woebken D, Lam P, Kuypers MM, Pommerening-Roeser A, Op den Camp HJ, Jetten MS (2008) Environmental detection of octahaemcytochrome c hydroxylamine/hydrazine oxidoreductase genes of aerobic and anaerobic ammonium-oxidizing bacteria. Environ Microbiol 10:3140–3149en_US
dc.relation.referencesShimamura M, Nishiyama T, Shinya K, Kawahara Y, Furukawa K, Fujii T (2008) Another multiheme protein, hydroxylamine oxidoreductase, abundantly produced in an anammox bacterium besides the hydrazine-oxidizing enzyme. J Biosci Bioeng 105:243–248en_US
dc.relation.referencesdoi: 10.1111/j.1462-2920.2008.01732.xen_US
dc.relation.referencesSchubert CJ, Durisch-Kaiser E, Wehrli B, Thamdrup B, Lam P, Kuypers MM (2006) Anaerobic ammonium oxidation in a tropical freshwater system (Lake Tanganyika). Environ Microbiol 8:1857–1863en_US
dc.relation.referencesdoi: 10.1111/j.1462-2920.2006.01074.xen_US
dc.relation.referencesShimamura M, Nishiyama T, Shigetomo H, Toyomoto T, Kawahara Y, Furukawa K, Fujii T (2007) Isolation of a multiheme protein with features of a hydrazine-oxidizing enzyme from an anaerobic ammoniumoxidizing enrichment culture. Appl Environ Microbiol 73:1065–1072en_US
dc.relation.referencesdoi: 10.1263/jbb.105.243en_US
dc.relation.referencesStrous M, Jetten MSM (2004) Anaerobic oxidation of methane and ammonium. Ann Rev Microbiol 58:99–117en_US
dc.relation.referencesdoi: 10.1146/annurev.micro.58.030603.123605en_US
dc.relation.referencesStrous M, van Gerven E, Kuenen JG, Jetten MSM (1997) Effects of aerobic and microaerobic conditions on anaerobic ammonium-oxidizing (anammox) sludge. Appl Environ Microbiol 63:2446–2448en_US
dc.relation.referencesTrimmer M, Nicholls JC, Deflandre B (2003) Anaerobic ammonium oxidation measured in sediments along the Thames estuary, United Kingdom. Appl Environ Microbiol 69:6447–6454en_US
dc.relation.referencesdoi: 10.1128/AEM.69.11.6447-6454.2003en_US
dc.relation.referencesvan de Vossenberg J, Rattray JE, Geerts W, Kartal B, van Niftrik L, van Donselaar EG, Sinninghe Damsté JS, Strous M, Jetten MSM (2008) Enrichment and characterization of marine anammox bacteria associated with global nitrogen gas production. Environ Microbiol 10:3120–3129en_US
dc.relation.referencesdoi: 10.1111/j.1462-2920.2008.01643.xen_US
dc.relation.referencesCao H, Hong Y, Li M, Gu J-D (2012) Lower abundance of ammonia-oxidizing archaea than ammonia-oxidizing bacteria in the subsurface sediments of the northern South China Sea. Geomicrobiol J 29:1–8en_US
dc.relation.referencesZhu G, Jetten MS, Kuschk P, Ettwig KF, Yin C (2010) Potential roles of anaerobic ammonium and methane oxidation in the nitrogen cycle of wetland ecosystems. Appl Microbiol Biotechnol 86:1043–1055en_US
dc.relation.referencesdoi: 10.1007/s00253-010-2451-4en_US
dc.relation.referencesZhu G, Wang S, Wang Y, Wang C, Risgaard-Petersen N, Jetten MSM, Yin C (2011) Anaerobic ammonia oxidation in a fertilized paddy soil. ISME J 5:1905–1912en_US
dc.relation.referencesdoi: 10.1038/ismej.2011.63en_US
dc.relation.referencesDang H, Chen R, Wang L, Guo L, Chen P, Tang Z, Tian F, Li S, Klotz MG (2010) Environmental factors shape sediment anammox bacterial communities in hypernutrified Jiaozhou Bay, China. Appl Environ Microbiol 76:7036–7047en_US
dc.relation.referencesHonghe nong chang (1986) Honehe nong chang zhi (Honghe State Farm Chronology), Jiamusi Shi Yin Shua Zong Chang, Jiamusi, Heilongjiang. pp 7–10 (in Chinese)en_US
dc.relation.referencesKoops H, Purkhold U, Pommerening-R A, Timmermann G, Wagner M (2003) The lithoautotrophic ammonia-oxidizing bacteria. The Prokaryotes 5:778–811en_US
dc.relation.referencesLozupone CA, Hamady M, Kelley ST, Knight R (2007) Quantitative and qualitative beta diversity measures lead to different insights into factors that structure microbial communities. Appl Environ Microbiol 73:1576–1585en_US
