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  • 8/14/2019 Enzymes in breadmaking: Economic relevance, markets & future perspectives

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    Digital Re-print - July | August 2009Feature: Enzymes

    Feature title: Enzymes in bread making: Economic relevance, markets and future perspectives

    www.gfmt.co.uk

    Grain & Feed Milling Technology is published six times a year by Perendale Publishers Ltd of the United Kingdom.All data is published in good faith, based on information received, and while every care is taken to prevent inaccuracies,

    the publishers accept no liability for any errors or omissions or for the consequences of action taken on the basis ofinformation published.Copyright 2009 Perendale Publishers L td. All rights reserved. No par t of this publication may be reproduced in any formor by any means without prior permission of the copyright owner. Printed by Perendale Publishers Ltd. ISSN: 1466-3872

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  • 8/14/2019 Enzymes in breadmaking: Economic relevance, markets & future perspectives

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    Global population

    growth is achallenge for thesuppliers of staple food.

    A projection from 2007

    to 2050 predicts an average

    population growth rate of 0.8

    percent from 6.7 billion to

    9.3 billion people (see Figure

    1). Provided that the per

    capita consumption of sta-

    ple crops remains constant,

    the production of wheat and

    rice will have to grow from

    600 million tonnes each to

    850 million tonnes, and corn

    production has to rise from

    currently 850 million tonnes to 1000

    millions tons (see Table 1).

    These figures do not take into account

    the growing demand for biofuel.

    As can be concluded from Figure2, there is still a long

    way to go for scien-

    tists and economists,

    since the produc-

    tion of wheat in the

    major wheat grow-

    ing area has been

    constant over the

    past decade. One

    approach could be

    to improve wheats

    tolerance towards

    drought, heat and

    rain in order to

    grow wheat in less

    favourable regions of this

    planet. Promising stepshave already been taken

    (see Figure 3).

    Chemicals can bereplaced

    The development of this

    market affects the whole

    food production chain

    including the suppliers of

    additives and enzymes.The current market

    for bakery enzymes is

    estimated to be about

    US$200 million (see Figure

    4). Although the share of

    bakery enzyme of the total

    enzyme market (five percent) will not

    increase, their consumption will rise with

    the increasing demand for enzymes in

    Enzymes in breadmaking:Economic relevance, markets, and future perspectives

    by Lutz Popper, Head of Research and Development,Mhlenchemie GmbH & Co KG, Ahrensburg, Germany

    Figure 1: Development of the global population (modifiedfrom Bhler AG, 2007)

    Table 1: Staple food crop production andconsumption 2007, estimated demandand required production 2050, based ona population growth of 0.8 percent p.a.

    Consumers ProductionConsumed

    as food

    B il li on M il li on t on s M il li on t on s

    2007

    Wheat 3.0 600 490

    Rice 3 .0 600 400

    Corn 1.0 700 220

    2050

    Wheat 4.2 845 690

    Rice 4 .2 845 563

    Corn 1.4 986 310

    Figure 2: Global wheat production, selected areas(modified from USDA, 2007)

    Grain&feed millinG technoloGy34 | Ju-augus 2009

    FeatureEnzymes

    general, to an estimated cost of almost

    US$300 million by 2011.

    In the same period, the total market for

    food enzymes is expected to grow at a rate

    of almost six percent to about US$1.2 billion.

    This growth is supported by the per-

    ception that enzymes are a natural way

    to improve efficiency and quality and that

    chemicals can be replaced, avoiding labelling

    or omitting e numbers. Declining prices due

    to competition of supply and consolidation of

    the food industry, provide additional impetus.

    Most of the new enzymes will be pro-

    duced with genetically modified organisms,

    and some of the enzymes will even be

    protein engineered, that is, their original

    sequence of amino acids will be modified,

    although there is some market resistance

    against enzymes from genetically modified

    organisms.

    As in the past years, the properties of

    existing enzymes

    and enzyme

    combinations are

    constantly being

    improved, creat-

    ing a wider field of

    use and increas-

    ing demand. The

    most efficient

    driving force for

    growth still will be

    innovation.

