Na Li,Rui Liu,Jianjun Chen,Jian Wang,Liqun Hou,Yuemei Zhou
This study investigated Fire Phoenix ( Festuca L.) and Echinacea purpurea (L.) Moench inoculated with a Mycobacterium strain N12 in remediation of soils contaminated with both polycyclic aromatic hydrocarbons (PAHs) and cadmium (Cd). Plant growth and PAH and Cd removal were monitored in 60, 120, and 150 days after transplanting. Results showed that Fire Phoenix plants grown in soil containing 200 mg/kg PAHs and 15 mg/kg Cd inoculated with N12 were able to remove 76.3% PAHs compared to removal of 68.3% of PAHs by the plants without N12 inoculation. On day 150, the underground biomass of Fire Phoenix plants grown in soil inoculated with N12 increased 59.40% compared to that without N12 inoculation. The enhanced removal of PAH by Fire Phoenix and N12 was related to the improved rhizosphere microbial activities . However, inoculation of N12 to E. purpurea grown soil did not significantly improve the removal of PAHs and Cd. Our results showed that phytoremediation of PAHs and Cd can be enhanced by a Mycobacterium strain N12, especially when PLFA concentrations of bacteria and fungi exceeded 60% of the initial concentrations, but the enhancement is plant species dependent.
Shanshan Sun,Haizhen Wang,Kang Yan,Jun Lou,Jiahui Ding,Shane A. Snyder,Laosheng Wu,Jianming Xu
A highly eff ;ective phenanthrene (PHE)-degrading co-culture containing Rhodococcus sp. WB9 and Mycobacterium sp. WY10 was constructed and completely degraded 100 mg L −1 PHE within 36 h, showing improved degradation rate compared to their monocultures. In the co-culture, strain WY10 played a predominant role in PHE degradation. 1-hydroxy-2-naphthoic acid was an end-product of PHE degradation by strain WB9 and accumulated in the culture medium to serve as a substrate for strain WY10 growth, thereby accelerating PHE degradation. In turn, strain WY10 degraded PHE and 1-hydroxy-2-naphthoic acid intracellularly to form phthalate and protocatechuate that were exported to the culture medium through efflux transporters. However, strain WY10 cannot take up extracellular phthalate due to the absence of phthalate transporters, restricting phthalate degradation and PHE mineralization. In the co-culture, phthalate and protocatechuate accumulated in the culture medium were taken up and degraded towards TCA cycle by strain WB9. Therefore, the metabolic cross-feeding of strains WB9 and WY10 accelerated PHE degradation and mineralization. These findings exhibiting the synergistic degradation of PHE in the bacterial co-culture will facilitate its bioremediation application.
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