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34720137ENVIRONMENTALSCIENCEVol.34No.7Jul.2013A2O1222212*2*1.1000832.100085.A2O17.16SrDNArep-PCR..16SrDNArep-PCRX172A0250-3301201307-2912-062013-02-212013-05-15KZCX2-YW-JC407-3KZZD-EW-09-31986~E-mailshagao152@163.com*E-mailxiaweipeng@163.comzhbai@rcees.ac.cnDiversityofCulturableFilamentousBacteriaintheActivatedSludgefromA2OWastewaterTreatmentProcessGAOSha12JINDe-cai2ZHAOZhi-rui2QIRong2PENGXia-wei12BAIZhi-hui21.CollegeofBiologicalSciencesandTechnologyBeijingForestryUniversityBeijing100083China2.ResearchCenterforEco-EnvironmentalSciencesChineseAcademyofSciencesBeijing100085ChinaAbstractTheanoxic-anaerobic-oxicA2Oprocessiswidelyusedinwastewatertreatmentplanthoweversludgebulkingandfoamingarethemostfrequentoperationalproblemsinthisprocess.ActivatedsludgebulkingiscausedbytheovergrowthofsometypesoffilamentousbacteriaespeciallyMicrothrixparvicella.Inthestudy17strainsoffilamentousbacteriawereisolatedfromthebulkingsludgeofA2OprocessusingGause'smedium.The16SrRNAgenesofthe17isolatesweresequencedtoanalyzetheirdiversity.Theresultsshowedallofthe17isolateswereStreptomyces.Furtheranalysisofthesestrainsbytherepetitivesequencebasedonpolymerasechainreactionrep-PCRtechnologyshowedthattherewasahighdiversityintheseisolatedStreptomyces.ThephysiologicalpropertiesofthemweredifferentfromMicrothrixparvicella.Thesettleabilityofactivatedsludgewasimprovedwhensomeoftheisolateswereinoculated.KeywordsbulkingsludgefilamentousbacteriaStreptomyces16SrDNArep-PCR12..34..5~8.910..NocardiaNocardiaamaraeNocardiapinensiss、FlexibacterType0092、CytophagaType0411、Thiothrix、Beggiatoa、Type0914、Haliscomenobacterhydrossis、Microthrixparvicella、Sphaerotilusnatans.Microthrixparvicella、pH、DO11~13..7A2O.14..11.1A2O-20℃.1.21520g1g0.5g0.5g0.5g0.01g20g1000mL50mgpH7.2~7.4..0.2g0.1g0.05g0.05g2g100mLpH7.2~7.4.100g1g0.5g0.5g0.5g0.01g20g1000mLpH7.2~7.4.1.35g45mL20min.10-4、10-5、10-6、10-7100μL28℃4~7d5.5~10d5~7d1000.1.4DNA16SrDNAPCRDNA.16SrDNA27f1492r.16SrDNA-PCR50μL5μL10×Buffer4μLdNTP2.5nmol·L-11μL1.2μLDNA1μg0.5μLTaqDNA.PCR95℃5min94℃1min55℃1min72℃2min3072℃7min.PCR-20℃.1.516SrDNA16SrDNAPCR.NCBIGenBankBlastMEGA4N-J16~18.1.6Rep-PCR19PCRBOXAIR5'-CTACGGCAAGGCGACGCTGACG-3'.25μL152.5μL10×Buffer2μLdNTP2.5nmol·L-12μL1.5μLDNA25μL.PCR95℃5min95℃45s44℃1min72℃3min3572℃10min.1112161.5%TBE6μL3μLloadingBuffer80V150min100V120min.1.727℃160r·min-12~3d.100mL150mL2%、5%、10%25℃60r·min-13hSVI10%.22.1171G+.17.191000DAPI.2.216SrDNA1716SrDNAGenBank1716SrDNA97%2.3192341Table1CulturefeaturesoftheisolatedfilamentousstrainsonGause'smediumGS01GS02GS03GS04GS05GS06GS07GS08GS09GS10GS11GS12GS13GS14GS15GS16GS17172.