A new classification system for bacterial Rieske non-heme iron aromatic ring-hydroxylating oxygenases
Rieske non-heme iron aromatic ring-hydroxylating oxygenases (RHOs) are multi-component enzyme systems that are remarkably diverse in bacteria isolated from diverse habitats. Since the first classification in 1990, there has been a need to devise a new classification scheme for these enzymes because...
Gespeichert in:
Veröffentlicht in: | BMC biochemistry 2008-04, Vol.9 (1), p.11-11, Article 11 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 11 |
---|---|
container_issue | 1 |
container_start_page | 11 |
container_title | BMC biochemistry |
container_volume | 9 |
creator | Kweon, Ohgew Kim, Seong-Jae Baek, Songjoon Chae, Jong-Chan Adjei, Michael D Baek, Dong-Heon Kim, Young-Chang Cerniglia, Carl E |
description | Rieske non-heme iron aromatic ring-hydroxylating oxygenases (RHOs) are multi-component enzyme systems that are remarkably diverse in bacteria isolated from diverse habitats. Since the first classification in 1990, there has been a need to devise a new classification scheme for these enzymes because many RHOs have been discovered, which do not belong to any group in the previous classification. Here, we present a scheme for classification of RHOs reflecting new sequence information and interactions between RHO enzyme components.
We have analyzed a total of 130 RHO enzymes in which 25 well-characterized RHO enzymes were used as standards to test our hypothesis for the proposed classification system. From the sequence analysis of electron transport chain (ETC) components of the standard RHOs, we extracted classification keys that reflect not only the phylogenetic affiliation within each component but also relationship among components. Oxygenase components of standard RHOs were phylogenetically classified into 10 groups with the classification keys derived from ETC components. This phylogenetic classification scheme was converted to a new systematic classification consisting of 5 distinct types. The new classification system was statistically examined to justify its stability. Type I represents two-component RHO systems that consist of an oxygenase and an FNRC-type reductase. Type II contains other two-component RHO systems that consist of an oxygenase and an FNRN-type reductase. Type III represents a group of three-component RHO systems that consist of an oxygenase, a [2Fe-2S]-type ferredoxin and an FNRN-type reductase. Type IV represents another three-component systems that consist of oxygenase, [2Fe-2S]-type ferredoxin and GR-type reductase. Type V represents another different three-component systems that consist of an oxygenase, a [3Fe-4S]-type ferredoxin and a GR-type reductase.
The new classification system provides the following features. First, the new classification system analyzes RHO enzymes as a whole. RwithSecond, the new classification system is not static but responds dynamically to the growing pool of RHO enzymes. Third, our classification can be applied reliably to the classification of incomplete RHOs. Fourth, the classification has direct applicability to experimental work. Fifth, the system provides new insights into the evolution of RHO systems based on enzyme interaction. |
doi_str_mv | 10.1186/1471-2091-9-11 |
format | Article |
