2010
DOI: 10.1264/jsme2.me09166
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Similarity of Bacterial Community Structure between Asian Dust and Its Sources Determined by rRNA Gene-Targeted Approaches

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Cited by 21 publications
(24 citation statements)
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References 32 publications
(29 reference statements)
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“…Realtime PCR was performed with universal primer sets EUB f933 (5′-GCA CAA GCG GTG GAG CAT GTG G-3′) and EUB r1387 (5′-GCC CGG GAA CGT ATT CAC CG-3′) 27) according to the procedure reported by Nishimura et al 28) To determine the recovery rate of DNA during extraction, known amounts of DNA fragment of the luciferase gene (luc) were inoculated into the samples before DNA extraction as an internal standard and quantified after DNA extraction.…”
Section: )mentioning
confidence: 99%
“…Realtime PCR was performed with universal primer sets EUB f933 (5′-GCA CAA GCG GTG GAG CAT GTG G-3′) and EUB r1387 (5′-GCC CGG GAA CGT ATT CAC CG-3′) 27) according to the procedure reported by Nishimura et al 28) To determine the recovery rate of DNA during extraction, known amounts of DNA fragment of the luciferase gene (luc) were inoculated into the samples before DNA extraction as an internal standard and quantified after DNA extraction.…”
Section: )mentioning
confidence: 99%
“…The transport of microbes by Asian dust has been reported Lee et al, 2009), and the presence of pathogens and allergens, with the potential to affect the health of downwind populations and ecosystems, was also revealed (Kellogg and Griffin, 2006). More than 2 × 10 13 to 4 × 10 16 bacterial cells km − 2 per month were estimated to be transported to Beijing by Asian dust (Nishimura et al, 2010). To identify bacteria in Asian dust, classical cultivation methods have been used to compare the differences in atmospheric colony-forming units (CFU) between normal and Asian dust days (Choi et al, 1997;Iwasaka et al, 2009).…”
Section: Introductionmentioning
confidence: 99%
“…As a minority of environmental bacteria can be cultured under standard laboratory conditions (Amann et al, 1995), the observed CFU counts likely represent a fraction of the actual bacterial diversity. Cultureindependent methods, such as denaturing gradient gel electrophoresis and terminal restriction fragment length polymorphism, are being increasingly used in these studies (Lee et al, 2009;Jeon et al, 2010;Nishimura et al, 2010). Using terminal restriction fragment length polymorphism analysis, Nishimura et al (2010) showed that the bacterial community structures in Asian dust samples differed greatly according to the scale of the dust event.…”
Section: Introductionmentioning
confidence: 99%
“…In particular, denaturing gradient gel electrophoresis (DGGE) 9) has been used to determine the genetic diversity of natural microbial communities and to identify the phylogenetic affiliation of community members. [10][11][12] Polymerase chain reaction (PCR)-amplified DNA fragments of the eubacterial 16S ribosomal RNA (rRNA) gene that have the same length but different sequences can be separated by DGGE. However, PCR-DGGE analysis is often difficult to implement with freshwater samples from eutrophic environments that contain PCR-inhibitors, such as humic acid.…”
mentioning
confidence: 99%