2018
DOI: 10.1016/j.apsoil.2018.04.013
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Green manure amendment enhances microbial activity and diversity in antibiotic-contaminated soil

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Cited by 50 publications
(19 citation statements)
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“…Proteobacteria, Actinobacteria, and Bacteroidetes play a part in organic mineralization and S-, N-, C-cycling (Ali et al 2019;Liang et al 2020), and the main bacterial communities that belong to them are associated with soil antibioticsresistant and antibiotics-degrading (Caban et al 2018). In our study, Proteobacteria and Acidobacteria were the dominant bacteria, accounting for 46.4% and 24.8% of soil bacteria, respectively ( Fig.…”
Section: Discussionmentioning
confidence: 51%
“…Proteobacteria, Actinobacteria, and Bacteroidetes play a part in organic mineralization and S-, N-, C-cycling (Ali et al 2019;Liang et al 2020), and the main bacterial communities that belong to them are associated with soil antibioticsresistant and antibiotics-degrading (Caban et al 2018). In our study, Proteobacteria and Acidobacteria were the dominant bacteria, accounting for 46.4% and 24.8% of soil bacteria, respectively ( Fig.…”
Section: Discussionmentioning
confidence: 51%
“…The DNA samples were extracted from 0.5 g of each sample with the FastDNA SPIN for Soil Kit (MP Biomedicals, Santa Ana, CA, USA), following the instructions of the manufacturer. The region of 16S rRNA V3‐V4 was reinforced for each specimen by utilizing primer sets of 338Fand 806R (Xu et al, 2017), and the internal transcribed spacer (ITS) primer regions of gene (ITS1F‐ITS2F) (Caban et al, 2018; Nottingham et al, 2018). The PCR components contained 25 μl of 5 μl of 5× Q5 reaction buffer, 5 μl of 5× Q5 High‐Fidelity GC buffer, 0.25 μl of Q5 High‐Fidelity DNA polymerase (5 U μl −1 ), 1 μl (10 uM) of each Forward and Reverse primers, 2 μl (2.5 mM) of dNTPs, 2 μl of DNA template, and 8.75 μl of ddH 2 O.…”
Section: Methodsmentioning
confidence: 99%
“…The DNA of samples was extracted from 0.5 g of soil with the FastDNA SPIN Kit for Soil (MP Biomedicals, Santa Ana, California), according to the manufacturer's instructions. The genomic DNA was amplified by PCR using the 16 S rRNA gene V3-V4 hypervariable region primers (338F and 806R) (Xu, Tan, Wang, & Gai, 2016), and the Internal Transcribed Spacer (ITS) gene region primers (ITS1F-ITS2) (Caban et al, 2018;Nottingham et al, 2018). PCR reactions: 8.75 μl of ddH 2 O; 5 μl of Q5 reaction buffer (×5) and Q5 High-Fidelity GC buffer (×5), respectively; 2 μl of dNTPs (2.5 mM) and DNA Template, respectively; 1 μl (10 uM) of forward and reverse primers, respectively; 0.25 μl (5 U/μl) of Q5 High-Fidelity DNA Polymerase, a total of 25 μl mixture (Deng, Yin, Zhu, & Zhou, 2018).…”
Section: Soil Dna Extraction and Amplification Of Sequencingmentioning
confidence: 99%