fermentation and enzymology as tool for functional whey

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Fermentation and enzymology as tool for functional whey ingredients/products Lutz Fischer Institute of Food Science and Biotechnology Department of BIOTECHNOLOGY University of Hohenheim, STUTTGART, Germany

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Fermentation and enzymologyas tool for functional whey

ingredients/products

Lutz Fischer

Institute of Food Science and BiotechnologyDepartment of BIOTECHNOLOGY

University of Hohenheim, STUTTGART, Germany

Water(938-943) Total Solids

(57-62)

Carbohydrates (47)-Lactose (47)

Milk Fat (0.5)- Triglycerides (0.25)- Phopholipids (0.15)- Diglycerids (0.05)- Free Fatty Acids (0.05)

Proteins (6.2)- β-Lactoglobulin (3.0)- α-Lactalbumin (1.2)- Immunoglobulin-G (0.7)- Proteose Peptone (0.6)- Serum Albumin (0.4)- Other Protein (0.3)

# Immunoglobulin-A (0.05)# Lactoferrin (0.045)# Lactoperoxidase (0.025)# Lysozyme (0.002)

Minerals (4.5)- Potassium (1.5)- Chloride (1.1)- Phosphorous (0.7)- Calcium (0.6)- Sodium (0.5)- Magnesium (0.1)- Trace Elements (0.03)

# Zinc (0.0015)# Iron (0.0006)# Iodine (0.0005)# Copper (0.0002)

NPN (0.132)- Urea (0.08)- Free Amino Acids (0.025)- Cholin (0.015)- Orotic Acid (0.012)

Vitamins (0.075)- Vitamin B5 (0.004)- Vitamin B2 (0.0015)- Vitamin C (0.0015)- Vitamin B6 (0.0005)

pH 5.9-6.6

Sweet cheese whey(components in g L-1)

Fermentation using whey

Comparison: typical chemically defined medium

glucose 10 gNH4Cl 1 gK2HPO4 0.5 gMgSO4 • 7 H2O 0.2 gFeSO4 • 7 H2O 0.01 gCaCl2• 2 H2O 0.01 gNaCl 0.5 gtrace element solution 1 ml

component amount/L

„molecular formula“ of a bacterial cell :C1 H1.6 O0.5 N0.15 P0.01 S0.001 (elemental analysis)

Whey is an undefined natural complex medium

The quality and/or quantity of the carbon/energy

source and the nitrogen source is an issue

The quality and/or quantity of the carbon/energy

source and the nitrogen source is an issue

- β-galactosidase activity- additional nitrogen source(s)

- β-galactosidase activity- additional nitrogen source(s)

pasteurizationor sterilization (?)

WP as fermentation medium

ò yeasts (GRAS) K. marxianus* YX/S 0.48-0.52

ò feedò (food)

ò yeasts (GRAS) K. marxianus* YX/S 0.48-0.52

ò feedò (food)

Processed whey concentrates(deproteinized)

Single cell protein(SCP)

Single cell oil(SCO)

Biosurfactants(SL)

ò yeasts, fungiCryptococcus curvatus

ò triglycerides (27 g L-1)

è N-limitationè unsaturated FA

(ca. 50% oleic acid)è possible use: biodiesel

ò yeastsCandida boidinii

ò biotensid (420 g L-1)

è on cell debris fromC. curvatus

Syldatk, C. (2006) Lecture Stuttgart*Schultz et al. (2006) AMB 69, 515

sophorose lipid

Chervaux et al. (2000) AEM 66. Vol. 12. 5306

Lactic acid bacteria and whey

ò lactic acid bacteria need a huge number of supplements (auxotrophic)

ò typical complex medium: MRS(peptone, meat extract, yeast extract, glucose, salts, minerals)

ò production of L. casei using supplemented and diluted, partly deproteinated wheya

(from powder)è supplements: ammonium salts (2.5 g L-1), yeast

extract (0.25 g L-1)

è biomass yield to lactose: YX/S =0.165 kg kg-1

ò lactic acid bacteria need a huge number of supplements (auxotrophic)

ò typical complex medium: MRS(peptone, meat extract, yeast extract, glucose, salts, minerals)

ò production of L. casei using supplemented and diluted, partly deproteinated wheya

