In Silico Analysis of the Phylogenetic and Physiological Characteristics of Sphingobium indicum B90A: A Hexachlorocyclohexane-Degrading Bacterium
The study focuses on the in silico genomic characterization of Sphingobium indicum B90A, revealing a wealth of genes involved in stress response, carbon monoxide oxidation, β-carotene biosynthesis, heavy metal resistance, and aromatic compound degradation, suggesting its potential as a bioremediatio...
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Veröffentlicht in: | Current microbiology 2024-08, Vol.81 (8), p.233, Article 233 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The study focuses on the in silico genomic characterization of
Sphingobium indicum
B90A, revealing a wealth of genes involved in stress response, carbon monoxide oxidation, β-carotene biosynthesis, heavy metal resistance, and aromatic compound degradation, suggesting its potential as a bioremediation agent. Furthermore, genomic adaptations among nine Sphingomonad strains were explored, highlighting shared core genes via pangenome analysis, including those related to the shikimate pathway and heavy metal resistance. The majority of genes associated with aromatic compound degradation, heavy metal resistance, and stress response were found within genomic islands across all strains.
Sphingobium indicum
UT26S exhibited the highest number of genomic islands, while
Sphingopyxis alaskensis
RB2256 had the maximum fraction of its genome covered by genomic islands. The distribution of
lin
genes varied among the strains, indicating diverse genetic responses to environmental pressures. Additionally, in silico evidence of horizontal gene transfer (HGT) between plasmids pSRL3 and pISP3 of the
Sphingobium
and
Sphingomonas
genera, respectively, has been provided. The manuscript offers novel insights into strain B90A, highlighting its role in horizontal gene transfer and refining evolutionary relationships among Sphingomonad strains. The discovery of stress response genes and the
czcABCD
operon emphasizes the potential of Sphingomonads in consortia development, supported by genomic island analysis. |
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ISSN: | 0343-8651 1432-0991 1432-0991 |
DOI: | 10.1007/s00284-024-03762-1 |