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当前位置:首页 > 商业/管理/HR > 质量控制/管理 > 采用实时荧光定量PCR技术比较提取土壤真菌DNA方法的差异王淑芳
PCRDNA1212*111.2220052.222005PCROMEGADNADNA。5Phytophthoracapsici。OMEGADNAPCR。DNAPCRDNA。2.78。OMEGADNADNA。。PCRDNAS151.9A0517-6611201133-20318-04ComparisonoftheDifferenceintheFungusDNAExtractedwiththeArtificialMethodandKitMethodWANGShu-fangetalHuaihaiInstituteofMarineCollegeLianyungangJiangsu222005AbstractObjectiveThedifferenceintheisolationoffungusDNAwithartificialandKitextractingmethodwascomparedbasedonthetestofthereal-timequantitativefluorescesPCRtechnique.MethodThehyphaeofPhytophthoracapsiciwithfivedifferentconcentrationsandtheCKwasinoculatedinthesterilesoilmediumandtheDNAfromsoilsampleswasextractedwithartificialandOMEGADNAkitrespectivelyandthenthePhytophthoracapsiciwasquantitativelydetectedwithreal-timequantitativePCRmethodanditsspecificprimers.ThecharacterofthetwoisolationDNAmethodswasanalyzedbasedonthecomparisonoftheresult.ResultItwasfoundthatthesoilfungusDNAwaslittleaf-fectedbyothermaterialsinthetwomethodsandthetemplateDNAofreal-timePCRtechniquecouldbeformed.ThequantitativeresultsofPhytophthoracapsiciobtainedbyKitmethodwas2.78timeshigherthanthatobtainedinaverage.ConclusionThekitmethodextractedmoreDNAanditsquantitativeresultsweremoreaccurateallreagentsneededbyartificialmethodwerecommonbiochemicalreagentswhichwereaffordableandeasytoacquire.Thereforebothmethodshadtheirownadvantagesthechoiceofthemshouldbebasedonpracticalconditions.KeywordsReal-timequantitativefluorescesPCRFungusDNAinsoilCARS-25-B-2Z2009044。1976-E-mailwangshufang2001@hotmail.com。*E-mailguizhenma@sohu.com。2011-08-15DNA。DNA。DNADNA1-7。DNADNA。TNEP-PBS6。、、、1-37、、K13-57。DNA。PCRDGGE。PCRDNA。DNA4PCRPhytophthoracapsiciDNA。11.11.1.1。。。1.1.2。PCRSYBRPremixExTaqTMPerfectRealTimeSigmaAR。DNABioTek。PCR。DNAOMEGA。1.1.3。Bio-RadiQ5PCRAmershamUltro-spec3300pro。1.21.2.1。1.2.1.1。80℃200。2h。1.2.1.2。PD25℃、150r/min2d4。10000r/min5min2.4g7.6mlJournalofAnhuiAgri.Sci.2011393320318-2032112ml16ml22ml26ml32ml36ml42ml46ml5。1.2.1.3。6。1~560.5g50.00、12.50、3.13、0.780.20mg/g。。1.2.2DNA。1.2.2.1LabMethod。3DNA4。CTAB-SDS0.5g10ml3mlTENPBufferTris50mmol/LEDTA20mmol/LNaCl100mmol/LPVP10g/LpH10.010min12000r/min5min3mlTENPBuffer23mlPBSBufferNaCl8g/LKCl0.2g/LNa2HPO41.44g/LKH2PO40.24g/LpH7.410min12000r/min5min3g0.5cm2ml2%CTABNaCl1.4mol/LTris-HCl100mmol/LpH8.0EDTA20mmol/LpH8.02%CTAB10min37℃1h15min35min1.5ml3%SDS5min65℃2h20min38000r/min15min/25∶241015000r/min15min0.1NaAc3mol/L0.61h15000r/min20min70%2150μlDNA。DNADNA3DNAPCR。1~6。1.2.2.2OMEGADNA。3DNA。