1998
DOI: 10.1128/aem.64.8.3075-3078.1998
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Screening of a Fosmid Library of Marine Environmental Genomic DNA Fragments Reveals Four Clones Related to Members of the Order Planctomycetales

Abstract: A fosmid library with inserts containing approximately 40 kb of marine bacterial DNA (J. L. Stein, T. L. Marsh, K. Y. Wu, H. Shizuya, and E. F. DeLong, J. Bacteriol. 178:591–599, 1996) yielded four clones with 16S rRNA genes from the orderPlanctomycetales. Three of the clones belong to thePirellula group and one clone belongs to thePlanctomyces group, based on phylogenetic and signature nucleotide analyses of full-length 16S rRNA genes. Sequence analysis of the ends of the genes revealed a consistent mismatch … Show more

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Cited by 150 publications
(67 citation statements)
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“…Béja et al, 2000). Environmental shotgun clone libraries were initially developed for analysis of prokaryote communities (Vergin et al, 1998), but are now being applied to complex, natural assemblages of marine viruses (Breitbart et al, 2002(Breitbart et al, , 2004Steward et al, 2002;Angly et al, 2006). These latter studies have shown that natural assemblages of DNA viruses are extraordinarily diverse, making the reconstruction of a genome by random sequencing an improbable event except with extraordinary sequencing effort (Angly et al, 2006).…”
Section: Metagenomicsmentioning
confidence: 99%
“…Béja et al, 2000). Environmental shotgun clone libraries were initially developed for analysis of prokaryote communities (Vergin et al, 1998), but are now being applied to complex, natural assemblages of marine viruses (Breitbart et al, 2002(Breitbart et al, , 2004Steward et al, 2002;Angly et al, 2006). These latter studies have shown that natural assemblages of DNA viruses are extraordinarily diverse, making the reconstruction of a genome by random sequencing an improbable event except with extraordinary sequencing effort (Angly et al, 2006).…”
Section: Metagenomicsmentioning
confidence: 99%
“…A negative control with no sample added was included in the extraction procedure and yielded no detectable DNA. Primers 27f-HEX (5-AGRGTTT-GATCMTGGCTCAG-3) (Vergin et al, 1998) and 519r (5-GWATTACCGCGGCKGCTG-3) (Lane et al, 1985) were used for amplification of 16S rRNA gene fragments. The forward primer was labelled with hexachloro-fluoroscein (HEX; Sigma-Aldrich, Suffolk, U.K.) at the 5¢ end to allow for fluorescent detection of terminal restriction fragments.…”
Section: Bacterial Community Compositionmentioning
confidence: 99%
“…Relationships were determined using the neighbour-joining method with Jukes-Cantor correction and checked for consistency using parsimony. The most variable regions (E. coli positions 452-463 and 849-850) were excluded from phylogenetic analyses of single representative Vergin et al (1998) by incorporating a degeneracy (T/C) at position 1508 (E. coli numbering).…”
Section: Sequence Analysismentioning
confidence: 99%
“…16S rRNA gene-targeted primers. TAC CTT GTT AYG ACT T Most Bacteria and ArchaeaLane (1991);Vergin et al (1998) a. 16S rRNA positions; E. coli numbering.…”
mentioning
confidence: 99%