EDITOR-IN-CHIEF BenjaminCaballero JohnsHopkinsUniversity CenterforHumanNutrition SchoolofHygieneandPublicHealth 615NorthWolfeStreet Baltimore,Maryland21205-2179 USA EDITORIAL ADVISORY BOARD EDITORS LuizCTrugo LaboratoryofFoodandNutritionBiochemistry DepartmentofBiochemistry,InstituteofChemistry FederalUniversityofRiodeJaneiro CTBlocoALab528-A IlhadoFundao,21949-900RiodeJaneiro Brazil PaulMFinglas InstituteofFoodResearch NorwichLaboratory ColneyLane Norwich,NR47UA UK PeterBelton PeterBerryOttaway AFRCInstituteofFoodResearch BerryOttawayAssociatesLtd NorwichLaboratory 1AFieldsYard ColneyLane PloughLane NorwichNR47UA HerefordHR40EL UK UK vi EDITORIALADVISORYBOARD RicardoBressani GeorgeDHill UniversidaddelValledeGuatemala LincolnUniversity InstitutedeInvestigaciones PlantSciencesGroup Aparto82 FieldServiceCentre Guatemala01901 Soil,PlantandEcologicalSciencesDivision POBox84 Canterbury BarbaraBurlingame NewZealand FoodandAgricultureOrganizationoftheUnitedNations VialedelleTermediCaracalla HarveyEIndyk Rome00100 AnchorProductsLimited Italy POBox7 Waitoa JerryCash NewZealand MichiganStateUniversity DepartmentofFoodScienceandHumanNutrition AnuraKurpad EastLansing StJohn’sMedicalSchool MI48824 DepartmentofNutrition USA Bangalore India ColinDennis JimFLawrence Campden&ChorleywoodRoodResearchAssociation SirFGBantingResearchCentre,Tunney’sPasture ChippingCampden HealthandWelfareCanada,HealthProtectionBranch GloucestershireGL556LD Ottawa UK OntarioK1A0L2 Canada JohannaTDwyer TuftsUniversity FXavierMalcata USDAHumanNutritionResearchCenter UniversidadeCatolicaPortugesa 711WashingtonStreet EscolaSuperiordeBiotecnologia USA RuaDrAntonioBernardinodeAlmeida TeeE-Siong Porto4200 InstituteofMedicalResearch Portugal DivisionofHumanNutrition JalanPahang KeshavanNiranjan KualaLumpur50588 UniversityofReading Malaysia DepartmentofFoodScienceandTechnology Whiteknights PatrickFFox POBox226 UniversityCollege Reading DepartmentofFoodChemistry BerkshireRG62AP Cork UK RepublicofIreland JohnRPiggott JesseGregory UniversityofStrathclyde UniversityofFlorida DepartmentofBioscienceandBiotechnology FoodScienceandHumanNutritionDepartment 204GeorgeStreet POBox110370 Glasgow NewellDrive ScotlandG11XW Gainesville UK FL32611-0370 USA VienoPiironen RJHamilton UniversityofHelsinki 10NorrisWay DepartmentofAppliedChemistry&Microbiology Formby POBox27 MerseysideL378DB HelsinkiFIN-00014 UK Finland EDITORIALADVISORYBOARD vii JanPokorny SteveLTaylor PragueInstituteofChemicalTechnology UniversityofNebraskaLincoln DepartmentofFoodScience DepartmentofFoodScienceandTechnology TechnickaStreet5 143HCFilleyHall CZ-16628Prague6 EastCampus CzechRepublic Lincoln NE68583-0919 USA TerryARoberts 59EdenhamCrescent JeanWoo Reading ChineseUniversityofHongKong BerkshireRG26HU DepartmentofMedicine UK PrinceofWalesHospital Shatin N.T De´liaBRodriguez-Amaya HongKong UniversityofCampinas DepartmentofFoodScience DavidCWoollard FacultyofFoodEngineering AgriQualityNZLtd POBox6121 LynfieldFoodServicesCentre Campinas 131BoundaryRoad SP13081-970 POBox41 Brazil Auckland1 NewZealand JacquesPRoozen StevenZeisel WageningenUniversity UniversityofNorthCarolinaatChapelHill AgrotechnologyandFoodSciences DepartmentofNutrition LaboratoryofFoodChemistry 2212McGavran-GreenbergHall POBox8129 ChapelHill 6700EVWageningen NC27599-7400 TheNetherlands USA FOREWORD Therearenodisciplinessoall-encompassinginhumanendeavoursasfoodscienceandnutrition.Whetheritbe biological, chemical, clinical, environmental, agricultural,physical– every science has a role and an impact. However, the disciplines of food science and nutrition do not begin or end with science. Politics and ethics, business and trade, humanitarian efforts, law and order, and basic human rights and morality all have somethingtodowithittoo. Asdisciplines,foodscienceandnutritionanswerquestionsandsolveproblems.Thequestionsandproblems arediverse,andcoverthefullspectrumofeveryissue.Lifespanisonesuchissue,coveredfromthenutritional basisforfetalandinfantdevelopment,tooptimalnutritionfortheelderly.Anothersuchissueisthetimespan of the ancient and wild agro-biodiversity