(from powder)è supplements: ammonium salts (2.5 g L-1), yeast

extract (0.25 g L-1)

è biomass yield to lactose: YX/S =0.165 kg kg-1

aMondragon-Parada et al. (2006) ABB 134, 223

by-products: lactic acid and EPSby-products: lactic acid and EPS

q production of pure L(+)- or D(-)-lactic acid*- 80.000 t anno-1, 90% by LAB fermentation- polylactic acid: biodegradable polymers- synthon in chemistry- food: preservative, flavour agent, acidity adjuster

q production of pure L(+)- or D(-)-lactic acid*- 80.000 t anno-1, 90% by LAB fermentation- polylactic acid: biodegradable polymers- synthon in chemistry- food: preservative, flavour agent, acidity adjuster

pH 5.5, 37°C, 4 g L-1 h-1

+ yeastextract

*Review see: Panesar et al. 2007, Food Chem. 105, 1

continuous production using immobilised cells (entrapment by gels)--> productivity

12 g L-1 h-1

continuous production using immobilised cells (entrapment by gels)--> productivity

12 g L-1 h-1

Lactic acid production in whey

Lactose(Gal-Glu)

enzymatic hydrolysis

Lactose-free milk, whey products- Increased digestibility, sweetness, solubility

chemicalisomerisation

Lactulose (Gal-Fru)- Most popular laxative- 10-times value of lactose- Prebiotic (FOSHU list)- Baby foods as bifidogenic factor- Increased sweetness, solubility

transgalactosylation

Galactosyl oligo-saccharides (GOS)- Increased solubility- Prebiotic (baby foods)- Laxative

Catalysis on lactose

Harju, M. (2001) Int. J. Dairy Technol. 54

Vivinal® GOS

enzymaticcatalysis ?

q reversed hydrolysis (thermodynamically controlled)

§ aw-value§ concentration

donor/acceptor

q transgalactosylation (kinetically controlled)

§ nucleophilic character

§ concentration of acceptors

trans-galactosylation

- R2OH (nucleophile)

Glycosidase

+ R2OH (nucleophile)

+ R1OH

*HO

O

O R1

OH

OH

HOCH2

HO

O

O

OH

OH

HOCH2

HO

O

O R2

OH

OH

HOCH2

Glycosidase+

reversed hydrolysis

- H2O

Glycosidase

+ H2O

+ R1OH

*HO

O

O R1

OH

OH

HOCH2

HO

O

O

OH

OH

HOCH2

HO

O

OH

OH

OH

HOCH2

Glycosidase+

Glycosidase

Synthesis using a hydrolase?

q Pyrococcus furiosus (extremophilic species of Archaea)

q enzyme CelB:

β-glucosidase as well as β-galactosidase activity

q stability: t1/2 (100°C) = 85h, t1/2 (110°C) = 13h

q CelB produced in E. coli (1 mkat L-1 = 16.6 Mill. U L-1)

geothermal heated marine sediments(Stetter, Uni Regensburg)

Quelle: ArchiMeDes

Unusual biocatalyst

- covalently immobilised Cel B- whey UF permeate- at 75°C

- covalently immobilised Cel B- whey UF permeate- at 75°C

1: column, optimum temperature

2: immobilised enzyme (Cel B)

3: substrate solution (processed whey)

4: water bath

5: pump

6: product solution

34

5

6

1

2

Expanded Bed =>Htotal

_________

Hbeads

Expanded bed reactor system

1.441.250.96Lactulose [g/L]

11.028.205.9345.61Lactose [g/L]

10.6216.2

10.6214.9

3.844.6

Lactulose [g/L]yield [%]

39.6162.3

33.6568.0

20.8180.2

105.13Lactose [g/L]hydrolysis [%]

+0.5 M Frc

1.752.8

1.712.5

2.363.1

Lactulose [g/L]yield [%]

48.0956.1

41.5662.1

34.1168.9

109.66Lactose [g/L]hydrolysis [%]concentr.

