11 research outputs found

    Possibility of using apple pomaces in the process of propionic-acetic fermentation

    Get PDF
    Background: In 2014, apple production in EU countries amounted to 11.8 million tonnes. A constant increase in the production of these fruits will lead to the accumulation of thousands of tonnes of apple pomace (production waste). The amount of industrial apples is the highest \u2014 their proportion on the market is estimated at 50\u201360%, of which over 95% is processed into juice. The proportion of pomace in the traditional pressing method accounts for 20% of fruits used. Results: Analysis of the growth dynamics of wild strain Propionibacterium freudenreichii T82 in micro-cultures using different carbon sources showed that the highest bacterial growth occurs in an environment with fructose and the most intense biosynthesis of metabolites was found in medium containing only saccharose. It has been found that P. freudenreichii T82 used apple pomaces as a source of carbon. Propionic acid biosynthesis reached its maximum value in the 120th hour of cultivation (1.771 g/L). At this time, the content of the acetic acid produced reached the level of 7.049 g/L. Conclusions: Utilization of by-products is a significant challenge for manufacturing sites and the natural environment. The solution to this problem may involve the use of pomace as a medium component for microorganism cultivation, which is a source of industrially useful metabolites. This study examined the possibility of using apple pomace as a carbon source in the process of propionic-acetic fermentation via wild strain Propionibacterium freudenreichii T82 bacteria

    Microbiological transglutaminase: Biotechnological application in the food industry

    No full text
    Microbial transglutaminases (mTGs) belong to the family of global TGs, isolated and characterised by various bacterial strains, with the first being Streptomyces mobaraensis. This literature review also discusses TGs of animal and plant origin. TGs catalyse the formation of an isopeptide bond, cross-linking the amino and acyl groups. Due to its broad enzymatic activity, TG is extensively utilised in the food industry. The annual net growth in the utilisation of enzymes in the food processing industry is estimated to be 21.9%. As of 2020, the global food enzymes market was valued at around 2.3billionUSD(mTGmarketwasestimatedtobearound2.3 billion USD (mTG market was estimated to be around 200 million USD). Much of this growth is attributed to the applications of mTG, benefiting both producers and consumers. In the food industry, TG enhances gelation and modifies emulsification, foaming, viscosity, and water-holding capacity. Research on TG, mainly mTG, provides increasing insights into the wide range of applications of this enzyme in various industrial sectors and promotes enzymatic processing. This work presents the characteristics of TGs, their properties, and the rationale for their utilisation. The review aims to provide theoretical foundations that will assist researchers worldwide in building a methodological framework and furthering the advancement of biotechnology research

    Possibility of using apple pomaces in the process of propionic-acetic fermentation

    Get PDF
    Background: In 2014, apple production in EU countries amounted to 11.8 million tonnes. A constant increase in the production of these fruits will lead to the accumulation of thousands of tonnes of apple pomace (production waste). The amount of industrial apples is the highest — their proportion on the market is estimated at 50–60%, of which over 95% is processed into juice. The proportion of pomace in the traditional pressing method accounts for 20% of fruits used. Results: Analysis of the growth dynamics of wild strain Propionibacterium freudenreichii T82 in micro-cultures using different carbon sources showed that the highest bacterial growth occurs in an environment with fructose and the most intense biosynthesis of metabolites was found in medium containing only saccharose. It has been found that P. freudenreichii T82 used apple pomaces as a source of carbon. Propionic acid biosynthesis reached its maximum value in the 120th hour of cultivation (1.771 g/L). At this time, the content of the acetic acid produced reached the level of 7.049 g/L. Conclusions: Utilization of by-products is a significant challenge for manufacturing sites and the natural environment. The solution to this problem may involve the use of pomace as a medium component for microorganism cultivation, which is a source of industrially useful metabolites. This study examined the possibility of using apple pomace as a carbon source in the process of propionic-acetic fermentation via wild strain Propionibacterium freudenreichii T82 bacteria

