natural hydrocolloids physicochemical properties to research … · 2018-08-25 · natural...
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Natural HydrocolloidsPhysicochemical
Properties to Research Initiatives
Srinivas Janaswamy, PhDWhistler Center for Carbohydrate ResearchDepartment of Food SciencePurdue UniversityWest Lafayette, IN 47907E-mail: [email protected]
March 29-30, 2016Itasca, Illinois, USA
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Outline• General introduction• Viscosity & Gelation• Structure-function relationships in a few
examples – Cellulose, Xanthan, Galactomannans, Gum Arabic, Alginate and Carrageenans
• Beyond food applications…
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Some food products maintain the structure, how?
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What are Hydrocolloids?• Natural • Water-soluble or -dispersible polysaccharides and
modified polysaccharides • Also called as Food Gums• Generally, they produce viscous dispersions and
gels (in some cases)
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Hydrocolloids: A few usesTo: - thicken- form gels- stabilize suspensions- bind/hold water- improve texture - stabilize emulsions- form films and coatings- encapsulate
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Hydrocolloids: A few applications• Emulsification (o/w or w/o)
– Salad dressing• Gum Arabic, xanthan
• Suspension/dispersion– Chocolate milk
• Carrageenan• Foams
– Whipped toppings• Locust bean gum
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• Protective films– Sausage casings
• Alginate• Syneresis inhibitor
– Processed cheeses• Locust bean gum, guar
Hydrocolloids: A few applications• Crystallization control
– Ice cream• many gums
• Flavor fixation– Powdered drink mixes
• Gum Arabic
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Amino
Chitosan
Sulfate
Carrageenan
CelluloseCurdlan
GalactomannanStarch
Arabinogalactan
AlginatePectin
Gellan FamilyXanthan
Carboxylate
Polysaccharides
NEUTRAL
Plant SeedSeaweed Bacterial
CHARGED
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Chemical RepeatsCellulose: 4)--D-Glc-(1
Amylose: 4)--D-Glc-(1
Curdlan: 3)--D-Glc-(1
Galactomannan: 4)--D-Man-(1 4)--D-Man-(16
1-D-Gal
Gellan: 3)--D-Glc-(14)--D-GlcA-(14)--D-Glc-(14)--L-Rha-(1
Welan: 3)--D-Glc-(14)--D-GlcA-(14)--D-Glc-(14)--L-Rha-(131
-L-Rha or -L-Man
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Hydrocolloids: Properties• Solutions behaviors are related to the
associative properties of hydrocolloids
• Hydrocolloid with regular repeating-unit sequence has a natural tendency to adopt a helical conformation
• Interactions between helices are affected by surrounding water molecules and cations (in the case of anionic hydrocolloids)
• Interactions between helices are responsible for the associative properties of hydrocolloids
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Viscosity
• Hydrocolloids become hydrated upon dispersion in water
• Hydrocolloids and water molecules interact via hydrogen bonds or ion-dipole interactions
• Upon hydration they interact with each other leading to viscosity
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Viscosity• Is dependent on molecular
size, shape and charge
• Influenced by the presence of polyelectrolytes and counter ions
• Linear chain requires more volume for tumbling (hydrodynamic volume) and gyration than branched molecule of the same molecular weight
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Junction Zones
• Junction zone bonds include– Hydrogen bonds– Ionic bonds– Covalent bonds
• If the interactions are substantialjunction zones are formed and might lead to gelation
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What controls the functionality, and How?
Molecular Shapes & Interactions!
