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1.
Astrobiology ; 9(4): 369-81, 2009 May.
Artigo em Inglês | MEDLINE | ID: mdl-19519213

RESUMO

Fluorescent in situ hybridization (FISH) and 16S rDNA analysis were used to characterize the endolithic colonization of silica-rich rhyolitic glass (obsidian) in a barren terrestrial volcanic environment in Iceland. The rocks were inhabited by a diverse eubacterial assemblage. In the interior of the rock, we identified cyanobacterial and algal 16S (plastid) sequences and visualized phototrophs by FISH, which demonstrates that molecular methods can be used to characterize phototrophs at the limits of photosynthetically active radiation (PAR). Temperatures on the surface of the dark rocks can exceed 40 degrees C but are below freezing for much of the winter. The rocks effectively shield the organisms within from ultraviolet radiation. Although PAR sufficient for photosynthesis cannot penetrate more than approximately 250 mum into the solid rock, the phototrophs inhabit cavities; and we hypothesize that by weathering the rock they may contribute to the formation of cavities in a feedback process, which allows them to acquire sufficient PAR at greater depths. These observations show how pioneer phototrophs can colonize the interior of volcanic glasses and rocks, despite the opaque nature of these materials. The data show that protected microhabitats in volcanic rocky environments would have been available for phototrophs on early Earth.


Assuntos
Cianobactérias/crescimento & desenvolvimento , Microbiologia Ambiental , Eucariotos/crescimento & desenvolvimento , Vidro , RNA Ribossômico 16S/genética , Cianobactérias/genética , DNA Ribossômico/química , Eucariotos/genética , Islândia , Hibridização in Situ Fluorescente , Luz , Microclima , Microscopia , Processos Fototróficos
2.
Trends Microbiol ; 16(3): 101-6, 2008 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-18280162

RESUMO

Microorganisms from diverse environments actively bore into rocks, contributing significantly to rock weathering. Carbonates are the most common substrate into which they bore, although there are also reports of microbial borings into volcanic glass. One of the most intriguing questions in microbial evolutionary biology is why some microorganisms bore. A variety of possible selection pressures, including nutrient acquisition, protection from UV radiation and predatory grazing could promote boring. None of these pressures is mutually exclusive and many of them could have acted in concert with varying strengths in different environments to favour the development of microorganisms that bore. We suggest that microbial boring might have begun in some environments as a mechanism against entombment by mineralization.


Assuntos
Bactérias/crescimento & desenvolvimento , Bactérias/metabolismo , Fenômenos Fisiológicos Bacterianos , Microbiologia Ambiental , Carbonatos/metabolismo , Vidro
3.
J Microbiol Methods ; 70(1): 1-12, 2007 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-17540467

RESUMO

The last decade has been marked by a large number of studies focused on understanding the distribution of microorganisms in volcanic environments. These studies are motivated by the desire to elucidate how the geochemically extreme conditions of such environments can influence microbial diversity both on the surface and in the subsurface of the Earth. The exploration of microbial community diversity has generally not relied on culture-dependent methods, but has been carried out using environmental DNA extraction. Because of the large diversity of chemically and physically complex samples, extracting DNA from volcanic environments is technically challenging. In view of the emerging literature, and our own experience in the optimisation of methods for DNA extraction from volcanic materials, it is timely to provide a methodological comparison. This review highlights and discusses new insights and methods published on DNA extraction methods from volcanic samples, considering the different volcanic environments. A description of a recent method for DNA extraction from basalt and obsidian glass rock samples from Iceland is included. Finally, we discuss these approaches in the wider context of modern work to understand the microbial diversity of volcanic environments.


Assuntos
Archaea/isolamento & purificação , Bactérias/isolamento & purificação , Biodiversidade , DNA Arqueal/isolamento & purificação , DNA Bacteriano/isolamento & purificação , Sedimentos Geológicos/microbiologia , Biologia Molecular/métodos , Microbiologia do Solo , Erupções Vulcânicas
4.
Environ Microbiol ; 8(2): 289-307, 2006 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-16423016

RESUMO

The microarray approach has been proposed for high throughput analysis of the microbial community by providing snapshots of the microbial diversity under different environmental conditions. For this purpose, a prototype of a 16S rRNA-based taxonomic microarray was developed and evaluated for assessing bacterial community diversity. The prototype microarray is composed of 122 probes that target bacteria at various taxonomic levels from phyla to species (mostly Alphaproteobacteria). The prototype microarray was first validated using bacteria in pure culture. Differences in the sequences of probes and potential target DNAs were quantified as weighted mismatches (WMM) in order to evaluate hybridization reliability. As a general feature, probes having a WMM > 2 with target DNA displayed only 2.8% false positives. The prototype microarray was subsequently tested with an environmental sample, which consisted of an Agrobacterium-related polymerase chain reaction amplicon from a maize rhizosphere bacterial community. Microarray results were compared to results obtained by cloning-sequencing with the same DNA. Microarray analysis enabled the detection of all 16S rRNA gene sequences found by cloning-sequencing. Sequences representing only 1.7% of the clone library were detected. In conclusion, this prototype 16S rRNA-based taxonomic microarray appears to be a promising tool for the analysis of Alphaproteobacteria in complex ecosystems.


Assuntos
Alphaproteobacteria/classificação , Análise de Sequência com Séries de Oligonucleotídeos/métodos , Filogenia , RNA Bacteriano/genética , RNA Ribossômico 16S/genética , Alphaproteobacteria/genética , Sequência de Bases , Dados de Sequência Molecular , Sensibilidade e Especificidade
5.
FEMS Microbiol Ecol ; 51(3): 333-40, 2005 Feb 01.
Artigo em Inglês | MEDLINE | ID: mdl-16329881

RESUMO

Neocaledonian mine spoils are considered as an extreme environment because of their edaphic conditions, which are unfavourable for life. The principal characteristics of this soil are the high nickel content (20,000 ppm) and the very low carbon (0.2%) and nitrogen (0.01%) levels, which are certainly among the major limiting factors for heterotrophic bacterial growth. The aim of this work was to determine what changes could occur in the bacterial community structure of the mine spoils when a carbon and a nitrogen source were added. Soil bacterial response to nutrient addition was examined in both the mine spoils and an agricultural soil, which is characterized by normal levels of nutrients. 16S rRNA gene clone libraries constructed to characterize changes occurring in the different soil bacterial communities showed an important selection of Actinobacteria in the mine spoils as a consequence of nutrient amendment: Actinobacteria represented 75% and 96% of the bacterial community structure after succinate and glucose addition, respectively. This was observed only in the mine spoils and is probably a consequence of the extreme environmental conditions. Carbon amendment in the agricultural soil led to an increase in Firmicutes, mainly Bacillus sp.


Assuntos
Actinobacteria/crescimento & desenvolvimento , Carbono/metabolismo , Ecossistema , Mineração , Níquel , Nitrogênio/metabolismo , Microbiologia do Solo , Actinobacteria/classificação , Actinobacteria/genética , Agricultura , DNA Bacteriano/análise , DNA Ribossômico/análise , Glucose/metabolismo , Dados de Sequência Molecular , Nova Caledônia , Filogenia , Reação em Cadeia da Polimerase , RNA Ribossômico 16S/genética , Solo/análise , Ácido Succínico/metabolismo
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