Search

Encapsulation is an innovative promising technique in the field of biotechnology, both for confining live microorganisms to promote their viability during processing and for the target delivery in the gastrointestinal tract, and for trapping active metabolites produced during a fermentation process within a carrier material, allowing their gradual release. During this work, a probiotic strain, Lacticaseibacillus paracasei CBA L74, was encapsulated using a hydrolyzed oatmeal suspension as a prebiotic carrier, by extrusion technique with CaCl2 a (1M) and alginate (1% w/v). The mini-bioreactors obtained were suspended in three different external liquids, (the same hydrolyzed oatmeal suspension used for the capsule production; a hydrolyzed oatmeal suspension with a modified pH equal to 3.3, and a hydrolyzed oatmeal suspension formulated by adding a specific concentration of dead bacteria) to evaluate whether the external liquid can help the confinement of the bacteria in the capsules. For this purpose, the fermentation process was carried out at 37°C for 24h; both capsules and external liquids were characterized by microbiological and chemical analyses. The maximum bacterial growth ( 109 CFU/mL) was reached in all the capsules, except for those suspended in the formulation with a modified pH where a bacterial charge of 3.5 x 108 CFU/mL was obtained; in any case, the bacterial confinement was not obtained. The highest lactic acid concentration (15.9 g/L) was observed for the capsules suspended in the same oatmeal suspension used for encapsulation, while the lowest one was obtained in the external oatmeal liquid with a modified pH. [ABSTRACT FROM AUTHOR]

Encapsulation is a commonly used tool in the pharmaceutical and nutraceutical fields to protect the compound of interest from adverse environmental conditions (i.e., production process, gastrointestinal transit, immune defense) or to ensure a target or controlled release of an active principle. However, capsules can also be used as reactors, by which probiotics can carry out a fermentation with improved process performances. In the present work, hydrolyzed oatmeal capsules were developed as mini-bioreactors, segregating the probiotic strain in active fermentation and allowing the metabolite release. The aim was to study how composition can influence the ability to ferment and the confinement of microorganisms. Four different capsules formulations were studied varying CaCl2 and alginate concentrations [(i) 0.5% alginate-0,1 M CaCl2; (ii) 1% alginate-1 M CaCl2; (iii) 1% alginate-3 M CaCl2; (iv) 1% alginate-5 M CaCl2]. The capsules were suspended in the same hydrolyzed oatmeal suspension used to produce them and left to ferment at 37°C for 24h. Microbiological and chemical analyses were carried out on both capsules and external liquids. An increase in the bacterial concentration of about 3 logs was recognized for all the first three formulations in the capsules, while a growth inhibition was observed for the (iv) formulation, the only formulation for which microorganism confinement was also noted. The highest lactic acid production (15.9 g/L) was observed for the (ii) formulation, while the lowest one was also recorded for formulation (iv). Optical analyses confirmed the different structural characteristics of the capsules. [ABSTRACT FROM AUTHOR]

Recently, the role of the gut microbiota in metabolic health, immunity, behavioral balance, longevity, and intestine comfort has been the object of several studies from scientific communities. They were encouraged by a growing interest from food industries and consumers toward novel fermented ingredients and formulations with powerful biological effects, such as pre, pro, and postbiotic products. Depending on the selected strains, the operating conditions, the addition of suitable reagents or enzymes, the equipment, and the reactor configurations, functional compounds with high bioactivity, such as short-chain fatty acids, gamma-aminobutyric acid, bioactive peptides, and serotonin, can be enhanced and/or produced through fermentation of several vegetable matrices. Otherwise, their formation can also be promoted directly in the gut after the dietary intake of fermented foods: In this case, fermentation will aim to increase the content of precursor substances, such as indigestible fibers, polyphenols, some amino acids, and resistant starch, which can be potentially metabolized by endogenous gut microorganisms and converted in healthy molecules. This review provides an overview of the main functional components currently investigated in literature and the associated gut health benefits. The current state of the art about fermentation technology as a promising functionalization tool to promote the direct or indirect formation of gut-health-enhancing components was deepened, highlighting the importance of optimizing microorganism selection, system setups, and process conditions according to the target compound of interest. The collected data suggested the possibility of gaining novel functional food ingredients or products rich in functional molecules through fermentation without performing additional extraction and purification stages, which are needed when conventional culture broths are used. [ABSTRACT FROM AUTHOR]

