| Literature DB >> 33344493 |
Antonio Morata1, Buenaventura Guamis2.
Abstract
Ultra-high pressure homogenization (UHPH) is a high pressure technique in which a fluid is pressurized by pumping at higher than 200 MPa and instantaneously depressurized at atmospheric pressure across a special valve. The full process takes <0.2 s and the in-valve time is <0.02 s. In the valve, extremely intense impacts and shear forces produce the nanofragmentation of biological tissue at a range of 100-300 nm. The antimicrobial effect is highly effective, reaching easily inactivation levels higher than 6-log cycles even at low in-valve temperatures. At in-valve temperatures of 140-150°C (0.02 s) the destruction of thermoresistant spores is possible. Even when the temperature in-valve can be elevated (70-150°C), it can be considered a gentle technology because of the tremendously short processing time. It is easy to get outlet temperatures after valve of 20-25°C by the expansion and assisted by heat exchangers. Thermal markers as hydroxymethylfurfural (HMF) are not formed, nor are deleterious effects observed in sensitive compounds as terpenes or anthocyanins, probably because of the low effect in covalent bonds of small molecules of the high-pressure techniques compared with thermal technologies. Additionally, intense inactivation of oxidative enzymes is observed, therefore protecting the sensory and nutritional quality of fruit juices and avoiding or reducing the use of antioxidants as sulphites. UHPH can be consider a powerful and highly effective continuous and sterilizing technology without thermal repercussions, able to keep fresh juices with most of their initial sensory and nutritional quality and allowing high-quality and natural fermented derivatives as wine.Entities:
Keywords: additives; colloidal stability; emerging technologies; grape must; oxidative enzymes; sulphites; winemaking
Year: 2020 PMID: 33344493 PMCID: PMC7746610 DOI: 10.3389/fnut.2020.598286
Source DB: PubMed Journal: Front Nutr ISSN: 2296-861X
Figure 1Range of pressures in conventional homogenization vs. UHPH. Effect on enzymes and microorganisms and nano-fragmentation in the UHPH valve.
Comparative features of UHPH and HHP.
| Operating mode | Continuous pumping. Treatment time 0.2 s | Discontinuous pressurization with water. Treatment time 3–10 min | ( |
| Effect on covalent bonds in small molecules with sensory impact | Unaffected | Unaffected | ( |
| Molds and yeasts control | Highly effective at 300 MPa | Highly effective at >400 MPa/5–10 min | ( |
| Bacteria | Highly effective at 300 MPa | Effective at >600 MPa/5–10 min | ( |
| Bacterial endospores | Highly effective at 300 MPa, if in-valve Temperature 140°C 0.2 s | Not applicable. Effective at >1,000 MPa/5–10 min | ( |
| Effect on biopolymers | Intense fragmentation. 100–300 nm. | Starch gelatinization. Protein denaturation. | ( |
| Oxidative enzymes | Strong inactivation at 300 MPa. PPO inactivation >90%. Absence of browning during more than 5 days in air exposed juices | Weak. Variable, usually needs temperature assistance | ( |
| Thermal markers (HMF) | Undetected | Lower than in thermal treatments | ( |
| Antioxidant capacity | Increased >150% | Non differences-slight reduction | ( |
| Vitamins | Preserved | Preserved | ( |
| Terpenes and aroma molecules | Unaffected | Unaffected | ( |
| Anthocyanins | Unaffected. Increased extraction from skin colloidal particles | Unaffected. Improved extraction from grapes | ( |
| Polyphenols | Improved extraction from apple and grapes | Non-significant differences in total phenolics and flavonoids. Improved extraction from grapes. | ( |
| Sensory profile | Unaffected. Better fruitiness | Unaffected | ( |
| New fermentative biotechnologies as use of non- | Better implantation and lesser competitiveness with indigenous microbiota | Better implantation and lesser competitiveness with indigenous microbiota | ( |
| Release of yeast assimilable nitrogen (YAN) and nutritional properties of must | Increased extraction from juice cell fragments. Favors the formation of fermentative esters. | Not described | ( |
| Protein digestibility | Improved | Improved | ( |
| Allergenicity | Decreased | Decreased | ( |
| Colloidal and color stability. | Improved. Higher stability of nanofragmented particles. Color stability. Better protein stability and lower haze formation. | Unaffected. Better protein stability and delayed protein haze. | ( |