that we are working to preserve, to the designer cultivars from biotechnology that we are trying to develop. Still another is the age-old food preparation methods now honoured by the ‘eco-gastronomes’ of the world, to the high tech food product development advances of recentyears. As with most endeavours, our scientific and technological solutions can and do create new, unforeseen problems. The technologies that gave us an affordable and abundantfoodsupplyled toobesityand chronic diseases.The‘‘greenrevolution’’ledtolossofsomeimportantagro-biodiversity.Thetechnologicalinnovation that gave us stable fats through hydrogenation, flooded the food supply with trans fatty acids. All these problems were identified through a multidisciplinary scientific approach and solutions are known. When technology created the problem and technology has found the solution, implementation is usually more successful.Reducingtransfattyacidsinthefoodsupplyiscaseinpoint.Beyondthetechnologies,thesolutions are more difficult to implement. We know how obesity can be reduced, but the solution is not directly technological.Hence,weshownosuccessintheendeavour. Ofalltheproblemsstillconfoundingusinfoodscienceandnutrition,noneissocompellingasreducingthe number of hungry people in the world. FAO estimates that there are 800 million people who do not have enough to eat. The World Food Summit Plan of Action, the Millennium Development Goals and other internationaleffortslook tofood science and nutrition toprovide thesolution. Yetwe only havepartof the solution—the science part. The wider world of effort in food science and nutrition needs to be more conscientiously addressed by scientists. This is the world of advocacy and action: advocacy for food and nutritionasbasichumanrights,coupledwithactiontogetfoodwhereitisneeded. Butallthoseeffortswouldbefutileiftheyarenotbasedonsoundscientificinformation.Thatiswhyworks such as this Encyclopedia are so important. They provide to a wide readership, scientists and non-scientists alike, the opportunity to quickly gain understanding on specific topics, to clarify questions, and to orient to furtherreading.Itisapleasuretobeinvolvedinsuchanendeavour,whereexpertsarewillingtoimparttheir knowledgeandinsightsonscientificconsensusandonexplorationofcurrentcontroversies.Allthewhile,this givesusoptimismforabrighterfoodandnutritionfuture. BarbaraBurlingame 25February2003 INTRODUCTION Thereisnofactormorevitaltohumansurvivalthanfood.Theonlysourceofmetabolicenergythathumans canprocessisfromnutrientsandbioactivecompoundswithputativehealthbenefits,andthesecomefromthe food that we eat. While infectious diseases and natural toxins may or may not affect people, everyone is inevitablyaffectedbythetypeoffoodtheyconsume. Inevolutionaryterms,humanshaveincreasedthecomplexityoftheirfoodchaintoanastoundinglevelina relativelyshorttime.Fromthefewstaplesofsomethousandyearsago,wehavemovedtoanextraordinarily richfoodchain,withmanyfooditemsthatwouldhavebeenunrecognizablejustsomehundredyearsago. In this evolution, scientific discovery and technical developments have always gone hand in hand. The identification of vitamins and other essential nutrients last century, and the development of appropriate technologies,ledtofoodfortification,andthusforthefirsttimehumanswereabletomodifyfoodstobetter fulfill their specific needs. As a result, nutritional deficiencies have been reduced dramatically or even eradicated in many parts of the world. This evolution is also yielding some undesirable consequences. The abundanceofhigh-density,cheapcaloriesources,andthemarketcompetitionhasfacilitatedoverconsumption andpromotedobesity,aproblemofglobalproportions. As the food chain grows in complexity, so does the scientific information related to it. Thus, providing accurate and integral scientific information on all aspects of the food chain, from agriculture and plant physiologytodietetics,clinicalnutrition,epidemiology,andpolicyisobviouslyamajorchallenge. The editors of the first edition of this encyclopedia took that challenge with, we believe, a great deal of success. This