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:*rRNA,E.coli;**cNIT3NIT3;***50mg·mL-1[6]10,80,,。,,,。l0,PCR、,。(fluorescenceinsituhybridization,FISH)、[1]。:,,DNA,。、。FISH,,,、、。11.11。FISH,,,(,215011):(FISH)。,FISH,:1×PBS;:①:46℃,5h,c(NaCl)55mmol/L;②:46℃,3h,c(NaCl)30~40mmol/L。:;;:X2:A:1674-4829(2009)04-0034-04:2009-05-19:(1979-),,,,:.EstablishmentofExperimentalConditionsandOptimizationofFluorescenceinsituHybridizationAssayforDetectingNitrifyingBacteriainBiofilmZHANGYong,SONGYin-ling,SHIJun,CHENYuAbstract:Experimentalconditionsoffluorescenceinsituhybridization(FISH)fordetectingnitrifyingbacteriainbiofilmisoptimizedthroughtest.Resultsshowthattheoptimizedpretreatmentandhybridizationconditionsfordetectingnitrifyingbacteriainclude:Samplesaren'tcleanedby1×PBSbeforeheatfixed.Hybridizationconditionsofdetectingnitrifyingbacteriainbiofilmareasfollows:①Nitrobacter:temperatureis46℃,hybridizationtimeis5h,andsodiumchlorideconcentrationintheeluateis55mmol/L.②Nitrosomonas:temperatureis46℃,hybridizationtimeis3h,andsodiumchlorideconcentrationintheeluateis30~40mmol/L.Keywords:Nitrifyingbacteria;Fluorescenceinsituhybridization(FISH);Hybridoptimization22420098EnvironmentalScienceandTechnologyVol.22No.4Aug.2009CCTGTGCTCCATGCTCCGCCTGTGCTCCAGGCTCCGCGATCCCCTGCTTTTCTCC16S,1035-105216S,189-2074055HEXFITCNIT3cNIT3**NSO190(5′-3′)*ω()/%5′***224(a),NSO190,2h.(b)NSO190,2h.(c),NIT3,2h.(d)NIT3,2h.1(100×)1.2,。1.32,3[3-4]。22.199%,,,。7d。2.299%,。2.3,50℃2h[5],4%(CH2O)20min,(C2H5OH),50%,80%,99%C2H5OH,3min。。2.4,。。5mm[6]。9μL,1μL,,。,。,。。2.5,48℃。,20min,,。,(CFM-500),CCD,、。BMP。33.13,10,3。。::ai1~ai10i。,A=(A1+A2+A3)/3,。3.2:(+++)、(++)、(+),。44.1,46℃。:,。:。NSO190NIT3/mL39245moLNaCl/mL1818/mL405510%SDS/mL111moLTris-HCl/mLpH=7.22223NIT3NSO1900.5moLEDTA/mL11.245moLNaCl/mL10%SDS/mL112moLTris-HCl/mLPH=7.211(i=1,2,3)Ai=ai1+ai2+……+ai1010FISH3520098051015202530(f)HEXNIT3,5h。(a)FITCNSO190,1h。(b)HEXNIT3,1h。(c)FITCNSO190,3h。(d)HEXNIT3,3h。(e)FITCNSO190,5h。123/A110,+15,++2,+A29,+13,+11,++A314,+15,++3,+/A11155123A28,+10,+,+++A11,+,+++10,+A34+8,++,+++//A41-(a),1-(b)NSO190,NSO190。1-(c)、1-(d)NIT3,NIT3。4.24.2.15ng/μL[7-8]46℃NaCl(NIT3:75mmoL;NSO190:30mmoL),。、,3。(1)2NSO190,NIT3。,1h2-(a)、,2-(b),,;3h2-(c),2-(d)、;5h2-(e),,2-(f),。2(100×)(2)4。43h,,NSO1903h。(3)5。53h5h,5h,NIT35h。4.2.2,Tm46℃[9],NSO190,NIT346℃。4.2.3NaCl,,。110]:F×0.5=18.51gM1-18.51gM2(2):F,%;M1,moL;M2,moL。NSO190c(NaCl)30mmoL,NIT3c(NaCl)75mmoL。NSO1903:c(A1)=20mmoL,c(A2)=30mmoL,c(A3)=40mmoL;NIT33,:c(B1)=55mmoL,c(B2)=75mmoL,c(B3)=95mmoL,3,。⑴3,,3-(c),3-(e);3-(b),3-(d),,3-(f)。36224(f)HEXNIT3,5h。c(NaCl)=95mmoL(a)FITCNSO190,3h。c(NaCl)=20mmoL(b)HEXNIT3,5h。c(NaCl)=55mmoL(c)FITCNSO190,3h。c(NaCl)=30mmoL(d)HEXNIT3,5h。c(NaCl)=75mmoL(e)FITCNSO190,3h。c(NaCl)=40mmoL123/A18,+,+++,+++A28,+15,++11,+++A319,+,+++4,+/A12123A110,++9,++6,+A217,+++,+++4,+A3,+++12,++14,++//A8C(Nace)=95mmoL3NaCl(100×)(2)NaCl6。6NaCl46℃,3h,c(NaCl)30~40mmol/L。(3)NaCl7。7NaCl46℃,5h,c(NaCl)55mmol/L。5,:(1)1×PBS。(2):①:46℃,5h,c(NaCl)55mmol/L;②:46℃,3h,c(NaCl)30~40mmol/L。[][1].[J].,2001,19(1):18-21.[2]BONDPL,ERHARTRM,WANNERGJR.Blackall.Identificationofsomeofthemajorgroupsofbacteriainefficientandnonefficientbiologicalphosphorusremovalactivatedsludgesystems[J].ApplEnvironMicrobiol,1999,65(9):4077-4084.[3]AMANNRW,LUDWIGKH,SCHLELFER.Phylogeneticidentificationandinsitudetectionofindividualmicrobialcellswithoutcultivation[J].MicrobiolRev,1995(59):143-169.[4]MOTERA,GOBELUB.Fluorescenceinsituhybridization(FISH)fordirectvisualizationofmicroorganisms[J].MicrobiolMethods,2000(41):85-112.[5],,,.FISHPCR[J].,2001,9(2):22-23.[6],,,.FISH[J].,2007,33(1):22-25.[7]KALMBACHSW,MANZB,BENDINGER.2000InsituprobingrevealsAquabacteriumcommuneasawidespreadandhighlyabundantbacterialspeciesindrinkingwaterbiofilms[J].WatRec,2000(34):575-581.[8]MANZWU,SZEWZYK.P.ETICXXON,RAMANN.Insituidentificationofbacteriaindrinkingwaterandadjoiningbiofilmsbyhybridizationwith16Sand23SRNA-directedfluorescentoligonucleotideprobes[J].ApplEnvironMicrobio,1993(59):2293-2298.[9]AMANNRI.Molecularnicrobialecologymanual:InsituidentificationofmicroorganismsbywholecellhybrizationwithRNAtargetedmucleicacidprobes[J].DordrechtKluwerAcademic,1995(6):1-15.[10]MANZW.InsituanalysisofmicrobialbiofilmsbyRNA-targetedoligonucleotideprobing[J].MethEnzymol,1999(310):79-91.()FISH37
本文标题:FISH法检测生物膜中硝化细菌流程的建立及优化张勇
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