In the actual scenario, characterised by a global crisis, sustainability is not a minor player; it has a crucial role in the global outlook. Sustainability at the environmental level evolves in recycling, reusing, upcycling, and no squandering policies. Nowadays, the incessant, excessive, and growing use of plastic has a strong impact on global warming and represents a threat to the Oceans and the Planet. The paper industry can play a crucial role in addressing this emergency, by substituting mostly or totally (where it is possible) this impacting material. To confer paper materials the same plastic resistances, some additives could be used. In detail, the feasibility of upcycling silk waste was investigated and paper products containing silk fibers were formulated to realize worthy substitutes for plastic materials. These alternative fibers were inserted as a filler (20%wt. and 30% wt) in the cellulosic matrix and the resulting suspension was used to produce special papers for packaging. Silk, in both cases, was subjected to a chemical pretreatment with NaOH before paper sheet formation, which guaranteed an appropriate silk-cellulose interaction, without compromising the final chemichal-physical properties. Moreover, the sheets were subjected to non-destructive and destructive testing, which confirmed respectively their high-quality degree and good mechanical resistances. Silk confers special characteristics, in particular, the resulting sheets with silk were fluffier to the touch than the reference in pure cellulose. The resulting materials can be used as semi-finished products to obtain more sustainable paper-based packaging materials and promote a plastic-to-paper transition. [ABSTRACT FROM AUTHOR]

Simple Summary: Chemotherapy and radiotherapy exposure cause a long-lasting low-grade inflammatory state that is responsible for inflamm-aging, with the early onset of different chronic diseases that usually appear later in life, i.e., cardiac damage, bone mass loss, and cellular senescence. To prevent inflamm-aging, there is a need to find new possible therapeutic strategies, targeting cells involved in the immune processes. Macrophages are mononuclear cells involved in immune and inflammatory responses that play a crucial role in iron metabolism. In addition, inflammation causes an increase in intracellular iron concentration, responsible for inducing inflammation as well. Our results show that CCS patients' macrophages are characterized by an increase in activated phenotype markers (M1) (inflammatory ones). We propose macrophages and iron metabolism as novel therapeutic targets to counteract inflamm-aging, and suggest the employment of different nutraceuticals (resveratrol, curcumin, and oil-enriched lycopene) to avoid other side effects of toxic regimens and to contain inflammation. The advancement of anti-cancer therapies has markedly improved the survival rate of children with cancer, making them long-term childhood cancer survivors (CCS). Nevertheless, these treatments cause a low-grade inflammatory state, determining inflamm-aging and, thus, favoring the early onset of chronic diseases normally associated with old age. Identification of novel and safer therapeutic strategies is needed to counteract and prevent inflamm-aging. Macrophages are cells involved in immune and inflammatory responses, with a pivotal role in iron metabolism, which is related to inflammation. We obtained macrophages from CCS patients and evaluated their phenotype markers, inflammatory states, and iron metabolism by Western blotting, ELISA, and iron assays. We observed a strong increase in classically activated phenotype markers (M1) and iron metabolism alteration in CCS, with an increase in intracellular iron concentration and inflammatory markers. These results suggest that the prevalence of M1 macrophages and alteration of iron metabolism could be involved in the worsening of inflammation in CCS. Therefore, we propose macrophages and iron metabolism as novel therapeutic targets to counteract inflamm-aging. To avoid toxic regimens, we tested some nutraceuticals (resveratrol, curcumin, and oil-enriched lycopene), which are already known to exert anti-inflammatory properties. After their administration, we observed a macrophage switch towards the anti-inflammatory phenotype M2, as well as reductions in pro-inflammatory cytokines and the intracellular iron concentration. Therefore, we suggest—for the first time—that nutraceuticals reduce inflammation in CCS macrophages through a novel anti-inflammatory mechanism of action, modulating iron metabolism. [ABSTRACT FROM AUTHOR]

