2018
DOI: 10.1016/j.foodres.2018.05.076
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Dynamics and diversity of microbial community succession during fermentation of Suan yu, a Chinese traditional fermented fish, determined by high throughput sequencing

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Cited by 130 publications
(72 citation statements)
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“…Dynamic changes to α-diversity indices indicated that the fungal diversity of Panxian ham fluctuated greatly during processing, while bacterial diversity tended to continually decrease ( Table 1). Similar trends have been reported during the Suan yu, a fermentation process for Chinese traditional fermented fish; Zang et al (2018) suggested that chitin (a characteristic component of the fungal cell wall) may be responsible for these results, providing a certain protection against environmental stress. Microbiota structural changes were analyzed using NMDS and PCoA based on Binary-Jaccard distances to evaluate variation and similarity (Figures 3C,D).…”
Section: Abundance and Diversity Of Bacterial And Fungal Microorganismssupporting
confidence: 77%
“…Dynamic changes to α-diversity indices indicated that the fungal diversity of Panxian ham fluctuated greatly during processing, while bacterial diversity tended to continually decrease ( Table 1). Similar trends have been reported during the Suan yu, a fermentation process for Chinese traditional fermented fish; Zang et al (2018) suggested that chitin (a characteristic component of the fungal cell wall) may be responsible for these results, providing a certain protection against environmental stress. Microbiota structural changes were analyzed using NMDS and PCoA based on Binary-Jaccard distances to evaluate variation and similarity (Figures 3C,D).…”
Section: Abundance and Diversity Of Bacterial And Fungal Microorganismssupporting
confidence: 77%
“…These discrepancies may be due to the shortcoming of the length of the sequencing fragment (average length 249.41 bp), and the limitation of the database's classification . Notably, similar phenomena have appeared in some published reports, indicating that there are still deficiencies in the field. Besides, according to culture studies, the number of LAB was at a high level, whereas the relative abundance of LAB was far lower than than that of Bacillus .…”
Section: Discussionmentioning
confidence: 99%
“…The amplification system included 0.3 μM of each primer, 40–60 ng template DNA, 1 μL KOD-FX-Neo (TOYOBO, Osaka, Japan), 1 × buffer and 0.4 mM dNTPs. The amplification conditions were 95°C for 5 min, followed by 15 cycles of 95°C for 1 min, 50°C for 1 min, and 72°C for 1 min, and a final step at 72°C for 7 min ( Zang et al, 2018 ). The amplification products were mixed with VAHTS DNA clean beads (Vazyme, Nanjing, China) for purification, and further amplified by solexa PCR using 0.25 μM of each primer (MPPI-a and MPPI-b), 10 μL purified amplification products, and 1 × Phusion (NEB, Ipswich, Massachusetts).…”
Section: Methodsmentioning
confidence: 99%
“…The amplification products were mixed with VAHTS DNA clean beads (Vazyme, Nanjing, China) for purification, and further amplified by solexa PCR using 0.25 μM of each primer (MPPI-a and MPPI-b), 10 μL purified amplification products, and 1 × Phusion (NEB, Ipswich, Massachusetts). The solexa PCR conditions were 98°C for 30 s, followed by 10 cycles of 98°C for 10 s, 65°C for 30 s, and 72°C for 30 s, and a final step at 72°C for 7 min ( Zang et al, 2018 ). The solexa PCR products were used for DNA library construction after quantification by Qubit 2.0 (Thermo Fisher Scientific, Waltham, MA, United States), mix 1:1 by mass, and DNA gel extraction.…”
Section: Methodsmentioning
confidence: 99%