    Three markets

    have been select-ed to visualise

    the development

    of the bakery

    enzyme segment,

    the US, the EU

    and China.

    For the US the

    average annual

    growth rate is

    interpolated to

    be 7.2 percent

    until 2010 (see

    Figure 5), with

    revenues of

    about US$70

    million at the

    end of the

    period.

    The EUstarts from a

    higher level,

    but due to a

    smaller growth

    of 4.5 percent

    the market will

    have a volume

    of only US$80

    million in 2010

    (see Figure 6).

    The

    expected

    growth

    rate of the

    Chinese mar-

    Figure 3: Tropicalised wheat in Tamil Nadu, India,close to the equator. Coconut and wheat growing in

    the same ecosystem (Nagarajan, 2006)

    Figure 4: Global enzyme market, 2006(left) and 2011 (right). Combined

    figures from Freedonia (2007) andMhlenchemie estimates

    Grain&feed millinG technoloGy Ju-augus 2009 | 35

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  • 8/14/2019 Enzymes in breadmaking: Economic relevance, markets & future perspectives

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    thevolumeyieldisthemaintarget

    copingwithvaryingwheatprop-

    erties is the major challenge

    compensationforperform-

    ance losses of compos-

    ite flours is requested.

    Recent enzyme developmentsThe enzymes currently being used most

    widely in the baking industry are more

    or less in order of decreasing importance

    fungal -amylase, hemicellulase (comprising

    pentosanase and xylanase), lipolytic enzymes

    (lipase, phospholipase, galactolipase etc.),glucose oxidase, protease (endo-peptidase),

    intermediate heat-stable -amylase, and glu-

    coamylase.

    Recent enzyme developments comprise

    asparaginase for avoiding acrylamide forma-

    tion, sulfhydryl oxidase as dough strength-

    ener, feruloyl esterase as rheological tool, f or

    improved flavour formation and possible for

    improved nutritional value of baked foods

    and more specific lipolytic enzymes not

    acting on triglycerides for bread and cake

    applications in recipes including shortening or

    butter or as egg replacement.

    Acrylamide is a potentially carcinogenic

    substance found in baked and fried food

    items. Potato products, wafers, biscuits and

    crispbread are most affected.

    It is formed during the Maillard (carameli-

    zation) reaction.At present there are no defined limits

    for acrylamide in food, but national warning

    thresholds exist.

    The amino acid aspargine is the key factor

    in acrylamide formation.

    In a Swedish study (Holmgren, 2007),

    adding aspargine-increased acrylamide from

    80ppb to as much as 6000ppb. It forms most-

    ly in the crust (99 percent), which indicates

    an influence of temperature and/or humidity.

    Darker products have higheracrylamide values.

    The addition of sugars or their enzymatic

    removal has no effect on acrylamide.

    2007) and on

    the authors

    data and esti-

    mates. The

    Asia-Pacific area

    is expected to

    grow at a similar

    rate as the US,

    while Africa and

    Latin Americas

    growth will be

    closer to the

    development of

    the European

    market.

    The general

    enzyme require-

    ments and trends

    differ signifi-

    cantly between

    developed and

    emerging mar-

    kets. Developed

    markets are

    mainly looking

    for:

    reductionof

    prices of clas-

    sical enzymes n ewenzymes with

    new func-

    tionalities

    enzymesforreplacement

    of chemicals

    enzymesfor increas-

    ing the shelf-

    life of baked

    goods with soft crumb

    segregationofenzymesfrom

    conventional and genetically

    modified micro-organisms

    In emerging markets:

    classicalenzymesareused

    breadpricesareregulatedin

    some areas, not allowing for

    ingredients adding to costs

    ket is stronger with an average of 9.5

    percent unti l 2013 (see Figure 7), but

    the starting point is also much lower,

    the revenues being only 13 percent of

    those in Europe (2003).

