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Applied and Environmental Microbiology, November 2001, p. 5343-5348, Vol. 67, No. 11
Institute of Ecology, University of Georgia,
Athens, Georgia 306021; Skidaway
Institute of Oceanography, Savannah, Georgia
314112; Ocean Sciences Department,
University of California, Santa Cruz, Santa Cruz, California
950643; and Department of Biology,
Rensselaer Polytechnic Institute, Troy, New York
12180-35904
Received 9 March 2001/Accepted 31 July 2001
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. Our results indicate that several groups of
heterotrophic bacterial nasA genes are common and widely
distributed in oceanic environments.
0099-2240/01/$04.00+0 DOI: 10.1128/AEM.67.11.5343-5348.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Diversity and Detection of Nitrate Assimilation
Genes in Marine Bacteria
*
Corresponding author. Mailing address: Skidaway
Institute of Oceanography, 10 Ocean Science Circle, Savannah, GA 31411. Phone: (912) 598-2441. Fax: (912) 598-2310. E-mail:
frischer{at}skio.peachnet.edu.
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