ⅠGS12、GS16、GS02、GS03、GS01、GS14、GS11、GS17、GS07ⅡGS15、GS13、GS05、GS09、GS08、GS04、GS10、GS06.ⅠGS12、GS16、GS02、GS03、GS01、GS14Streptomycesmicroflavus126196JN180208、Streptomycescavourensis173883EU570437、Streptomycesmicroflavus2429JN180194、StreptomycesmicroflavusPM258JQ42216399%.GS03StreptomycesmicroflavusPM258100%GS11GS17StreptomycesrubiginosohelvolusNXPT24JN99992099.5%118Fig.1MicroscopicphotographoftheculturedisolatesandMicrothrixparvicella216SrDNATable216SrDNAsequenceanalysisoftheculturablefilamentousbacteria16SrDNAGenBankGenBank/%GS01JX430438StreptomycesflavofuscusJQ92441099.9GS02JX430439Streptomycesmicroflavus2429JN18019499.8GS03JX430440StreptomycesmicroflavusJQ422163100GS04JX430441StreptomycesphaeochromogenesEU59447199.5GS05JX430442Streptomycessp.XAS589GQ39524399.6GS06JX430443Streptomycessp.OA20JN94213299.9GS07JX430444Streptomycessp.CPE393JN96903499.6GS08JX430445Streptomycessp.CPE338JN96902599.5GS09JX430446StreptomycesrocheiFJ79257799.5GS10JX430447Streptomycessp.195018GU26387599.9GS11JX448396StreptomycesrubiginosohelvolusNXPT24JN99992099.5GS12JX679243StreptomycesmicroflavusJN18020897.8GS13JX465725Streptomycessp.XAS589GQ39524399.7GS14JX465726Streptomycessp.QZGY-A23JQ81208097.7GS15JX679244Streptomycessp.MJM3859EU60334799.7GS16JX679245StreptomyceslavendulaeAB18407999.9GS17JX465724StreptomycesrubiginosohelvolusNXPT24JN99992099.841927A2O216SrDNAN-JFig.2Neighborjoiningphylogenetictreeananlysisof16SrDNAofStreptomyces99.8%.GS07ⅠStreptomycessp.CPE393JN96903499.6%.Ⅱ82.GS157.GS15Streptomycessp.MJM3859EU60334799.7%799%.16SrDNA16SrDNAGenBank.2.3Rep-PCRBOXAIR17rep-PCR3.4.ⅠGS10、GS06、GS08ⅡGS17、GS15ⅢGS07、GS11、GS03、GS12ⅣGS09、GS04、GS05、GS01、GS02、GS16.DNA、rep-PCR.rep-PCR.2.41720~23..SVISVI60~100mL·g-1SVI150mL·g-1SVI300mL·g-124.2%、5%、10%17.GS05、GS14、GS175%4.45%GS05、GS14、GS17SVI3h.SVI...5192343BOX-PCRFig.3FingerprintsofBOXAIR-PCRelectrophoresis45%SVIFig.4EffectoftheisolatedStreptomycesstrainsonSVIofactivatedsludge2526.、pH、、、..31.21716SrDNA.rep-PCR.3.致谢:.1.J.20123393197-3201.2.J.2007283546-550.3GuoFZhangT.ProfilingbulkingandfoamingbacteriainactivatedsludgebyhighthroughputsequencingJ.WaterResearch20124682772-2782.61927A2O4MartinsAMPPagillaKHeijnenJJetal.Filamentousbulkingsludge-acriticalreviewJ.WaterResearch2004384793-817.5CaravelliAGiannuzzLZaritzkyN.EffectofchlorineonfilamentousmicroorganismspresentinactivatedsludgeasevaluatedbyrespirometryandINT-dehydrogenaseactivityJ.WaterResearch20043892395-2405.6.J.201228315-19.7.J.2010361
本文标题:A2O工艺活性污泥中可培养丝状细菌的多样性
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