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Complete genome sequence of Pseudomonas alcaliphila JAB1 (=DSM 26533), a versatile degrader of organic pollutants

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    0501882 - ÚMG 2019 RIV GB eng J - Journal Article
    Rídl, Jakub - Šuman, J. - Fraraccio, S. - Hradilová, Miluše - Strejček, M. - Cajthaml, Tomáš - Zubrova, A. - Macek, Tomáš - Strnad, Hynek - Uhlík, O.
    Complete genome sequence of Pseudomonas alcaliphila JAB1 (=DSM 26533), a versatile degrader of organic pollutants.
    Standards in Genomic Sciences. Roč. 13, February (2018), č. článku 3. ISSN 1944-3277
    R&D Projects: GA ČR GA13-28283S
    Institutional support: RVO:68378050 ; RVO:61388971
    Keywords : Pseudomonas alcaliphila JAB1 * Pseudomonadaceae * Genome * Dioxygenase * Monooxygenase * Biodegradation * Aromatic compounds * Biphenyl * Polychlorinated biphenyls (PCBs) * Chlorobenzoic acids (CBAs) * cis-1,2-dichloroethylene (cDCE) * Phenol * bph genes * ben genes * phe genes * maldi-tof ms
    OECD category: Biochemistry and molecular biology; Microbiology (MBU-M)
    Impact factor: 1.458, year: 2018

    In this study, following its isolation from contaminated soil, the genomic sequence of Pseudomonas alcaliphila strain JAB1 (=DSM 26533), a biphenyl-degrading bacterium, is reported and analyzed in relation to its extensive degradative capabilities. The P. alcaliphila JAB1 genome (GenBank accession no. CP016162) consists of a single 5.34 Mbp-long chromosome with a GC content of 62.5%. Gene function was assigned to 3816 of the 4908 predicted genes. The genome harbors a bph gene cluster, permitting degradation of biphenyl and many congeners of polychlorinated biphenyls (PCBs), a ben gene cluster, enabling benzoate and its derivatives to be degraded, and phe gene cluster, which permits phenol degradation. In addition, P. alcaliphila JAB1 is capable of cometabolically degrading cis-1,2-dichloroethylene (cDCE) when grown on phenol. The strain carries both catechol and protocatechuate branches of the beta-ketoadipate pathway, which is used to funnel the pollutants to the central metabolism. Furthermore, we propose that clustering of MALDI-TOF MS spectra with closest phylogenetic relatives should be used when taxonomically classifying the isolated bacterium, this, together with 16S rRNA gene sequence and chemotaxonomic data analyses, enables more precise identification of the culture at the species level.
    Permanent Link: http://hdl.handle.net/11104/0293864

     
     
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