Metabolic pathway and cell adaptation mechanisms revealed through genomic, proteomic and transcription analysis of a Sphingomonas haloaromaticamans strain degrading ortho-phenylphenol
Ortho -phenylphenol (OPP) is a fungicide contained in agro-industrial effluents produced by fruit-packaging plants. Within the frame of developing bio-strategies to detoxify these effluents, an OPP-degrading Sphingomonas haloaromaticamans strain was isolated. Proteins/genes with a putative catabolic...
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Veröffentlicht in: | Scientific reports 2017-07, Vol.7 (1), p.6449-14, Article 6449 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Ortho
-phenylphenol (OPP) is a fungicide contained in agro-industrial effluents produced by fruit-packaging plants. Within the frame of developing bio-strategies to detoxify these effluents, an OPP-degrading
Sphingomonas haloaromaticamans
strain was isolated. Proteins/genes with a putative catabolic role and bacterium adaptation mechanisms during OPP degradation were identified via genomic and proteomic analysis. Transcription analysis of all putative catabolic genes established their role in the metabolism of OPP. The formation of key transformation products was verified by chromatographic analysis. Genomic analysis identified two orthologous operons encoding the
ortho
-cleavage of benzoic acid (BA) (
ben/cat
). The second
ben/cat
operon was located in a 92-kb scaffold along with (i) an operon (
opp
) comprising genes for the transformation of OPP to BA and 2-hydroxypenta-2,4-dienoate (and genes for its transformation) and (ii) an incomplete biphenyl catabolic operon (
bph
). Proteomics identified 13 up-regulated catabolic proteins when
S. haloaromaticamans
was growing on OPP and/or BA. Transcription analysis verified the key role of the catabolic operons located in the 92-kb scaffold, and flanked by transposases, on the transformation of OPP by
S. haloaromaticamans
. A flavin-dependent monoxygenase (OppA1), one of the most up-regulated proteins in the OPP-growing cells, was isolated via heterologous expression and its catabolic activity was verified
in vitro
. |
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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-017-06727-6 |