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NON-THERMAL PROCESSING TECHNOLOGIES AND DAIRY PRODUCT QUALITY Geoffrey Smithers , Cornelius (Kees) Versteeg, and Jay Sellahewa CSIRO/Food Science Australia FIL-IDF Dairy Science and Technology Week Québec City, Québec, Canada May 14th, 2008
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NON-THERMAL PROCESSING TECHNOLOGIES AND DAIRY PRODUCT QUALITY

Geoffrey Smithers, Cornelius (Kees) Versteeg, and Jay Sellahewa

CSIRO/Food Science Australia

FIL-IDF Dairy Science and Technology WeekQuébec City, Québec, Canada

May 14th, 2008

OUTLINEBrief history of dairy processing

The ‘dairy tree’‘Foundation’ dairy products/commoditiesremain backbone – differentiation criticalNew millennium dairy products/ingredients – processing innovation

Future dairy processing technologiesHigh pressure processing (HPP)Power ultrasonics (‘powersonics’)Pulsed electric field (PEF)Cold plasma

Summation – what’s on/over the horizon

MILK – THE RAW MATERIAL WE PRIZE!

Protein and fat components impart a range of desirable properties to food, foundation for dairy products/ingredients, nutritionOther components (minor lipids, peptides, minerals, lactose) andprocessing can modulate their functionality

0.32Minor (vitamins, acids)

0.65Minerals

3.9Fat

4.6Lactose

3.3Protein (casein, whey)

87.3Water

Content(%, w/w)

Component

BRIEF HISTORY OF DAIRY PROCESSINGMilk, whey and colostrum considered valuable foods for thousands of years

~800 BC – calves' stomachs used to transport milk

Protein coagulation, through action of natural enzyme chymosin, spawns start of the cheese (and whey) industry

Processing, often thermal, used to:Ensure safety and quality, extend shelf-lifeAllow for storage, transport and distributionReveal/transform functionality of components – products and ingredients

Modern food industry demanding more:Functional dairy proteins/peptides, lactose, lipids, minerals

EVOLVING ‘DAIRY TREE’Milk Ingredients

Liquid Milk, Milk ConcentratesMilk Powders, Milk Powder Replacers

Milk Protein Products/IngredientsCheese, yoghurt, other fermented productsTotal Milk Proteins, CoprecipitatesWhey-based and Casein products

Milkfat ProductsCream, butter, anhydrousmilkfat

Newer Dairy IngredientsSpecialized powder blendsBioactive peptidesProtein fractions (eg, lactoferrin)

Australian Dairy (1996)

processing science & technology

‘FOUNDATION’ DAIRY PRODUCTS –FUTURE OF PROCESSINGEfficiency gains, quality improvements, differentiation

Cheese, other fermented productsNew coagulants, better startersBetter tasting, low fatSpeedier, predictable maturationQuality enhancements, lower cost

PowdersCost-effectiveness improvements –membrane processing, evaporationMembrane processing and spray dryingenhancements – better and newfunctionality

“Consumers are demanding ‘miracle foods’that are totally natural, have zero calories, zero fats and cholesterol,

delicious taste, total nutrition, low price,environmentally-friendly production,

‘green’ packaging . . . and that guaranteeperfect bodies, romance and immortality”

– Carol Brookins

FOOD MARKETPLACE IS FAST MOVING AND DEMANDING!

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FUNCTIONAL FOODS REVOLUTION!Global market size >$75b (Just-food.com, 2006/07)

USA > $20b, 14% growthOther markets – EU, Japan8% growth/yr globally

Global market size forecast > $100b by 2010

Industry demands quality, economical, novel and substantiated ingredients

Dairy ingredients excellent choice – nutritious, functional, widely available

Science and technology of dairy component processing and transformation forms essential foundation to successful commercial products

Global functional foods market

“(Increasing) consumer demand for new foods and changes in eating habits and food safety risks are

affecting the food processing industry. The population is becoming older on average; moreover, consumers want fresh and minimally processed foods without

synthetic chemical preservatives. To address the need for safer food and compete for consumer acceptance, manufacturers are exploring new food processing and

preservation methods.”– Don Zink, Nestlé

FUTURE FOOD (DAIRY) PROCESSING

“High Pressure

Processing”

WHAT IS HIGH PRESSURE PROCESSING (HPP)?

