2020
DOI: 10.1080/01490451.2020.1822959
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Diversity and Abundance of Denitrifying Bacteria in the Sediment of a Eutrophic Estuary

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Cited by 14 publications
(6 citation statements)
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References 49 publications
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“…The differential abundance between nirS and nirK may be due to the competition for the substrates required by different enzyme synthesis (Huang et al, 2011). Moreover, compared to nirK-encoding denitrifiers, the variety of nirS-encoding denitrifiers was also greater, which is consistent with previous studies (Shi et al, 2019b;Ming et al, 2021). In general, nirS-and nirK-encoding denitrifiers had different respond to environmental parameters, and nirS denitrifiers had better adaptation to the coastal environments (Jones and Hallin, 2010;Likhitrattanapisal et al, 2021).…”
Section: Discussionsupporting
confidence: 86%
“…The differential abundance between nirS and nirK may be due to the competition for the substrates required by different enzyme synthesis (Huang et al, 2011). Moreover, compared to nirK-encoding denitrifiers, the variety of nirS-encoding denitrifiers was also greater, which is consistent with previous studies (Shi et al, 2019b;Ming et al, 2021). In general, nirS-and nirK-encoding denitrifiers had different respond to environmental parameters, and nirS denitrifiers had better adaptation to the coastal environments (Jones and Hallin, 2010;Likhitrattanapisal et al, 2021).…”
Section: Discussionsupporting
confidence: 86%
“…In the case of nitrite reductase, the most remarkable aspect is that all the retrieved sequences code for copper-nitrite reductases type (NirK); consequently, none of them are cytochrome cd 1 -nitrite reductase type (NirS). Interestingly, many previous studies investigating the distribution of nirS and nirK along different ecosystems indicate that environmental conditions such as low oxygen availability, high water content or high salinity are favourable for the nirS carrying communities [ 23 , 48 , 49 , 50 , 51 ]. Furthermore, in these studies it is also pointed out that nirK gene is not even detectable in samples at “high salinity” [ 49 , 52 , 53 ].…”
Section: Resultsmentioning
confidence: 99%
“…Interestingly, many previous studies investigating the distribution of nirS and nirK along different ecosystems indicate that environmental conditions such as low oxygen availability, high water content or high salinity are favourable for the nirS carrying communities [ 23 , 48 , 49 , 50 , 51 ]. Furthermore, in these studies it is also pointed out that nirK gene is not even detectable in samples at “high salinity” [ 49 , 52 , 53 ]. However, it is worth highlighting that these studies are neither carried out nor focused on hypersaline environments, such as salt marshes or salty ponds, whose microbial communities differ from other less saline ecosystems and in which the Archaea domain populations are predominant [ 2 , 54 , 55 ].…”
Section: Resultsmentioning
confidence: 99%
“…The 16S NGS results showed that the distribution of potentially pathogenic bacteria in the Liaohe estuary was mainly abundant in the nearshore N area. According to previous studies (Ming et al, 2020), the estuary had the characteristics of high sewage discharge, high population density, and eutrophication which could be the main reason for the high abundance of potentially pathogenic bacteria in the nearshore N area. Our study detected Vibrio with high abundance using both 16S NGS and qPCR techniques.…”
Section: Distribution Of Potential Pathogens In the Estuarymentioning
confidence: 99%