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Veterinaarmeditsiini ja loomakasvatuse instituut

Selle valdkonna püsiv URIhttp://hdl.handle.net/10492/2469

Sirvi

Sirvi Veterinaarmeditsiini ja loomakasvatuse instituut Autor "Abramova, Liubov" järgi

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  • Pisipilt
    Kirje
    Adenosine Triphosphate and Adenylate Energy Charge in Ready-to-Eat Food
    (MDPI, 2024) Konoplev, Georgii; Sünter, Alar; Kuznetsov, Artur I.; Raudsepp, Piret; Püssa, Tõnu; Toom, Lauri; Rusalepp, Linda; Anton, Dea; Stepanova, Oksana V.; Lyalin, Daniil; Abramova, Liubov; Kozin, Andrey; Stepanova, Oksana S.; Frorip, Aleksandr; Roasto, Mati
    It is commonly accepted that dietary nucleotides should be considered as essential nutrients originating mainly but not exclusively from meat and fish dishes. Most research in food science related to nutrition nucleotides is focused on raw products, while the effects of thermal processing of ready-to-eat food on nucleotide content are largely overlooked by the scientific community. The aim of this study is to investigate the impact of thermal processing and cold storage on the content of dietary nucleotides in freshly prepared and canned ready-to-eat meat and fish food. The concentrations of ATP, ADP, AMP, IMP, Ino, and Hx were determined using NMR, HPLC, FPMLC, and ATP bioluminescence analytical techniques; freshness indices K and K1 and adenylate energy charge (AEC) values were estimated to assess the freshness status and confirm a newly unveiled phenomenon of the reappearance of adenylate nucleotides. It was found that in freshly prepared at 65 ◦C ≤ T ≤ +100 ◦C and canned food, the concentration of free nucleotides was in the range of 0.001–0.01 μmol/mL and remained unchanged for a long time during cold storage; the correct distribution of mole fractions of adenylates corresponding to 0 < AEC < 0.5 was observed compared to 0.2 < AEC < 1.0 in the original raw samples, with either a high or low content of residual adenylates. It could be assumed that heating at nonenzymatic temperatures T > 65 ◦C can rupture cell membranes and release residual intracell nucleotides in quite a meaningful concentration. These findings may lead to a conceptual change in the views on food preparation processes, taking into account the phenomenon of the free adenylates renaissance and AEC bioenergetics.
  • Pisipilt
    Kirje
    Fast Protein and Metabolites (Nucleotides and Nucleosides) Liquid Chromatography Technique and Chemical Sensor for the Assessment of Fish and Meat Freshness
    (MDPI, 2023) Kuznetsov, Artur; Frorip, Aleksandr; Sünter, Alar; Kasvand, Nensi; Korsakov, Vadim; Konoplev, Georgii; Stepanova, Oksana; Rusalepp, Linda; Anton, Dea; Püssa, Tõnu; Roasto, Mati; Abramova, Liubov; Kozin, Andrey; Toom, Lauri; Hirsch, Soeren; Mukhin, Nikolay
    Fast protein and metabolite liquid chromatography (FPLMC) was introduced years ago to enable the easy separation of high-molecular compounds such as proteins from small molecules and the identification of the low-molecular substances. In this paper, the method is applied for the rapid evaluation of freshness and monitoring the aging of animal meat and fish. A novel chromatographic sensor was developed with a deep UV LED-based photometric detection unit (255–265 nm), an original flow cuvette and registration scheme; the processing of a chromatogram with the sensor takes approximately 15 min. Strict isochronism between the elution of ATP metabolites, mainly hypoxanthine (Hx) and inosine monophosphate (IMP), and the time of maturation of meat or fish, was discovered. A new freshness index H* = [Hx]/[IMP] was introduced, which is proportional to the instrumental delay time in the FPMLC chromatograms: the H* index < 0.5 indicates the presence of inosine monophosphate (IMP) and the high quality of the meat or fish. Reasonably strong correlations were revealed between data obtained by FPMLC and total volatile basic nitrogen TVB-N (for fish) or volatile fatty acids VFA (for meat) content. Moreover, putative nucleotide salvage and an increase in the concentration of IMP were observed in fish after heat treatment using the FPMLC sensor and NMR technique.