    Figure 8 summarises the world bakery

    enzyme market in 2006 and projected

    to 2011, based on market research data

    (Frost & Sullivan, 2004, 2005, Fredonia,

    Figure 5: Bakery Enzymes Market U.S.Revenue Forecasts, 2000-2010 (modified from Frost &

    Sullivan, 2004)

    Figure 6: Bakery Enzymes Market Europe. RevenueForecasts, 2001-2011 (modified from Frost & Sullivan,

    2005)

    Figure 7: Bakery Enzymes Market ChinaRevenue Forecasts, 2003-2013 (modified from Frost &

    Sullivan, 2007)

    Figure 8: Bakery Enzymes Market WorldRevenue Forecasts, 2006-2011

    Grain&feed millinG technoloGy36 | Ju-augus 2009

    FeatureEnzymes

    dough-strengthening disulfide bridges.

    In addition, oxidation gelation of pen-

    tosans via feruloyl residues may occur,

    increasing the water absorption. An

    undesirable side-effect of the above

    oxidases is their action on unsaturated

    lipids, which creates an unpleasant off-

    flavour.

    In particular bakery items from frozen

    and sheeted dough, such as croissants, may

    be severely affected. Therefore, the use of

    glyco-oxidases as a general flour-improvingenzyme is not recommended.

    Sulfhydryl oxidase (SOX, EC 1.8.3.2)

    specifically oxidizes sulfhydryl groups in

    protein and peptides. Hydrogen peroxide is

    also formed in this reaction. But in relation

    to the number of oxidized sulfhydryl groups,

    much less hydrogen peroxide is formed by

    SOX than by glycoside oxidases.

    In baking trials, SOX from S. cerevi-

    siae showed good potential, in particular in

    applications involving lamination steps and

    prolonged fermentation.

    Figure 10 shows a comparison of glucose

    oxidase and SOX in steamed bread baking trials.

    Furthermore, a partial replacement

    of ascorbic acid used as a dough stabi-

    Improving baking propertiesSeveral oxidases have been proposed

    and are being used for improving the baking

    properties of flour, in particular dough stabil-

    ity and mechanical tolerance.

    The common principle of most oxidases

    applied in baking is their action on mono- or

    oligosaccharides or other glycosides, creating

    a carboxyl group and hydrogen peroxides.

    The hydrogen peroxide then acts as a non-

    specific oxidant, oxidizing available electron

    donors in dough, including sulfhydryl groups.

    This

    results in the

    creation or

    protection of

    Temperatures above 200C, lower final

    product humidity and baking powder, in par-

    ticular with ammonium bicarbonate, increase

    acrylamide values, whereas yeast fermenta-

    tion reduces them.

    The decomposition of the precursor

    asparagine by asparaginase, Innovase ASP,

    is an effective means to reduce the acryla-

    mide formation. The enzyme is active in a

    pH range of 5-8.5 and at 30-65C hence in

    an optimum range for most baking applica-

    tions. In crispbread trials Innovase ASP

    reduced acrylamide to less than 25 per-

    cent, and in wafers Innovase ASP reduced

    it to about 10 percent of the original level(see Figure 9).

    Figure 9: Acrylamide reduction by Innovase ASP incrispbread and wafers

    Figure 10: Comparison of glucose oxidase andsulfhydryl oxidase in steamed bread. Wheat flour:

    DNS/CWRS; basic treatment: 40 ppm ascorbic acid(AAc); over-proofed samples only

    Table 2: Effect of FAE on the Alveogram

    Resting time 28 min Resting time 120 min

    % P L W P/L le P L W P/L le ldp

    0.00 102 100 351 1.02 59.6 81 123 334 0 .66 60.3 4.8

    0.02 101 101 349 1.00 59.9 83 122 329 0 .69 59.0 5.6

    0.04 106 88 333 1.20 60.4 85 115 324 0 .66 58.8 3.2

    0.08 100 110 364 0.91 5 9.1 79 132 325 0.60 5 8.2 1 0.6

    0.12 95 113 351 0.84 58.5 74 136 309 0 .55 57.2 11.8

    0.14 94 126 374 0.75 58.7 71 140 309 0 .51 57.9 17.3

    0.16 88 133 359 0.66 57.9 6 8 1 49 3 07 0 .4 6 5 6. 8 1 4. 4

    0.20 81 130 320 0. 62 57.1 63 145 268 0 .44 55.6 15.8

    Grain&feed millinG technoloGy Ju-augus 2009 | 37

    Feature Enzymes

    - RUMINANTS

    Enzymes Phosphorus

    requirements ofdairy cows

    Practical grazingsystems

    Dairy Heifer survival Omega-3 fatty

    acids and fertility

    PIGS

    Minerals Tryptophan

    requirements Feed processing

    technology Starter piglet

    systems Organic acids in

    pig diets

    RAPESEEDCO-PRODUCTS

    Feeding toruminants Feedi ng to pigs

    Commodity trends

    GENERAL PAPERS

    Oxidative stressand animalperformance

    Mycotoxins &mycotoxin binders

    Assessment ofnutritive value offeeds

    Potentialapplications of GMtechnology

    Legislation onenvironmentalimpact

    Impacts of climatechange on livestocksystems

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  • 8/14/2019 Enzymes in breadmaking: Economic relevance, markets & future perspectives

    4/5

    Future growthFigure 13 summarises potential reasons

    for future growth of the bakery enzyme

    market.

    In the first place, replacement of gluten

    is mentioned.

    The globally rising wheat price increase

    the tendency to replace expansive wheat

    with high gluten content and good baking

    properties by cheaper wheat. The lack in

    gluten content and baking performance can

    a least partially be replaced by adding func-tional ingredients such as enzymes.

    The second position in Figure 13 is taken

    by the term shelf life, in this case comprising

    microbial stability as well as crumb soft-

    ness. Both are increasingly required due to

    the continuing trends of bakeries merging

    to larger units with centralised production,

    hence longer distances from factory to shop.

    ReferencesBhler AG, 2007. Personal communication.

    Freedonia, 2007. Freedonia Focus on enzymes

    (FF35017). The Freedonia Group Inc, Cleveland, USA.

    Frost & Sullivan, 2004. European Markets for

    Enzymes in Food Applications (B460-88). Frost &

    Sullivan Ltd., London, UK.

    Frost & Sullivan, 2005. The U.S. Enzymes for Food

    Applications Markets (A660-88). Frost & Sullivan

    Ltd., London, UK.

    Frost & Sullivan, 2007. Strategic Analysis of

    Chinese Food Enzymes Markets (P074-88). Frost &

    Sullivan Ltd., London, UK.

    Holmgren, L., 2007. Control of acrylamide

    formation by processing and formulation. 3rd Int.

    Mhlenchemie Symposium, June 14-15. Hamburg,

    Germany.

    Hoseney, R.C. and Faubion, J.M., 1981. A

    mechanism for the oxidative gelation of wheat

    flour water-soluble pentosans. Cereal Chem. 58(5),

    421-424.

    Nagarajan, S., 2006. Quality Characteristics

    of Indian Wheat. In: Future of Flour. Popper, L.,

    Freund, W. and Schfer, W. (Eds.), Agrimedia Verlag

    Hamburg, Germany.

    USDA, 2007. Grain: World Markets and Trade.

    www.fas.usda.gov/psdonline.

    Ferulic acidcontributes to themechanical stability

    In wheat or rye flour

    dough, ferulic acid con-

    tributes to the mechanical

    stability by absorption of

    water and the stabilisation

    of gluten. An excess of sta-

    bility can result in a limited

    volume yield during the

    bread making process.

    As other hemicellulases,

    ferulic acid esterase is able

    to soften the xylan/gluten

    complex by the release of

    water from the gel and by

    the breakdown of covalent

    linkages.