In recent years, scientific research and industries have been focusing on the application of biological treatments aimed at imparting functional properties to waste products from food industries according to the principles on which the circular economy model is based, namely, the recovery, valorisation, and reuse of wastes. This work aimed at exploring the possibility of valorising waters from the blanching process of dried navy beans through lactic acid fermentation using Lacticaseibacillus paracasei CBA L74 as a starter. Two samples at different solid concentrations (0.75 °Bx and 1.25 °Bx) were fermented, and, in both cases, a bacterial load of 8 Logs and a lactic acid concentration of approximately 1.3 g/L were reached, despite the lack of nutrients. An unusual pH trend, characterised by an initial decrease and unexpected final rise, was observed during the fermentation of both samples: simultaneously, an increase in protein content was observed, suggesting that the proteolytic action of the microorganism could be responsible for the release of pH-increasing substances. In both cases, a slight increase in total polyphenols (approximately 23.3–33.72%) and flavonoids (approximately 42.3–52%) due to fermentation was observed, with a corresponding improvement in antioxidant capacity (approximately 25.32–37.72%). A significant increase in saponin concentration was determined for the most concentrated blanching water (from 2.87 ± 0.28 to 6.68 ± 0.69 mgOAE/mL), leading to an improvement in foaming properties and an enhanced capacity to produce stable emulsions. The obtained results confirmed the possibility of reducing water consumption from blanching operations, as well as finding valorisation opportunities for this side stream through a safe and inexpensive fermentation treatment. [ABSTRACT FROM AUTHOR]

The concept of postbiotic has been attracting the attention of the scientific community and several industrial realities to develop new claims and new market segments for functional fermented products. The aim of this work was to develop a process to produce an oat-based postbiotic ingredient to be used in personal care cosmetic formulations. A hydrolyzed oatmeal suspension was fermented using Lacticaseibacillus paracasei CBA L74 as starter culture, at 37 °C for 48 h by controlling the pH; then the bacterial charge was inactivated by a mild thermal treatment at 80 °C for 30 s, obtaining a postbiotic. The effect of different process steps, hydrolysis, sterilization, fermentation, and inactivation phases, on lactic acid concentration, total polyphenolic content, antioxidant activity, tyrosinase inhibition activity and Sun Protection Factor value was investigated, demonstrating the potential cosmetic applications. The maximum bacterial growth and lactic acid production were achieved after 24 h of process, with a cell density and a lactic acid concentration of 3.05 × 109 CFU/mL and 8.60 g/L, respectively. The total phenolic content and the antioxidant activity reached their maximum values (2.5 mgGAE/mL, EC50 = 2.2 mg/mL and 1.38 × 10−2 mmol Fe2+/g and 7.3 × 10−3 mmol TE/g, respectively) after the sterilization treatment; the maximum tyrosinase inhibition of 50.6%, corresponding to a sample concentration of 16 mg/mL, was found after 24 h of fermentation process. Fermentation did not show an impact on UV shielding ability and the SPF value decreased during the process. [ABSTRACT FROM AUTHOR]

In recent years, the use of hop extracts in industrial and home brewing processes as an alternative to hop cones or pellets usually added to wort during boiling has become increasingly popular. These extracts represent concentrated sources of bitter compounds, i.e., α- and β-acids, which are involved in some of the main reactions that take place in the wort and are responsible for the bitterness and the final quality of beer. This work aims at proposing a novel extraction technique, using a hydrofluorocarbon solvent in subcritical conditions; this process provided an extraction yield of 19% and an α-acid recovery of approximately 49% in 120 min of process. The α-acid isomerization kinetics of thermally treated hop extracts were studied and compared with those of both hop pellets and a CO2 extract. Laboratory scale tests showed that shorter boiling times were needed using hydrofluorocarbon and CO2 extracts (approximately 25 min and 34 min, respectively) to reach the same isomerization efficiency of 16.73%, achieved in 50 min of boiling with pellets. Moreover, the process was scaled up and the possibility of considerably reducing the conventional treatment times using hydrofluorocarbon extracts was confirmed: the same isomerization yield (9.1%) obtained after 50 min using the traditional procedure with hop pellets was reached in a shorter time of approximately 35 min in a pilot apparatus. [ABSTRACT FROM AUTHOR]

