Dairy matrices: effect of processing and composition on microstructure and nutritional properties Sylvie Turgeon, Laure Rinaldi, Erik Ayala-Bribiesca

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Dairy matrices: effect of processing and composition on microstructure and nutritional properties Sylvie Turgeon, Laure Rinaldi, Erik Ayala-Bribiesca 30 mai 2011

Michel Britten, Sylvie Gauthier, André Marette Laure, Erik, stagiaires Personnel de recherche AAC et U. Laval (STELA- INAF) Projet Action concertée Novalait, AAC, FQRNT, MAPAQ

Context Effect of food structure on nutritional value Diversity of dairy products structural organization Aim of the research project Two major dairy components studied: Proteins and lipids and possible effect of kinetics of their digestion and absorption Conclusion/ perspective

Nutritionist and gut physiologist study foods based on their composition Structure is usually not considered Digestion is a complex process Definitions

Bioaccessibility -Release of the nutrient from the food matrix into the GI tract Bioavailability -Portion of nutrient that is absorbed and actually reach the systemic circulation

Well-known examples: Fiber reduces glycemia (rate of glucose appearance in serum); Increase in viscosity; Modification of enzymatic activity/ access to substrate, etc. Protein release vs glycemia and satiety; Lipemia (rate of lipid appearance in serum) Depends on amount and nature of dietary triglycerides and the presence of other nutrients

Diversity of dairy products structural organization Aguilera, 2005

Slow Vs fast proteins Total leucine rate of appearance in serum after ingestion Boirie et al 1997

Establish the link between physical characteristics of various dairy matrices and protein and lipid bioaccessibility and bioavailability.

Study of protein digestion in two milks with different heat treatment Laure Rinaldi

Digestion model liquid matrix Dynamic mecanical actions Digestion steps (37 C) Digestion products treatment Mixing Orbital stirring 9g of dairy product 6mL saliva - ph 6,8-20s 12mL (twice 6mL) gastric solution ph 1,3-30min 12mL duodenal soln 6mL bile 2mL NaHCO 3 ph 8,2-60min Homogenization (9500rpm, 20s) To stop enzymatic activity Adapted fromversantvoort et al. 2005

Digestion model liquid matrix Commercial milks: Pasteurised and traited by Ultra High Temperature Dairy matrix studied by Lacroix et al., 2008: different protein digestion kinetics

Gastric digestion (SDS-PAGE) results Are caseins totally digested? cns β- lg 2 repns, 10-6 g proteins/well Undig. gastric 4min Past. UHT

Gastric digestion (SDS-PAGE) results UHT cns β- lg α- la Undig. Gast.: 2min 15min 30min Pasteurised 2 repns, 4.10-5 g proteins/well Undig.: 10-6 g cns β- lg α- la

Digestion model conclusion Gastro-intestinal digestion model in vitro: able to distinguish milk digestion kinetics differences upon different industrial process

Amino acids bioaccessibility results UHT Pasteurised gastric duodenal gastric duodenal Digestion time (min) AA unbioaccessible in stomach Digestion time (min) 0,9 Free AA quickly from the beginning 2-3 times more free AA for UHT milk than pasteurised

Peptide bioaccessibility materials & methods Products of digestion from pasteurised vs sterilised milks Study of peptides with LC/MS Complex chromatograms Different appearance kinetics of peptides upon: milk selected peptide Poster 14

Digestions of milks with different heat treatment conclusion In vitro model: different digestion kinetics upon UHT vs pasteurised milk tendency agreed with in vivo study future Study of semi-liquid matrix: commercial yogurts and yogurts with controlled process study in vivo, rats

Erik Ayala Bribiesca

Importance of the food matrix Modulate nutrient release Cheddar cheese: model dairy matrix Well-known solid matrix Commercial and industrial importance Standardized production parameters Source of calcium and lipids

Cheese as a model matrix Interaction between calcium and proteins Structuring of the paracasein gel 1 Cheese under digestive conditions Interactions between calcium and lipids Pancreatic lipase effiency 2 Calcium soap production 3 Long chain fatty acids excretion 3 1 Metzger and Mistry, 1994; 1995 2 Hu et al., 2010 3 Denke et al., 1993

Calcium enrichment of the cheddar cheese matrix increases its resistance to physical disintegration during in-vitro digestion. Calcium content in cheddar cheese has an impact on lipolysis during in-vitro digestion.

Cheddar cheese production calcium enrichment CaCl 2 added during the salting process In-vitro 1 digestion of cheeses in conical tubes head-over-heels agitation with glass beads Analysis of chymes physical disintegration of cheeses pass through metal mesh (1.5 mm x 1.5 mm) lipolysis rate free fatty acids 1 adapted from Versanvoort et al. 2004

Results and discussion Physical disintegration of calcium-enriched cheddar cheeses during in-vitro digestion 100 Disintegration (%) 80 60 40 20 Gastric phase 0 4 12 mg Ca / g curds 0 Duodenal phase 0 60 120 180 240 300 Digestion progress (minutes)

Results and discussion Lipolysis of calcium-enriched cheddar cheeses during in-vitro digestion 60 60 59 Lipolysis rate (%) 50 40 30 20 10 mg Ca / g curds Duodenal phase 0 4 12 53 0 90 120 150 180 210 240 270 300 Digestion progress (minutes)

Effect of calcium supplement Slower disintegration of the matrix Faster lipolysis of accessible fat Calcium enriched cheeses had higher lipolysis rates although they presented slower disintegration rates. 100 Physical disintegration (%) 80 60 Lipolysis (%) 40 20 0 0 4 12 90 120 150 180 210 240 270 300 minutes

Analyses in process Fatty acid profiles (gas chromatography) Fatty acids present as calcium soaps Cheese matrices characterization Texture profile analysis Colloidal calcium Future works Cheese with different milk-fat fractions Potential reach Modulation of lipid bioaccessibility Possible impact on metabolic responses