    Unlike the most often

    used hemicellulases exert-

    ing an endo-1, 4--xylano-

    lytic actions on the xylan

    polymer, ferulic acid este-

    rase cleaves the side-chains

    between the galactose

    residue and the ferulic acid.

    Both activities improve the

    expandability of the dough

    and hence can be used to

    increase the volume yield.

    The enzyme has a

    significant effect on the

    dough rheology.

    When applied in the

    Alveograph, it was pos-

    sible to achieve a signifi-

    cant reduction of the P/L

    ratio while the energy

    remained constant over a

    wide dosage range (Table

    2). At prolonged resting

    times (120 minutes) the

    energy was close to that of

    untreated flour even when

    the P/L was diminished to

    0.46 instead of the initial

    ratio of 0.66.

    The extensibility of the

    dough could be increased

    by about 30 percent, as

    shown in Figure 12.

    Obviously, the

    enzyme is capable to

    partially hydrolyze the

    linkages between gluten

    and arabinoxylan (Hoseney and Faubion,

    1981) and/or to break-down the pen-

    tosan gel, resulting in the release of

    water from the gel, which is then avail-

    able for gluten hydration and softening.

    The enzyme also reduces the viscosity

    of flour suspensions, e.g. wafer batters

    (not shown).

    liser was possible. Steamed bread with

    reduced ascorbic acid had a brighter

    crumb colour (see Figure 11). The reason

    for this effect is not yet known. In but-

    ter croissants made from frozen dough,

    no formation of off-flavour was noted,

    while GOX-treated samples developed a

    strange smell.

    Figure 12: Effect of ferulic acid esterase fromStreptomyces sh10 on the extensibility in the

    Alveogram

    Figure 13: Potential reasons for futuregrowth of the bakery enzyme market

    Figure 11: Effect of sulfhydryl oxidase on crumbcolour of steamed bread. Wheat flour: DNS/

    CWRS; normal proof

    forMoreinforMation:

    Mhlenchemie GmbH & Co KG

    Kurt-Fischer-Str. 55

    22926 Ahrensburg

    Germany

    Tel: +49 4102 202-001

    Fax: +49 4102 202-010

    Email: [email protected]

    Website: www.muehlenchemie.de

    Grain&feed millinG technoloGy38 | Ju-augus 2009

    FeatureEnzymes

    I ll r i i rl l r r F ir i ,I i , l

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  • 8/14/2019 Enzymes in breadmaking: Economic relevance, markets & future perspectives

    5/5

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    Asubscriptionmagazine for the global flour &feedmillingindustries-first publishedin1891

    August 2009

    Growingconcerns overmycotoxins

    Enzymes inbreadmaking:Economic relevance,markets,and futureperspectives

    In this issue:

    V acuumpla ysanimportantrolein

    deliveringmicro-ingredients

    tolivestock

    A re y ou r ea dyfor newcrop?

    F OC US :E ur op e

    Flouradeliverysystem

    for vitaminsandmineralsreceivesWHO

    endorsement

    Preservingfeedmaterialsafter harvesta multifaceted

    approach tomycotoxins

    GFMT0904.indd 1 9/07/ 009 15:48

    ThisdigitalRe-printispartoftheJuly|August2009editionofGrain&FeedMillingTechnologymagazine.

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    general, to an estimated cost of almostUS$300 million by 2011.

    Inthesameperiod, thetotalmarket forfood enzymesisexpected to growat a rateofalmost sixpercent to about US$1.2 billion.

    Thisgrowthissupportedby theper-ceptionthatenzymesarea naturalway

    toimproveefficiencyandqualityandthatchemicalscanbereplaced,avoidinglabellingoromittingenumbers. ecliningpricesdue

    tocompetitionofsupplyandconsolidationofthefoodindustry,provideadditionalimpetus.

    ost ofthenewenzymeswillbe pro-duced withgenetically modified organisms,and someofthe enzymeswillevenbeproteinengineered, that is, theiroriginalsequenceofamino acidswillbemodified,althoughthereissomemarket resistanceagainst enzymesfromgenetically modifiedorganisms.

    sinthe past years, thepropertiesof

    existing enzymesand enzymecombinationsareconstantly beingimproved, creat-ing a widerfield ofuseand increas-ing demand. Themost efficientdriving force forgrowthstillwillbeinnovation.

