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Background & Aims: High hydrostatic pressure (HHP) processing is a non-thermal method proposed as an alternative to Holder pasteurization (HoP) for the treatment of human milk. HHP preserves numerous milk bioactive components that are degraded by HoP, but no data are available for milk oligosaccharides (HMOs) or the formation of Maillard reaction products, which may be deleterious for preterm newborns., Methods: We evaluated the impact of HHP processing of human milk on 22 HMOs measured by liquid chromatography with fluorescence detection and on furosine, lactuloselysine, carboxymethyllysine (CML) and carboxyethyllysine (CEL) measured by liquid chromatography with tandem mass spectrometric detection (LC-MS/MS), four established indicators of the Maillard reaction. Human raw milk was sterilized by HoP (62.5 °C for 30 min) or processed by HHP (350 MPa at 38 °C)., Results: Neither HHP nor HoP processing affected the concentration of HMOs, but HoP significantly increased furosine, lactuloselysine, CML and CEL levels in milk., Conclusions: Our findings demonstrate that HPP treatment preserves HMOs and avoids formation of Maillard reaction products. Our study confirms and extends previous findings that HHP treatment of human milk provides safe milk, with fewer detrimental effects on the biochemically active milk components than HoP., Competing Interests: Conflict of interest The authors declare no conflict of interest. NS is an employee of Société des Produits Nestlé S.A. Switzerland., (Copyright © 2021 Elsevier Ltd and European Society for Clinical Nutrition and Metabolism. All rights reserved.)

Campylobacteriosis has been recognized as the major bacterial food-borne infection worldwide. Campylobacter, especially C. jejuni, contaminate mainly poultry meat. Although more sensitive than other food-borne pathogens to many stresses, C. jejuni can survive food processing and go on to reach its final reservoir (the human gut). Genomic analyses of this organism indicate a lack of genes described in other gram-negative bacteria to overcome stresses. The high-pressure recovery response of C. jejuni 81-176 was analyzed from two-dimensional electrophoretic profiles of the cytoplasmic proteome. The main cellular mechanisms controlling the down- and upregulated proteins are discussed.

High pressure processing is a novel food preservation technology, applied for over 15 years in the food industry to inactivate spoilage and pathogenic microorganisms. Many studies have shown the differential resistance of bacterial cells to high pressure. Listeria monocytogenes is a bacterium able to grow at refrigerated temperature and to survive for a long time in minimally processed foods such as raw smoked fish. The freezing process does not cause significant decline of L. monocytogenes. The phase diagram of water under pressure permits a pressure treatment under subzero temperature, without the disadvantages of freezing for food quality. The aim of this study was to estimate if combined effects of pressure and subzero temperature could increase the destruction of L. monocytogenes in buffer and in smoked salmon. We investigated effects of high pressure processing (100, 150, and 200 MPa) combined with subzero temperatures (-10, -14, and -18 degrees C) and pH (7.0 and 4.5). Results showed that the most effective high-pressure treatment to inactivate L. monocytogenes was 200 MPa, -18 degrees C, and pH 4.5. The relevance of pressure holding time and the synergistic effect of pressure coupled with the subzero temperature to inactivate bacteria are highlighted. Modifications of physical properties (color and texture) were a lightening of color and an increase of toughness, which might be accepted by consumers, since safety is increased.

Effects of pressure-shift freezing and/or pressure-assisted thawing on the quality of sea bass muscle were evaluated and compared with conventional (air-blast) frozen and thawed samples. Microstructural analysis showed a marked decrease of muscle cell damage for pressure-assisted frozen samples. According to differential scanning calorimetry (DSC), protein extractability, and SDS-PAGE results, high-pressure treatment (200 MPa) produced a partial denaturation with aggregation and insolubilization of the myosin, as well as alterations of the sarcoplasmic proteins. Only small differences between high-pressure processes (freezing or/and thawing) were registered. High-pressure-treated systems led to a decrease of water holding capacity but differences between high-pressure and conventional methods disappeared after cooking. Muscle color showed important alterations due to high-pressure treatments (increasing L* and b*).

Calpains (calcium-activated neutral proteases) of sea bass (Dicentrarchus labrax L.) muscle may participate in the degradation of muscle tissue during postmortem storage. These enzymes are regulated by calpastatin, their endogenous specific inhibitor. The objective of this study was to evaluate the changes encountered by the calpain system during the postmortem storage of fish muscle after high-pressure treatment. From 100 MPa, high-pressure treatment of purified calpains results in a loss of their activity as well as in the dissociation of the heterodimeric form. In muscle, the high-pressure processing decreases the initial activity of calpain. This loss in activity may be due to an inactivation by a change of structure. Initial calpastatin activity is not modified by the high-pressure treatment, but it decreases during the storage from the beginning for a treatment at 300 MPa after which calpastatin is stable during 2 d. Therefore, this study also suggests that high-pressure treatment could be a useful way to improve fish flesh quality.

High-pressure processing is finding a growing interest in the food industry. Among the advantages of this emerging process is the ability to favorably freeze and thaw food. This study aims at comparing the effect of different freezing and thawing processes on the quality of Atlantic salmon fillets. Atlantic salmon (Salmo salar) samples were frozen by Pressure-Shift Freezing (PSF, 200 MPa, -18 degrees C) and Air-Blast Freezing (ABF, -30 degrees C, 4 m/s). Samples were stored 1 mo at -20 degrees C and then subjected to different thawing treatments: Air-Blast Thawing (ABT, 4 degrees C, 4 m/s), Immersion Thawing (IMT, 20 degrees C), and Pressure-Assisted Thawing (PAT, 200 MPa, 20 degrees C). Changes in texture, color, and drip loss were investigated. The toughness of the PSF samples was higher than that of the ABF sample. The modification of color was more important during high-pressure process than during the conventional process. The PSF process reduced thawing drip compared with ABF. The presence of small ice crystals in the pressure-shift frozen sample is probably the major reason leading to the reduced drip volumes. The freezing process was generally much more influent on quality parameters than the thawing process. These results show the interaction between freezing and thawing processes on selected quality parameters.

High pressure processing is recently applied in the food industry to inactivate spoilage and pathogenic microorganisms. Bacterial cells exhibit various barosensibility, and the role of pressurization, depressurization and constant pressure stage remain unknown. We investigated the effect of high pressure processing on Salmonella typhimurium and Listeria monocytogenes cells at 400 and 500 MPa respectively in buffer pH 7 at 20 degrees C. We applied various pressurization/depressurization kinetic rates (1, 5 and 10 MPa/s for pressurization and 250, 20 and 5 MPa/s for depressurization), and various pulse series or pressure holding times. Results show that high pressure pulses reduced linearly the number of bacterial cells according to the product of pressure and time: we defined this product as a Barometric Power (BP). Reduction of both microorganisms increased when holding time increased from 5 to 20 min, and better results were obtained when the rate of pressurization and depressurization were increased.