fullrecord | <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2358900</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A178468466</galeid><sourcerecordid>A178468466</sourcerecordid><originalsourceid>FETCH-LOGICAL-b5521-36cc19e3331589450a31dd9d215d03d0af7f5793cba99e602d871f670e97d6ce3</originalsourceid><addsrcrecordid>eNqFkt-L1DAQx4Mo3nn66qMEBd96Zpo2bV6E5fAXHAiizyFNJt1om5xJV93_3pRdzjs8kQQyzHzmx5cJIU-BnQP04hU0HVQ1k1DJCuAeOb123L9hn5BHOX9lDLqeNQ_JCfS870C2pwQ3NOBPaiads3fe6MXHQPM-LzhTFxMdtFkweT3RTx7zN6QhhmqLM1KfCqlTnEuOocmHsdrubYq_9lPxhJEWa8SgM-bH5IHTU8Ynx_eMfHn75vPF--ry47sPF5vLamjbGioujAGJnHNoe9m0THOwVtoaWsu4Zdp1ru0kN4OWEgWrbVHhRMdQdlYY5Gfk9aHu1W6Y0RoMS9KTukp-1mmvovbqdiT4rRrjD1Xz0pCxUuD5oUDMi1fZ-AXN1sQQ0CwKRC17Lgu0OUCDj__ocjti4qzWXah1F0oqgFLj5XHSFL_vMC9q9tngNOmAcZeVkNBIJvl_QZBl7q4RBXxxAEc9ofLBxdLbrLDalL03otyVOr-DKsfi7ItQdL7470owKeac0F3rBKbWL_i3smc3d_AHP_45_htlLddI</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>19900746</pqid></control><display><type>article</type><title>A new classification system for bacterial Rieske non-heme iron aromatic ring-hydroxylating oxygenases</title><source>MEDLINE</source><source>BioMedCentral</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><source>Springer Nature OA/Free Journals</source><source>PubMed Central Open Access</source><creator>Kweon, Ohgew ; Kim, Seong-Jae ; Baek, Songjoon ; Chae, Jong-Chan ; Adjei, Michael D ; Baek, Dong-Heon ; Kim, Young-Chang ; Cerniglia, Carl E</creator><creatorcontrib>Kweon, Ohgew ; Kim, Seong-Jae ; Baek, Songjoon ; Chae, Jong-Chan ; Adjei, Michael D ; Baek, Dong-Heon ; Kim, Young-Chang ; Cerniglia, Carl E ; Oak Ridge Institute for Science and Education (ORISE), Oak Ridge, TN (United States)</creatorcontrib><description>Rieske non-heme iron aromatic ring-hydroxylating oxygenases (RHOs) are multi-component enzyme systems that are remarkably diverse in bacteria isolated from diverse habitats. Since the first classification in 1990, there has been a need to devise a new classification scheme for these enzymes because many RHOs have been discovered, which do not belong to any group in the previous classification. Here, we present a scheme for classification of RHOs reflecting new sequence information and interactions between RHO enzyme components.
We have analyzed a total of 130 RHO enzymes in which 25 well-characterized RHO enzymes were used as standards to test our hypothesis for the proposed classification system. From the sequence analysis of electron transport chain (ETC) components of the standard RHOs, we extracted classification keys that reflect not only the phylogenetic affiliation within each component but also relationship among components. Oxygenase components of standard RHOs were phylogenetically classified into 10 groups with the classification keys derived from ETC components. This phylogenetic classification scheme was converted to a new systematic classification consisting of 5 distinct types. The new classification system was statistically examined to justify its stability. Type I represents two-component RHO systems that consist of an oxygenase and an FNRC-type reductase. Type II contains other two-component RHO systems that consist of an oxygenase and an FNRN-type reductase. Type III represents a group of three-component RHO systems that consist of an oxygenase, a [2Fe-2S]-type ferredoxin and an FNRN-type reductase. Type IV represents another three-component systems that consist of oxygenase, [2Fe-2S]-type ferredoxin and GR-type reductase. Type V represents another different three-component systems that consist of an oxygenase, a [3Fe-4S]-type ferredoxin and a GR-type reductase.
