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Donoso, R.A.; Ruiz, D.; Garate-Castro, C.; Villegas, P.; Gonzalez-Pastor, J.E.; de Lorenzo, V.; Gonzalez, B.; Perez-Pantoja, D. |
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Identification of a self-sufficient cytochrome P450 monooxygenase from Cupriavidus pinatubonensis JMP134 involved in 2-hydroxyphenylacetic acid catabolism, via homogentisate pathway |
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Year |
2021 |
Publication |
Microbial Biotechnology |
Abbreviated Journal |
Microb. Biotechnol. |
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14 |
Issue |
5 |
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1944-1960 |
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Keywords |
COMPLETE GENOME SEQUENCE; ELECTRON-TRANSFER; GENE; DEGRADATION; SYSTEM; STRAIN; P450BM3; GROWTH; DOMAIN; HYDROXYLATION |
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Abstract |
The self-sufficient cytochrome P450 RhF and its homologues belonging to the CYP116B subfamily have attracted considerable attention due to the potential for biotechnological applications based in their ability to catalyse an array of challenging oxidative reactions without requiring additional protein partners. In this work, we showed for the first time that a CYP116B self-sufficient cytochrome P450 encoded by the ohpA gene harboured by Cupriavidus pinatubonensis JMP134, a beta-proteobacterium model for biodegradative pathways, catalyses the conversion of 2-hydroxyphenylacetic acid (2-HPA) into homogentisate. Mutational analysis and HPLC metabolite detection in strain JMP134 showed that 2-HPA is degraded through the well-known homogentisate pathway requiring a 2-HPA 5-hydroxylase activity provided by OhpA, which was additionally supported by heterologous expression and enzyme assays. The ohpA gene belongs to an operon including also ohpT, coding for a substrate-binding subunit of a putative transporter, whose expression is driven by an inducible promoter responsive to 2-HPA in presence of a predicted OhpR transcriptional regulator. OhpA homologues can be found in several genera belonging to Actinobacteria and alpha-, beta- and gamma-proteobacteria lineages indicating a widespread distribution of 2-HPA catabolism via homogentisate route. These results provide first time evidence for the natural function of members of the CYP116B self-sufficient oxygenases and represent a significant input to support novel kinetic and structural studies to develop cytochrome P450-based biocatalytic processes. |
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1751-7915 |
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WOS:000664134700001 |
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UAI @ alexi.delcanto @ |
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1426 |
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Valenzuela-Heredia, D.; Henriquez-Castillo, C.; Donoso, R.; Lavin, P.; Ulloa, O.; Ringel, M.T.; Bruser, T.; Campos, J.L. |
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An unusual overrepresentation of genetic factors related to iron homeostasis in the genome of the fluorescent Pseudomonas sp. ABC1 |
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2021 |
Publication |
Microbial Biotechnology |
Abbreviated Journal |
Microb. Biotechnol. |
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14 |
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3 |
Pages |
1060-1072 |
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Abstract |
Members of the genus Pseudomonas inhabit diverse environments, such as soil, water, plants and humans. The variability of habitats is reflected in the diversity of the structure and composition of their genomes. This cosmopolitan bacterial genus includes species of biotechnological, medical and environmental importance. In this study, we report on the most relevant genomic characteristics of Pseudomonas sp. strain ABC1, a siderophore-producing fluorescent strain recently isolated from soil. Phylogenomic analyses revealed that this strain corresponds to a novel species forming a sister clade of the recently proposed Pseudomonas kirkiae. The genomic information reveals an overrepresented repertoire of mechanisms to hoard iron when compared to related strains, including a high representation of fecI-fecR family genes related to iron regulation and acquisition. The genome of the Pseudomonas sp. ABC1 contains the genes for non-ribosomal peptide synthetases (NRPSs) of a novel putative Azotobacter-related pyoverdine-type siderophore, a yersiniabactin-type siderophore and an antimicrobial betalactone; the last two are found only in a limited number of Pseudomonas genomes. Strain ABC1 can produce siderophores in a low-cost medium, and the supernatants from cultures of this strain promote plant growth, highlighting their biotechnological potential as a sustainable industrial microorganism. |
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1751-7915 |
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WOS:000611185100001 |
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UAI @ alexi.delcanto @ |
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1326 |
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