2021
DOI: 10.1007/s00284-021-02419-7
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Anaerobic Degradation of Propanil in Soil and Sediment Using Mixed Bacterial Culture

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Cited by 7 publications
(3 citation statements)
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“…The degradation rate of propanil reached 60% at 2 h and the highest degradation rate of 84% at 8 h. Furthermore, the degradation product of propanil by AmiH52 was determined as 3,4-dichloroaniline (3,4-DCA), which is consistent with previous studies (Herrera-Gonzalez et al 2013 ; Zhang et al 2011 , 2019 ). In contrast, a mixed culture of four bacterial strains, which were isolated from the sediment slurry, transformed 90% of propanil within 10 days in liquid media (Oanh and Duc 2021 ). Another study reported that 81% of propanil was degraded after 100 days of incubation in an anaerobic soil environment (Pettigrew et al 1985 ).…”
Section: Discussionmentioning
confidence: 99%
“…The degradation rate of propanil reached 60% at 2 h and the highest degradation rate of 84% at 8 h. Furthermore, the degradation product of propanil by AmiH52 was determined as 3,4-dichloroaniline (3,4-DCA), which is consistent with previous studies (Herrera-Gonzalez et al 2013 ; Zhang et al 2011 , 2019 ). In contrast, a mixed culture of four bacterial strains, which were isolated from the sediment slurry, transformed 90% of propanil within 10 days in liquid media (Oanh and Duc 2021 ). Another study reported that 81% of propanil was degraded after 100 days of incubation in an anaerobic soil environment (Pettigrew et al 1985 ).…”
Section: Discussionmentioning
confidence: 99%
“…1.0 g of soil collected from every single experiment was diluted with sterile distilled water (1:10; w/v), from which bacterial DNA was isolated using the UltraCleanTM Soil DNA Isolation Kit (Mo Bio Laboratories, Inc., Solana Beach, CA, USA). The relative abundance of the bacterial community in soil was determined through Illumina MiSeq sequencing of 16 S rRNA genes as described in a previous study (Oanh & Duc, 2021). The relative abundances of the bacterial species in the soil slurries were determined by sequencing 16 S rRNA genes using an Illumina MiSeq bench-top sequencer.…”
Section: Diversity and Relative Abundance Of Soil Bacterial Communitymentioning
confidence: 99%
“…16S rRNA and ITS sequences of distinct regions (16S V3-V4, ITS1) were amplified using specific primers with a barcode. The forward primer 338F (5 -ACTCCTACGGGAGGCAG CAG-3 ) and the reverse primer 806R (5 -GGACTACHVGGGTWTCTAAT-3 ) were used to amplify the V3-V4 region of 16S rRNA genes [25]. The ITS1 region of fungal nuclear DNA was amplified with primers ITS1F (5 -CTTGGTCATTTAGAGGAAGTAA-3 ) and ITS2 (5 -GCTGCGTTCTTCATCGATGC-3 ) [26].…”
Section: Gene Amplicons and Illumina Miseq Sequencingmentioning
confidence: 99%