Very high pressure exerted by water (up to 700 MPa = 100,000 psi)

Distributed evenly and instantly throughout (water-based) foodKeeps food from being crushed

Microbial (and some enzyme) inactivation without off-flavors, color degradation, and other quality loss associated with heat

EFFECTS OF HIGH PRESSURE

As above, plus equilibria may changeFood systems

Some change in conformationMacromolecules

Generally not affectedSmall molecules (eg, flavors)

Selectively inactivated or activatedEnzymes

Many inactivated, some easilyViruses

Vegetative cells – inactivatedBacterial spores – not inactivated (yet)Fungal spores – some inactivated

Microorganisms

InactivatedParasites

EffectMaterial

HPP INACTIVATION OF SALMONELLAValencia juice, pH 4.2

Pressure (MPa)

Initial cf

u/mL

103

105

107

300 450 600525375

> 300 sec

< 15 sec15 sec

30 sec45 sec

LISTERIA UNDER PRESSURE Leakage of cell contents through holes in membrane

Control450 MPa, 300 s 600 MPa, 180 s

PROTEIN STATES UNDER PRESSURE

Atmospheric pressure 100-200 MPa

>300 MPa

>1000 MPa >3000 MPa

Effects on covalent bonds

Molten globuleMonomerOligomer Unfolded

Note: Water turns into ice >1000 MPa at room temperature

Aggregation

HPP EFFECT ON CASEINSIncreased supernatant caseins – dissociation/shrinkage of micellesPartially reversible with time (and temp.) change

(a)

0

20

40

60

80

UM HM PM200 PM400 PM600% N

on-s

edim

enta

ble

Indi

vidu

al P

rote

in

(w/w

in

UM)

Supernatant a-casein (green),κ-casein (purple), ß-casein (red/brown)

HPP EFFECT ON WHEY PROTEINS

0.0

1.0

2.0

3.0

0 10 20 30Time (min)

Con

cent

ratio

n (g

/L)

alfa 600 beat 600alfa 300 beta 300alfa 150 beta 150

0

0.1

0.2

0.3

0.4

0.5

0 10 20 30Time (min)

Con

cent

ratio

n (g

/L)

PeptidesBSAlactoferrin

Stockmann et al. (2004)

Substantial (~75%) denaturation of ß-lactoglobulin at 600 MPa, 10 min

HPP EFFECT ON ANTIMICROBIAL ACTIVITY OF LACTOFERRIN

0.0

1.0

2.0

3.0

4.0

5.0

6.0

7.0

culture control LF untreated control LF 600MPa, 5 min

LF sample

Viab

le c

ount

of S

alm

. Typ

him

uriu

m

(Log

CFU

/ml)

Wan et al. (2005)

High pressure has no measurable effect on

anti-microbial function of Lf

HPP EFFECT ON LACTOPEROXIDASE

0.00

0.05

0.10

0.15

0.20

0.25

0.30

0.35

0.40

0.45

0 5 10 15 20 25 30 35

Time (min)

Abs

orba

nce

(405

nm

)LP untreated controlLP 600 MPa, 5 min

Wan et al. (2005)

At cold pasteurization conditions using high

pressure, 75% of LP is retained

SEMI-CONTINUOUS HPP PROCESSING OF LIQUIDS

Typical output = 3,000 L/hr

COMMERCIAL DEVELOPMENTS Dairy-based sandwich fillings from SpainCold pasteurized colostrum products from New Zealand

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COMMERCIAL DEVELOPMENTS Dairy desserts from Meidi-Ya in Japan Cold pasteurized probiotic cultures withextended shelf-life from New Zealand

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‘SNAPSHOT’ OF HPP CAPABILITY AT FOOD SCIENCE AUSTRALIA

Screening Trial

Time (s)

0 10 20 30 40 50 60 70

CFU

/ml

100

101

102

103

104

105

106

107

2472 2655 2657 2345 2340 2343 2542 2341 2342

35L, 100,000 psi, 0 –121oC, food grade pilot factory

2 & 3L (contained), 90,000 psi, challenge studies (real pathogens, real foods)

5 mL kinetic, 100,000psi, -20 – 121oC

Multidisciplinary team of experts!

