The aroma transformation of Japanese sea bass (Lateolabrax japonicas) through endogenous enzyme incubation during the lag phase of attached microorganisms.
Food Chem
; 463(Pt 2): 141215, 2024 Sep 10.
Article
em En
| MEDLINE
| ID: mdl-39278078
ABSTRACT
Endogenous enzymes play a crucial role in determining fish product aroma. However, the attached microorganisms can promote enzyme production, making it challenging to identify specific aromatic compounds resulting from endogenous enzymes. Thus, we investigated the aroma transformation of Japanese sea bass through enzymatic incubation by controlling attached microorganisms during the lag phase. Our results demonstrate that enzymatic incubation significantly enhances grassy and sweet notes while reducing fishy odors. These changes in aroma are associated with increased levels of 10 volatile compounds and decreased levels of 3 volatile compounds. Among them, previous studies have reported enzyme reaction pathways for octanal, 1-nonanal, vanillin, indole, linalool, geraniol, citral, and 6-methyl-5-hepten-2-one; however, the enzymatic reaction pathways for germacrene D, beta-caryophyllene, pristane, 1-tetradecene and trans-beta-ocimene remain unclear. These findings provide novel insights for further study to elucidate the impact of endogenous enzymes on fish product aromas.
(−)-Alpha-terpineol (PubChem CID: 443162); 1-Nonanal (PubChem CID: 31289); 1-Octen-3-ol (PubChem CID: 18827); 1-Tetradecene (PubChem CID: 14260); 2,4-Di-tert-butylphenol (PubChem CID: 7311); 2-Ethylhexanol (PubChem CID: 7720); 2-cyclopentenone (PubChem CID: 13588); 3-Heptylacrolein (PubChem CID: 5283345); 6-methyl-5-hepten-2-one (PubChem CID: 9862); Acetoin (PubChem CID: 179); Acetophenone (PubChem CID: 7410); Alpha-caryophyllene (PubChem CID: 5281520); Alpha-pinene (PubChem CID: 6654); Attached microorganism; Benzaldehyde (PubChem CID: 240); Benzodihydrofuran (PubChem CID: 10329); Beta-caryophyllene (PubChem CID: 5281515); Beta-myrcene (PubChem CID: 31253); Beta-pinene (PubChem CID: 14896); Butylated hydroxytoluene (PubChem CID: 31404); Butyldiglycol (PubChem CID: 8177); Caryophyllene oxide (PubChem CID: 1742210); Cis-linalool oxide (PubChem CID: 22310); Citral (PubChem CID: 638011); Decyl aldehyde (PubChem CID: 8175); Dl-limonene (PubChem CID: 22311); Endogenous enzyme; Eugenol (PubChem CID: 3314); Geraniol (PubChem CID: 637566); Geranylacetone (PubChem CID: 1549778); Germacrene d (PubChem CID: 5317570); Heptaldehyde (PubChem CID: 8130); Hexadecanal (PubChem CID: 984); Hexanal (PubChem CID: 6184); Hexanoic acid (PubChem CID: 8892); Indole (PubChem CID: 798); Isophorone (PubChem CID: 6544); Lag phase; Lateolabrax japonicas Aroma; Linalool (PubChem CID: 6549); Methyl palmitate (PubChem CID: 8181); Naphthalene (PubChem CID: 931); Nerol (PubChem CID: 643820); Nonanoic acid (PubChem CID: 8158); O-xylene (PubChem CID: 7237); Octanal (PubChem CID: 454); P-xylene (PubChem CID: 7809); Palmitic acid (PubChem CID: 985); Palmitic acid ethyl ester (PubChem CID: 12366); Phenethyl alcohol (PubChem CID: 6054); Phytane (PubChem CID: 12523); Pristane (PubChem CID: 15979); Styrene (PubChem CID: 7501); Trans-beta-ocimene (PubChem CID: 5281553); Trans-linalool oxide (PubChem CID: 6432254); Vanillin (PubChem CID: 1183)
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Idioma:
En
Revista:
Food Chem
Ano de publicação:
2024
Tipo de documento:
Article
País de afiliação:
China