The new classification system provides the following features. First, the new classification system analyzes RHO enzymes as a whole. RwithSecond, the new classification system is not static but responds dynamically to the growing pool of RHO enzymes. Third, our classification can be applied reliably to the classification of incomplete RHOs. Fourth, the classification has direct applicability to experimental work. Fifth, the system provides new insights into the evolution of RHO systems based on enzyme interaction.</description><identifier>ISSN: 1471-2091</identifier><identifier>EISSN: 1471-2091</identifier><identifier>DOI: 10.1186/1471-2091-9-11</identifier><identifier>PMID: 18387195</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Aromatic compounds ; Bacteria ; Bacterial Proteins - chemistry ; Bacterial Proteins - classification ; Bacterial Proteins - genetics ; BASIC BIOLOGICAL SCIENCES ; Databases, Protein ; Ferredoxins - chemistry ; Health aspects ; Identification and classification ; Oxidases ; Oxygenases - chemistry ; Oxygenases - classification ; Oxygenases - genetics ; Phylogeny</subject><ispartof>BMC biochemistry, 2008-04, Vol.9 (1), p.11-11, Article 11</ispartof><rights>COPYRIGHT 2008 BioMed Central Ltd.</rights><rights>Copyright © 2008 Kweon et al; licensee BioMed Central Ltd. 2008 Kweon et al; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b5521-36cc19e3331589450a31dd9d215d03d0af7f5793cba99e602d871f670e97d6ce3</citedby><cites>FETCH-LOGICAL-b5521-36cc19e3331589450a31dd9d215d03d0af7f5793cba99e602d871f670e97d6ce3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2358900/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2358900/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,24780,27901,27902,53766,53768,75480,75481</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18387195$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/servlets/purl/1629839$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Kweon, Ohgew</creatorcontrib><creatorcontrib>Kim, Seong-Jae</creatorcontrib><creatorcontrib>Baek, Songjoon</creatorcontrib><creatorcontrib>Chae, Jong-Chan</creatorcontrib><creatorcontrib>Adjei, Michael D</creatorcontrib><creatorcontrib>Baek, Dong-Heon</creatorcontrib><creatorcontrib>Kim, Young-Chang</creatorcontrib><creatorcontrib>Cerniglia, Carl E</creatorcontrib><creatorcontrib>Oak Ridge Institute for Science and Education (ORISE), Oak Ridge, TN (United States)</creatorcontrib><title>A new classification system for bacterial Rieske non-heme iron aromatic ring-hydroxylating oxygenases</title><title>BMC biochemistry</title><addtitle>BMC Biochem</addtitle><description>Rieske non-heme iron aromatic ring-hydroxylating oxygenases (RHOs) are multi-component enzyme systems that are remarkably diverse in bacteria isolated from diverse habitats. Since the first classification in 1990, there has been a need to devise a new classification scheme for these enzymes because many RHOs have been discovered, which do not belong to any group in the previous classification. Here, we present a scheme for classification of RHOs reflecting new sequence information and interactions between RHO enzyme components.
We have analyzed a total of 130 RHO enzymes in which 25 well-characterized RHO enzymes were used as standards to test our hypothesis for the proposed classification system. From the sequence analysis of electron transport chain (ETC) components of the standard RHOs, we extracted classification keys that reflect not only the phylogenetic affiliation within each component but also relationship among components. Oxygenase components of standard RHOs were phylogenetically classified into 10 groups with the classification keys derived from ETC components. This phylogenetic classification scheme was converted to a new systematic classification consisting of 5 distinct types. The new classification system was statistically examined to justify its stability. Type I represents two-component RHO systems that consist of an oxygenase and an FNRC-type reductase. Type II contains other two-component RHO systems that consist of an oxygenase and an FNRN-type reductase. Type III represents a group of three-component RHO systems that consist of an oxygenase, a [2Fe-2S]-type ferredoxin and an FNRN-type reductase. Type IV represents another three-component systems that consist of oxygenase, [2Fe-2S]-type ferredoxin and GR-type reductase. Type V represents another different three-component systems that consist of an oxygenase, a [3Fe-4S]-type ferredoxin and a GR-type reductase.
