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1.
J Biotechnol ; 157(1): 148-53, 2012 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-21983235

RESUMO

Delftia tsuruhatensis BM90, previously isolated from Tyrrhenian Sea and selected for its ability to degrade a wide array of phenolic compounds, was immobilized in chemically modified macro porous cellulose. The development of bacterial adhesion on the selected carrier was monitored by scanning electron microscopy. Evident colonization started already after 8h of incubation. After 72h, almost all the carrier surface was covered by the bacterial cells. Extracellular bacterial structures, such as pili or fimbriae, contributed to carrier colonization and cell attachment. Immobilized cells of D. tsuruhatensis were tested for their ability to biodegrade a pool of 20 phenols in repeated batch process. During the first activation batch (72h), 90% of phenols degradation was obtained already in 48h. In the subsequent batches (up to 360h), same degradation was obtained after 24h only. By contrast, free cells were slower: to obtain almost same degradation, 48h were needed. Thus, process productivity, achieved by the immobilized cells, was double than that of free cells. Specific activity was also higher suggesting that the use of immobilized D. tsuruhatensis BM90 could be considered very promising in order to obtain an efficient reusable biocatalyst for long-term treatment of phenols containing effluents.


Assuntos
Reatores Biológicos/microbiologia , Células Imobilizadas/citologia , Delftia/citologia , Polifenóis/metabolismo , Análise de Variância , Biodegradação Ambiental , Células Imobilizadas/química , Células Imobilizadas/metabolismo , Celulose/química , Delftia/química , Delftia/metabolismo , Reutilização de Equipamento , Porosidade
2.
PLoS One ; 6(6): e20725, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-21687732

RESUMO

BACKGROUND: Bacterial outer membrane vesicles (OMV) are packets of periplasmic material that, via the proteins and other molecules they contain, project metabolic function into the environment. While OMV production is widespread in proteobacteria, they have been extensively studied only in pathogens, which inhabit fully hydrated environments. However, many (arguably most) bacterial habitats, such as soil, are only partially hydrated. In the latter, water is characteristically distributed as films on soil particles that are, on average thinner, than are typical OMV (ca. ≤10 nm water film vs. 20 to >200 nm OMV;). METHODOLOGY/PRINCIPAL FINDINGS: We have identified a new bacterial surface structure, termed a "nanopod", that is a conduit for projecting OMV significant distances (e.g., ≥6 µm) from the cell. Electron cryotomography was used to determine nanopod three-dimensional structure, which revealed chains of vesicles within an undulating, tubular element. By using immunoelectron microscopy, proteomics, heterologous expression and mutagenesis, the tubes were determined to be an assembly of a surface layer protein (NpdA), and the interior structures identified as OMV. Specific metabolic function(s) for nanopods produced by Delftia sp. Cs1-4 are not yet known. However, a connection with phenanthrene degradation is a possibility since nanopod formation was induced by growth on phenanthrene. Orthologs of NpdA were identified in three other genera of the Comamonadaceae family, and all were experimentally verified to form nanopods. CONCLUSIONS/SIGNIFICANCE: Nanopods are new bacterial organelles, and establish a new paradigm in the mechanisms by which bacteria effect long-distance interactions with their environment. Specifically, they create a pathway through which cells can effectively deploy OMV, and the biological activity these transmit, in a diffusion-independent manner. Nanopods would thus allow environmental bacteria to expand their metabolic sphere of influence in a manner previously unknown for these organisms.


Assuntos
Delftia/citologia , Membranas Intracelulares/metabolismo , Proteínas de Bactérias/metabolismo , Lipopolissacarídeos/metabolismo , Periplasma/metabolismo , Microbiologia do Solo
3.
Syst Appl Microbiol ; 28(1): 66-76, 2005 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-15709367

RESUMO

A novel, plant growth-promoting bacterium Delftia tsuruhatensis, strain HR4, was isolated from the rhizoplane of rice (Oryza sativa L., cv. Yueguang) in North China. In vitro antagonistic assay showed this strain could suppress the growth of various plant pathogens effectively, especially the three main rice pathogens (Xanthomonas oryzae pv. oryzae, Rhizoctonia solani and Pyricularia oryzae Cavara). Treated with strain HR4 culture, rice blast, rice bacterial blight and rice sheath blight for cv. Yuefu and cv. Nonghu 6 were evidently controlled in the greenhouse. Strain HR4 also showed a high nitrogen-fixing activity in N-free Döbereiner culture medium. The acetylene reduction activity and 15N2-fixing activity (N2FA) were 13.06 C2H4 nmolml(-1) h(-1) and 2.052 15Na.e.%, respectively. The nif gene was located in the chromosome of this strain. Based on phenotypic, physiological, biochemical and phylogenetic studies, strain HR4 could be classified as a member of D. tsuruhatensis. However, comparisons of characteristics with other known species of the genus Delftia suggested that strain HR4 was a novel dizotrophic PGPB strain.


Assuntos
Antibiose , Delftia/fisiologia , Reguladores de Crescimento de Plantas/biossíntese , Composição de Bases , China , Cromossomos Bacterianos/genética , DNA Bacteriano/química , DNA Bacteriano/isolamento & purificação , DNA Ribossômico/química , DNA Ribossômico/isolamento & purificação , Delftia/química , Delftia/citologia , Delftia/genética , Ácidos Graxos/análise , Ácidos Graxos/isolamento & purificação , Genes Bacterianos/genética , Genes Fúngicos , Genes de RNAr , Magnaporthe/efeitos dos fármacos , Magnaporthe/crescimento & desenvolvimento , Dados de Sequência Molecular , Fixação de Nitrogênio/genética , Oryza/microbiologia , Filogenia , Doenças das Plantas/microbiologia , RNA Bacteriano/genética , RNA Ribossômico 16S/genética , Rhizoctonia/efeitos dos fármacos , Rhizoctonia/crescimento & desenvolvimento , Análise de Sequência de DNA , Microbiologia do Solo , Xanthomonas/efeitos dos fármacos , Xanthomonas/crescimento & desenvolvimento
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