    Research on Thermal Imaging Usage as a Method for Detecting <i>Bacillus subtilis</i> Bacteria in Mortadella

    No full text
    Meat and meat products are important sources of valuable proteins and other nutrients, but they are also a conducive environment for microorganisms’ growth and can easily corrupt. In order to ensure the safety and quality of these products throughout its entire shelf-life, reliable microbial contamination assessment techniques must be used. Despite their effectiveness, traditional diagnostics methods are expensive and time consuming. Therefore, new timesaving, reliable techniques are searched for. Infrared thermography could be a good alternative method in this area. As a quick technique to detect microorganisms, it can overcome the limitations of traditional microbiological food-quality assessment methods. It has numerous advantages, such as the possibility of taking immediate temperature measurements and short processing times for obtaining a thermal image, non-contact and non-destructive measurements, and, unlike other methods, real-time measurement monitoring. Real-time monitoring is particularly important for modern production systems. The purpose of this research study is to develop a methodology for microbiological quality control of mortadella inoculated with Bacillus subtilis ATCC 6633 bacteria using a thermal imaging camera with an uncooled microbolometric detector. It was found that the thermal imaging measurements used in this research study enabled the distinction of contaminated samples (min. 106 CFU/g) from sterile samples. The tests should only record the temperature of the samples during the first 25 s after previously performing activations at −18 °C ± 1 °C for 60 s. This is where differences between the samples are most pronounced. Estimating the trend line of the sample’s cooling process is advisable

    Research on Thermal Imaging Usage as a Method for Detecting Bacillus subtilis Bacteria in Mortadella

    No full text
    Meat and meat products are important sources of valuable proteins and other nutrients, but they are also a conducive environment for microorganisms&rsquo; growth and can easily corrupt. In order to ensure the safety and quality of these products throughout its entire shelf-life, reliable microbial contamination assessment techniques must be used. Despite their effectiveness, traditional diagnostics methods are expensive and time consuming. Therefore, new timesaving, reliable techniques are searched for. Infrared thermography could be a good alternative method in this area. As a quick technique to detect microorganisms, it can overcome the limitations of traditional microbiological food-quality assessment methods. It has numerous advantages, such as the possibility of taking immediate temperature measurements and short processing times for obtaining a thermal image, non-contact and non-destructive measurements, and, unlike other methods, real-time measurement monitoring. Real-time monitoring is particularly important for modern production systems. The purpose of this research study is to develop a methodology for microbiological quality control of mortadella inoculated with Bacillus subtilis ATCC 6633 bacteria using a thermal imaging camera with an uncooled microbolometric detector. It was found that the thermal imaging measurements used in this research study enabled the distinction of contaminated samples (min. 106 CFU/g) from sterile samples. The tests should only record the temperature of the samples during the first 25 s after previously performing activations at &minus;18 &deg;C &plusmn; 1 &deg;C for 60 s. This is where differences between the samples are most pronounced. Estimating the trend line of the sample&rsquo;s cooling process is advisable

    Accumulation of Selenium in Candida utilis Growing in Media of Increasing Concentration of this Element

    No full text
    Selenium is considered an essential component of all living organisms. Studies on the enrichment of yeast cells with selenium, using the ability of cell biomass to bind this element, are being reported more and more. Yeast cultures were cultivated in YPD medium enriched with Na2SeO3 salts for 72 h at 28 &deg;C on a shaker utilizing reciprocating motion. Selenium in cell biomass was determined with the use of ICP&ndash;MS. It was observed that the addition of selenium to the experimental medium (in the range of 4&ndash;100 mg/L) increased the content of this element in the yeast cell biomass. During the extension of cultivation time, the number of yeast cells and biomass yield exhibited a decreasing trend. Based on the obtained results, it was concluded that yeast cells exhibited the ability to accumulate selenium in both logarithmic and stationary growth phases. The dose of 20 and 30 mg/L of selenium in the culture medium meets the expectations in terms of both the content of selenium bound to yeast cells (1944 &plusmn; 110.8 &mu;g/g dry weight) under 48-h cultivation. The obtained results confirmed that the Candida utilis ATCC 9950 strain exhibits the ability to bind selenium, which means that the biomass of these yeasts may be used as a natural source of selenium in the diet of humans and animals