The new classification system provides the following features. First, the new classification system analyzes RHO enzymes as a whole. RwithSecond, the new classification system is not static but responds dynamically to the growing pool of RHO enzymes. Third, our classification can be applied reliably to the classification of incomplete RHOs. Fourth, the classification has direct applicability to experimental work. Fifth, the system provides new insights into the evolution of RHO systems based on enzyme interaction.</description><subject>Aromatic compounds</subject><subject>Bacteria</subject><subject>Bacterial Proteins - chemistry</subject><subject>Bacterial Proteins - classification</subject><subject>Bacterial Proteins - genetics</subject><subject>BASIC BIOLOGICAL SCIENCES</subject><subject>Databases, Protein</subject><subject>Ferredoxins - chemistry</subject><subject>Health aspects</subject><subject>Identification and classification</subject><subject>Oxidases</subject><subject>Oxygenases - chemistry</subject><subject>Oxygenases - classification</subject><subject>Oxygenases - genetics</subject><subject>Phylogeny</subject><issn>1471-2091</issn><issn>1471-2091</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkt-L1DAQx4Mo3nn66qMEBd96Zpo2bV6E5fAXHAiizyFNJt1om5xJV93_3pRdzjs8kQQyzHzmx5cJIU-BnQP04hU0HVQ1k1DJCuAeOb123L9hn5BHOX9lDLqeNQ_JCfS870C2pwQ3NOBPaiads3fe6MXHQPM-LzhTFxMdtFkweT3RTx7zN6QhhmqLM1KfCqlTnEuOocmHsdrubYq_9lPxhJEWa8SgM-bH5IHTU8Ynx_eMfHn75vPF--ry47sPF5vLamjbGioujAGJnHNoe9m0THOwVtoaWsu4Zdp1ru0kN4OWEgWrbVHhRMdQdlYY5Gfk9aHu1W6Y0RoMS9KTukp-1mmvovbqdiT4rRrjD1Xz0pCxUuD5oUDMi1fZ-AXN1sQQ0CwKRC17Lgu0OUCDj__ocjti4qzWXah1F0oqgFLj5XHSFL_vMC9q9tngNOmAcZeVkNBIJvl_QZBl7q4RBXxxAEc9ofLBxdLbrLDalL03otyVOr-DKsfi7ItQdL7470owKeac0F3rBKbWL_i3smc3d_AHP_45_htlLddI</recordid><startdate>20080403</startdate><enddate>20080403</enddate><creator>Kweon, Ohgew</creator><creator>Kim, Seong-Jae</creator><creator>Baek, Songjoon</creator><creator>Chae, Jong-Chan</creator><creator>Adjei, Michael D</creator><creator>Baek, Dong-Heon</creator><creator>Kim, Young-Chang</creator><creator>Cerniglia, Carl E</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><scope>OIOZB</scope><scope>OTOTI</scope><scope>5PM</scope></search><sort><creationdate>20080403</creationdate><title>A new classification system for bacterial Rieske non-heme iron aromatic ring-hydroxylating oxygenases</title><author>Kweon, Ohgew ; Kim, Seong-Jae ; Baek, Songjoon ; Chae, Jong-Chan ; Adjei, Michael D ; Baek, Dong-Heon ; Kim, Young-Chang ; Cerniglia, Carl E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b5521-36cc19e3331589450a31dd9d215d03d0af7f5793cba99e602d871f670e97d6ce3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Aromatic compounds</topic><topic>Bacteria</topic><topic>Bacterial Proteins - chemistry</topic><topic>Bacterial Proteins - classification</topic><topic>Bacterial Proteins - genetics</topic><topic>BASIC BIOLOGICAL SCIENCES</topic><topic>Databases, Protein</topic><topic>Ferredoxins - chemistry</topic><topic>Health aspects</topic><topic>Identification and classification</topic><topic>Oxidases</topic><topic>Oxygenases - chemistry</topic><topic>Oxygenases - classification</topic><topic>Oxygenases - genetics</topic><topic>Phylogeny</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kweon, Ohgew</creatorcontrib><creatorcontrib>Kim, Seong-Jae</creatorcontrib><creatorcontrib>Baek, Songjoon</creatorcontrib><creatorcontrib>Chae, Jong-Chan</creatorcontrib><creatorcontrib>Adjei, Michael D</creatorcontrib><creatorcontrib>Baek, Dong-Heon</creatorcontrib><creatorcontrib>Kim, Young-Chang</creatorcontrib><creatorcontrib>Cerniglia, Carl E</creatorcontrib><creatorcontrib>Oak Ridge Institute for Science and Education (ORISE), Oak Ridge, TN (United States)</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>OSTI.GOV - Hybrid</collection><collection>OSTI.GOV</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BMC biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kweon, Ohgew</au><au>Kim, Seong-Jae</au><au>Baek, Songjoon</au><au>Chae, Jong-Chan</au><au>Adjei, Michael D</au><au>Baek, Dong-Heon</au><au>Kim, Young-Chang</au><au>Cerniglia, Carl E</au><aucorp>Oak Ridge Institute for Science and Education (ORISE), Oak Ridge, TN (United States)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A new classification system for bacterial Rieske non-heme iron aromatic ring-hydroxylating oxygenases</atitle><jtitle>BMC biochemistry</jtitle><addtitle>BMC Biochem</addtitle><date>2008-04-03</date><risdate>2008</risdate><volume>9</volume><issue>1</issue><spage>11</spage><epage>11</epage><pages>11-11</pages><artnum>11</artnum><issn>1471-2091</issn><eissn>1471-2091</eissn><abstract>Rieske non-heme iron aromatic ring-hydroxylating oxygenases (RHOs) are multi-component enzyme systems that are remarkably diverse in bacteria isolated from diverse habitats. Since the first classification in 1990, there has been a need to devise a new classification scheme for these enzymes because many RHOs have been discovered, which do not belong to any group in the previous classification. Here, we present a scheme for classification of RHOs reflecting new sequence information and interactions between RHO enzyme components.
