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Environ Sci Pollut Res Int. 2015 Dec;22(24):19408-16. doi: 10.1007/s11356-015-4471-1. Epub 2015 Apr 15.

Phytoremediation using microbially mediated metal accumulation in Sorghum bicolor.

Author information

1
Microbial Communication, Institute of Microbiology, Friedrich Schiller University, Neugasse 25, 07743, Jena, Germany.
2
Applied Geology, Institute of Earth Science, Friedrich Schiller University, Burgweg 11, 07749, Jena, Germany.
3
Bio Pilot Plant, Leibniz Institute for Natural Product Research and Infection Biology - Hans Knöll-Institute, Beutenbergstraße 11a, 07745, Jena, Germany.
4
Microbial Communication, Institute of Microbiology, Friedrich Schiller University, Neugasse 25, 07743, Jena, Germany. Erika.Kothe@uni-jena.de.

Abstract

Reclaiming land that has been anthropogenically contaminated with multiple heavy metal elements, e.g., during mining operations, is a growing challenge worldwide. The use of phytoremediation has been discussed with varying success. Here, we show that a careful examination of options of microbial determination of plant performance is a key element in providing a multielement remediation option for such landscapes. We used both (a) mycorrhiza with Rhizophagus irregularis and (b) bacterial amendments with Streptomyces acidiscabies E13 and Streptomyces tendae F4 to mediate plant-promoting and metal-accumulating properties to Sorghum bicolor. In pot experiments, the effects on plant growth and metal uptake were scored, and in a field trial at a former uranium leaching heap site near Ronneburg, Germany, we could show the efficacy under field conditions. Different metals could be extracted at the same time, with varying microbial inoculation and soil amendment scenarios possible when a certain metal is the focus of interest. Especially, manganese was extracted at very high levels which might be useful even for phytomining approaches.

KEYWORDS:

Field trial; Heavy metals; Phytoremediation; Pot experiments; Rhizophagus; Sorghum bicolor; Streptomyces

PMID:
25874434
DOI:
10.1007/s11356-015-4471-1
[Indexed for MEDLINE]

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