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Molecular Shapes
• Helices are the preferred structures
• Nuclear Magnetic Resonance (solution)
• Atomic Force Microscopy: low resolution
• Diffraction techniques: high resolution
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Chemical StructuresArise from different
• Monosaccharides such as glucose, mannose and galactose• Configurations (e.g. L, D, and ) • Linkages (e.g. 13, 14 and 16) • Distributions of all of the above
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Hydrocolloids: A few examples
3. Galactomannans: Guar gum & Locust bean gum
4. Gum Arabic
5. Alginate
6. Carrageenans
2. Xanthan
1. Cellulose
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Cellulose: Chemical structure
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Cellulose
• Four crystalline allomorphs: I, II, III and IV• I: Native fibers from Valonia, ramie, cotton and wood • II: Fibers produced after regeneration (using alkali)
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Cellulose: Molecular structure
• 2-fold helix of pitch 10.4 Å• Stabilized by O3H···O5 bonds across
each glycosidic bridge oxygen atom
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Cellulose I vs. II
I
II
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Cellulose: Effect of Substitution
Cellulose Hydroxypropylmethylcellulose (HPMC)
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Xanthan• A bacterial gum• Source
– Xanthomonas campestris• Structure
– Basically a derivatized cellulose
Cellulosebackbone
Side chain
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Xanthan
Bulkyside
group
Bulkyside
group
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Xanthan• Uses
− Temperature and pH independent viscosity− Beverages
Good flavor releaseCloud stabilizer
− Frozen foodsPie fillings-increases freeze-thaw stability
− RelishesGood acid stability (0.1%)
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• Mannan backbone contains (1→6)-linked -D-galactose residues as random side groups
• Galactose/Mannose ratio: Varies from 0.3 in carob, 0.6 in guaranto 0.9 in fenugreek
• Solubility: Most galactomannans are water soluble and produce highly viscous solutions. Used as thickening agents in a variety of food systems
Galactomannans
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Guar gum• Source
– Grown in India, Pakistan and the U.S. – seed endosperm
A guar plant: Cyamopsis tetragonolobus
• Structure– Mannose:Galactose = 2:1– MW = 1-2 x 106 Daltons
• Hydrates rapidly in water and yields highly viscous dispersions
• Neutral gum & pH has little effect
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• Uses– Ice cream– Baked goods– Meat– Beverages– Dressings and sauces
Guar gum
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Locust bean gum
• Structure– A galactomannan (Man:Gal = 4:1)– MW 300,000 to 360,000 Daltons– Side chains are not uniformly distributed– Some parts of the backbone are highly substituted:
“hairy” regions, while other parts are not substituted at all: “bare” regions
• Source– Grows in the near East and
Mediterranean
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Locust bean gum• Uses
– Ice cream– Cheese products– Meat products– Chocolate substitute
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Galactomannan: Molecular structure• Mannan-like 2-fold helix of pitch 10.4 Å; the side group is turned towards
the reducing end
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Cellulose Mannan
Considerable increase in chain width causes voids in thesheet structure; ability to trap water leads to solubility
Galactomannan: Molecular structure
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Galactomannan: Packing arrangemen
a
o b
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Gum Arabic
• Structure– D-galactose, L-arabinose,
L-rhamnose, D-glucuronic acid– MW 50,000 to 3,500,000 Daltons
• An exudate gum• Source
– Acacia trees– Sudan and other African countries– Produced naturally as teardrop
shaped globules from tree barks
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Gum Arabic• Uses
– Candies: decreases sugar crystallization – Baked goods: reduces moisture absorption– Frozen desserts: formation and maintenance of
small ice crystals– Flavor fixation: retains volatile flavors and
protects from degradation
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Alginate• Source
– Brown algae, Macrocystis pyrifera• Structure
– D-mannuronic acid, L-guluronic acid– Poly(M) blocks– Poly(G) blocks– Alternating M-G blocks– M/G ratio differs depending on the source
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Alginate• Uses
– Ice cream– Bakery icings– Bakery jelly– Meringues– Salad dressings– Pimento stuffed olives– Frozen reformed onion rings
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Carrageenans• Fifteen Carrageenans: and
• -, - and -carrageenans are utilized extensively due to their greater versatility
• - and -carrageenan gel in the presence of mono (K+) and divalent (Ca2+) cations but trivalent ions (Fe3+) are needed for -carrageenan
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Structure-function relationships: Iota-carrageenan
SO3-
23
45
6
14
56
3
1
2
SO3-
3)--D-Gal-4-SO3--(14)-3,6-anhydro--D-Gal-2-SO3
- (1
Na+ form Ca2+ form
Janaswamy et al., Unpublished results
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Iota-carrageenan: Molecular Structure
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13.9 Å 13.6 Å
Na+ Ca2+Iota-carrageenan: Helix-Helix association
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Carrageenans• Uses
Puddings–“Eggless” custards
Chocolate milk–Particle suspension
Cheese products–Prevents whey separation
Ice cream–Crystallization control
Meat–Protective coating
Salad dressing–Stabilizer
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Sprinkle Supplements on Foods
Functionalized Hydrocolloids
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Recap
• Defined & Categorized Polysaccharides• Discussed hydration, viscosity and junction zones • Discussed chemical structure and solution
properties of a few Hydrocolloids• Role of hydrocolloids in developing novel
functional foods, food supplements and medicinal foods
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Food for Thought
• Do you think alginate and carrageenans would display cation dependent solution properties? If so, why?
• In a food product development, if you were given an opportunity to choose between carrageenan and xanthan which one you would prefer and why?
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