Abstract

Milk proteins genetic variants have long attracted interest as they are associated with important issues relating to milk composition and technological properties. An important debate has recently opened at an international level on the role of β-casein (β-CN) A1 and A2 polymorphisms, toward human health. For this reason, a lot of efforts has been put into the promotion of A2 milk by companies producing and selling A1-free milk, leading the farmers and breeders to switch toward A2 milk production without paying attention on the potential effect of the processability of milk into cheese. The aim of the present work was to evaluate the effects of β-CN, specifically the A1 and A2 allelic variants, on the detailed milk protein profile and cheese-making traits in individual milk samples of 1,133 Holstein Friesian cows. The protein fractions were measured with reversed-phase (RP)-HPLC (expressed in g/L and % N), and the cheese-making traits, namely milk coagulation properties, cheese yield, and curd nutrient recoveries assessed at the individual level, with a nano-scale cheese-making procedure. The β-CN (CSN2), κ-CN (CSN3), and β-lactoglobulin (LGB) genetic variants were first identified through RP-HPLC and then confirmed through genotyping. Estimates of the effects of protein genotypes were obtained using a mixed inheritance model that considered, besides the standard nuisance variables (i.e., days in milk, parity, and herd-date), the milk protein genes located on chromosome 6 (CSN2, CSN3) and on chromosome 11 (LGB), and the polygenic background of the animals. Milk protein genes (CSN2, CSN3, and LGB) explained an important part of the additive genetic variance in the traits evaluated. The β-CN A1A1 was associated with a significantly lower production of whey proteins, particularly of β-lactoglobulin (-8.2 and -6.8% for g/L and % N, respectively) and α-lactalbumin (-4.7 and -4.4% for g/L and % N, respectively), and a higher production of β-CN (6.8 and 6.1% for g/L and % N, respectively) with respect to the A2A2 genotype. Regarding milk cheese-making ability, the A2A2 genotype showed the worst performance compared with the other genotypes, particularly with respect to the BA1, with a higher rennet coagulation time (7.1 and 28.6% compared with A1A1 and BA1, respectively) and a lower curd firmness at 30 min. Changes in milk protein composition through an increase in the frequency of the A2 allele in the production process could lead to a worsening of the coagulation and curd firming traits.

Highlights

  • Milk protein composition is an important factor in the nutritional and technological characteristics of milk

  • The aim of this work was to evaluate, for the first time, the effects of β-CN, and in particular the A1 and A2 alleles, on (1) milk yield and composition, (2) milk detailed protein profile expressed both quantitatively (g/L) and qualitatively (% N), and (3) 18 technological traits, including milk coagulation properties (MCP), curd-firming traits (CF), cheese yields (CY), and curd nutrient recoveries (REC), in a population of 1,133 Holstein cows, using a mixed inheritance model taking into account β-CN, κ-CN, and β-LG protein genotypes together with the additive polygenic background of the animals

  • The present study found that the CSN2 genotypes exert an effect on the MCP and cheese yield-related traits

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Summary

Introduction

Milk protein composition is an important factor in the nutritional and technological characteristics of milk. Milk protein polymorphisms are the result of SNP, nucleotide insertion or deletion, or post-translational modification (Caroli et al, 2009). These have been extensively studied in recent decades as they have a significant effect on milk yield, the protein profile, and functional properties, being responsible for changes in the quantities and proportions of the protein components of milk (Amalfitano et al, 2020) and affecting. One of the most important milk protein fractions is β-CN, which accounts for almost one-third of the total milk protein content (Huppertz, 2013) It can be found in different genetic variants, the most common are A1 and A2 (Guantario et al, 2020). Pal et al (2015) concluded that the release of β-casomorphin-7 had effects on gastrointestinal motility and proinflammatory and immunomodulatory outcomes, in both in vitro models and in vivo animal experiments

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