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Book
Les herbicides et leurs emploi
Authors: ---
ISBN: 2801100528 2706600241 2705600241 9782801100523 Year: 1975 Publisher: Gembloux Duculot [J.]

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Dissertation
Fiber-optic SPR bioassays for detection of bacteria and viruses
Authors: ---
ISBN: 9789088263323 Year: 2013 Publisher: Leuven Katholieke Universiteit Leuven

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In food quality, healthcare and biotechnology the presence of bacteria a nd viruses can have considerable consequences both willing and unwilling . Accurate identification and quantification of the bacteria and virusse s is key in this context. Currently, there are only a limited number of truly fast and reliable methods available. Sensitive diagnostic tests co uld have a large impact on several crucial healthcare problems such as a ntibiotic resistance or could further improve food quality control. Ther efore the aim of this disseration was to develop innovative, fast and hi ghly sensitive bioassays on a compact fiber optic SPR biosensor platform (FO-SPR), that can be used to identify and quantify bacteria and viruse s in a multiplexed way. First, the FO-SPR sensor was used to st udy the affinity and binding kinetics of small viral particles. These so -called bacteriophages, can display peptide libraries with affinity for almost any target molecule. The target molecule, in this case eGFP, was immobilized on the FO-SPR biosensor surface and afterwards exposed to th e bacteriophage library, allowing real-time monitoring of their interact ions. Although the bioassay based on the detection of the entire viruses showed limited sensitivity, it proved to be a valuable tool for compari ng binding kinetics of different viral particles, which expressed affini ty peptides in different densities on the surface. Following, k eeping in mind the need for both detecting and identifying pathogens wit hin the same test, a more universal bioassay was created using the genet ic material of micro-organisms. The thermal denaturation of DNA complexe s was measured using the FO-SPR technology. Here, the target DNA was use d to form complexes between two hybridization probes, each complementary to one half of the target molecule and immobilized both on the gold nan oparticles (Au NPs) and the sensor surface. Amplification with gold nano particle labels resulted in a clear signal, which superimposed the SPR s ignal caused by temperature changes during DNA melting analysis. This assay was then validated by measuring genetic variability in two genes of L. pneumophila, which is a common human pathoge n responsible for atypical pneumonia. Although the two selected genes ar e frequently used for the quantification of these bacteria, one of them is well documented as highly variable and therefore prone to introducing amplification bias in PCR based molecular diagnostic tests. The FO-SPR biosensor proved to be reliable for detecting mutations in those samples that previously displayed ambiguous qPCR quantification results. Moreov er, it showed advantages as a high resolution and fast genetic screening tool that can compete with the current standard techniques for single p oint mutation (SNP) detection.Next, the possibilities of the FO-SPR DNA biosensor were explored for target quantification. The FO-SPR biosen sor was able to monitor in real-time quantitative ligation. The gradualincrease in signal over multiple DNA ligation cycles was used to determi ne DNA concentrations in a broad dynamic range with a detection limit of 100 fM. Even more importantly, the obtained melting signal during each cycle of the ligation was sufficiently accurate to discriminate an SNP i n the amplified target molecule. Finally, the FO-SPR melting as say was applied to directly detect two bacterial species in one sample. To allow multiplex detection on FO-SPR, hybridization probes complementa ry to two regions of interest in different bacteria were immobilized on a single FO-SPR sensor and Au NPs. By choosing target regions with non-o verlapping melting curves in each bacteria, the presence of one or both bacteria could easily be identified. Even DNA targets with SNPs could be differentiated from the wild type targets. This achievement is a significant step towards a FO-SPR biosensor for pathogenic bacteria . Further development of this platform concerning both the FO-SPR biosen sor hardware and the implemented bioassays could make this technology an ideal candidate for the next generation point of care biosensor


Book
Bacterial wilt disease in Asia and the South Pacific : proceedings of an international workshop held at Los Banos, 8-10 October 1985
Authors: ---
ISBN: 094951120X Year: 1986 Volume: vol 13

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Dissertation
Ecophysiological and biochemical responses of two olive tree cultivars 'Olea europaea L. 'Meski' and 'Koroneiki') under drought stress and nitrogen deficiency
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ISBN: 9789059893023 Year: 2009 Publisher: Gent Universiteit Gent. Faculteit Bio-Ingenieurswetenschappen

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Dissertation
Effect of synthetic surfactants on the fate of pesticides and trace metals in soil
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ISBN: 9789088261039 Year: 2009 Volume: 858 Publisher: Leuven Katholieke Universiteit Leuven

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Dissertation
Molecular & physiological responses to drought stress in Fragaria sp.
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ISBN: 9789059895706 Year: 2012 Publisher: Gent Universiteit Gent. Faculteit Bio-Ingenieurswetenschappen

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Dissertation
A quantitative microbiological exposure assessment of Bacillus cereus in cooked-chilled foods
Authors: ---
ISBN: 9789059896468 Year: 2013 Publisher: Gent : UGent,

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Dissertation
Sustainable insect control in vegetables through optimized applications of entomopathogenic nematodes
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ISBN: 9789059896512 Year: 2013 Publisher: Gent : UGent,

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Dissertation
Genetic assessment of pesticide-degrading bacteria in the Mekong delta of Vietnam
Authors: ---
ISBN: 9789088263705 Year: 2014 Volume: 1195 Publisher: Leuven Katholieke Universiteit Leuven

