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Journal of Bacteriology, February 2000, p. 825-828, Vol. 182, No. 3
Department of Fermentation Technology,
Hiroshima University, Higashi-Hiroshima, Hiroshima 739-8527, Japan
Received 27 August 1999/Accepted 3 November 1999
Pulsed-field gel electrophoresis of PmeI digests of the
Nitrosomonas sp. strain ENI-11 chromosome produced four
bands ranging from 1,200 to 480 kb in size. Southern hybridizations
suggested that a 487-kb PmeI fragment contained two copies
of the amoCAB genes, coding for ammonia monooxygenase
(designated amoCAB1 and amoCAB2), and three copies of the
hao gene, coding for hydroxylamine oxidoreductase
(hao1, hao2, and
hao3). In this DNA fragment,
amoCAB1 and amoCAB2
were about 390 kb apart, while hao1,
hao2, and hao3 were
separated by at least about 100 kb from each other. Interestingly, hao1 and hao2 were
located relatively close to amoCAB1 and
amoCAB2, respectively. DNA sequence analysis
revealed that hao1 and
hao2 shared 160 identical nucleotides
immediately upstream of each translation initiation codon. However,
hao3 showed only 30% nucleotide identity in
the 160-bp corresponding region.
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Physical Map Location of the Multicopy Genes Coding for Ammonia
Monooxygenase and Hydroxylamine Oxidoreductase in the
Ammonia-Oxidizing Bacterium Nitrosomonas sp. Strain
ENI-11
*
Corresponding author. Mailing address: Department of
Fermentation Technology, Hiroshima University, Higashi-Hiroshima,
Hiroshima 739-8527, Japan. Phone: 81-824-24-7756. Fax: 81-824-22-3758. E-mail: hohtake{at}ipc.hiroshima-u.ac.jp.
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