second edition builds on that success while updating and expanding in several areas. A large numberofentrieshavebeenrevised,andnewentriesadded,amountingtotwoadditionalvolumes.Thesenew entries include new developments and technologies in food science, emerging issues in nutrition, and addi- tionalcoverageofkeyareas.Asalways,wehavemadeeffortstopresenttheinformationinaconciseandeasy toreadformat,whilemaintainingrigorousscientificquality. We trust that a wide range of scientists and health professionals will find this work useful. From food scientistsin search of a methodological detail,to policymakers seeking updateon a nutrition issue, we hope that you will find useful material for your work in this book. We also hope that, in however small way, the Encyclopedia will be a valuable resource for our shared efforts to improve food quality, availability, access, andultimately,thehealthofpopulationsaroundtheworld. BenjaminCaballero LuizTrugo PaulFinglas A Acceptability of Food SeeFoodAcceptability:AffectiveMethods;MarketResearchMethods ACESULFAME/ACESULPHAME JFLawrence,HealthandWelfareCanada,Ontario, Production and Physical and Chemical Canada Properties Copyright2003,ElsevierScienceLtd.AllRightsReserved. Acesulfame K (Figure 1) is structurally related to 0003 saccharin. Italso has many of the same physicaland chemicalproperties. Background Acesulfame was one of a series of sweet-tasting 0004 Acesulfame K (potassium salt of 6-methyl-1,2,3- substances synthesized by Hoechst AG in the late 0001 oxathiazine-4(3H)-one-2,2-dioxide; Figure 1) is a 1960s.Allofthesehadincommontheoxathiazinone high-intensity artificial sweetener which is about dioxide ring structure. The synthesis involved reac- 200 times as sweet as sucrose (compared to a 3% tionoffluorosulfonylisocyanatewitheitheracetylene aqueous sucrose solution). It was accidentally dis- derivativesorwithactivemethylenecompoundssuch covered in 1967 by Dr. Karl Clauss, a researcher as a-diketones, a-keto acids, or esters. The latter re- with Hoechst AG in Frankfurt, FRG, during his ex- action is used for the commercial production of ace- periments on new materials research. The sweetener sulfame K. A generalized reaction scheme for isnotmetabolizedbythehumanbodyandthuscon- synthesis of the oxathiazinone dioxide ring structure tributesnoenergytothediet.Itisnowapproved for is shown in Figure 2. Many analoges have been pre- useinmorethan20countries. pared and evaluated for taste properties. The potas- sium salt of the 6-methyl derivative, acesulfame K, displayedthebestsensoryandphysicalpropertiesand Sweetness thus it has received extensive testing aimed at ThesweetnesspropertiesofacesulfameKaresimilar obtainingapprovalforitsuseindietfoods. 0002 tosaccharin.Ithasaclean,sharp,sweettastewitha AcesulfameKisawhitecrystallinematerialwhich 0005 rapidonsetofsweetnessandnolingeringaftertasteat isstableupto250(cid:1)C,atwhichtemperatureitdecom- normal use levels. However, at high concentrations, poses. The free acid form of the sweetener has a equivalent to 5% or 6% sucrose solutions, acesul- distinctmeltingpointof123.5(cid:1)C. fame K does possess a bitter, chemical aftertaste. AcesulfameKhasaspecificdensityof1.83.When 0006 The intensity of sweetness of acesulfame K, in dissolved in water it produces a nearly neutral solu- common with other artificial sweeteners, varies tionwhilethefreeacidisstronglyacidic(pHofa0.1 depending upon its concentration and the type of moll(cid:2)1aqueoussolutionbeing1.15).Thesweetener foodapplication. Forexample, itis90 times sweeter is very soluble in water; a 27% solution can be thana6%sucrosesolution,160timessweeterthana prepared at 20(cid:1)C. The solubility of acesulfame K 4%sucrosesolutionand250timessweeterthana2% increases significantly with temperature. At 80(cid:1)C, sucrose solution. Mixtures of acesulfame K with 50% solutions can be prepared; because of this, otherintensesweeteners,suchasaspartameorcycla- greater than 99% purity can be obtained by mate, result in some synergistic increases in sweet- crystallization. It is substantially less soluble in ness. Mixtures with saccharin are somewhat less common solvents such as ethanol, methanol, or synergistic. acetone. 