Unveiling degradation mechanism of PAHs by a Sphingobium strain from a microbial consortium.
Lige ZhangHuan LiuJunbiao DaiPing XuHongzhi TangPublished in: mLife (2022)
Polycyclic aromatic hydrocarbons (PAHs) are a class of persistent pollutants with adverse biological effects and pose a serious threat to ecological environments and human health. The previously isolated phenanthrene-degrading bacterial consortium (PDMC) consists of the genera Sphingobium and Pseudomonas and can degrade a wide range of PAHs. To identify the degradation mechanism of PAHs in the consortium PDMC, metagenomic binning was conducted and a Sphingomonadales assembly genome with 100% completeness was obtained. Additionally, Sphingobium sp. SHPJ-2, an efficient degrader of PAHs, was successfully isolated from the consortium PDMC. Strain SHPJ-2 has powerful degrading abilities and various degradation pathways of high-molecular-weight PAHs, including fluoranthene, pyrene, benzo[a]anthracene, and chrysene. Two ring-hydroxylating dioxygenases, five cytochrome P450s, and a pair of electron transfer chains associated with PAH degradation in strain SHPJ-2, which share 83.0%-99.0% similarity with their corresponding homologous proteins, were identified by a combination of Sphingomonadales assembly genome annotation, reverse-transcription quantitative polymerase chain reaction and heterologous expression. Furthermore, when coexpressed in Escherichia coli BL21(DE3) with the appropriate electron transfer chain, PhnA1B1 could effectively degrade chrysene and benzo[a]anthracene, while PhnA2B2 degrade fluoranthene. Altogether, these results provide a comprehensive assessment of strain SHPJ-2 and contribute to a better understanding of the molecular mechanism responsible for the PAH degradation.
Keyphrases
- polycyclic aromatic hydrocarbons
- electron transfer
- human health
- escherichia coli
- risk assessment
- climate change
- heavy metals
- transcription factor
- gene expression
- emergency department
- high resolution
- biofilm formation
- oxidative stress
- binding protein
- dna repair
- long non coding rna
- cystic fibrosis
- dna methylation
- klebsiella pneumoniae
- health risk assessment
- multidrug resistant
- candida albicans