Determination of nucleotide and enzyme degradation in haddock ( Melanogrammus aeglefinus ) and herring ( Clupea harengus ) after high pressure processing

• Published in: PeerJ (San Francisco, CA) CA), 2019-08, Vol.7, p.e7527-e7527, Article e7527
• Main Authors: Karim, Nurul Ulfah, Kennedy, James Terence, Linton, Mark, Patterson, Margaret, Watson, Sally, Gault, Norman
• Format: Article
• Language: English
• Subjects: 5-nucleotidase; Adenosine monophosphate; Adenosine triphosphate; AMP; Aquaculture, Fisheries and Fish Science; ATP; ATP (Adenosine triphosphate); Biochemistry; Biodegradation; Clupea harengus; Death; Dephosphorylation; Enzymatic activity; Enzymes; Fish; Flavor; Food Science and Technology; Gadinae; Haddock; Herring; Hypoxanthine; Melanogrammus aeglefinus; Muscle proteins; Nucleoside phosphorylase; Nucleosides; Nucleotidase; Nucleotidases; Nucleotides; Nucleotides degradation; Nutrition; Phosphorylase; Pressure; Purines; Shelf life; Species; Uric acid; Xanthine
• ISSN: 2167-8359; 2167-8359
• DOI: 10.7717/peerj.7527

The degradation of nucleotides and their enzymes had been widely used to evaluate fish freshness. Immediately after fish death, adenosine triphosphate (ATP) degrades into inosine-5-monophosphate (IMP) via adenosine-5-diphosphate (ADP) and adenosine-5-monophosphate (AMP). IMP degradation continues to produce inosine (ino) and hypoxanthine (Hx) and further deteriorates the fish by producing xanthine and uric acid. The dephosphorylation of IMP to Ino is carried out by the enzyme 5'-nucleotidase (5'-NT), whereas the degradation of Ino to Hx is carried out by the enzyme nucleoside phosphorylase (NP). This study assesses the application of high pressure processing (HPP) in two species of fishes; haddock ( ) and herring ( ) as a means to extend the shelf-life by slowing down the rate of nucleotides degradation. Haddock and herring fillets were subjected to HPP at 200, 250 and 300 MPa for 1 and 3 min before being stored for 14 days. In addition, 5'-NT and NP enzyme activities were determined on both fish species that were subjected to 100-600 MPa for 1 and 3 min. Adenosine triphosphate, ADP and AMP in both haddock and herring were lower at higher pressure levels. Inosine (Ino) increased ( < 0.05) after treatment at higher pressures in both species. Hx in herring decreased significantly ( < 0.05) at higher pressures but not in haddock. values are the ratio of Ino and Hx to all nucleotides. values in haddock were not significantly ( > 0.05) affected by the pressure treatment. values are ratio of Hx to the sum of IMP, Ino and Hx. values in haddock were significantly decreased ( < 0.05) with increasing pressure level. values are ratio of IMP to the sum of IMP, Ino and Hx. value showed no significant effects ( > 0.05) after pressure treatment. Furthermore, value in control herring were significantly higher ( < 0.05) than those of the pressure-treated samples. values in herring decreased significantly ( < 0.05) with increasing pressure level. value in herring showed no significant effects ( > 0.05) after pressure treatment. Pressure treatment brought a significant decrease ( < 0.05) in protein content in both haddock and herring. 5'-NT activity was 20-35 fold higher compared to NP activity in haddock and 15-44 fold higher than NP activity in herring. 5'-NT and NP activities decreased significantly with increasing pressure level in both species. High pressure processing effectively slows down the conversion of Ino to Hx, delaying the undesirable flavour that develops in