POTENTIAL DAIRY APPLICATIONS FOR HPP

Not a panacea, niche products and/or applications for specific marketsYogurt/dairy dessert/smoothies manufacture

less syneresis, firmer texture, less solidsshelf-life, enhance probiotic activity

CheeseIncrease speed of maturation, arrest at specific timeImprove textureRaw milk cheese with safety (requires regulatory approval)Fresh curd cheeses, cheese based spreads – extend shelf-life

Enhance functionality of specific/specialized powders (eg, solubility)Milk, colostrum and whey bioactives (eg, lactoferrin and others)

Cold pasteurization while maintaining bioactivity

“Power Ultrasound”

PRINCIPLES OF ULTRASOUND

Ultrasound causes tiny bubbles, naturally present in a liquid, to expand and contract thousands of times every second to the point where the bubble collapsesAt the time of cavitation, the temperature inside the bubble reaches 5,000°K and 2,000 bar pressure ‘The Bubble’

POWER ULTRASONICS – FAST MOVING!

Sound waves over 18 kHzNeed medium to propagateEquipment from 20 to 1,000 kHzVery specialized engineering design and application understandingPower(sonics) increasing – High Power Ultrasonics (HPU)Commercially scaleable

ULTRASONICS IN BIOLOGICAL SYSTEMS

Colloidal disintegration and dispersion

Cell wall/particulate dispersion – rheology

Cell rupture - bioavailability, extraction

Intracellular disruption Viability

Mass transfer Extraction, infusion

Excitement Fermentations

Incr

easi

ng in

tens

ity

The bubble cloud at tip of sonotrode

EFFECTS OF ULTRASONICS

Size reduction and reactions can occurFood systems

Structures disrupted, functionality may be affected

Macromolecules

Reactions and free radicals, flavor may be affected

Small molecules

Selectively inactivated/activatedEnzymes

NoViruses

Little effect in isolationCan significantly enhance effects of other treatments (eg, low heat)

Microorganisms

YesParasites

EffectMaterial

ULTRASONIC PRODUCT MODIFICATION – DAIRY EXAMPLE I

Viscositymanagement

Thickeningand thinningGelationWaterbinding

Particle sizereduction and agglomeration

Hydrocolloid polymer cleaving – “nano-milling”

Crystallization management

Particle Size Distribution

0.01 0.1 1 10 100 1000 3000 Particle Size (µm)

0

1

2

3

4

5

6

7

8

9

10

Volume

(%)

Untreated whole milkUltrasound homogenization of whole milk

Mawson, Simons, Bates et al. (2005)

UF OF WHEY – ULTRASONIC FLUX IMPROVEMENT – DAIRY EXAMPLE II

0

5

1 0

1 5

2 0

2 5

5 0 0 5 5 0 6 0 0 6 5 0 7 0 0 7 5 0 8 0 0 8 5 0 9 0 0 9 5 0 1 0 0 0

C ro s s f lo w ra te (m l/m in )

Perm

eate

Flu

x (l/

m2 h)

w ith U ltra s o u n d

w ith o u t U ltra s o u n d

Steady-state flux after 4 h permeation of 6% whey at 300 kPa transmembrane pressure

Production cycle enhancements of 20 - 70%, some benefits during cleaningNo apparent damage to membranes or whey solutions

with ultrasound

without ultrasound

Mawson, Simons et al. (2006)

