scholarly journals The inconsistent microbiota of Budu, the Malaysian fermented anchovy sauce, revealed through 16S amplicon sequencing

PeerJ ◽  
2021 ◽  
Vol 9 ◽  
pp. e12345
Author(s):  
Muhammad Zarul Hanifah Md Zoqratt ◽  
Han Ming Gan

Budu is a Malaysian fermented anchovy sauce produced by immersing small fishes into a brine solution for 6 to 18 months. Microbial enzymes are known to contribute to fermentation; however, not much is known about the microbial community in Budu. Therefore, a better understanding of the Budu microbiome is necessary to improve the quality, consistency, and safety of the Budu products. In this study, we collected 60 samples from 20 bottles of Budu produced by seven manufacturers. We analyzed their microbiota using V3–V4 16S rRNA amplicon sequencing when we first opened the bottle (month 0), as well as 3 and 7 months post-opening (months 3 and 7). Tetragenococcus was the dominant genus in many samples, reaching a maximum proportion of 98.62%, but was found in low abundance, or absent, in other samples. When Budu samples were not dominated by a dominant taxa, we observed a wider genera diversity such as Staphylococcus, Acinetobacter, Halanaerobium and Bacillus. While the taxonomic composition was relatively stable across sampling periods, samples from two brands showed a sudden increase in relative abundance of the genus Chromobacterium at month 7. Based on prediction of metagenome functions, non-Tetragenococcus-dominated samples were predicted to have enriched functional pathways related to amino acid metabolism and purine metabolism compared to Tetragenococcus-dominated samples; these two pathways are fundamental to fermentation quality and health attributes of fish sauce. Among the non-Tetragenococcus-dominated samples, contributions towards amino acid metabolism and purine metabolism were biased towards the dominant taxa when species evenness is low, while in samples with higher species evenness, the contributions towards the two pathways were predicted to be evenly distributed between taxa. Our results demonstrated that the utility of 16S sequencing to assess batch variation in fermented food production. The distinct microbiota was shown to correlate with characteristic metagenome function including functions potentially related to fermented food nutrition and quality.

1976 ◽  
Vol 54 (9) ◽  
pp. 938-948 ◽  
Author(s):  
Ming Sai Liu ◽  
Johan A. Hellebust

The amino acid metabolism of Cyclotella cryptica is strongly influenced by changes in salinity of the medium. A sudden increase in salinity (water stress) reduces the total uptake of amino acids by the cells and also their assimilation into proteins. Under water-stress conditions, proline is readily synthesized from glutamate, arginine, and ornithine. and proline synthesized under these conditions turns over very slowly and accumulates.Increases in osmolarity of the medium, whether caused by salts, mannitol, or sucrose (but not by glycerol), is followed immediately by rapid synthesis of proline. Proteolysis is not observed under water-stress conditions. The high level of proline accumulated under these conditions is rapidly reduced when the cells are transferred back to low osmolarity media. The loss of 14C from proline is accompanied by rapid incorporation into proteins and also conversion of proline into other cell constituents.The proline level is relatively low in high-salinity-adapted cells, and proline turns over rapidly in such cells. This indicated that the accumulation of proline occurs mainly in response to abrupt changes of intracellular ionic strength during adaptation to increased salinities. Additions of salts and organic substances to cell suspensions in low-salinity media cause plasmolysis followed by rapid deplasmolysis. However, when cells are transferred to high-osmolarity solutions of single salts or organic substances, deplasmolysis is only observed in media containing KCl or glycerol. Increases of external osmolarity cause increases in concentrations of intracellular potassium and free amino acids.


1979 ◽  
Vol 7 (1) ◽  
pp. 261-262
Author(s):  
E. V. ROWSELL

1985 ◽  
Vol 4 ◽  
pp. 141-146 ◽  
Author(s):  
K VESTERBERG ◽  
J BERGSTROM ◽  
P FURST ◽  
U LEANDER ◽  
E VINNARS

Diabetes ◽  
1993 ◽  
Vol 42 (12) ◽  
pp. 1868-1877 ◽  
Author(s):  
L. Luzi ◽  
A. S. Petrides ◽  
R. A. De Fronzo

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