Black garlic (BG) can be found on menus everywhere, but this unique ingredient isn’t anything new. Traditional and natural BG is, simply put, the product of aging regular garlic bulbs leaving them for weeks and months at typical ambient temperatures and high humidity (about 40°C and 90-100% RH) without addition of any preservatives achieving its typical colour and sticky texture. In this work, in order to speed up the complex Maillard reactions at the base of the organoleptic, textural and nutritional characteristics of the BG. The optimal process conditions and time were determined and the time of the browning of the cloves have been reduced considerably; the tests to produce black garlic are carried out with different temperature values (70-80-90°C) and different relative humidity values (70-80-90% RH). The process time can be consistently reduced ranging between 2-4 days. Samples produced at higher temperature (90°C) and low humidity (70%RH) were dry, friable and with low content of water while samples produced at high humidity (80-90%RH) and low temperature presented a gum-like consistency. The allicin has been totally transformed by the treatment losing the typical smell of the garlic. Moreover, there is also an increasing of the polyphenols and flavonoids contents if compared to the raw fresh garlic (respectively ranging between 32 -26 and 18 -13 mgGAE/gdr). Higher fructose content (250÷ 500 mg / g dry) - that confers sweetness - was measured at the end of the thermal processing as a possible consequence of the hydrolysis of long chain of the fructans. [ABSTRACT FROM AUTHOR]

Lactic acid fermentation of legume-based matrices has been gaining an increasing interest in recent years to produce pro- and post-biotic functional foods at high protein content. The optimization of the main process conditions is necessary to improve bacterial growth, microbial metabolic activity, thus the consequent functional properties of the resulting fermented products. A preliminary study of feasibility about the potential of using a leguminous substrate as growth medium for Lactobacillus paracasei CBA L74 was already conducted in previous experimentations. In this work, the effect of improving mixing conditions of a cooked navy bean suspension during the lactic acid fermentation process was investigated and some chemical and physical properties of the resulting fermented products were studied to verify their potential application as functional ingredients in food formulations. The mixing system was optimized by designing an impeller that guarantees a more homogeneous distribution of nutrients and avoids concentration gradients that could inhibit the microorganism proliferation. Bacterial growth, lactic acid production, sugar, and starch consumption were compared with those obtained during previous experimentations carried out with a different impeller. The major availability of nutrients in the fermenting medium reached with the customized impeller allowed a faster achievement of the maximum microbial load (1×109 CFU/mL after 14 h of process) and a lower doubling time of 1.53 h. Furthermore, fermentation led to a reduction in water absorption, oil binding, and foam capacity of the fermented bean powders. Total phenolic and flavonoid content and their antioxidant capacity were not influenced by the fermentation process itself but favored by the previous thermal treatment of sterilization. [ABSTRACT FROM AUTHOR]

Oil bodies (OBs) dispersed in an aqueous medium form a natural emulsion with high physical and microbiological stability. This work was focused on the development of a new protocol for extracting OBs from olive paste, through the extraction of an olive oil body cream (OOBC) with a yield of about 43% (wt/wt) in approximately 2 h. The proximate analysis revealed the presence of moisture, lipids and proteins as well as the contents of polyphenols and flavonoids, and the antioxidant powers were determined. The rheological and tribological performances of the OOBC were evaluated. Moreover, we measured a size distribution in the range of 0.7–1.7 m, by using a standard optical microscope. The results have demonstrated clearly that the OOBC extracted from the olive paste can be used as a functional and vegan ingredient in food emulsions. [ABSTRACT FROM AUTHOR]

ABSTRACT An experimental investigation on sulfur dioxide removal in a pilot-scale spray dryer from the flue gas generated by combustion of low-sulfur (S) heavy oil is reported. A lime-water slurry [...]

Celiac disease (CD) is an autoimmune disease characterized by an altered immune response stimulated by gliadin peptides that are not digested and cause damage to the intestinal mucosa. The aim of this study was to investigate whether the postbiotic Lactobacillus paracasei (LP) could prevent the action of gliadin peptides on mTOR, autophagy, and the inflammatory response. Most of the experiments performed were conducted on intestinal epithelial cells Caco-2 treated with a peptic-tryptic digest of gliadin (PTG) and P31-43. Furthermore, we pretreated the Caco-2 with the postbiotic LP before treatment with the previously described stimuli. In both cases, we evaluated the levels of pmTOR, p70S6k, and p4EBP-1 for the mTOR pathway, pNFkβ, and pERK for inflammation and LC 3 and p62 for autophagy. For autophagy, we also used immunofluorescence analysis. Using intestinal organoids derivate from celiac (CD) patients, we analyzed the effect of gliadin after postbiotic pretreatment with LP on inflammation marker NFkβ. Through these experiments, we showed that gliadin peptides are able to induce the increase of the inflammatory response in a more complex model of intestinal epithelial cells. LP postbiotic was able to induce autophagy in Caco-2 cells and prevent gliadin effects. In conclusion, postbiotic pretreatment with LP could be considered for in vivo clinical trials. [ABSTRACT FROM AUTHOR]

