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簡介:1中文中文3780字畢業(yè)論文外文資料翻譯學院生物科學與工程學院專業(yè)食品科學與工程姓名學號070301109外文出處JOURNALOFCHROMATOGRAPHYA,7641997177–182附件外文資料原文指導教師評語簽名年月日用外文寫2動注射分析的電化學檢測法(ECD法),使各種脂肪和油樣中游離脂肪酸的測定更加簡便快捷。因為脂肪酸含量可以由測量流動信號峰高和面積得出,該方法也適用于液相色譜電化學檢測法測定脂肪酸含量。高效液相色譜電化學檢測法被認定為一種不用衍生物檢測高級脂肪酸的簡便方法。2.實驗.實驗21.試劑棕櫚酸995、硬脂酸995、油酸99、亞油酸99,均購自和光試劑公司日本大阪。標準酸溶液都用乙醇乙腈1090混合溶液溶解。以下油樣都是從市場上購得山茶油資生堂牌,日本東京、玉米油和油菜籽油林時計化工,日本東京、橄欖油宮澤醫(yī)藥,日本東京,大豆油關東化學,日本東京。乙醇乙腈1090混合溶液和一個裝有6MM維生素K376MM高氯酸鋰的柱子分別作為流動相和醌溶液。電解液中的高氯酸鋰可以減少電化學電池的電阻。圖1高效液相系統(tǒng)流動相是乙醇乙腈混合溶劑,醌溶液為6MM維生素K76MM高氯酸鋰的乙醇乙腈溶液,DG是除氣裝置,P1、P2是泵,S是樣品注射器(20ΜL),分離柱(色譜柱100RP18,250MM4MM,5微米);MC是混合柱線圈(50厘米),D是電化學檢測器、電化學電池和電位儀,R是記錄儀。22儀器高效液相色譜電化學檢測系統(tǒng)如圖1所示,包括除氣器分光公司DG98050型,日本東京、泵P1和P2分光PU980型、樣品注射器羅丹尼7125型,美國加利福尼亞、結構性柱(ODS柱色譜柱100RP18,250MM34MM5MM,CICAMERCK公司,日本東京、電化學電池分光EC840型,電位儀皇氏電化學系統(tǒng)311B型,日本川崎、記錄儀分光807IT型。電化學電池由玻碳工作電極、飽和甘汞電極
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上傳時間:2024-03-11
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簡介:JOURNALOFCHROMATOGRAPHYA,7641997177–182DETERMINATIONOFHIGHERFATTYACIDSINOILSBYHIGHPERFORMANCELIQUIDCHROMATOGRAPHYWITHELECTROCHEMICALDETECTIONTFUSE,FKUSU,KTAKAMURASCHOOLOFPHARMACY,TOKYOUNIVERSITYOFPHARMACYANDLIFESCIENCE14321,HORINOUCHI,HACHIOJI,TOKYO19203,JAPANRECEIVED15APRIL1996REVISED15AUGUST1996ACCEPTED22OCTOBER1996ABSTRACTASYSTEMOFHIGHPERFORMANCELIQUIDCHROMATOGRAPHYWITHELECTROCHEMICALDETECTIONWASDEVELOPEDFORTHESEPARATIONANDDETERMINATIONOFHIGHERFATTYACIDSANOCTADECYLSILICAODSCOLUMNWASUSEDASTHESTATIONARYPHASEANDANETHANOL–ACETONITRILE1090MIXTUREASTHEMOBILEPHASETHEELUATEWASMIXEDWITHAQUINONESOLUTIONWHICHWASCOMPOSEDOF6MM2METHYL1,4NAPHTHOQUINONEAND76MMLICLOINETHANOL–ACETONITRILE1090THROUGHAMIXINGCOILPEAKHEIGHTFOR4HIGHERFATTYACIDSMEASUREDAT2415MVVSSATURATEDCALOMELELECTRODESCEWASLINEARAGAINSTTHEAMOUNTOFACIDBETWEEN20AND1200PMOLFREEFATTYACIDSINVARIOUSOILSAMPLESWEREDETERMINEDBYTHISMETHOD,WHICHWASFOUNDNOTONLYSENSITIVEANDREPRODUCIBLEBUTALSOASIMPLEMEANSFORSEPARATINGANDDETERMININGFREEFATTYACIDSINOILSKEYWORDSELECTROCHEMICALDETECTIONFATTYACIDS1INTRODUCTIONPHOREPRIORTHECOLUMNSEPARATIONISREQUIREDFORSENSITIVEDETECTIONINHPLCMANYDERIVATIZINGMANYATTEMPTSHAVEBEENMADEFORTHESEPARATIONLABELLINGREAGENTSHAVEBEENDEVELOPEDFORTHISANDDETERMINATIONOFFATTYACIDSBYGASCHROMATOGPURPOSE4–13ACATALYSTINSOMECASESISREQUIREDRAPHYGC1–3ANDHIGHPERFORMANCELIQUIDCHROFORCOMPLETEDERIVATIZATIONOWINGTOTHEPOORREACMATOGRAPHYHPLC4–13INCURRENTGCANALYSISTIVITYOFCARBOXYLGROUPS4FORTHEDERIVATIZATIONCOMMONLYEMPLOYEDTODAY,FREEFATTYACIDSAREOFFATTYACIDSWITHSUCHREAGENTS,THEAMOUNTOFGENERALLYCONVERTEDTOTHEIRMETHYLESTERSANDTHENREAGENT,REACTIONTEMPERATUREANDTIMEARECRITICALFORINJECTEDINTOACAPILLARYGCMETHYLATIONANDGCHIGHREACTIONEFFICIENCYANDAVOIDINGANYSIDEPRODCONDITIONS,SUCHASPROGRAMMEDTEMPERATURE,SPLITUCTFORMATIONWATERISOFTENANINCOMPATIBLEENINJECTION,ASWELLASTYPEOFCAPILLARYCOLUMN,CARRIERVIRONMENTFORDERIVATIZATIONREACTIONSANDTOFINDAGAS,ANDDETECTOR,AREALLIMPORTANTDETERMINANTSOFSOLUTIONTOTHISPROBLEM,EXAMINATIONWASMADEOFHIGHACCURACYANDPRECISIONTHEMAINADVANTAGEOFTHEUSEOFAQUEOUSMICELLARSYSTEMSFORDERIVATIZAHPLCWITHFLUORESCENTDETECTIONHPLCFLOFFATTYTION5ALTHOUGHFLUORIMETRICDETECTIONISQUITEACIDSISHIGHSENSITIVITYHOWEVER,OWINGTOTHEWEAKSENSITIVE,FLUORESCENTINTENSITYISLIABLETOVARYOWINGABSORPTIONANDFLUORESCENTPROPERTIESOFFATTYACIDS,TOTHEPRESENCEOFSUBSTANCESINCOMPLICATEDSAMPLESDERIVATIZATIONWITHASTRONGCHROMOPHOREORFLUOROUNLESSTHEREISACLEANUPPROCEDUREFORTHEIRELIMINATIONITISTHUSHIGHLYDESIRABLETODEVELOPASIMPLECORRESPONDINGAUTHORANDRAPIDMETHODTHATREQUIRESNOSUCHPROCEDURE00219673/97/1700COPYRIGHT?1997ELSEVIERSCIENCEBVALLRIGHTSRESERVEDPIIS0021967396009065TFUSEETAL/JCHROMATOGRA7641997177–1821793RESULTSANDDISCUSSIONTHATAPPLIEDPOTENTIALTHATWOULDGIVETHEREDUCTIONCURRENTOFPROTONATEDQUINONETHEREDUCTIONPOTENTIALOFPROTONATEDQUINONEWAS31VOLTAMMETRICREDUCTIONOFVKINTHEPRESENCELESSNEGATIVETHANTHATOFDISSOLVEDOXYGENTHE3OFFATTYACIDSHALFPEAKPOTENTIALOFTHEFIRSTREDUCTIONWAVEOFOXYGENINETHANOLCONTAINING38MMLICLOWAS4PROTONATIONOFQUINONEATTHEELECTRODESURFACE2730MVVSSCEHOWEVER,THEREMAYHAVEBEENOCCURSPRIORTOITSELECTRONTRANSFERPROTONATEDBACKGROUNDCURRENTDUETOTHEDISSOLVEDOXYGEN,QUINONEISREDUCEDATAPOTENTIALLESSNEGATIVETHANSINCETHEOXYGENWASREDUCEDATPOTENTIALSMORETHATOFQUINONETOGIVEANEWPEAKONTHEVOLTNEGATIVETHAN2300MVVSSCEAMMOGRAMOFQUINONE17,18HIGHERFATTYACIDS,SUCHASPALMITICACID,INANETHANOLSOLUTIONCON32HPLCECDTAININGVKANDLICLOWEREPREVIOUSLYFOUNDTO34GIVERISETOAPEAKOFPROTONATEDVKONTHEINCONSIDERATIONOFTHEABOVE,HPLCECDOFFATTY3VOLTAMMOGRAMOFVKATAPOTENTIALLESSNEGATIVEACIDSWASCARRIEDOUTREVERSEDPHASESEPARATIONOF3THANTHEREDUCTIONPOTENTIALOFVKVKITSELFGAVEHIGHERFATTYACIDSWASDONEUSINGANODSCOLUMN33ACLEARREDUCTIONPEAKAT2720MVVSSCE,ANDAANDAMPOFANETHANOL–ACETONITRILEMIXTURETHEPEAKOFPROTONATEDVKWASNOTEDAT2320MVVSDISSOLVEDOXYGENINMPANDTHEQUINONESOLUTION3SCEAFTERADDINGPALMITICACIDTOTHESOLUTIONTHEWASREMOVEDBYTHEDEGASSORA20MLALIQUOTOFPEAKHEIGHTWASPROPORTIONALTOADDEDACIDCONSOLUTIONCONTAININGFATTYACIDSWASINJECTEDINTOTHECENTRATION16COLUMNTHEELUATEWASMIXEDWITHTHEQUINONETHEHALFPEAKPOTENTIALOFAPEAKOFPROTONATEDSOLUTIONANDTHEFATTYACIDSWASDETECTEDWITHECDVKWASPREVIOUSLYSHOWNTOSHIFTTOAMOREEXAMINATIONWASMADEOFHOWTHERATIOOFACETONI3NEGATIVEPOTENTIALACCOMPANIEDBYANINCREASEINPKTRILETOETHANOLINTHEMPINFLUENCEDTHESEPARATIONAOFTHEADDEDACID17HOWEVER,HALFPEAKPOTENTIALSANDSENSITIVITYFORACIDDETERMINATIONINFIG2,THEOFPREPEAKSFORDIFFERENTHIGHERFATTYACIDSWERERETENTIONTIMEAANDTHEPEAKHEIGHTSBOFSIGNALSESSENTIALLYTHESAME,SINCEACIDSTRENGTHWASNEARLYFOR200PMOLLINOLEIC,OLEIC,PALMITICANDSTEARICACIDTHESAMEEACHFATTYACIDCOULDTHUSBEDETECTEDATWEREPLOTTEDAGAINSTTHERATIOOFTHETWOSOLVENTS,INFIG2RETENTIONTIMEAANDPEAKHEIGHTBASFUNCTIONSOFSOLVENTRATIOOFTHEMOBILEPHASEALINOLEICACID,BOLEICACID,CPALMITICACID,DSTEARICACIDAMOUNTOFACID5200PMOLHPLCCONDITIONSQUINONESOLUTION,6MMVK176MMLICLOINETHANOL–ACETONITRILE34MIXTURESAMPLEVOLUME,20MLCOLUMN,LICHROSPHER100RP18250MM34MMID,5MMCOLUMNTEMPERATURE,ROOMTEMPERATUREFLOWRATE,11ML/MINAPPLIEDPOTENTIAL,2415MVVSSCE
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上傳時間:2024-03-13
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簡介:HINDAWIPUBLISHINGCORPORATIONINTERNATIONALJOURNALOFAGRONOMYVOLUME2012,ARTICLEID543230,7PAGESDOI101155/2012/543230RESEARCHARTICLEIMPROVEMENTOFSOYBEANOILSOLVENTEXTRACTIONTHROUGHENZYMATICPRETREATMENTFVGRASSO,1PAMONTOYA,1CCCAMUSSO,1,2ANDBGMAROTO1,21FACULTADDECIENCIASEXACTAS,F′ISICASYNATURALES,UNIVERSIDADNACIONALDEC′ORDOBA,AVENUEVELEZSARSFIELD1200,5000C′ORDOBA,ARGENTINA2FACULTADDECIENCIASAGROPECUARIAS,UNIVERSIDADNACIONALDEC′ORDOBA,AVENUEVALPARA′ISOS/NO,5000C′ORDOBA,ARGENTINACORRESPONDENCESHOULDBEADDRESSEDTOFVGRASSO,FGRASSOAGROUNCEDUARRECEIVED5NOVEMBER2011REVISED14FEBRUARY2012ACCEPTED6MARCH2012ACADEMICEDITORBERTRANDMATTH¨AUSCOPYRIGHT?2012FVGRASSOETALTHISISANOPENACCESSARTICLEDISTRIBUTEDUNDERTHECREATIVECOMMONSATTRIBUTIONLICENSE,WHICHPERMITSUNRESTRICTEDUSE,DISTRIBUTION,ANDREPRODUCTIONINANYMEDIUM,PROVIDEDTHEORIGINALWORKISPROPERLYCITEDTHEPURPOSEOFTHISSTUDYISTOEVALUATEMULTIENZYMEHYDROLYSISASAPRETREATMENTOPTIONTOIMPROVESOYBEANOILSOLVENTEXTRACTIONANDITSEVENTUALADAPTATIONTOCONVENTIONALPROCESSESENZYMATICACTIONCAUSESTHEDEGRADATIONOFTHECELLSTRUCTURESTHATCONTAINOILIMPROVEMENTSINTERMSOFEXTRACTION,YIELD,ANDEXTRACTIONRATEAREEXPECTEDTOBEACHIEVEDSOYBEANFLAKESANDCOLLETSWEREUSEDASMATERIALSANDHEXANEWASUSEDASASOLVENTTEMPERATURE,PH,ANDINCUBATIONTIMEWEREOPTIMIZEDANDDIFFUSIONCOEFFICIENTSWEREESTIMATEDFOREACHSOLIDEXTRACTIONSWERECARRIEDOUTINACOLUMN,OILCONTENTWASDETERMINEDACCORDINGTOTIME,ANDAMATHEMATICALMODELWASDEVELOPEDTODESCRIBETHESYSTEMTHEOPTIMUMCONDITIONSOBTAINEDWEREPH54,38?C,AND97H,ANDPH58,44?C,AND58HOFTREATMENTFORFLAKESANDCOLLETS,RESPECTIVELYHYDROLYZEDSOLIDSEXHIBITEDAHIGHERYIELDDIFFUSIONCOEFFICIENTSWEREESTIMATEDBETWEEN10?11AND10?10THEHIGHESTDIFFUSIONCOEFFICIENTWASOBTAINEDFORHYDROLYZEDCOLLETS073GOIL/MLAND07GOIL/MLWEREOBTAINEDAT240SINACOLUMNFORCOLLETSANDFLAKES,RESPECTIVELYHYDROLYZEDSOLIDSEXHIBITEDAHIGHERYIELDTHEENZYMATICINCUBATIONACCELERATESTHEEXTRACTIONRATEANDALLOWSFORHIGHERYIELDTHEPROPOSEDMODELPROVEDTOBEAPPROPRIATE1INTRODUCTIONSEEDOILSREPRESENT70OFGLOBALOILPRODUCTION,OFWHICH30ISSOYBEANOILOILSEEDSARETHEMOSTIMPORTANTEXPORTITEMSINARGENTINA1INOILSEEDS,THEVACUOLESWITHINCELLSCONTAINOIL,ANDBOTHCELLWALLSANDVACUOLESHAVETOBEBROKENINORDERTOIMPROVESOLVENTEXTRACTIONTHEREFORE,THEPREPARATIONOFTHESEEDBEFORESOLVENTEXTRACTIONISCRITICALTOMAXIMIZEOILRECOVERYANALTERNATIVEPRETREATMENTTOFACILITATETHERELEASEOFOILFROMTHESEEDCOULDBEENZYMATICDEGRADATIONINTHISWAY,THEPARTIALHYDROLYSISOFSOYBEANSEEDCELLSTRUCTURESWITHAPPROPRIATEENZYMESWOULDINCREASEPERMEABILITY,WHICHWOULDINTURNINCREASEMASSTRANSFER2ANENZYMATICTREATMENTSTAGECOULDBEINCORPORATEDFORINDUSTRIALPURPOSESWITHOUTSIGNIFICANTCHANGESTOCONVENTIONALPROCESSESTHEOILRELEASEOBTAINEDUSINGTHISMETHODCOULDRESULTINAHIGHEREXTRACTIONYIELDAND/ORSMALLERQUANTITIESOFTHEORGANICSOLVENTSUSED3INSOLVENTEXTRACTION,PRETREATEDOILSEEDSPOROUSSOLIDMATRIXCOMEINTOCONTACTWITHAPURESOLVENTORASOLVENTMIXTUREMISCELLATOTRANSFERTHEOILFROMTHESOLIDMATRIXTOTHELIQUIDMEDIUMWHILETHEPRINCIPLEOFEXTRACTIONISRELATIVELYSIMPLE,ITISACOMPLEXMECHANISM4INORDERTODESCRIBETHISPROCESS,THEMASSTRANSFERPHENOMENAINVOLVEDANDTHEEVENTUALRESISTANCETOMASSTRANSFERINTHESOLIDPHASESOLIDSOYBEANANDINTHELIQUIDPHASEHEXANESHOULDBEANALYZEDTHISPROCESSINVOLVESSEVERALPHENOMENAOILISDIFFUSEDTHROUGHTHEINTERNALPORESTOTHESURFACEOFTHESOLIDINTERNALMASSTRANSPORTANDISTHENPASSEDTOTHEBULKLIQUIDBYMEANSOFACONVECTIVEMECHANISMPRODUCEDBYTHECONCENTRATIONDIFFERENCEBETWEENTHESOLUTIONOCCLUDEDINTHEPORESANDTHEBULKSOLUTIONEXTERNALTRANSPORTBECAUSETHEOILTOBEEXTRACTEDISCONTAINEDWITHINANINSOLUBLESOLIDNETWORKWITHOCCLUDEDMISCELLA,THEDIFFUSIONOCCURSMAINLYBETWEENTHEOCCLUDEDSOLUTIONANDTHESOLID,GREATLYAFFECTINGTHEEXTRACTIONRATESINCETHESOLIDMATRIXRESISTSDIFFUSIVETRANSPORT5INTERNATIONALJOURNALOFAGRONOMY3PROPOSEDBYMANYAUTHORS12–14,ANDCARR′INANDCRAPISTE4?C?TDEF?2C?X21WITHTHEFOLLOWINGINITIALANDBOUNDARYCONDITIONSFORANUNLIMITEDANDPERFECTLYAGITATEDVOLUMEOFBULKLIQUIDFORT0,CCO,FORT0,C0,INX?L,XL2THESOLUTIONTO1WASOBTAINEDFORPLATEANDSPHERE,ACCORDINGTOTHESOLIDTHATWASCONSIDEREDTHEFOLLOWINGWASOBTAINEDBYINTEGRATINGEACHSOLUTIONANDTAKINGINTOACCOUNTTHATTHESERIESOBTAINEDCONVERGERAPIDLYFORPLATEWITHTHICKNESS2L,QQ08Π2E?Π2DT/2L23FORSPHEREWITHRADIUSR,QQ06Π2E?Π2DEFT/R24BECAUSETHETRIGLYCERIDESPRESENTINVEGETABLEOILHAVEDIFFERENTMOLECULARWEIGHTSANDSTRUCTURES,ITISEASIERTOMEASURETHEAMOUNTOFOILINRELATIONTOSOLIDMASSTHEREFORE,THEC/COCONCENTRATIONRATIOWASTURNEDINTOAQ/Q0QUANTITYRATIOINBOTHEQUATIONS12EQUATIONS3AND4WERELINEARIZEDANDREPRESENTEDACCORDINGTOTIMETTHESLOPEOFBOTHLINESWASUSEDTOEVALUATETHEEFFECTIVEDIFFUSIONCOEFFICIENTSMATHEMATICALMODELFORCOLUMNEXTRACTIONTHEFIXEDBEDWASREGARDEDASASECTIONOFANEXTRACTIONCOLUMNTOWHICHASTEADYSTREAMOFHEXANE,QLO,ISSUPPLIEDANDFROMWHICHTHESAMEFLOWOFMISCELLA,QL,ISEXTRACTEDTHEMASSBALANCESFOREACHPHASEWERETHEFOLLOWINGSOLID?DCSDTKSAVS??CS?KEQCL?5LIQUIDDCLDT?QLCLVLKLAVL??CSKEQ?CL?6INTHEMASSBALANCEESTIMATION,ITWASASSUMEDTHATTHEBEDWASMADEUPOFPOROUSPARTICLESISOTROPICANDSPHERICALPARTICLESFORCOLLETSWITHANDWITHOUTENZYMATICPRETREATMENTANDFORFLAKESWITHENZYMATICTREATMENTTHEOILCONTENTINEACHOFTHESOLIDSISUNIFORMINALLPARTICLES,ANDTHEOILBEHAVESASASINGL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上傳時間:2024-03-13
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上傳時間:2024-05-21
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上傳時間:2024-03-13
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上傳時間:2024-01-07
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簡介:中文中文6000字,字,4000單詞,單詞,22600英文字符英文字符出處出處DESHPANDERP,CHINNANMS,PHILLIPSRDPROCESSDEVELOPMENTOFACHOCOLATE‐FLAVOUREDPEANUT–SOYBEVERAGEJINTERNATIONALJOURNALOFFOODSCIENCETECHNOLOGY,2008,435886894本科畢業(yè)設計(論文)本科畢業(yè)設計(論文)外文參考文獻譯文及原文外文參考文獻譯文及原文學院輕工化工學院輕工化工學院專業(yè)食品科學與工程食品科學與工程11外文文獻譯文外文文獻譯文巧克力味花生大豆飲料的研制巧克力味花生大豆飲料的研制摘要摘要利用兩種富含蛋白的含油種子資源即花生和大豆開發(fā)一種新型飲料產品。中度烘烤的花生粉和巧克力粉配合使用以產生怡人風味。相對于純花生產品,花生和大豆的組合提高必需氨基酸含量,尤其是賴氨酸。試驗工廠規(guī)模的飲料生產草案包括重要操作步驟過濾、均質和巴氏滅菌法。飲料制備包括一個三因素限制混合設計。在賴氨酸的含量、粘度和可視穩(wěn)定指數能分別達到51MG/G蛋白質、369MPAS和100的基礎上,其限制因素的上限和下限確定為花生(306-587)、大豆(283-435)以及巧克力糖漿(130-259)。改進的飲料配方和加工草案是對新型巧克力味花生大豆飲料的消費者認可度做進一步研究的基礎。關鍵詞關鍵詞飲料加工草案,巧克力味花生大豆飲料,巧克力糖漿,賴氨酸含量,大豆,花生,三組分混合設計,粘度,可視化穩(wěn)定指數1111前言前言開發(fā)一系列的傳統(tǒng)花生產品的趨勢目前越發(fā)明顯,最近,采用花生生產蛋白飲料產品成為焦點。對蔬菜調和乳、巧克力味花生飲料,UHT滅菌花生飲料和部分脫脂烤花生飲料的調查研究顯示花生奶已經成為奶類產品中的熱門。蛋白質的飲食不足尤其在發(fā)展中國家,是促進食品科學家和營養(yǎng)師研制營養(yǎng)均衡蛋白食品的因素之一?;ㄉ鞍椎臓I養(yǎng)價值在于它的蛋白質含量、必需氨基酸組成以及蛋白質消化率。花生蛋白缺乏某些必需氨基酸如賴氨酸、色氨酸、蘇氨酸和含硫氨基酸,但它的消化率卻與動物蛋白相當。當植物蛋白作為食物被攝入時,需要引起重視的是從營養(yǎng)角度,谷物和豆類的混合組合設計可彌補必需氨基酸間的不平衡。飲食被認為是加強營養(yǎng)以滿足已知的必需營養(yǎng)物質的缺乏的最佳途徑,而其中豆制品所占比例越來越高。這種配方通常在兒童及特殊人群的飲料中作為全面營養(yǎng)補充劑。此外,還能為傳統(tǒng)食品提供別樣的選擇,大豆蛋白正與很多膳食替代飲料融為一體,從而為忙碌的消費者帶來便利。大豆是含所有9中必需氨基酸且其含量能滿足人類需求的唯一豆科植物,被歸類到與肉類、牛奶、魚和雞蛋同等的優(yōu)質蛋白資源。大豆原料具有不同的
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上傳時間:2024-03-12
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上傳時間:2023-07-21
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下載積分: 13 賞幣
上傳時間:2023-07-21
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