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Survival of a novel endophytic fungus Phomopsis liquidambari B3 in the indole-contaminated soil detected by real-time PCR and its effects on the indigenous microbial community.

Authors :
Wang HW
Dai CC
Zhu H
Wang XX
Source :
Microbiological research [Microbiol Res] 2014 Dec; Vol. 169 (12), pp. 881-7. Date of Electronic Publication: 2014 Jun 06.
Publication Year :
2014

Abstract

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.<br /> (Copyright © 2014 Elsevier GmbH. All rights reserved.)

Details

Language :
English
ISSN :
1618-0623
Volume :
169
Issue :
12
Database :
MEDLINE
Journal :
Microbiological research
Publication Type :
Academic Journal
Accession number :
24958248
Full Text :
https://doi.org/10.1016/j.micres.2014.05.006