2001
DOI: 10.1128/aem.67.11.5343-5348.2001
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Diversity and Detection of Nitrate Assimilation Genes in Marine Bacteria

Abstract: A PCR approach was used to construct a database of nasA genes (called narB genes in cyanobacteria) and to detect the genetic potential for heterotrophic bacterial nitrate utilization in marine environments. A nasA-specific PCR primer set that could be used to selectively amplify the nasA gene from heterotrophic bacteria was designed. Using seawater DNA extracts obtained from microbial communities in the South Atlantic Bight, the Barents Sea, and the North Pacific Gyre, we PCR amplified and sequenced nasA genes… Show more

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Cited by 111 publications
(89 citation statements)
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“…In a study of coral mucus additions to seawater (Allers et al, 2008), a rapid increase in the abundance of Alteromonas bacteria concomitant with significant decreases in the C:N ratio of particulate organic matter was found, suggesting that they rapidly assimilated dissolved organic carbon. Marinobacter is the most common heterotrophic organism associated with libraries of the assimilatory nitrate uptake gene nasB in nitraterich waters (Allen et al, 2001). Trichodesmium is known to exude fixed N and C into surrounding waters (Capone et al, 1994;Mulholland et al, 2006).…”
Section: Metatranscriptome Library Characteristicsmentioning
confidence: 99%
“…In a study of coral mucus additions to seawater (Allers et al, 2008), a rapid increase in the abundance of Alteromonas bacteria concomitant with significant decreases in the C:N ratio of particulate organic matter was found, suggesting that they rapidly assimilated dissolved organic carbon. Marinobacter is the most common heterotrophic organism associated with libraries of the assimilatory nitrate uptake gene nasB in nitraterich waters (Allen et al, 2001). Trichodesmium is known to exude fixed N and C into surrounding waters (Capone et al, 1994;Mulholland et al, 2006).…”
Section: Metatranscriptome Library Characteristicsmentioning
confidence: 99%
“…The universal bacterial primers 27F (5 0 -AGAGTTTGATCCTGGCTCAG-3 0 ) and 1492R (5 0 -GGTTACCTTGTTACGACTT-3 0 ) were used to amplify community DNA. The nitrate assimilation gene nasA was amplified using the primers nas964 and nasA1735 [15] and newly designed primer set: nasF30 (5 0 -TAYTGYGGBGTNGGNTG-3 0 ) and nasR1080 (5 0 -CCCATNGCRTTNGGYTG-3 0 ) in this study, with the following cycling conditions: 95°C for 4 min, followed by 30 cycles, 95°C for 50 s, 30 s at 53°C, 50 s at 72°C, with a 7 min final extension. The PCR products were gel-purified and ligated into pMD18-T vectors, then transformed into Escherichia coli DH5a competent cells (TaKaRa, Dalian, China).…”
Section: Sample Collectionmentioning
confidence: 99%
“…The concentration of nitrate was high in the deep ocean. The spacial distribution of nitrate-assimilating bacteria (NAB) has been investigated using the nasA gene in various oceanic surface waters [15][16][17]. However, these studies were not emphasized on the difference of NAB in the vertical dimension.…”
Section: Introductionmentioning
confidence: 99%
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“…Res., 9 (5): 223-236, 2015 Bacterial Genomic DNA extraction kit (Bio Basic, Canada) according to the manufacturer's instruction. The partial DNA fragment of bacterial 16S rRNA gene was amplified by PCR using a forward primer fd1 (5'-AGAGTTTGATCCTGGCTCAG-3') and a reverse primer rp2 (5'-ACGGCTACCTTGTTACGACTT-3') (Allen et al, 2001). For the ITS region, the highly conserved sequences were designed based on published sequences with adjacent 3' end region of the 16S rRNA and 5' end region of the 23S rDNA using a forward primer ITS-16SF (5'-CGGTGAATACGTTCCCGGGYCTTG-3') and a reverse primer ITS-23SR (5'-TTTCRCCTTTCCCTCACGGTA-3').…”
Section: Amplification Of 16s Rrna and Internal Transcribed Region (Imentioning
confidence: 99%