    Threemarketshavebeenselect-ed to visualise

    thedevelopmentof the bakeryenzymesegment,

    theUS, theEUand China.

    FortheUS theaverage annualgrowth rate isinterpolated tobe7.2 percentuntil2010 (seeFigure 5), withrevenues ofabout US$70million at theend of theperiod.

    The EUstarts from ahigher level,but due to asmaller growthof .5 percent

    the market willhave a volumeof only US$80million in 2010(see Figure 6).

    Theexpectedgrowthrate of theChinese mar-

    Figure3:Tropicalised heatinTamil adu,India,closetotheequator.Coconutand heatgroin gin

    thesameecosystem(agarajan,2006)

    Figure4:Globalenzymemarket,2006(left)and2011(right).Combined

    figuresfromFreedonia(2007)andhlenchemieestimates

    G r in&feed illinG techn lGy Ju- ugus 2009|35

    Fe ture Enzymes

    Beapart ofthe

    4TH ANNUAL IAOM

    EURASIADISTRICT

    CONFERENCE& EXPO

    TechnicalProgram

    Whats New Program

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    RegisterToday!

    Whats inStore?

    Organized bythe

    InternationalAssociationofOperativeMillers

    and the

    InternationalIndustrialAcademy

    September 23-25,2009

    InternationalIndustrialAcademy

    Moscow,RussianFederation

    GFMT0904.indd 35 9/07/ 009 15:56

    dough-strengthening disulfidebridges.

    In addition, oxidation gelation of pen-

    tosans via feruloyl residues may occur,

    increasing the water absorption. n

    undesirable side-effect of the above

    oxidases is their action on unsaturated

    lipids, which creates an unpleasant off-

    flavour.

    Inparticular bakery itemsfromfrozen

    and sheeted dough, suchascroissants, may

    beseverely affected. Therefore, theuseof

    glyco-oxidasesasa generalflour-improving

    enzymeisnot recommended.

    Sul fhydr y l o x i da se( S , EC 1. 8. 3.2)

    specifically oxidizes sulfhydryl groups in

    proteinand peptides. Hydrogenperoxideis

    also formed inthisreaction. But inrelation

    to thenumberofoxidized sulfhydrylgroups,

    muchless hydrogenperoxideis formed by

    S t ha nby g l y c os i deo xi da ses .

    I nba k i ng t r i al s , S f r o m S . c er ev i-

    siaeshowed good potential, inparticularin

    applicationsinvolving laminationsteps and

    prolonged fermentation.

    Figure10shows acomparisonofglucose

    oxidaseandS insteamedbreadbakingtrials.

    Furthermore, a partial replacement

    of ascorbic acid used as a dough stabi-

    I r v in i n r r tiSev er al o x i da sesha v ebeenpro po sed

    and arebeing used forimproving thebaking

    propertiesofflour, inparticulardoughstabil-

    ity and mechanicaltolerance.

    Thecommonprinciple ofmost oxidases

    applied inbaking istheiractiononmono-or

    oligosaccharidesorotherglycosides, creating

    a carboxylgroup and hydrogenperoxides.

    Thehydrogenperoxide thenactsas a non-

    specific oxidant, oxidizing availableelectron

    donorsindough, including sulfhydrylgroups.

    This

    r esult s i nt hecreation or

    protectionof

    Temperaturesabove200 C, lowerfinal

    product humidity and baking powder, inpar-

    ticularwithammoniumbicarbonate, increase

    acrylamidevalues, whereasyeast fermenta-

    tionreducesthem.