The enrichment of oils with nutraceutical bioactive phytomolecules allows the achievement of functional oil-based products of great interest in the food, pharmaceutical, and cosmetic fields. Carotenoids, such as lycopene and β-carotene, are available at a high concentration in tomatoes and tomato waste products, as peels, seeds, and pulp; their recovery is recently attracting growing interest and economic importance in the food industry, and also in consideration of the huge amount of industrial waste produced. The aim of this work is to study the production of an oil functionalized with carotenoids from tomato peels. The extractions were carried out using an innovative process based on the use of commercial Norflurane as solvent in subcritical conditions. Extraction trials were performed on dried tomato peels, with the addition of tomato seeds or wheat germ flour as sources of oily co-solvents, capable of also preserving the biological characteristics of the carotenoids extracted. Although lycopene solubility in Norflurane is quite low, the solvent recirculation and regeneration were allowed to reach a concentration in the oily extracts of approximately 0.3 mg/goil after 2 h of the process. The enrichment in β-carotene was more pronounced, and concentrations of 0.733 mg/goil and 0.952 mg/goil were observed in wheat germ and tomato seed oils, respectively. The results obtained in this study were compared with those obtained by traditional and supercritical CO2 extraction methods. [ABSTRACT FROM AUTHOR]

Synbiotic products are a type of functional food with great potential due to consumer interest in foods that improve health and/or reduce the risk of certain diseases. In this study, synbiotic macrocapsules were developed using Lactobacillus paracasei CBA L74 as probiotic and lactobionic acid (LBA) as prebiotic. Firstly, the probiotic was proven to be able to use LBA as the only substrate source checking their growth and lactic acid production. Then, four different types of capsules were produced using sodium alginate as matrix and different hardener solutions (CaCl2 and chitosan). The macrocapsules were characterised regarding their strength, and the best performing ones were used for further analysis. In order to obtain a synbiotic capsule characterized by a longer stability time due to low water activity, the capsules were dried using freeze and thermal drying. Successively, to revitalize the microorganisms, the capsules were rehydrated in two different media (saline solution and yogurt), subjected to simulated in vitro digestion tests and visually characterised. In addition, their viability over time was assessed. As a result, L. paracasei was able to grow using LBA as the only source of carbon with better production of lactic acid for prolonged periods. The more resistant freeze- and thermal-dried capsules showed differences in rehydration kinetics, and visual changes were also observed. In simulated in vitro digestion tests, capsules rehydrated in yogurt showed the best results in terms of survival. Regarding their viability over time, the importance of the use of chitosan was noted. [ABSTRACT FROM AUTHOR]

Celiac Disease (CD) is an autoimmune disease characterized by inflammation of the intestinal mucosa due to an immune response to wheat gliadins. It presents in subjects with genetic susceptibility (HLA-DQ2/DQ8 positivity and non-HLA genes) and under the influence of environmental triggers, such as viral infections and intestinal microbiota dysbiosis. The only treatment currently available in CD is a gluten-free diet for life. Despite this, the intestinal dysbiosis that is recorded in celiac subjects persists, even with adherence to dietary therapy. In this review, we have analyzed the literature over the past several decades, which have focused on the use of pro-, pre- and post-biotics in vitro and in vivo in CD. The study of probiotics and their products in CD could be interesting for observing their various effects on several different pathways, including anti-inflammatory properties. [ABSTRACT FROM AUTHOR]

Banana puree, due to its nutritional composition, is a good substrate for fermentation in the development of probiotic products. The production of banana puree mainly consists of three phases, i.e., raw material pretreatment, heat treatment, and the addition of anti-browning agents. In this study, we conducted three experimental protocols to evaluate the effect of ripeness grade, heat treatment, and ascorbic acid addition on fermentation performance. At the end of each protocol, the substrate was subjected to the fermentation process (37 °C, 48 h), and then measurements of pH reduction, microbial growth, and lactic acid production were used as markers in the analysis of fermentation performance. Ripe bananas produced better results than unripe bananas whose fermentation appeared to be inhibited. Therefore, ripe bananas were used to test the effect of two different heat treatments (sterilization (121 °C, 20 min) versus tyndallization (70 °C, 30 min; 37 °C, 30 min; 70 °C, 30 min)) on banana puree fermentation, and no significant differences were observed. Finally, 500 or 1000 ppm of ascorbic acid, normally used as an anti-browning agent, was added to ripe tyndallized bananas. No differences in fermentation results were observed between the two tested conditions, though values obtained for growth and lactic acid production were significantly lower than those from fermentation of banana puree without ascorbic acid. [ABSTRACT FROM AUTHOR]

The mathematical modeling of fermentation processes allows for the formulation of predictions about the kinetics of biomass growth and metabolite production as well as setting or verifying the best operative conditions in view of the economical convenience of the process. For this purpose, we performed a kinetic study of a rice flour fermentation process using Lactobacillus paracasei CBA L74 with and without pH control; the pH value was set to 5.8 under pH control. Monod, Logistic, and Contois models were proposed to describe the bacterial growth rate in both conditions. The best mathematical model, which was able to describe the experimental data obtained without pH control, was the Contois model, as the specific growth rate was influenced by both the glucose reduction (from 14.31 g/L to 10.22 g/L) and the biomass production (2 log growth) that occurred during fermentation. Conversely, when pH control was implemented, both Monod and Contois models satisfactorily described the specific growth rate trend. The estimated kinetic parameters confirmed that biomass production (2 log growth) and glucose consumption (from 14.31 g/L to 6.06 g/L) did not affect the microorganism's growth capacity when the fermenting medium was maintained at an optimal pH. The lactic acid production rate described by the Luedeking–Piret model did not appear to be linked to growth in the absence of pH control while, on the other hand, this model was unsuitable for describing the experimental lactic acid concentration when pH control was applied. The kinetic modeling of lactic acid production and the percentage of added glucose in the protocol with controlled pH will be optimized in the future. [ABSTRACT FROM AUTHOR]

Cereals are becoming interesting substrates to be fermented to obtain new functional foods. For this reason, an enzymatic pretreatment of a wheat flour suspension using amylase was investigated in order to guarantee the feasibility to ferment a cereal‐based substrate at a solid content higher than that used in past experimentations. Trials with and without amylase pretreatment, using a 52% w/v wheat flour water suspension, were carried out to evaluate the fermentation feasibility; mixing tests with a food dye were performed to verify the suspension homogeneity. The pretreated suspension, whose starch was hydrolyzed for about 80% by α‐amylase, was then fermented (37°C, 24h) by Lactobacillus paracasei CBA‐L74. Starting from pH value 5.75, microbial concentration 1.89 × 106 CFU/ml and lactic acid 0 mg/L, final values of 3.93, 3 × 108 CFU/ml and 6,251 mg/L were found after 24 hr of fermentation. The untreated suspension went to gelation and was impossible to ferment because its consistency was like a dough and the mixing system was not suitable to ensure mixing. Practical applications: The aim of the present study was the handling and the fermentation of cereal‐based substrate at high solid content (52% w/v), through a preliminary amylase pretreatment. The fermentation of such a solid content could guarantee the production of a greater quantity of solid fermented matrix and this could considerably reduce drying times with greater productivity at a low cost. [ABSTRACT FROM AUTHOR]

