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2.
Appl Environ Microbiol ; 72(9): 5982-9, 2006 Sep.
Article in English | MEDLINE | ID: mdl-16957219

ABSTRACT

We investigated bacterial diversity in different aquatic environments (including marine and lagoon sediments, coastal seawater, and groundwater), and we compared two fingerprinting techniques (terminal restriction fragment length polymorphism [T-RFLP] and automated ribosomal intergenic spacer analysis [ARISA]) which are currently utilized for estimating richness and community composition. Bacterial diversity ranged from 27 to 99 phylotypes (on average, 56) using the T-RFLP approach and from 62 to 101 genotypes (on average, 81) when the same samples were analyzed using ARISA. The total diversity encountered in all matrices analyzed was 144 phylotypes for T-RFLP and 200 genotypes for ARISA. Although the two techniques provided similar results in the analysis of community structure, bacterial richness and diversity estimates were significantly higher using ARISA. These findings suggest that ARISA is more effective than T-RFLP in detecting the presence of bacterial taxa accounting for <5% of total amplified product. ARISA enabled also distinction among aquatic bacterial isolates of Pseudomonas spp. which were indistinguishable using T-RFLP analysis. Overall, the results of this study show that ARISA is more accurate than T-RFLP analysis on the 16S rRNA gene for estimating the biodiversity of aquatic bacterial assemblages.


Subject(s)
Bacteria/genetics , DNA Fingerprinting/methods , DNA, Bacterial/genetics , DNA, Ribosomal Spacer/genetics , Polymorphism, Restriction Fragment Length , Water Microbiology , Bacteria/classification , Bacteria/isolation & purification , Biodiversity , DNA, Bacterial/isolation & purification , DNA, Ribosomal Spacer/isolation & purification , Ecosystem , Fresh Water/microbiology , Geologic Sediments/microbiology , Molecular Sequence Data , Pseudomonas/classification , Pseudomonas/genetics , Pseudomonas/isolation & purification , Seawater/microbiology
3.
Appl Environ Microbiol ; 71(11): 6719-29, 2005 Nov.
Article in English | MEDLINE | ID: mdl-16269702

ABSTRACT

A polyphasic approach has been developed to gain knowledge of suitable key indicators for the evaluation of environmental impact of genetically modified Bt 11 and Bt 176 corn lines on soil ecosystems. We assessed the effects of Bt corn (which constitutively expresses the insecticidal toxin from Bacillus thuringiensis, encoded by the truncated Cry1Ab gene) and non-Bt corn plants and their residues on rhizospheric and bulk soil eubacterial communities by means of denaturing gradient gel electrophoresis analyses of 16S rRNA genes, on the nontarget mycorrhizal symbiont Glomus mosseae, and on soil respiration. Microcosm experiments showed differences in rhizospheric eubacterial communities associated with the three corn lines and a significantly lower level of mycorrhizal colonization in Bt 176 corn roots. In greenhouse experiments, differences between Bt and non-Bt corn plants were detected in rhizospheric eubacterial communities (both total and active), in culturable rhizospheric heterotrophic bacteria, and in mycorrhizal colonization. Plant residues of transgenic plants, plowed under at harvest and kept mixed with soil for up to 4 months, affected soil respiration, bacterial communities, and mycorrhizal establishment by indigenous endophytes. The multimodal approach utilized in our work may be applied in long-term field studies aimed at monitoring the real hazard of genetically modified crops and their residues on nontarget soil microbial communities.


Subject(s)
Bacterial Proteins/genetics , Bacterial Toxins/genetics , Ecosystem , Endotoxins/genetics , Plants, Genetically Modified , Soil Microbiology , Zea mays/microbiology , Bacillus thuringiensis/genetics , Bacillus thuringiensis/metabolism , Bacillus thuringiensis Toxins , Bacteria/classification , Bacteria/genetics , Bacteria/growth & development , Bacterial Proteins/metabolism , Bacterial Toxins/metabolism , DNA, Ribosomal/analysis , Endotoxins/metabolism , Fungi/growth & development , Hemolysin Proteins , Molecular Sequence Data , Mycorrhizae , Plant Roots/microbiology , RNA, Ribosomal, 16S/genetics , Restriction Mapping/methods , Sequence Analysis, DNA , Soil/analysis , Zea mays/genetics
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