‘SNAPSHOT’ OF HPU CAPABILITY AT FOOD SCIENCE AUSTRALIA

25 kHz Laboratory focused and radialsonotrodes (400 W and 1 kW)Laboratory flow-through cellsLaboratory kinetic reaction vesselSonifier spray nozzleCommercial scale flow-through,focused and radial sonotrodes (8 kW)Pilot-scale tank system (8 kW)

40 kHz20 litre tank (500 W)Commercial scale, pentagonal focused flow-through cell (500 W)

1 MHzTank plate transducer

Ultrasonic cutting knife (1 kW, 20 kHz)

FUNCTIONAL APPLICATIONS OF HPU IN DAIRY PROCESSING

Extraction, separationEmulsification, mixingEnzyme activation, inactivationCrystallizationDegassing and defoamingSpraying/coatingEncapsulationHigh-shear mixing, homogenization, viscosity modulationLow temperature dryingPasteurization at lower temperature?

The ‘bubble cloud’ at tip of sonotrode

Cost-effective!

“Pulsed Electric Field”

WHAT IS PULSED ELECTRIC FIELD (PEF) PROCESSING?

Application of high voltage pulses (up to 50 kV/cm) to target product/liquid

Product/liquid becomes part of ‘electrical circuit’Several short pulses, treatment times of microsecondsVarious wave shapes possible, differ in effectivenessMainly inactivates vegetative microbial cells

Some concurrent heating, temp. control importantSuitable for liquid streams, continuous operationSmall (2,000 L/h) and larger (10,000 L/h) commercial units available - commercialization in progress (juice and water) . . . is dairy next?

PEF PROCESSING SYSTEM

Intensity 20 - 50 kV/cmPulse duration 1 - 10 µsecTotal treatment time 10 – 50 µsec

Charging Resistor High Voltage Switch

Supply Power

Food

CapacitorEnergy Storage

Chamber Treatment

PumpTemp Control

Temp. Control

Feedingtanks

Collectiontank

Pulse Generator

TreatmentChamber

HV PowerSupply

Capacitor

CELL DAMAGE AFTER PEF TREATMENT

Control Cell PEF Treated CellBarbosa-Canovas, Washington State Univ.

Saccharomyces cerevisiae (yeast) in apple juice

Inactivation of natural microflora in raw milk: PEF vs. untreated vs. heat only

0.0

2.0

4.0

6.0

8.0

34.2 32.5 28.1 24.0 PEF off 72°C 15sec

63°C 30min

PEF treatment (kV/cm) on incubated raw milk , monopulse, 55°C, 1 ml/sec

Viab

le c

ount

(log

cfu

/ml)

0

15

30

45

60

LP (m

g/L)

TPC Y&M Eb LP

Wan et al. (2006)

PEF IN DAIRY SYSTEMS – I

Inactivation of introduced microflora in skim milk: PEF vs. heat only

0

2

4

6

8

25 30 35 40 45 50 55 60 65

Temperature (°C)

Res

idua

l VC

(log

CFU

/ml)

PEF offPEF

0

2

4

6

8

25 30 35 40 45 50 55 60 65

Temperature (°C)

Res

idua

l VC

(log

CFU

/ml)

PEF offPEF

0

2

4

6

8

50 55 60 65 70 75 80 85

Temperature (°C)

Res

idua

l VC

(log

CFU

/ml)

PEF offPEF

Pseudomonas fluorescens ATCC948

Salmonella typhimurium ATCC14028

Enterobacter faecalis ATCC19433

0

2

4

6

8

45 50 55 60 65 70 75 80 85Temperature (°C)

Res

idua

l VC

(log

CFU

/ml)

PEF offPEF

Listeria monocytogenes NCTC11994

PEF IN DAIRY SYSTEMS – II

Wan et al. (2006)

5 log reduction <50˚C

6 log reduction <70˚C

6 log reduction <60˚C

5 log reduction <55˚C

PEF CAPABILITY AT FOOD SCIENCE AUSTRALIA

Laboratory-scale system (from Ohio State Univ.), suitable for initial scoping work

Up to 10 L/hr

Laboratory-scale system (from Ohio State Univ.), suitable for initial scoping work

