嗜热真菌Thermomyceslanuginosus耐热木聚糖酶性质及应用研究

嗜热真菌Thermomyceslanuginosus耐热木聚糖酶性质及应用研究

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时间:2019-05-10

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1、中国农业大学博士学位论文嗜热真菌Thermomyceslanuginosus耐热木聚糖酶性质及应用研究姓名:李秀婷申请学位级别:博士专业:食品科学指导教师:李里特;江正强20040601中国农业大学博十学位论文AbstmctAbstractXylanasecanhydrolyze13-1,4lgJycosidiclinkagesofthexylanbackbonetoproduceshortchainxylo‘oligosacchridesofvariouslengths.Hence.endo-G-xylanaseisthecruc

2、ialenzymecomponentsofmicrobialxylanolyticenzymesystems.Microbialxylanaseshaveattractedconsiderableresearchinterestinrecentyearsbecausetheirpotentialapplicationinthefood,animalfeed,paperandpulpindustries.Inthepresentdissertation,athermostablexylanasofromThermomyceslanug

3、inosusCBS288.54wereinvestigated.TheeffectsofdifferentfactorsOnxylanaseproduction印ZlanuginosusCBS288,54inshakeflaskconditionEightimprovedxylanaseproducingstrainswerescreenedbyshakena咄cultivationaftersporesofThermomyceslanuginosusCBS288.54weretreatedwithUV-irradiationand

4、ethyl-methanesulfonate.CultivationconditionsofthethermophilicfungusThermomyceslanuginosusCBS288.54·M18forthermostablexylanaseproductionwel"einvestigated.Corn-cobxylan(water·insoluble)wasfoundtobethebestinducerandcarbonSOUl'Ce.Tryptone+yeastextractWaSthebestnitrogensoum

5、es.TheoptimaltemperatureandtheinitialpHoftheculturesforxylanaseproductionwe[e50"CandpH7.0,respectively.Thehighestxylanaseactivityof1,834u/mLwasachievedundertheseoptimalconditions.Theeffectsofdifferent扣ctorsonxylanaseproductionbyT.1anuginosusCBS288.54-M18undersolidstate

6、culture(ssc)ThecultivationconditionsfortheproductionofthermostablexylanasefromThermomyceslanuginosusCBS288.54-M18undersolidstateculture(ssc)weTcinvestigated.Theeffectsofcarbonandnitrogensources,carbonSOUlVⅪtomineralsolutionratio,fermentationtemperatureandinitialpHofcul

7、tureonenzymeproductionwerestudied.Resultsshowedthat,byusingwheatbranandoomcubattheratioof8:2asthecarbonsonrce)yeastextractandtryptoneattheratioof1:1asthenitrogensource.amountofxylanaseproducedbythecultureincreased200%comparedtothosewithoutoptimizedcarbonandnitrogensour

8、ces.TheoptimalcarbonsourcetomineralsolutionratioandtheinitialpHofculturesforenzymeproductionwas1:3andpH7.0,respective

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