A PCR approach was used to construct a database of nasA genes (called narB
genes in cyanobacteria) and to detect the genetic potential for heterotroph
ic bacterial nitrate utilization in marine environments. A nasA-specific PC
R primer set that could be used to selectively amplify the nasA gene from h
eterotrophic bacteria was designed. Using seawater DNA extracts obtained fr
om microbial communities in the South Atlantic Bight, the Barents Sea, and
the North Pacific Gyre, we PCR amplified and sequenced nasA genes. Our resu
lts indicate that several groups of heterotrophic bacterial nasA genes are
common and widely distributed in oceanic environments.