Up to 10 L/hr

Pilot-scale system (from Diversified Technologies), suitable for ‘proof-of-concept’and piloting work

Up to 300 L/hr; 1,000 L/hr for low conductivity fluids

Pilot-scale system (from Diversified Technologies), suitable for ‘proof-of-concept’and piloting work

Up to 300 L/hr; 1,000 L/hr for low conductivity fluids

POTENTIAL DAIRY APPLICATIONS FOR PEF

Lower temperature pasteurization

Extending shelf-life of pasteurized liquids

Maintenance of biological activity/efficacy of ‘bioactive’ dairy ingredients (eg, lactoferrin, lactoperoxidase, immunoglobulins) during ‘pasteurization’

Improved heat stability of some dairy proteins?

Enhanced extraction of components (possible role in fractionation of MFGM?)

“Cold Plasma”

ver069 3

WHAT IS COLD PLASMA?

Plasma is gas excited to the point where it releases electrons

Fully ionized gas of low density

Also known as the fourth state of matter

Generally contains ions, atoms, singlets, photons and electrons

Cold plasma is partially ionized gas at 30 - 60°C

Usually maintained under vacuum, although atmospheric pressure cold plasma is achievable

COLD PLASMA SYSTEMSPrototype system in The Netherlands (courtesy HennieMastwijk, ATO, The Netherlands)

Prototype system in The Netherlands (courtesy HennieMastwijk, ATO, The Netherlands)

Prototype microwave cold plasma bench unit developed by Prof Tran and Innovative Foods Centre at FSA

Prototype microwave cold plasma bench unit developed by Prof Tran and Innovative Foods Centre at FSA

MICROWAVE COLD PLASMA

Atmospheric and low pressure cool plasma treatment of B.subtilis

012345678

0 200 400 600 800

Treatment time (seconds)

Red

uctio

n lo

g nu

mbe

r

Atmospheric,Loughborough (UK)UV, Loughborough (UK)Low pressure,Swinburne (AUS)

Prototype microwave cold plasma pilot unit developed by Prof. Tran and Innovative Foods Centre at FSA

Prototype microwave cold plasma pilot unit developed by Prof. Tran and Innovative Foods Centre at FSA

Cold plasma inactivates microbial spores!Cold plasma inactivates microbial spores!Different size units (lab, bench and pilot)

Enhanced hygiene/ treatment of pathogens on equipment and food surfaces (meat, fruit), and powders (dairy)

ADVANTAGES AND CHALLENGES

Effective microbial inactivation on irregular surfacesShort exposure time requiredLow energy requirementNo chemical residuesMinimal surface change

Barriers . . .Depth of penetrationScale up of the effectSurface oxidation could limit application

Attractiveness . . .

POTENTIAL DAIRY APPLICATIONS FOR COLD PLASMA

Surface pasteurization and disinfection of:Irregular shapesDairy powdersDairy processing equipmentPackaging materials

Surface coating Deposition of vitamins and sensitive bioactive compounds to food surfaces (dairy and non-dairy)

SUMMING UP . . .Food marketplace demanding, fast moving

Functional foods revolution, burgeoning opportunity

Process efficiencies, quality enhancements will continue

Processing innovations will form foundation for new and differentiated dairy products/ingredients

HPP, powersonics, PEF, cold plasma

On/over the horizon . . .High pressure sterilization of heat-sensitiveproductsModulation of ingredient behavior using emergingtechnologies becomes ‘mainstream’PEF for extraction

ACKNOWLEDGEMENTSScience and technology colleagues and their teams

‘IFC team’, Mary Ann Augustin, Jason Wan, Kirthi De Silva, Louise Bennett, Roderick Williams, Lloyd Simons, Raymond Mawson, Sandani Udabage, Peerasak Sanguansri, Darren Bates, and others

Funding supportCSIRO, Food Science Australia,Victorian Govt., Dairy Australia,Monash Univ., Melbourne Univ.,Swinburne, Food Futures Flagship

Australian dairy companies

MERCI!


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