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Petroleum-contaminated terrestrial ecosystems require effective bioremediation strategies. In this study, genomic analysis revealed key biodegradation genes on the 21# chromosome: alkane hydroxylases (, , ) and aromatic ortho-cleavage pathway genes (). Phylogenetic and multiple sequence alignment analyses of the gene in strain 21# revealed the presence of signature motifs characteristic of Baeyer-Villiger monooxygenase. Functional annotation analysis demonstrated stronger phylogenetic affinity of this protein to previously characterized BVMOs than to hydroxylases. Therefore, it is suggested that the AlmA protein in 21# exhibits BVMO activity and participates in the subterminal oxidation pathway of alkane degradation. Wild-type 21# degraded both n-Octacosane (24.47%) and pyrene (34.03%). Engineered 21#-A3 showed significantly enhanced n-Octacosane degradation (28.68%). To validate AlmA function and assess impacts of exogenous gene integration, we expressed the gene from KJ-1 via pET-28a(+)- vector. Enzymatic assays demonstrated no activity toward long-chain alkanes but high activity for 2-decanone (0.39 U/mg) and 2-dodecanone (0.37 U/mg). Metabolite analysis confirmed recombinant AlmA functions through subterminal oxidation. This study establishes a foundational framework for advancing the optimization of petroleum-degrading bacteria. To engineer more efficient hydrocarbon-degrading strains, future research should integrate meta-cleavage pathways to expand their substrate utilization range for polycyclic aromatic hydrocarbons.
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http://dx.doi.org/10.3390/microorganisms13081953 | DOI Listing |
Microorganisms
August 2025
Shandong Provincial Key Laboratory of Applied Microbiology, Ecology Institute, Qilu University of Technology (Shandong Academy of Sciences), Jinan 250103, China.
Petroleum-contaminated terrestrial ecosystems require effective bioremediation strategies. In this study, genomic analysis revealed key biodegradation genes on the 21# chromosome: alkane hydroxylases (, , ) and aromatic ortho-cleavage pathway genes (). Phylogenetic and multiple sequence alignment analyses of the gene in strain 21# revealed the presence of signature motifs characteristic of Baeyer-Villiger monooxygenase.
View Article and Find Full Text PDFAppl Environ Microbiol
January 2024
State Key Laboratory of Microbial Metabolism, Joint International Research Laboratory of Metabolic & Developmental Sciences, and School of Life Sciences & Biotechnology, Shanghai Jiao Tong University, Shanghai, China.
Many species can grow on -alkanes of varying lengths (≤C40). AlmA, a unique flavoprotein in these strains, is the only enzyme proven to be required for the degradation of long-chain (LC) -alkanes, including C32 and C36 alkanes. Although it is commonly presumed to be a terminal hydroxylase, its role in -alkane degradation remains elusive.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
April 2024
School of Chemistry, The University of Manchester, Manchester Institute of Biotechnology (MIB), 131 Princess Street, Manchester, M1 7DN, UK.
Selective, one-step C-H activation of fatty acids from biomass is an attractive concept in sustainable chemistry. Biocatalysis has shown promise for generating high-value hydroxy acids, but to date enzyme discovery has relied on laborious screening and produced limited hits, which predominantly oxidise the subterminal positions of fatty acids. Herein we show that ancestral sequence reconstruction (ASR) is an effective tool to explore the sequence-activity landscape of a family of multidomain, self-sufficient P450 monooxygenases.
View Article and Find Full Text PDFMol Cell Biochem
June 2024
Faculty of Pharmacy & Pharmaceutical Sciences, 2142J Katz Group-Rexall Centre for Pharmacy and Health Research, University of Alberta, Edmonton, AL, T6G 2E1, Canada.
Angew Chem Int Ed Engl
February 2023
Department of Biocatalysis, Institute of Catalysis, CSIC, C/Marie Curie 2, 28049, Madrid, Spain.
The hydroxylation of fatty acids is an appealing reaction in synthetic chemistry, although the lack of selective catalysts hampers its industrial implementation. In this study, we have engineered a highly regioselective fungal peroxygenase for the ω-1 hydroxylation of fatty acids with quenched stepwise over-oxidation. One single mutation near the Phe catalytic tripod narrowed the heme cavity, promoting a dramatic shift toward subterminal hydroxylation with a drop in the over-oxidation activity.
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