dc.relation.referencesQuan ZX, Rhee SK, Zuo JE, Yang Y, Bae JW, Park JR, Lee ST, Park YH (2008) Diversity of ammonium-oxidizing bacteria in a granular sludge anaerobic ammonium-oxidizing (anammox) reactor. Environ Microbiol 10:3130–3139en_US
dc.relation.referencesSchmid M, Twachtmann U, Klein M, Strous M, Juretschko S, Jetten M, Metzger JW, Schleifer KH, Wagner M (2000) Molecular evidence for genus level diversity of bacteria capable of catalyzing anaerobic ammonium oxidation. Syst Appl Microbiol 23:93–106en_US
dc.relation.referencesdoi: 10.1080/01490451.2011.559304en_US
dc.relation.referencesvan de Graaf AA, de Bruijn P, Robertson LA, Jetten MS, Kuenen JG (1996) Autotrophic growth of anaerobic ammonium-oxidizing micro-organisms in a fluidized bed reactor. Microbiology (UK) 142:2187–2196en_US
dc.relation.referencesvan de Graaf AA, Mulder A, de Bruijn P, Jetten MSM, Robertson LA, Kuenen JG (1995) Anaerobic oxidation of ammonium is a biologically mediated process. Appl Environ Microbiol 61:1246–1251en_US
dc.relation.referencesWeidner S, Arnold W, Pühler A (1996) Diversity of uncultured microorganisms associated with the seagrass Halophila stipulacea estimated by restriction fragment length polymorphism analysis of PCR-amplified 16S rRNA genes. Appl Environ Microbiol 62:766–771en_US
dc.relation.referencesXing B, Dudas MJ, Zhang Z, Xu Q (1994) Pedogenetic characteristics of albic soils in the Three River Plain, Heilongjiang province. Acta Pedologica Sinica 31:95–104en_US
dc.relation.referencesDale OR, Tobias CR, Song B (2009) Biogeographical distribution of diverse anaerobic ammonium oxidizing (anammox) bacteria in Cape Fear River estuary. Environ Microbiol 11:1194–1207en_US
dc.relation.referencesdoi: 10.1111/j.1462-2920.2008.01850.xen_US
dc.relation.referencesDalsgaard T, Canfield DE, Petersen J, Thamdrup B, Acuna-Gonzalez J (2003) N2 production by the anammox reaction in the anoxic water column of Golfo Dulce, Costa Rica. Nature 422:606–608en_US
dc.relation.referencesdoi: 10.1038/nature01526en_US
dc.relation.referencesDalsgaard T, Donald BT, Canfield E (2005) Anaerobic ammonium oxidation (anammox) in the marine environment. Res Microbiol 156:457–464en_US
dc.relation.referencesdoi: 10.1016/j.resmic.2005.01.011en_US
dc.relation.referencesFrancis CA, Beman JM, Kuypers MM (2007) New processes and players in the nitrogen cycle: the microbial ecology of anaerobic and archaeal ammonia oxidation. ISME J 1:19–27en_US
dc.relation.referencesdoi: 10.1038/ismej.2007.8en_US
dc.relation.referencesHofstra N, Bouwman AF (2005) Denitrification in agricultural soils: summarizing published data and estimating global annual rates. Nutr Cycl Agroecosys 72:267–278en_US
dc.relation.referencesdoi: 10.1007/s10705-005-3109-yen_US
dc.relation.referencesHong Y, Li M, Cao H, Gu J-D Hong (2011a) Residence of habitat-specific anammox bacteria in the deep-sea subsurface sediments of the South China Sea: analyses of marker gene abundance with physical chemical parameters. Microb Ecol 62:36–47en_US
dc.relation.referencesdoi: 10.1007/s00248-011-9849-0en_US
dc.relation.referencesHong Y, Yin B, Zheng TL (2011b) Diversity and abundance of anammox bacterial community in the deep-ocean surface sediment from equatorial Pacific. Appl Microbiol Biotechnol 89:1233–1241en_US
dc.relation.referencesdoi: 10.1007/s00253-010-2925-4en_US
dc.relation.referencesHumbert S, Tarnawski S, Fromin N, Mallet M-P, Aragno M, Zopfi J (2010) Molecular detection of anammox bacteria in terrestrial ecosystems: distribution and diversity. ISME J 4:450–454en_US
dc.identifier.spage1785en_HK
dc.identifier.epage1798en_HK
dc.identifier.eissn1432-0614en_US
dc.identifier.isiWOS:000314407300035-
dc.publisher.placeGermanyen_HK
dc.description.otherSpringer Open Choice, 28 May 2012en_US
dc.identifier.scopusauthoridWang, J=55191621900en_HK
dc.identifier.scopusauthoridGu, JD=7403129601en_HK
dc.identifier.citeulike10639525-
dc.identifier.issnl0175-7598-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats