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The aroma transformation of Japanese sea bass (Lateolabrax japonicas) through endogenous enzyme incubation during the lag phase of attached microorganisms.
Liu, Xinru; Guan, Junlan; Yang, Yuanfan; Wu, Ling; Ni, Hui; Li, Qingbiao; Chen, Feng.
Afiliação
  • Liu X; College of Food and Biological Engineering, Jimei University, Xiamen 361021, China.
  • Guan J; College of Food and Biological Engineering, Jimei University, Xiamen 361021, China.
  • Yang Y; College of Food and Biological Engineering, Jimei University, Xiamen 361021, China; Fujian Provincial Key Laboratory of Food Microbiology and Enzyme Engineering, Xiamen 361021, China; Research Center of Food Biotechnology of Xiamen City, Xiamen 361021, China.
  • Wu L; College of Food and Biological Engineering, Jimei University, Xiamen 361021, China; Fujian Provincial Key Laboratory of Food Microbiology and Enzyme Engineering, Xiamen 361021, China; Research Center of Food Biotechnology of Xiamen City, Xiamen 361021, China.
  • Ni H; College of Food and Biological Engineering, Jimei University, Xiamen 361021, China; Fujian Provincial Key Laboratory of Food Microbiology and Enzyme Engineering, Xiamen 361021, China; Research Center of Food Biotechnology of Xiamen City, Xiamen 361021, China; Xiamen Ocean Vocational College, Xiamen
  • Li Q; College of Food and Biological Engineering, Jimei University, Xiamen 361021, China; Fujian Provincial Key Laboratory of Food Microbiology and Enzyme Engineering, Xiamen 361021, China; Research Center of Food Biotechnology of Xiamen City, Xiamen 361021, China.
  • Chen F; Department of Food Science, Nutrition and Packaging, Clemsin University, Clemsin City of South Carolina 29631, USA Department of Food, Nutrition and Packaging Sciences, Clemson University, Clemson, SC 29634, USA.
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.
Palavras-chave
(−)-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

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