2 ACESULFAME/ACESULPHAME CH Table1 TypicaluselevelsofacesulfameKindietfoods tbl0001 3 Foodproducts Concentration(mgkg(cid:2)1) O C O Softdrinks 1000 N− SO Coffeeandtea 267 K+ 2 Jamsandmarmalades 3000 Ready-to-eatdesserts 1000 fig0001 Figure1 StructureofacesulfameK.ReproducedfromAcesul- Chewinggum 2000 phame/Acesulfame, Encyclopaedia of Food Science, Food Tech- nology and Nutrition, Macrae R, Robinson RK and Sadler MJ (eds),1993,AcademicPress. desserts,breakfastcereals,andchewinggum.Table1 lists approximate concentration levels of acesulfame O O Ktypicallyusedinseveraltypesoffoods. ∆ C + O O N O O O Safety and Regulatory Status SO F 2 O NH SO2F AcesulfameKhasbeensubjectedtoextensivefeeding 0010 Fluoro- studies in mice, rats, and dogs. The substance is not sulfonyl- H3C O considered to be carcinogenic, mutagenic, or terato- isocyanate SO NaOH 2 genic. It is excreted unmetabolized in test animals O O NH or humans. The current maximum acceptable daily N SO F 2 intake (ADI: the maximum amount that can be con- H O sumed daily for a lifetime without appreciable risk) established by the Food and Agriculture Organiza- fig0002 Figure 2 Synthesis of the acesulfame ring structure using fluorosulfonyl isocyanate and tert-butylacetoacetate as start- tion/World Health Organization (FAO/WHO) Joint ing materials. Reproduced from Acesulphame/Acesulfame,En- ExpertCommitteeonFoodAdditivesin1990is5mg cyclopaedia of Food Science, Food Technology and Nutrition, perkgbodyweight.Thisvalueisbasedonthehighest Macrae R, Robinson RK and Sadler MJ (eds), 1993, Academic amountfedtoanimalsforwhichtherewasnoeffect. Press. ThefirstregulatoryapprovalforacesulfameKwas 0011 bytheUKin1983.Sincethenithasreceivedapproval forspecificusesinmorethan20countries. The stability of acesulfame K in the solid state is 0007 verygood.Itcanbestoredatambienttemperaturefor 10 years without decomposition. Aqueous solutions Analysis at pH 3 or greater may also be stored for extended Thin-layer chromatography, isotachorphoresis, and 0012 periods without detectable decomposition or loss of high-performance liquid chromatography (HPLC) sweetness.However,belowpH3,significanthydroly- have been evaluated for the determination of ace- sismayoccuratelevatedtemperatures.Forexample, sulfame K in a variety of matrices, including liquid atpH2.5anaqueousbufferedsolutionofacesulfame and solid food products, animal feed, and biological Kwoulddecomposebyabout30%after4monthsof fluids.Ofthethree,HPLCisperhapsthemostuseful storage at 40(cid:1)C, whereas no decomposition occurs since the efficiency of the chromatography coupled under the same conditions within the pH range of with selective detection (ultraviolet absorbance) 3–8. At 20(cid:1)C, less than 10% decomposition of ace- enable quantitative measurements to be made in sulfame K occurs after 4 months’storage at pH 2.5, rathercomplexfoodsamples.Inaddition,thesample indicating that under normal storage conditions preparation is minimal, usually involving a water aqueoussolutionsofthesweetenerareverystable. extraction for solid samples or a filtration and dilu- AcesulfameKisstableundermostfood-processing 0008 tion of liquid samples before direct HPLC analysis. conditions, including the elevated temperature treat- Acesulfame K has been incorporated into a multi- mentsencounteredinpasteurizationandbaking. sweeteneranalyticalmethodemployingHPLC. Food Uses Seealso:Carbohydrates:SensoryProperties; Chromatography:High-performanceLiquid 0009 Becauseofitsstability,acesulfameKhasbeenevalu- Chromatography;GasChromatography;Legislation: atedinawidevarietyofdietfoodproducts,including ContaminantsandAdulterants;Saccharin;Sweeteners: table-top sweeteners, soft drinks, fruit preparations, Intensive ACIDOPHILUSMILK 3 Further Reading reverse-phase liquid chromatography with absorbance detection. Journal of the Association of Official FrantaRandBeckB(1986)Alternativestocaneandbeet AnalyticalChemists71:934–937. sugar.FoodTechnology40:116–128. O’Brien-Nabors