17 research outputs found

    Evaluation of a cereal milling by-product for the low cost production of Bacillus thuringiensis kurstaki in submerged fermentation

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    With the idea of finding a cheap medium for the mass production of Bacillus thuringiensis (Bt), a cereal milling by product (CMB) was evaluated and was shown efficient to be used as a source of carbohydrates, proteins and minerals for the production of δ-endotoxins in submerged fermentation of a new strain of Bacillus thuringiensis kurstaki “Lip”. The results obtained in 1000 mL shake flasks experiments showed that the toxin proteins concentration produced in the 6% (w/v) CMB medium was 2.4 fold and 1.54 fold greater than the values reached in the Anderson medium and in a standard semi synthetic medium respectively, while there was no significant difference between the cell, spore and crystal counts or between the protein profiles of the “Lip” spore/crystal complex obtained in the three mediums. Considering all three factors, relative yield, productivity and cost, the use of the CMB mono-component medium was proved much more economical for an industrial production of “Lip” than the references mediums. Moreover, the suitability of the medium for large scale production of Bt based bio insecticide was evidenced in a 5 L lab bioreactor

    A simple method for the separation of Bacillus thuringiensis spores and crystals

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    A simple new method, for separating Bacillus thuringiensis crystals from spores and cell debris, is described. The developed purification method uses hexane and low speed centrifugation and does not require any expensive material or reagents

    Diversity of Bacillus cereus sensu lato mobilome

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    Bacillus cereus sensu lato s.l.) is a group of bacteria displaying close phylogenetic relationships but a high ecological diversity. The three most studied species are Bacillus anthracis, Bacillus cereus sensu stricto and Bacillus thuringiensis. While some species are pathogenic to mammals or associated with food poisoning, Bacillus thuringiensis is a well-known entomopathogenic bacterium used as biopesticide worldwide. B. cereus s.l. also contains a large variety of mobile genetic elements (MGEs)

    IS 982 and kin: new insights into an old IS family.

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    Insertion sequences (IS) are ubiquitous transposable elements with a very simple organization: two inverted repeats flanking a transposase coding gene. IS is one of 26 insertion sequence families known so far. With 70 registered members in the ISFinder database, this family remains somewhat unexplored, despite the association of many of its members with important features such as antibiotic resistance. IS has a fairly simple organization with a mean length of ca. 1 Kb, two inverted repeats with conserved 5' AC 3' ends flanking a transposase coding gene and direct repeats of variable lengths. Its transposase has a RNAse-H like chemistry with an atypical DDE motif. In this study, we first highlight the current knowledge on the IS family by dissecting its registered members and their characteristics. Secondly, we bring new insights into this old, yet uncharted IS family, by exploring its registered elements, as well as the genomic and proteomic databases of bacterial and archaeal strains. This probing showed that the presence and distribution of this family goes far beyond the clear-cut registry of ISFinder database

    Analyse moléculaire des gènes cry1A d'une souche de Bacillus thuringiensis et étude de l'interaction des toxines correspondantes dans une modèle de membrane biomimétique

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    Bacillus thuringiensis (Bt) est une bactérie produisant des inclusions protéiques cristallines à pouvoir insecticide et elle est largement exploitée à l'échelle industrielle. Dans cette étude, des souches de Bt ont été isolées du sol libanais. Nous avons étudié en premier la présence des principaux gènes cry1A codant pour des -endotoxines actives sur les lépidoptères. Les souches possédant ces gènes ont été testées pour leur toxicité sur des larves d'Ephestia kuehniella (E. kuehniella). Une souche nommée Lip, étant quatre fois plus toxique sur ces larves que la référence mondiale Bt subsp. kurstaki HD1, fut sélectionnée pour une étude plus approfondie. Après clonage et séquençage, nous avons identifié une nouvelle toxine de type Cry1Aa : Cry1Aa22 et une nouvelle variante de la toxine Cry1Ac. Ces dernières se sont montrées plus toxiques sur des larves d'E. kuehniella, et plus stables en présence des protéases intestinales de ces larves que Cry1Aa et Cry1Ac de HD1 permettant d'expliquer la toxicité élevée de la souche sauvage. D'autre part, nous avons optimisé la construction d'un modèle de membrane biomimétique incluant la membrane de la bordure en brosse intestinale (BBM) des larves d'E. kuehniella. Ces membranes nous ont servi à l'étude de l'interaction des toxines Cry1Aa et Cry1Ac de Lip et celles de HD1. Les toxines de Lip ont interagit différemment et avec une plus grande affinité avec ces modèles que celles de HD1.Tous ces résultats montrent que Lip est une souche intéressante pour une exploitation industrielle et que le modèle de membrane biomimétique est une alternative permettant la prédiction de l'affinité des toxines Cry.Bacillus thuringiensis (Bt) is a bacterium that synthesizes insecticidal proteic crystallin inclusions and is widely used at an industrial scale. In this study, Bt strains were isolated from Lebanese soil. We studied the presence of the main cry1A genes encoding for -endotoxins active on Lepidoptera. Strains harboring these genes were tested for their toxicity against Ephestia kuehniella (E. kuehniella) larvae. The strain named Lip, being four folds more toxic to the larvae than the reference strain Bt subsp. kurstaki HD1, was selected for further study. We identified a novel Cry1Aa toxin, Cry1Aa22, and a variety of the Cry1Ac toxin after cloning and sequencing of the corresponding genes. These toxins were more toxic to E. kuehniella larvae and more stable in the presence of these larvae's intestinal midgut juice than Cry1Aa and Cry1Ac of HD1. Moreover, we optimized the construction of a biomimetic membrane model based on the intestinal brush border membrane (BBM) of E. kuehniella larvae. These models were used to study the interaction of Cry1Aa and Cry1Ac of Lip and HD1. Toxins of Lip interacted differently and with a greater affinity with these model membranes than toxins of HD1.These results show that Lip is an interesting Bt strain that could be exploited at an industrial scale. On another hand, the biomimetic membrane constructed in this study could be an alternative allowing the prediction of the Cry toxin's affinity.MONTPELLIER-BU Sciences (341722106) / SudocSudocFranceF