We have analyzed a total of 130 RHO enzymes in which 25 well-characterized RHO enzymes were used as standards to test our hypothesis for the proposed classification system. From the sequence analysis of electron transport chain (ETC) components of the standard RHOs, we extracted classification keys that reflect not only the phylogenetic affiliation within each component but also relationship among components. Oxygenase components of standard RHOs were phylogenetically classified into 10 groups with the classification keys derived from ETC components. This phylogenetic classification scheme was converted to a new systematic classification consisting of 5 distinct types. The new classification system was statistically examined to justify its stability. Type I represents two-component RHO systems that consist of an oxygenase and an FNRC-type reductase. Type II contains other two-component RHO systems that consist of an oxygenase and an FNRN-type reductase. Type III represents a group of three-component RHO systems that consist of an oxygenase, a [2Fe-2S]-type ferredoxin and an FNRN-type reductase. Type IV represents another three-component systems that consist of oxygenase, [2Fe-2S]-type ferredoxin and GR-type reductase. Type V represents another different three-component systems that consist of an oxygenase, a [3Fe-4S]-type ferredoxin and a GR-type reductase.
The new classification system provides the following features. First, the new classification system analyzes RHO enzymes as a whole. RwithSecond, the new classification system is not static but responds dynamically to the growing pool of RHO enzymes. Third, our classification can be applied reliably to the classification of incomplete RHOs. Fourth, the classification has direct applicability to experimental work. Fifth, the system provides new insights into the evolution of RHO systems based on enzyme interaction.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>18387195</pmid><doi>10.1186/1471-2091-9-11</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1471-2091 |
ispartof | BMC biochemistry, 2008-04, Vol.9 (1), p.11-11, Article 11 |
issn | 1471-2091 1471-2091 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2358900 |
source | MEDLINE; BioMedCentral; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Alma/SFX Local Collection; Springer Nature OA/Free Journals; PubMed Central Open Access |
subjects | Aromatic compounds Bacteria Bacterial Proteins - chemistry Bacterial Proteins - classification Bacterial Proteins - genetics BASIC BIOLOGICAL SCIENCES Databases, Protein Ferredoxins - chemistry Health aspects Identification and classification Oxidases Oxygenases - chemistry Oxygenases - classification Oxygenases - genetics Phylogeny |
title | A new classification system for bacterial Rieske non-heme iron aromatic ring-hydroxylating oxygenases |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T08%3A07%3A57IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20new%20classification%20system%20for%20bacterial%20Rieske%20non-heme%20iron%20aromatic%20ring-hydroxylating%20oxygenases&rft.jtitle=BMC%20biochemistry&rft.au=Kweon,%20Ohgew&rft.aucorp=Oak%20Ridge%20Institute%20for%20Science%20and%20Education%20(ORISE),%20Oak%20Ridge,%20TN%20(United%20States)&rft.date=2008-04-03&rft.volume=9&rft.issue=1&rft.spage=11&rft.epage=11&rft.pages=11-11&rft.artnum=11&rft.issn=1471-2091&rft.eissn=1471-2091&rft_id=info:doi/10.1186/1471-2091-9-11&rft_dat=%3Cgale_pubme%3EA178468466%3C/gale_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=19900746&rft_id=info:pmid/18387195&rft_galeid=A178468466&rfr_iscdi=true |