Jiangsu Key Laboratory for Microbes and Functional Genomics, Jiangsu Engineering and Technology Research Center for Industrialization of Microbial Resources, College of Life Science, Nanjing Normal University, Jiangsu Province 210023, China.
Jiangsu Key Laboratory for Microbes and Functional Genomics, Jiangsu Engineering and Technology Research Center for Industrialization of Microbial Resources, College of Life Science, Nanjing Normal University, Jiangsu Province 210023, China; College of Teacher Education, Nanjing Normal University, Jiangsu Province 210023, China.
Microbiol Res. 2014 Dec;169(12):881-7. doi: 10.1016/j.micres.2014.05.006. Epub 2014 Jun 6.
The recently isolated fungal strain Phomopsis liquidambari B3 can degrade high concentrations of indole, indicating its potential for the bioremediation of indole-contaminated soil. In this study, a specific real-time PCR was developed to detect the survival of P. liquidambari B3 in soil. Subsequently, degradation activity of strain B3 and its effects on indigenous microbial community were analyzed. Results showed the amount of P. liquidambari B3 genomic DNA increased to a maximum 5.67 log (pgg(-1) dry soil) 10 days after inoculation of 5.04 log (pgg(-1) dry soil), and then gradually decreased with time and after 40 days it was below the detection limit. By the end of the experiment (day 40), bioaugmented microsoms showed a 93.7% decrease in indole, while the values for biostimulated and control microcosms were much lower. Higher microbial biomass and enzyme activities were observed in bioaugmented soil. Denaturing gradient gel electrophoresis analysis showed bioaugmentation increased richness of resident microbial community. These results indicate that P. liquidambari B3 is effective for the remediation of indole-contaminated soil and also provides valuable information about the behavior of the inoculant population during bioremediation, which could be directly used in the risk assessment of inoculant population and optimization of bioremediation process.
最近分离的真菌菌株 Phomopsis liquidambari B3 可以降解高浓度的吲哚,表明其在吲哚污染土壤的生物修复中具有潜力。在本研究中,开发了一种特定的实时 PCR 来检测 P. liquidambari B3 在土壤中的存活情况。随后,分析了菌株 B3 的降解活性及其对土著微生物群落的影响。结果表明,在接种 5.04 log (pgg(-1) 干土)后 10 天内,P. liquidambari B3 的基因组 DNA 数量增加到最大 5.67 log (pgg(-1) 干土),然后随着时间的推移逐渐减少,40 天后降至检测限以下。实验结束时(第 40 天),生物强化的微生物体显示吲哚减少了 93.7%,而生物刺激和对照微宇宙的数值要低得多。生物强化土壤中的微生物生物量和酶活性更高。变性梯度凝胶电泳分析表明,生物强化增加了土著微生物群落的丰富度。这些结果表明,P. liquidambari B3 可有效修复吲哚污染土壤,同时为接种剂种群在生物修复过程中的行为提供了有价值的信息,这些信息可直接用于接种剂种群的风险评估和生物修复过程的优化。