    The decomposition of the precursor

    asparagine by asparaginase, Innovase SP,

    is an effective means to reduce the acryla-

    mide formation. The enzyme is active in a

    pH range of 5-8.5 and at 30-65C hence in

    an optimum range for most baking app lica-

    tions. In crispbread trials Innovase SP

    reduced acrylamide to less than 25 per-

    cent, and in wafers Innovase SP reduced

    it to about 10 percent of the original level

    (see Figure 9).

    Figure9: crylamidereductionbyInnovase SPincrispbreadandafers

    Figure10:Comparisonofglucoseoxidaseandsulfhydryloxidaseinsteamedbread. heatflour:

    S/CRS; basictreatment:40ppmascorbicacid( c);over-proofedsamplesonly

    T l 2 :E ff c t f F E n t h l v r m

    s ti n ti m 2 mi n s ti n ti m 12 m in

    % L /L l L /L l l

    . 1 2 1 3 51 1 . 2 5 . 8 1 1 23 3 34 . . 3 4. 8

    . 2 1 1 1 1 3 4 1 . 5 . 8 3 1 22 3 2 . 5 . 5 .

    . 4 1 8 8 3 3 3 1 . 2 . 4 8 5 1 15 3 24 . 5 8 .8 3 .2

    . 8 1 1 1 3 4 . 1 5 . 1 1 32 3 25 . 5 8. 2 1 .

    .12 5 1 1 3 3 5 1 . 8 4 5 8 .5 4 1 3 3 . 5 5 5 .2 1 1. 8

    .14 4 1 2 3 4 . 5 58 . 1 1 4 3 . 51 5 . 1 .3

    .1 8 8 1 33 3 5 . 5 . 8 1 4 3 . 4 5 .8 1 4. 4

    .2 8 1 1 3 3 2 . 2 5 .1 3 1 4 5 2 8 . 4 4 5 5. 1 5 . 8

    Gr in feed i llinG techn lGy Ju- ugus 2009 | 37

    Fe t u e En

    -RUMINANTS

    EnzymesPhosphorus

    requirements ofdairy cows

    Practicalgrazingsystems

    DairyHeifersurvivalOmega-3fatty

    acids andfertility

    PIGS

    MineralsTryptophan

    requirementsFeedprocessing

    technologyStarterpiglet

    systemsOrganicacids in

    pigdiets

    RAPESEEDCO-PRODUCTS

    Feedingtoruminants

    FeedingtopigsCommodity trends

    GENERALPAPERS

    Oxidative stressandanimalperformance

    Mycotoxins &mycotoxinbinders

    Assessmentofnutritive value offeeds

    Potentialapplications of GMtechnology

    Legislationonenvironmentalimpact

    Impacts of climatechange onlivestocksystems

    9th 10th September2009SuttonBoningtonCampus

    InternationalFeedConference

    Nowinits43 rd year& stillgoingstrong

    This meeting has beenheldannuallysince 1967atthe University ofNottinghamSuttonBoningtonCampus(Schoolof Biosciences;the bestSchoolofitskindinthe UK).

    The meetingattracts delegates fromallparts of the FeedIndustry as wellas University /ResearchPersonnelandGovernmentpersonnel.Itis anexcellentexample of Technology Transfer.

    The Programme Committee consists ofUniversity staff andcolleagues fromtheAnimalFeedIndustry.

    Between16and18invitedpapers arechosenrelevanttoboththe scienceandthe practice of AnimalNutritionpresentedby recognisedauthorities fromEurope butalsoworldwide.

    Details may be foundat:

    www.nottingham.ac.uk/feedconf/

    What can conference delegates expect?

    Topicalsubjects|Speakersof thehighestquality| Interactiveatmosphereallowingex cellent l iais onb et w eendeleg at es &speakers|NEWensuite bedrooms|Free24/7Internet access| Extremelywell-stockedLibrary|State-of-the-ArtConferenceCentre|Bar/Social complex|BrandnewSportsHallwithmulti-gym,etc

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    Youropportunitytolearnaboutlatestdevelop-mentsofGLOBALGAPandhaveaninputintotheStandard!1.Joininand haveyour sayontherevised contentfor

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