0.5g、500g1mlBufferSLXMlus3~5min100μlBufferDS70℃10min3000r/min3min2ml270μlBufferSP25min13000r/min、4℃5min2ml0.720~30-20℃1h13000r/min、4℃10min200μlElutionBuffer10s65℃10~20min50~100μlHTRReagent10s2min13000r/min2min2mlXP2Buffer10000r/min1min2ml300μlXP2Buffer10000r/min1min2ml700μlSPWWashBuffer10000r/min1min12ml13000r/min2min1.5ml30~100μlElutionBuffer65℃10~15min13000r/min1minDNA。3DNA1’~6’。DNA260nmA260nmA260nm/A280nm。1.2.3PCR。PCRSYBRGREENI。P1-F5’-AGGTGCACACAAAC-TTCCC-3’P1-R5’-GCAAAGCCGATTCAAAAG-3’。He8。PCRSYBRbuffer10μl0.3μmolDNA1μl1~10ng20μl。3DNA。95℃30s95℃5s60℃30s40iQ595℃60s55℃60s55℃30s。1.2.4。PCRiQ5Bio-RadiQ5OpticalSystemSoftware。22.1DNAOMEGADNA3DNA5μl1%。1DNA3DNA0.780.20mg/g2DNA。350.00、12.50、3.13mg/g。DNA。OMEGADNA5DNA130.780.20mg/g。66’DNA。2.2PCRITSDNA101.000×109~1.000×102/μl。“1.2.3”PCRPCR1μl1~61’~6’DNA。3Y=-3.295X+44.485R20.9801.000×109~1.000×1028。-3.295913023933PCRDNAM1Takaraλ-HindⅢdigestDNAMarker23130bpM2Tranks2KDNAMarker2000bp1~61~6DNA。NoteM1.Takara-λHindⅢdigestDNAMarkerthelargestbandwas23130bpM2isTranks2KDNAMarkerthelargestbandwas2000bp1-6.Soilsamplesfrom1to6.1DNAFig.1SoilDNAisolatedbylabmethodMTakaraλ-HindⅢdigestDNAMarker23130bp1~61’~6’DNA。NoteM.Takaraλ-HindⅢdigestDNAMarkerthelargestbandwas23130bp1~6.Soilsamplesfrom1’to6’.2OMEGADNAFig.2SoilDNAisolatedbyOMEGAkitmethod101.1%2.01PCR2PCR。3PCRFig.3Standardcurveofreal-timePCRofP.capsiciCt。1DNA3.87±0.19×104/μl2.78±0.13×102/μl。OMEGADNA9.51±0.47×104/μl1.01±0.06×103/μl。66’PCR。DNA。OMEGADNADNA52.46、2.56、3.09、2.173.632.78。DNA70%~80%OMEGADNA1.35~1.53。1PCRTable1Resultsofreal-timePCRbylabmethodandkitmethodMyceliumamount∥mglglgmyceliumamountLabextractionNo.Quantitativeresultscopy/μllglgMeanofquantitativeresultsOMEGAKitextractionNo.Quantitativeresultscopy/μllglgMeanofquantitativeresults50.001.69913.87±0.19×1044.5881'9.51±0.47×1044.97812.501.09721.67±0.09×1044.2232'4.27±0.01×1044.0293.130.49634.01±0.22×1033.6033'1.24±0.04×1043.4910.78-0.10947.36±0.40×1023.4614'1.60±0.09×1033.2040.20-0.69952.78±0.13×1023.4445'1.01±0.06×1033.00406--6'--1~41’~4’DNA。4、51~41’~4’DNA。DNAY=0.6639X+3.4405R20.9526OME-GADNADNAY=0.9724X+3.1517R20.9389。DNA9PCRDNA。4、5OMEGADNAOME-GADNADNA023022011。DNA。4DNAFig.4StandardcurveofsoilDNAextractionbylabmethod5OMEGADNADNAFig.5StandardcurveofsoilDNAisolationbykitmethod3DNADNA。DNA。DNADNA。DNA。OMEGADNADNAPCROMEGADNAPCRDNADNADNADNA2.78。。。1.DNAJ.20092299-302.2.DNAJ.200811703-705.3.DNAJ.20074611-616.4.DNAJ.20055854-860.5.DNAJ.200839112-16.6.TENP-PBSDNAJ.2010382412978-12980.7.DNAJ.20098151-155.8HEJZSHENJPZHANGLMetal.Quantitativeanalysesoftheabun-danceandcompositionofammonia-oxidizingbacteriaandammonia-oxidi-zingarchaeaofaC
本文标题:采用实时荧光定量PCR技术比较提取土壤真菌DNA方法的差异王淑芳
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