Diversity of ammonia monooxygenase operon in autotrophic ammonia-oxidizing bacteria

@article{citeulike:2783640, abstract = {Autotrophic ammonia-oxidizing bacteria use the essential enzyme ammonia monooxygenase (AMO) to transform ammonia to hydroxylamine. The amo operon consists of at least three genes, amoC, amoA, and amoB; amoA encodes the subunit containing the putative enzyme active site. The use of the amo genes as functional markers for ammonia-oxidizing bacteria in environmental applications requires knowledge of the diversity of the amo operon on several levels: (1) the copy number of the operon in the genome, (2) the arrangement of the three genes in an individual operon, and (3) the primary sequence of the individual genes. We present a database of amo gene sequences for pure cultures of ammonia-oxidizing bacteria representing both the \&\#35- and the \&\#37-subdivision of Proteobacteria in the following genera: Nitrosospira (6 strains), Nitrosomonas (5 strains) and Nitrosococcus (2 strains). The amo operon was found in multiple (2-3) nearly identical copies in the \&\#35-subdivision representatives but in single copies in the \&\#37-subdivision ammonia oxidizers. The analysis of the deduced amino acid sequence revealed strong conservation for all three Amo peptides in both primary and secondary structures. For the amoA gene within the \&\#35-subdivision, nucleotide identity values are approximately 85\% within the Nitrosomonas or the Nitrosospira groups, but approximately 75\% when comparing between these groups. Conserved regions in amoA and amoC were identified and used as primer sites for PCR amplification of amo genes from pure cultures, enrichments and the soil environment. The intergenic region between amoC and amoA is variable in length and may be used to profile the community of ammonia-oxidizing bacteria in environmental samples. Electronic supplementary material to this paper can be obtained by using the Springer LINK server located at http://dx.doi.org/10.1007/s00203-001-0369-z.}, author = {Norton, Jeanette and Alzerreca, Javier and Suwa, Yuichi and Klotz, Martin }, citeulike-article-id = {2783640}, doi = {10.1007/s00203-001-0369-z}, journal = {Archives of Microbiology}, keywords = {amoa, autotrophs, lh-pcr}, month = {February}, number = {2}, pages = {139--149}, posted-at = {2008-05-11 03:49:43}, priority = {2}, title = {Diversity of ammonia monooxygenase operon in autotrophic ammonia-oxidizing bacteria}, url = {http://dx.doi.org/10.1007/s00203-001-0369-z}, volume = {177}, year = {2002} }

TY - JOUR ID - citeulike:2783640 L3 - citeulike-article-id:2783640 TI - Diversity of ammonia monooxygenase operon in autotrophic ammonia-oxidizing bacteria JF - Archives of Microbiology VL - 177 IS - 2 SP - 139 EP - 149 N2 - Autotrophic ammonia-oxidizing bacteria use the essential enzyme ammonia monooxygenase (AMO) to transform ammonia to hydroxylamine. The amo operon consists of at least three genes, amoC, amoA, and amoB; amoA encodes the subunit containing the putative enzyme active site. The use of the amo genes as functional markers for ammonia-oxidizing bacteria in environmental applications requires knowledge of the diversity of the amo operon on several levels: (1) the copy number of the operon in the genome, (2) the arrangement of the three genes in an individual operon, and (3) the primary sequence of the individual genes. We present a database of amo gene sequences for pure cultures of ammonia-oxidizing bacteria representing both the &#35- and the &#37-subdivision of Proteobacteria in the following genera: Nitrosospira (6 strains), Nitrosomonas (5 strains) and Nitrosococcus (2 strains). The amo operon was found in multiple (2-3) nearly identical copies in the &#35-subdivision representatives but in single copies in the &#37-subdivision ammonia oxidizers. The analysis of the deduced amino acid sequence revealed strong conservation for all three Amo peptides in both primary and secondary structures. For the amoA gene within the &#35-subdivision, nucleotide identity values are approximately 85% within the Nitrosomonas or the Nitrosospira groups, but approximately 75% when comparing between these groups. Conserved regions in amoA and amoC were identified and used as primer sites for PCR amplification of amo genes from pure cultures, enrichments and the soil environment. The intergenic region between amoC and amoA is variable in length and may be used to profile the community of ammonia-oxidizing bacteria in environmental samples. Electronic supplementary material to this paper can be obtained by using the Springer LINK server located at http://dx.doi.org/10.1007/s00203-001-0369-z. KW - amoa KW - autotrophs KW - lh-pcr AU - Norton, Jeanette AU - Alzerreca, Javier AU - Suwa, Yuichi AU - Klotz, Martin PY - 2002/02/01/ UR - http://dx.doi.org/10.1007/s00203-001-0369-z ER -