ÿþ<HTML><HEAD><TITLE>25º Congresso Brasileiro de Microbiologia </TITLE><link rel=STYLESHEET type=text/css href=css.css></HEAD><BODY aLink=#ff0000 bgColor=#FFFFFF leftMargin=0 link=#000000 text=#000000 topMargin=0 vLink=#000000 marginheight=0 marginwidth=0><table align=center width=700 cellpadding=0 cellspacing=0><tr><td align=left bgcolor=#cccccc valign=top width=550><font face=arial size=2><strong><font face=Verdana, Arial, Helvetica, sans-serif size=3><font size=1>25º Congresso Brasileiro de Microbiologia </font></font></strong><font face=Verdana size=1><b><br></b></font><font face=Verdana, Arial,Helvetica, sans-serif size=1><strong> </strong></font></font></td><td align=right bgcolor=#cccccc valign=top width=150><font face=arial size=2><strong><font face=Verdana, Arial, Helvetica, sans-serif size=1><font size=1>ResumoID:1846-2</font></em></font></strong></font></td></tr><tr><td colspan=2><br><br><table align=center width=700><tr><td>Área: <b>Microbiologia Geral e Meio Ambiente ( Divisão L )</b><p align=justify><strong><P>MICRORGANISMS WITH ANAMMOX ACTIVITY IN SLUDGE ACCLIMATED FROM A SWINE MANURE TREATMENT LAGOON</P></strong></p><p align=justify><b>Aline Viancelli </b> (<i>UFSC</i>); <b>Airton Kunz </b> (<i>CNPSA</i>); <b>Paulo Augusto Esteves </b> (<i>CNPSA</i>); <b>T. Fujii </b> (<i>Dept SLS</i>); <b>Matias Vanotti </b> (<i>ARS/USDA</i>); <b>T Nishiyama, </b> (<i>Dept SLS</i>); <b>Regina Vasconcellos Antônio </b> (<i>UFSC</i>)<br><br></p><b><font size=2>Resumo</font></b><p align=justify class=tres><font size=2><P class=MsoNormal style="MARGIN: 0cm 0cm 0pt; TEXT-ALIGN: justify"><B style="mso-bidi-font-weight: normal"><SPAN lang=EN-US style="mso-ansi-language: EN-US">Introduction: </SPAN></B><SPAN lang=EN-US style="mso-ansi-language: EN-US">ANAMMOX (anaerobic ammonium oxidation) process is an alternative technology in nitrogen removal from wastewater and consists on the oxidation of NH<SUB>4</SUB> to N<SUB>2</SUB>. The advantages of ANAMMOX over conventional nitrification/denitrification process are less oxygen and no organic carbon requirement. The bacteria responsible for ANAMMOX process belong to phylum Planctomycetes and have a widespread distribution. There are five uncultured genus<I style="mso-bidi-font-style: normal"> C. Brocadia; C. Kuenenia; C.</I> <I style="mso-bidi-font-style: normal">Scalindua; C. Anammoxoglobus </I>and <I style="mso-bidi-font-style: normal">C. Jettenia</I>. The present study aimed to analyze the bacterial community from an ANAMMOX reactor by molecular methods. <B style="mso-bidi-font-weight: normal">Material and methods: </B>Reactor was inoculated with sludge from an anaerobic lagoon in experimental swine manure treatment at EMBRAPA - Swine and Poultry. After 20 months operating on ANAMMOX activity, samples were collected; DNA was extracted and treated with phenol/chloroform isoamylalcohol. Amplification of 16S rDNA gene was performed with KOD -plus- DNA polymerase using primers <?xml:namespace prefix = st1 ns = "urn:schemas-microsoft-com:office:smarttags" /><st1:metricconverter w:st="on" ProductID="6F">6F</st1:metricconverter> 5 -GGAGAGTTAGATCTTGGCTCAG-<st1:metricconverter w:st="on" ProductID="3 ">3 </st1:metricconverter> and 1492R 5 -GGTTACCTTGTTACGACT-<st1:metricconverter w:st="on" ProductID="3 ">3 </st1:metricconverter>. PCR was carried out according to: 2 min at <st1:metricconverter w:st="on" ProductID="94&#65456;C">94°C</st1:metricconverter>, 25 cycles (15 sec at <st1:metricconverter w:st="on" ProductID="94&#65456;C">94°C</st1:metricconverter>, 30 sec at <st1:metricconverter w:st="on" ProductID="58&#65456;C">58°C</st1:metricconverter>, 30 sec at <st1:metricconverter w:st="on" ProductID="68&#65456;C">68°C</st1:metricconverter>). Amplified fragments were inserted into pBluescript <st1:place w:st="on"><st1:City w:st="on">II</st1:City> <st1:State w:st="on">KS+</st1:State></st1:place> and transformed with <I style="mso-bidi-font-style: normal">Escherichia coli</I> DH10B. Plasmidial DNA extracted was sequenced with BigDye terminator v3.1 methodology and compared with sequences from nr-database using BLAST. <B style="mso-bidi-font-weight: normal">Results and Discussion: </B>Seventeen clones were obtained. Three of these clones had 97% homology with organisms belonging to Anammox group (Planctomycete KSU-1 and <I style="mso-bidi-font-style: normal">Candidatus </I>Jettenia asiatica). One clone, showed homology with phylum <I style="mso-bidi-font-style: normal">Chlorobium</I> (93%) that lives in anoxic aquatic settings and in phototrophic consortiums with </SPAN><I style="mso-bidi-font-style: normal">â</I><I style="mso-bidi-font-style: normal"><SPAN lang=EN-US style="mso-ansi-language: EN-US">-proteobacteria</SPAN></I><SPAN lang=EN-US style="mso-ansi-language: EN-US">. Twelve clones had 99% homology with <I style="mso-bidi-font-style: normal">Janthinobacterium</I>. <B style="mso-bidi-font-weight: normal">Conclusion: </B>Bacteria with ANAMMOX activity in a laboratory reactor was confirmed by the present study. Were identified organisms homologous to <I style="mso-bidi-font-style: normal">Candidatus</I> <I style="mso-bidi-font-style: normal">Jettenia asiatica</I>, Planctomycete KSU-1, <I style="mso-bidi-font-style: normal">Chlorobium </I>and <I style="mso-bidi-font-style: normal">Janthinobacterium</I>.<B style="mso-bidi-font-weight: normal"><?xml:namespace prefix = o ns = "urn:schemas-microsoft-com:office:office" /><o:p></o:p></B></SPAN></P></font></p><br><b>Palavras-chave: </b>&nbsp;Swine manure, 16S rDNA, ANAMMOX</td></tr></table></tr></td></table></body></html>