2018
DOI: 10.5194/bg-15-1815-2018
|View full text |Cite
|
Sign up to set email alerts
|

Plant <i>n</i>-alkane production from litterfall altered the diversity and community structure of alkane degrading bacteria in litter layer in lowland subtropical rainforest in Taiwan

Abstract: Abstract. n-Alkane and alkane-degrading bacteria have long been used as crucial biological indicators of paleoecology, petroleum pollution, and oil and gas prospecting. However, the relationship between n-alkane and alkane-degrading bacteria in natural forests is still poorly understood. In this study, long-chain n-alkane (C 14 -C 35 ) concentrations in litterfall, litter layer, and topsoil as well as the diversity and abundance of n-alkane-degrading bacterial communities in litter layers were investigated in … Show more

Help me understand this report
View preprint versions

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

0
3
0

Year Published

2021
2021
2024
2024

Publication Types

Select...
6

Relationship

1
5

Authors

Journals

citations
Cited by 8 publications
(3 citation statements)
references
References 27 publications
0
3
0
Order By: Relevance
“…The DNA library was prepared via the template out of genomic DNA using region of interest-specific primers. The primers (341F: 5’-CCTACGGGNGGCWGCAG-3’/805R:5’-GACTACHVGGGTATCTAATCC-3’) were designed to target the V3 and V4 regions of 16S rDNA [ 55 ]. The PCR reaction solution was composed of 50 ng microbial DNA (5 ng/µL), 5 µL each forward and reverse primer (1 µM), and 12.5 µL 2x Phusion Hot start flex Master Mix, with ddH 2 O added up to 25µL.…”
Section: Methodsmentioning
confidence: 99%
“…The DNA library was prepared via the template out of genomic DNA using region of interest-specific primers. The primers (341F: 5’-CCTACGGGNGGCWGCAG-3’/805R:5’-GACTACHVGGGTATCTAATCC-3’) were designed to target the V3 and V4 regions of 16S rDNA [ 55 ]. The PCR reaction solution was composed of 50 ng microbial DNA (5 ng/µL), 5 µL each forward and reverse primer (1 µM), and 12.5 µL 2x Phusion Hot start flex Master Mix, with ddH 2 O added up to 25µL.…”
Section: Methodsmentioning
confidence: 99%
“…Additionally, sequence data ligation of forward and reverse reads was performed using the CLC bio plate form (Genomic Workbench v.8.5). FASTA files were generated as described by Huang et al [ 26 ]. We used QIIME2 as a sequence analysis tool to further analyze the FASTA files.…”
Section: Methodsmentioning
confidence: 99%
“…For both water and sediment microorganisms, Proteobacteria displayed a relatively high abundance of up to 81.04% (in propanol batch culture) for water microorganisms and 78.44% (in butyric acid batch culture) for sediment microorganisms after the first day of biodegradation (day 1). Proteobacteria have been reported as prominent hydrocarbon-utilizing bacteria in previous studies [52][53][54]. Proteobacteria species contain the alkB-encoded alkane hydroxylase enzyme responsible for the biodegradation of alkanes and their derivatives [55].…”
Section: Relative Abundance At Phyla Levelmentioning
confidence: 99%