In recent years, scientific interest in the development of non‐dairy‐based functional foods is increasing progressively and the fermentation of cereals, legumes, fruits and vegetable‐based foods is becoming an important scientific research topic for the production of new probiotic products. In particular, legumes represent a possible alternative to protein foods from animal origins and an adequate fermentation substrate as they contain high amount of nutrients, such as proteins, carbohydrates, fibres, vitamins, and minerals, which are all useful to the growth and metabolic activity of certain microorganisms. This work focuses on the feasibility of developing a dry legume‐based functional product using a fermentation process carried out on a 10% w/v navy bean suspension, in a lab‐scale stirred batch reactor. After soaking and cooking dried navy beans, the fermentation tests performed on the resulting medium using Lactobacillus paracasei CBA L74 showed a maximum bacterial count of 109 CFU/mL after 20 hours and a maximum lactic acid concentration of 1.9 g/L after 16 hours of process time. A freeze‐drying process was performed on the fermented bean suspension, showing a 2‐log microbial reduction and a bacterial viability in the resulting probiotic powder of 3.7 × 108 CFU/g. [ABSTRACT FROM AUTHOR]

Coeliac disease is an increasingly recognised pathology, induced by the ingestion of gluten in genetically predisposed patients. Undigested gliadin peptide can induce adaptive and innate immune response that unleash the typical intestinal mucosal alterations. A growing attention is paid to alternative therapeutic approaches to the gluten-free diet: one of these approaches is the use of probiotics and/or postbiotics. We performed lactic fermentation of rice flour with and without pH control, using Lactobacillus paracasei CBA L74 as fermenting strain. We evaluated bacterial growth, lactic acid production during fermentation and gliadin peptide P31-43 entrance in CaCo-2 cells with and without pH control. When pH control was applied no differences were observed in terms of bacterial growth; on the contrary, lactic acid production was greater, as expected. Both samples could inhibit the P31-43 entrance in CaCo-2 cells but the effect was significantly greater for samples obtained when the pH control was applied. [ABSTRACT FROM AUTHOR]

The concept of functional food has evolved throughout the years. These days we define a food to be functional when it confers a benefit to human health. Lactic acid fermentation is one of the most important and used food processing technologies to produce this type of food. Fermentation of Lactobacillus Paracasei CBA L74 - a homofermentative, gram positive probiotic - on rice flour suspension has been proved to be a successful route to produce functional foods. However, the process was characterized by high energy consumption, low air sparging and complex expensive metabolite separation. A research program has been developed to carry out L. Paracasei fermentation using a low viscosity medium based on rice flour suspension. Fractionation of rice flour suspension provided a medium characterized by low amounts of solids and nutrients at concentration high that support the microorganism growth. Fermentations were carried in a 1L batch reactor equipped with an agitation systems designed to provide uniform mixing. The composition of the medium; cells, glucose, protein, pH, metabolite production as well as L. Paracasei' growth trend was analysed throughout the process. Fermentation on supernatant obtained from rice flour and water suspension through centrifugation were possible to produce a potential probiotic functional food with a good bacterial charge. [ABSTRACT FROM AUTHOR]

Background: In vivo assays cannot always be conducted because of ethical reasons, technical constraints or costs, but a better understanding of the digestive process, especially in infants, could be of great help in preventing food-related pathologies and in developing new formulas with health benefits. In this context, in vitro dynamic systems to simulate human digestion and, in particular, infant digestion could become increasingly valuable. Objective: To simulate the digestive process through the use of a dynamic model of the infant gastroenteric apparatus to study the digestibility of starch-based infant foods. Design: Using M.I.D.A (Model of an Infant Digestive Apparatus), the oral, gastric and intestinal digestibility of two starch-based products were measured: 1) rice starch mixed with distilled water and treated using two different sterilization methods (the classical method with a holding temperature of 121°C for 37 min and the HTST method with a holding temperature of 137°C for 70 sec) and 2) a rice cream with (premium product) or without (basic product) an aliquot of rice flour fermented by Lactobacillus paracasei CBA L74. After the digestion the foods were analyzed for the starch concentration, the amount of D-glucose released and the percentage of hydrolyzed starch. Results: An in vitro dynamic system, which was referred to as M.I.D.A., was obtained. Using this system, the starch digestion occurred only during the oral and intestinal phase, as expected. The D-glucose released during the intestinal phase was different between the classical and HTST methods (0.795 grams for the HTST versus 0.512 for the classical product). The same analysis was performed for the basic and premium products. In this case, the premium product had a significant difference in terms of the starch hydrolysis percentage during the entire process. Conclusions: The M.I.D.A. system was able to digest simple starches and a more complex food in the correct compartments. In this study, better digestibility of the premium product was revealed. [ABSTRACT FROM AUTHOR]