{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,24]],"date-time":"2026-10-24T02:20:20Z","timestamp":1792808420247,"version":"4.5.0"},"reference-count":38,"publisher":"Microbiology Society","issue":"5","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2007,5,1]]},"abstract":"<jats:p>Three bacterial strains, designated MT1<jats:sup>T<\/jats:sup>, RW10<jats:sup>T<\/jats:sup>and IpA-2<jats:sup>T<\/jats:sup>, had been isolated previously for their ability to degrade chlorosalicylates or isopimaric acid. 16S rRNA gene sequence analysis demonstrated that these bacteria are related to species of the genus<jats:italic>Pseudomonas<\/jats:italic>. Analysis of the results of DNA\u2013DNA hybridization with several close phylogenetic neighbours revealed a low level of hybridization (less than 57\u200a%). On the basis of phenotypic characteristics, phylogenetic analysis, DNA\u2013DNA relatedness data and chemotaxonomic analysis, it is concluded that these isolates represent separate novel species, for which the names<jats:italic>Pseudomonas reinekei<\/jats:italic>sp. nov. (type strain MT1<jats:sup>T<\/jats:sup>=DSM 18361<jats:sup>T<\/jats:sup>=CCUG 53116<jats:sup>T<\/jats:sup>),<jats:italic>Pseudomonas moorei<\/jats:italic>sp. nov. (type strain RW10<jats:sup>T<\/jats:sup>=DSM 12647<jats:sup>T<\/jats:sup>=CCUG 53114<jats:sup>T<\/jats:sup>) and<jats:italic>Pseudomonas mohnii<\/jats:italic>sp. nov. (type strain IpA-2<jats:sup>T<\/jats:sup>=DSM 18327<jats:sup>T<\/jats:sup>=CCUG 53115<jats:sup>T<\/jats:sup>) are proposed.<\/jats:p>","DOI":"10.1099\/ijs.0.64703-0","type":"journal-article","created":{"date-parts":[[2007,5,1]],"date-time":"2007-05-01T20:03:01Z","timestamp":1178049781000},"page":"923-931","source":"Crossref","is-referenced-by-count":62,"title":["Pseudomonas reinekei sp. nov., Pseudomonas moorei sp. nov. and Pseudomonas mohnii sp. nov., novel species capable of degrading chlorosalicylates or isopimaric acid"],"prefix":"10.1099","volume":"57","author":[{"given":"Beatriz","family":"C\u00e1mara","sequence":"first","affiliation":[{"name":"Division of Microbiology, HZI \u2013 Helmholtz Zentrum f\u00fcr Infektionsforschung, Inhoffenstrasse 7, 38124 Braunschweig, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Carsten","family":"Str\u00f6mpl","sequence":"additional","affiliation":[{"name":"Division of Microbiology, HZI \u2013 Helmholtz Zentrum f\u00fcr 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