+0.1 M Frc

6.8320.6

6.4718.1

5.6615.1

Lactulose [g/L]yield [%]

10.9575.2

8.4980.8

6.6884.9

44.17Lactose [g/L]hydrolysis [%]

+0.5 M Frc

4.23.32.4yield [%]

75.882.087.0hydrolysis [%]diluted+0.1 M Frc

2.01.61.3start t0

Htotal/HbeadssugarWhey-UF-permeate

Continuous lactulose synthesis

Selective protein hydrolysis

ò whole cell fermentation

ò commercially available enzymes(pancreatic proteases, etc.)

ò proteases from dairy starter cultures

ò whole cell fermentation

ò commercially available enzymes(pancreatic proteases, etc.)

ò proteases from dairy starter cultures

Japan: CalpisCalpisSwiss, Finland:EvolusEvolus

dairy products with dairy products with ACE ACE inhibitorsinhibitors

Native-PAGE of the soluble proteolytic enzymes from Lactobacillus helveticus: active-staining (H-Ala-Pro-pNA; H-Ala-pNA) and silver-staining (A: active-staining, B: silver-staining; PhastTM-Gradient-Gel 8-25, GE Healthcare Bio-Science, Uppsala, Sweden).

L. helveticus: proteolyticenzymes

relative activity [%]whole cell soluble enzymes

H-Ala-Pro-pNA 100* 100**H-Ala-pNA 8.9 67H-Pro-pNA 2.9 3.4

H-Val-pNA 0.67 3.2*100% = 81 nkat/mL **100% = 60 nkat/mL

NH2

O

N

O N

O

OH

NH2

O

N

O N

O

OH

Isoleucine-Proline-Proline (IPP) Valine-Proline-Proline (VPP)

Structural formula of the bioactive, anti-hypertensive tripeptides produced in skim milk

Structural formula of the bioactive, anti-hypertensive tripeptides produced in skim milk

N

COOH

CH3

SH

O

NN

OH COOH

(CH2)4

NH2OOH

Captopril Lisinopril

Examples of drug ACE-inhibitors [Estler and Schmidt, 2007]Examples of drug ACE-inhibitors [Estler and Schmidt, 2007]

Substrate specificity

EQLTKCEVFRELKDLKGYGGVSLPEWVCTTFHTSGYDTEAIVENNQSTDYGLFQINNKIWCKNDQDPHSSNICNISCDKFLNNDLTNNIMCVKKILDKVGINYWLAHKALCSEKLDQWLCEKL

α-Lactalbumin B (123 amino acids)α-Lactalbumin B (123 amino acids)

LIVTQTMKGLDIQKVAGTWYSLAMAASDISLLDAQSAPLRVYVEELKPTPEGDLEILLQKWENGECAQKKIIAEKTKIPAVFKIDALNENKVLVLDTDYKKYLLFCMENSAEPEQSLACQCLVRTPEVDDEALEKFDKALKALPMHIRLSFNTPQLEEQCHI

β-Lactoglobulin B (162 amino acids)β-Lactoglobulin B (162 amino acids)

Sequences of whey proteins

Conclusions

ò whey and its various formulations (permeates, powders, concentrates) can be regarded as versatile raw materials for further refinement by microbial cells or/and selective enzymes

ò there is and probably will not be „the one big process“ but a wide varity of bright biocatalytic applications to produce new functional valuablesè food industryè cosmetic industryè pharmaceutical industryè chemical industry

ò entrepreneurial decisiveness is demanded from the dairy industry in order to introduce new methods and expertise and to expand theirinterdisciplinary activities

ò whey and its various formulations (permeates, powders, concentrates) can be regarded as versatile raw materials for further refinement by microbial cells or/and selective enzymes

ò there is and probably will not be „the one big process“ but a wide varity of bright biocatalytic applications to produce new functional valuablesè food industryè cosmetic industryè pharmaceutical industryè chemical industry

ò entrepreneurial decisiveness is demanded from the dairy industry in order to introduce new methods and expertise and to expand theirinterdisciplinary activities

... and the financial support by the BMBF- AiF-FV 14787 (via FEI, Bonn)- BioChance PLUS-3 FKZ 0313137

Karin Jaindl, Timo Stressler, Thomas Eisele,Anja Manns, Sabine Lutz-Wahl, Bertolt Kranz, Wolfgang Claaßen

Prof. Dr.-Ing. Jörg Hinrichs and his group

Acknowledgement