Plant-microorganism interactions in bioremediation of polychlorinated biphenyl-contaminated soil
Language English Country Netherlands Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
22728721
DOI
10.1016/j.nbt.2012.06.004
PII: S1871-6784(12)00132-X
Knihovny.cz E-resources
- MeSH
- Bacteria cytology genetics isolation & purification metabolism MeSH
- Genes, Bacterial genetics MeSH
- Biodegradation, Environmental MeSH
- Soil Pollutants metabolism MeSH
- Microbial Interactions * MeSH
- Polychlorinated Biphenyls metabolism MeSH
- Ribosomal Proteins metabolism MeSH
- RNA, Ribosomal, 16S genetics MeSH
- Solanum metabolism MeSH
- Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization MeSH
- Nicotiana metabolism MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Soil Pollutants MeSH
- Polychlorinated Biphenyls MeSH
- Ribosomal Proteins MeSH
- RNA, Ribosomal, 16S MeSH
During the second half of the last century a large amount of substances toxic for higher organisms was released to the environment. Physicochemical methods of pollutant removal are difficult and prohibitively expensive. Using biological systems such as microorganisms, plants, or consortia microorganisms-plants is easier, cheaper, and more environmentally friendly. The aim of this study was to isolate, characterize and identify microorganisms from contaminated soil and to find out the effect of plants on microbial diversity in the environment. Microorganisms were isolated by two approaches with the aim to find all cultivable species and those able to utilise biphenyl as a sole source of carbon and energy. The first approach was direct extraction and the second was isolation of bacteria after enrichment cultivation with biphenyl. Isolates were biochemically characterized by NEFERMtest 24 and then the composition of ribosomal proteins in bacterial cells was determined by MALDI-TOF mass spectrometry. Ribosomal proteins can be used as phylogenetic markers and thus MALDI-TOF MS can be exploited also for taxonomic identification because the constitution of ribosomal proteins in bacterial cells is specific for each bacterial species. Identification of microorganisms using this method is performed with the help of database Bruker Daltonics MALDI BioTyper. Isolated bacteria were analyzed from the point of the bphA gene presence. Bacteria with detected bphA gene were then taxonomically identified by 16S rRNA sequence. The ability of two different plant species, tobacco (Nicotiana tabacum) and nightshade (Solanum nigrum), to accumulate PCBs was studied as well. It was determined that various plant species differ in the PCBs accumulation from the contaminated soil. Also the content of PCBs in various plant tissues was compared. PCBs were detected in roots and aboveground biomass including leaves and berries.
References provided by Crossref.org
Hunting Down Frame Shifts: Ecological Analysis of Diverse Functional Gene Sequences
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