ArticleScientific reports2017
Salt Adaptation and Evolutionary Implication of a Nah-related PAHs Dioxygenase cloned from a Halophilic Phenanthrene Degrading Consortium.
Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed, 27 citations in OpenAlex.
- The syntrophic network of pyrene degradation by the synthetic halophilic consortium PES.Frontiers in microbiology · 2026Article
- Degradation Mechanism of Phenanthrene by the Halophilic Strain Altererythrobacter sp. Y3.Applied biochemistry and biotechnology · 2025Article
- Prospects in the bioremediation of petroleum hydrocarbon contaminants from hypersaline environments: A review.Environmental science and pollution research international · 2022Review
- Insights Into Mechanism of the Naphthalene-Enhanced Biodegradation of Phenanthrene byFrontiers in microbiology · 2021Article
- Salinity effect on the metabolic pathway and microbial function in phenanthrene degradation by a halophilic consortium.AMB Express · 2018Article
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Authors and funding
5 authors at 2 institutions in 1 country.
Funding
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Abstract
Polycyclic aromatic hydrocarbons (PAHs) pollutions often occur in marine and other saline environment, largely due to anthropogenic activities. However, study of the PAHs-degradation genotypes in halophiles is limited, compared with the mesophilic terrestrial PAHs degraders. In this study, a bacterial consortium (CY-1) was enriched from saline soil contaminated with crude oil using phenanthrene as the sole carbon source at 10% salinity. CY-1 was dominated by the moderate halophilic Marinobacter species, and its dominant PAHs ring-hydroxylating dioxygenase (RHD) genotypes shared high identity to the classic nah-related RHDs found in the mesophilic species. Further cloning of a 5.6-kb gene cluster from CY-1 unveiled the existence of a new type of PAHs degradation gene cluster (hpah), which most probably evolves from the nah-related gene clusters. Expression of the RHD in this gene cluster in E. coli lead to the discovery of its prominent salt-tolerant properties compared with two RHDs from mesophiles. As a common structural feature shared by all halophilic and halotolerant enzymes, higher abundance of acidic amino acids was also found on the surface of this RHD than its closest nah-related alleles. These results suggest evolution towards saline adaptation occurred after horizontal transfer of this hpah gene cluster into the halophiles.
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