2001
DOI: 10.1128/aem.67.11.5308-5314.2001
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Recovery and Phylogenetic Analysis of nifH Sequences from Diazotrophic Bacteria Associated with Dead Aboveground Biomass of Spartina alterniflora

Abstract: DNA was extracted from dry standing dead Spartina alterniflora stalks as well as dry Spartina wrack from the North Inlet (South Carolina) and Sapelo Island (Georgia) salt marshes. Partial nifH sequences were PCR amplified, the products were separated by denaturing gradient gel electrophoresis (DGGE), and the prominent DGGE bands were sequenced. Most sequences (109 of 121) clustered with those from ␣-Proteobacteria, and 4 were very similar (>99%) to that of Azospirillum brasilense. Seven sequences clustered wit… Show more

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Cited by 65 publications
(67 citation statements)
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“…It appears that the sequence diversity in the system was relatively low compared to most estuarine and benthic systems, but the community included components that reflected open ocean, benthic and estuarine origins. Open ocean photic layer microbial communities appear to have lower nifH diversity and different community composition (Zehr et al, 1998) from coastal and estuarine (Jenkins et al, 2004), and benthic communities, including microbial mats (Omoregie et al, 2005), coral reefs (Hewson et al, 2007b) and salt marshes (Lovell et al, 2001;Moisander et al, 2005). However, in the high-diversity coastal and benthic systems, a large proportion of the community nifH genes is not expressed, at least not at detectable levels (Moisander et al, 2006;Man-Aharonovich et al, 2007;Short and Zehr, 2007).…”
Section: Discussionmentioning
confidence: 99%
“…It appears that the sequence diversity in the system was relatively low compared to most estuarine and benthic systems, but the community included components that reflected open ocean, benthic and estuarine origins. Open ocean photic layer microbial communities appear to have lower nifH diversity and different community composition (Zehr et al, 1998) from coastal and estuarine (Jenkins et al, 2004), and benthic communities, including microbial mats (Omoregie et al, 2005), coral reefs (Hewson et al, 2007b) and salt marshes (Lovell et al, 2001;Moisander et al, 2005). However, in the high-diversity coastal and benthic systems, a large proportion of the community nifH genes is not expressed, at least not at detectable levels (Moisander et al, 2006;Man-Aharonovich et al, 2007;Short and Zehr, 2007).…”
Section: Discussionmentioning
confidence: 99%
“…Hsu and Buckley (2009) found that the nitrogen-fixing bacterial community structure differed across treatments as a function of vegetation biomass. Lovell et al (2001) also demonstrated that differences in the nitrogen-fixing bacterial community are closely associated with vegetation biomass. In the meadow soil beneath Carex, the nifH gene diversity was primarily affected by altitude, while abundance was primarily affected by soil-available K. Zhang et al (2006) found that altitude was one of the key factors influencing the nitrogen-fixing bacterial community in alpine prairie soil.…”
Section: Discussionmentioning
confidence: 99%
“…CV4 was amplified from offshore and oligotrophic stations A, D, E and F and has 99.7% nucleotide sequence similarity to sequences reported in the North Pacific (e.g., EU159536; Fong et al, 2008) and Gulf of Aqaba (DQ825729; Foster et al, 2009a). CV5 (5.1%) is most closely related (90% nucleotide similarity) to a nifH sequence from an uncultivated a-proteobacteria (AF389713) associated with a marsh cordgrass, Spartina alterniflora (Lovell et al, 2001). This phylotype is closely related (88% nucleotide similarity) to a-24809A06, which Moisander et al (2008) used in the design of a qPCR assay, but has too many mismatches in the primer/ probe region to be amplified.…”
Section: Resultsmentioning
confidence: 99%