2008
DOI: 10.1111/j.1574-6968.2007.01029.x
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Does capillary racetrack-based enrichment reflect the diversity of uncultivated magnetotactic cocci in environmental samples?

Abstract: The racetrack-based PCR approach is widely used in phylogenetic analysis of magnetotactic bacteria (MTB), which are isolated from environmental samples using the capillary racetrack method. To evaluate whether the capillary racetrack-based enrichment can truly reflect the diversity of MTB in the targeted environmental sample, phylogenetic diversity studies of MTB enriched from the Miyun lake near Beijing were carried out, using both the capillary racetrack-based PCR and a modified metagenome-based PCR approach… Show more

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Cited by 31 publications
(32 citation statements)
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“…These cocci might be Alphaproteobacteria MTB that often coexist with "Ca. Magnetobacterium bavaricum"-like bacteria in Lake Miyun as described previously (14)(15)(16)(17). Transmission electron microscopic analysis demonstrated that these cells had different magnetosome morphologies and arrangements (see Fig.…”
Section: Fig 1 (A)mentioning
confidence: 59%
“…These cocci might be Alphaproteobacteria MTB that often coexist with "Ca. Magnetobacterium bavaricum"-like bacteria in Lake Miyun as described previously (14)(15)(16)(17). Transmission electron microscopic analysis demonstrated that these cells had different magnetosome morphologies and arrangements (see Fig.…”
Section: Fig 1 (A)mentioning
confidence: 59%
“…Nearly complete 16S rRNA genes were amplified directly from magnetically enriched MTB cells in which MWB-1 was dominant by using the universal bacterial primers 27F (5=-AGAGTTTGATCCTGGCTCAG-3=) and 1492R (5=-GGTTACCTTG TTACGACTT-3=) as described previously (31,34). PCR was performed using a T-Gradient thermocycler (Whatman Biometra, Göttingen, Germany).…”
Section: Methodsmentioning
confidence: 99%
“…The bacterial universal primers 27F (5Ј-AGAGTTTGATCCTGGCTCAG-3Ј) and 1492R (5Ј-GGTTACCTTGTTACGACTT-3Ј) (5) were used to amplify 16S rRNA genes directly from the 20 l of magnetically enriched MTB. PCR amplification and cloning procedures for construction of a 16S rRNA genes clone library were performed as previously reported (22,23). Twenty clones were randomly picked up and subjected to sequencing.…”
Section: Methodsmentioning
confidence: 99%