L and Gelardi RC (1991) Alternative KretchmerNandHollenbeckCB(1991)SugarsandSweet- Sweeteners.NewYork:M.Dekker. eners.BocaRaton:CRCPress. LawrenceJFandCharbonneauCF(1988)Determinationof seven artificial sweeteners in diet food preparations by ACIDOPHILUS MILK WKneifelandCBonaparte,Universityof derivedfromacido(acid)andphilus(loving)andthis AgriculturalSciences,Vienna,Austria designationreflectstheacidotolerantpotentialofthis species. In 1959, Rogosa and Sharpe presented a Copyright2003,ElsevierScienceLtd.AllRightsReserved. detaileddescriptionofthisbacterium. Background and History Fundamental Characteristics of Since the first documentation of the beneficial role 0001 Lactobacillusacidophilus of Lactobacillus acidophilus in correcting disorders of the human digestive tract in 1922, products con- Together with 43 other species, L. acidophilus is 0004 taining L. acidophilus, especially various types of listed as a member of the genus Lactobacillus which Acidophilusmilk,havebecomeincreasinglypopular. belongs to the heterogeneous category of lactic acid Today,amultitudeofsuchproductsarecommercially bacteria. Lactobacilli are Gram-positive, nonmotile, available,manyofthembeingassignedtothecategory catalase-negative, nonspore-forming rods with vary- ofprobioticfoods.Mostoftheseprobioticspossessa ingshapes,rangingfromslender,longrodstococco- bacterial microflora of well-documented and scienti- bacillary forms. They are considered as (facultative) fically proven bacterial strains with several benefical anaerobes withmicroaerophilicproperties. L.acido- properties.Besidesothercategoriesoffoodscontain- philus usually appears as rods with rounded ends, ing special ingredients, these products have also with asize of0.6–0.9(cid:3)1.5–6mm, mainly organized recently been subclassified under the umbrella of singly or in pairs or short chains (Figure 1). The cell functionalfoods. wallpeptidoglycanisoftheLys-d-Asptype;themean Ingeneral,thehumanbodyisinhabitatedbymore proportion of guanine and cytosine in the DNA 0002 than 500 different bacterial species; among them, ranges between 34 and 37%. With rare exceptions, the lactobacilli play an important ecological role. this bacterium shows good growth at 45(cid:1)C but not Besidestheirimportantgut-associatedfunction,lacto- below15(cid:1)C,havinganoptimumgrowthtemperature bacilli are also part of various other human-specific in the range of 35–38(cid:1)C. Substrates with pH values microbialecosystems,e.g.,skin,vagina,mouth,nasal, of5.5–6.0arepreferred.Metabolically,itisatypical andconjunctivalsecretions.L.acidophilusisthebest obligatelyhomofermentativebacteriumandproduces known of the health-promoting lactobacilli of racemiclacticacid(boththelþandthed(cid:2)enantio- mammals and a naturally resident species of the mericforms)fromlactose,glucose,maltose,sucrose, humangastrointestinaltract.Itcolonizessegmentsof and other carbohydrates. Usually, it follows the thelowersmall intestine andpartsofthelargeintes- Embden–Meyerhof–Parnas pathway for glucose tine, together with other lactobacilli species, such metabolism. Important growth factor requirements as L. salivarius, L. leichmanii, and L. fermentum. It are acetic or mevalonic acid, riboflavin, pantothenic isinterestingtonotethattheseresidentLactobacillus acid, niacin, folic acid and calcium, but not cobala- speciesshouldbedistinguishedfromthespectrumof min, pyridoxine, and thymidine. Starch and cello- so-called transient Lactobacillus species, which are biose are fermented by most strains. Another representedbyL.casei. differential key criterion for the distinction from Historically, in 1900, Australian researchers isol- other lactobacilli (e.g., L. delbrueckii subsp. bulgar- 0003 ated L. acidophilus from fecal samples of bottle-fed icus) is its capability of cleaving esculin. Further infants for thefirst time and named it ‘Bacillus acid- differential criteria are the utilization of trehalose, ophilus.’ The actual nomenclature L. acidophilus is melibiose, raffinose, ribose, and lactose. While
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