Addition of allochthonous fungi to a historically contaminated soil affects both remediation efficiency and bacterial diversity

被引:30
作者
Federici, Ermanno
Leonardi, Vanessa
Giubilei, Maria A.
Quaratino, Daniele
Spaccapelo, Roberta
D'Annibale, Alessandro
Petruccioli, Maurizio
机构
[1] Univ Tuscia, Dipartimento Agrobiol & Agrochim, I-01100 Viterbo, Italy
[2] Univ Perugia, Dip Med Sperimentale Sci Biochim, Perugia, Italy
[3] Interuniv Natl Consortium Chem Environm, Venice, Italy
关键词
mycoremediation; bioaugmentation; historically contaminated soil; DGGE; microbial interactions; aromatic hydrocarbons;
D O I
10.1007/s00253-007-1143-1
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Botryosphaeria rhodina DABAC P82 and Pleurotus pulmonarius CBS 664.97 were tested for their ability to grow and to degrade aromatic hydrocarbons in an aged contaminated soil. To evaluate the impact of indigenous microflora on the overall process, incubations were performed on both fumigated and nonfumigated soils. Fungal colonization by B. rhodina was unexpectedly lower in the fumigated than in the nonfumigated soil while the growth of P. pulmonarius showed an opposite response. Degradation performances and detoxification by both fungi in the nonfumigated soil were markedly higher than those observed in the fumigated one. Heterotrophic bacterial counts in nonfumigated soil augmented with either B. rhodina or P. pulmonarius were significantly higher than those of the corresponding incubation control (6.7+/-0.3 x 10(8) and 8.35 +/- 0.6 x 10(8), respectively, vs 9.2 +/- 0.3 x 10(7)). Bacterial communities of both incubation controls and fungal-augmented soil were compared by numerical analysis of denaturing gradient gel electrophoresis profiles of polymerase chain reaction (PCR)-amplified 16S ribosomal RNA (rRNA) genes and cloning and sequencing of PCR-amplified 16S rRNA genes. Besides increasing overall diversity, fungal augmentation led to considerable qualitative differences with respect to the pristine soil.
引用
收藏
页码:203 / 211
页数:9
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