    The aspects of microbial biomass use in the utilization of selected waste from the agro-food industry

    No full text
    Cellular biomass of microorganisms can be effectively used in the treatment of waste from various branches of the agro-food industry. Urbanization processes and economic development, which have been intensifying in recent decades, lead to the degradation of the natural environment. In the first half of the 20th century, problems related to waste management were not as serious and challenging as they are today. The present situation forces the use of modern technologies and the creation of innovative solutions for environmental protection. Waste of industrial origin are difficult to recycle and require a high financial outlay, while the organic waste of animal and plant origins, such as potato wastewater, whey, lignin, and cellulose, is dominant. In this article, we describe the possibilities of using microorganisms for the utilization of various waste products. A solution to reduce the costs of waste disposal is the use of yeast biomass. Management of waste products using yeast biomass has made it possible to generate new metabolites, such as β-glucans, vitamins, carotenoids, and enzymes, which have a wide range of industrial applications. Exploration and discovery of new areas of applications of yeast, fungal, and bacteria cells can lead to an increase in their effective use in many fields of biotechnology

    Use of Propionibacterium freudenreichii T82 Strain for Effective Biosynthesis of Propionic Acid and Trehalose in a Medium with Apple Pomace Extract and Potato Wastewater

    No full text
    Propionic acid bacteria are the source of many metabolites, e.g., propionic acid and trehalose. Compared to microbiological synthesis, the production of these metabolites by petrochemical means or enzymatic conversion is more profitable. The components of microbiological media account for a large part of the costs associated with propionic fermentation, due to the high nutritional requirements of Propionibacterium. This problem can be overcome by formulating a medium based on the by-products of technological processes, which can act as nutritional sources and at the same time replace expensive laboratory preparations (e.g., peptone and yeast extract). The metabolic activity of P. freudenreichii was investigated in two different breeding environments: in a medium containing peptone, yeast extract, and biotin, and in a waste-based medium consisting of only apple pomace and potato wastewater. The highest production of propionic acid amounting to 14.54 g/L was obtained in the medium containing apple pomace and pure laboratory supplements with a yield of 0.44 g/g. Importantly, the acid production parameters in the waste medium reached almost the same level (12.71 g/L, 0.42 g/g) as the medium containing pure supplements. Acetic acid synthesis was more efficient in the waste medium; it was also characterized by a higher level of accumulated trehalose (59.8 mg/g d.s.). Thus, the obtained results show that P. freudenreichii bacteria exhibited relatively high metabolic activity in an environment with apple pomace used as a carbon source and potato wastewater used as a nitrogen source. This method of propioniate production could be cheaper and more sustainable than the chemical manner

    Metabolic Response of the Yeast Candida utilis During Enrichment in Selenium

    No full text
    Selenium (Se) was found to inhibit the growth of the yeast Candida utilis ATCC 9950. Cells cultured in 30 mg selenite/L supplemented medium could bind 1368 &micro;g Se/g of dry weight in their structures. Increased accumulation of trehalose and glycogen was observed, which indicated cell response to stress conditions. The activity of antioxidative enzymes (glutathione peroxidase, glutathione reductase, thioredoxin reductase, and glutathione S-transferase) was significantly higher than that of the control without Se addition. Most Se was bound to water-insoluble protein fraction; in addition, the yeast produced 20&ndash;30 nm Se nanoparticles (SeNPs). Part of Se was metabolized to selenomethionine (10%) and selenocysteine (20%). The HPLC-ESI-Orbitrap MS analysis showed the presence of five Se compounds combined with glutathione in the yeast. The obtained results form the basis for further research on the mechanisms of Se metabolism in yeast cells
    corecore