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The Mekong delta is the largest agricultural region of Vietnam. To meet the food demand for the local inhabitants and export, intensive crop cultivation results in a steady increase in application of chemical fertilizers and pesticides. Diverse chemical classes of herbicides, fungicides and insecticides have been used in the delta resulting in contamination of surface water and sediments. However, the fate of residual pesticides and capacity for microbial degradation in soils of the Mekong delta are largely unknown. It was hypothesized that the continuous selection pressure of pesticides in agricultural fields in the Mekong delta has resulted into an adapted community that is able to degrade and/or mineralize intensively used pesticides. Therefore, the overall objective of the study was to gain knowledge on the biodegradation of some currently used pesticides in the delta and the genetics involved in the catabolism of these compounds.Biodegradation and mineralization of four currently used pesticides were examined in a pristine soil and in agricultural soil samples that had a history of pesticide treatment and that were collected from two distant provinces in the Mekong delta. The examined pesticides included one herbicide, i.e., the chlorinated phenoxyacetic acid 2,4-D, and three insecticides, i.e., the chlorinated cyclodiene endosulfan, the synthetic pyrethroid cypermethrin and the methylcarbamate carbofuran. 2,4-D and cypermethrin were degraded/mineralized in all soil samples including the control soil while endosulfan was not mineralized in any of the soil samples. Carbofuran was only mineralized in soils that had been exposed to the compound. From soils showing 2,4-D degradation or carbofuran mineralization activity, ten distinct strains that use 2,4-D as sole source of carbon and energy and one strain that uses carbofuran as sole source of nitrogen, carbon and energy were isolated. The 2,4-D-degrading isolates were identified as members of the ß-proteobacterial genera Burkholderia, Cupriavidus and Ralstonia while the carbofuran-degrading strain belongs to the alfa-proteobacterial genus Novosphingobium. 2,4-D degradation in the 2,4-D-degrading isolates was plasmid encoded and the phenotype could be transferred by conjugation to a plasmid-free derivative of Cupriavidus metallidurans CH34. The plasmids were sequenced and the sequences analyzed. All plasmids contained homologues of the previously described tfd genes that code for the biodegradation of 2,4-D. Eight of the nine plasmids analyzed were identified as IncP-1ß plasmids with backbone sequences that are highly similar to those of the prototype 2,4-D-catabolic plasmid pJP4. These plasmids show minor differences in structure between each other indicating that they are variants of a similar ancestor. In one strain, the tfd genes were located on a plasmid, designated as pPO4, which appears to be a member of a poorly characterized plasmid group. The tfd genes on the IncP-1ß plasmids are highly similar in organization and sequence to the tfd genes identified on pJP4 although minor differences were detected. As on pJP4, the tfd genes are organized in two isofunctional catabolic clusters (tfd-I and tfd-II) that determine the conversion of 2,4-dichlorophenol into ß-ketoadipate and a separated tfdA gene that determines the conversion of 2,4-D to 2,4-dichlorophenol. Plasmid pPO4 carries a tfdA homologue and only one of the dichlorophenol catabolic gene modules. However, the strong similarity in sequence and organization of the tfd genes on pPO4 and the IncP-1ß plasmids suggest that the inter-plasmid exchange of tfd genes has taken place in the rice field bacterial community where the plasmids originated from. Moreover, the occurrence of the genes primarily on conjugative genetic elements with broad host range features shows the mobile character of the 2,4-D-catabolic phenotype in the examined soil community which can contribute to adaptation of its populations towards recruiting 2,4-D biodegradation genotypes. Novosphingobium sp. KN65.2 has the capability to use carbofuran as sole carbon and nitrogen source for growth that is accompanied by the mineralization of the aromatic ring structure of the compound. The genes involved in carbofuran degradation as well as the corresponding metabolic pathway in Novosphingobium sp. KN65.2 were analyzed. A collection of plasposon mutants impaired in carbofuran degradation and mineralization was isolated and representative mutants were subjected to proteomic and metabolite analyses. Metabolic profiling revealed several new metabolic intermediates, in addition to the initial hydrolysis product carbofuran phenol. The promiscuous carbofuran-hydrolyzing enzyme Mcd, which is present in several bacteria partially degrading carbofuran but lacking ring mineralization capacity, is not encoded by the KN65.2 genome. An alternative hydrolase gene required for this step was not yet identified, but the constitutively expressed genes of the unique cfd operon, including the oxygenase genes cfdC and cfdE, could be linked to further degradation of the phenolic metabolite. A third oxygenase gene cfdI and the transporter gene cftA encoding a TonB-dependent outer membrane receptor with potential regulatory function are located outside the cfd cluster, but appear also to be involved in carbofuran mineralization. The study has revealed the first dedicated carbofuran-catabolic genes and provides insight in the early steps of benzofuran ring degradation. The isolation of a carbofuran-mineralizing Novosphingobium sp. KN65.2 only from a carbofuran-treated field and the unique genetic make-up of carbofuran degradation genes in the strain supports the proposed hypothesis that continuously applied selection pressure of carbofuran in agricultural fields in the Mekong delta has resulted into a genetically adapted bacterial community that is able to degrade this intensively used insecticide.


Book
Die nichtparasitären Krankheiten
Authors: --- ---
ISBN: 3489773268 3489768264 3489769260 Year: 1970 Publisher: Berlin : Parey,

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