    Bacillus cereus Biofilms—same, only different

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    Bacillus cereus displays a high diversity of lifestyles and ecological niches and include beneficial as well as pathogenic strains. These strains are widespread in the environment, are found on inert as well as on living surfaces and contaminate persistently the production lines of the food industry. Biofilms are suspected to play a key role in this ubiquitous distribution and in this persistency. Indeed, B. cereus produces a variety of biofilms which differ in their architecture and mechanism of formation, possibly reflecting an adaptation to various environments. Depending on the strain, B. cereus has the ability to grow as immersed or floating biofilms, and to secrete within the biofilm a vast array of metabolites, surfactants, bacteriocins, enzymes, and toxins, all compounds susceptible to act on the biofilm itself and/or on its environment. Within the biofilm, B. cereus exists in different physiological states and is able to generate highly resistant and adhesive spores, which themselves will increase the resistance of the bacterium to antimicrobials or to cleaning procedures. Current researches show that, despite similarities with the regulation processes and effector molecules involved in the initiation and maturation of the extensively studied Bacillus subtilis biofilm, important differences exists between the two species. The present review summarizes the up to date knowledge on biofilms produced by B. cereus and by two closely related pathogens, Bacillus thuringiensis and Bacillus anthracis. Economic issues caused by B. cereus biofilms and management strategies implemented to control these biofilms are included in this review, which also discuss the ecological and functional roles of biofilms in the lifecycle of these bacterial species and explore future developments in this important research area

    Optimization of Culture Conditions and Wheat Bran Class Selection in the Production of Bacillus thuringiensis-Based Biopesticides

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    International audienceBacillus thuringiensis is the leading microbial-based biopesticide, thanks to its parasporal crystal proteins or δ-endotoxins, which are toxic to insect larvae upon ingestion. Once in the insect larvae midgut, the crystal is solubilized by the alkaline pH and the δ-endotoxins activated by proteolytic cleavage. Thanks to its high efficiency as a biopesticide, several efforts have been made to enhance its growth and δ-endotoxins production, in various types of culture media. In this study, a culture medium based on wheat bran (WB), the by-product of cereal grain milling, was used to grow Bacillus thuringiensis and produce δ-endotoxins. Using the response surface methodology (RSM), the effects of three variables were evaluated: WB particles granulometry, their concentration, and their agitation in a 48-h shake-flask culture at 30 °C. Three response parameters were targeted: δ-endotoxins production, final culture pH, and dry-matter consumption. According to the RSM results, the optimum would be at 3.7 g WB/50 mL, with a granulometry above 680 μm and agitation between 170 and 270 rpm. This study is key to developing natural and cheap culture media that can be used at an industrial level for Bacillus thuringiensis-based biopesticides

    A Novel Antidipteran Bacillus thuringiensis Strain: Unusual Cry Toxin Genes in a Highly Dynamic Plasmid Environment

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    Bacillus thuringiensis has emerged as a major bioinsecticide on the global market. It offers a valuable alternative to chemical products classically utilized to control pest insects. Despite the efficiency of several strains and products available on the market, the scientific community is always on the lookout for novel toxins that can replace or supplement the existing products. In this study, H3, a novel B. thuringiensis strain showing mosquitocidal activity, was isolated from Lebanese soil and characterized in vivo at genomic and proteomic levels. H3 parasporal crystal is toxic on its own but displays an unusual killing profile with a higher 50% lethal concentration (LC50) than the reference B. thuringiensis serovar israelensis crystal proteins. In addition, H3 has a different toxicity order: it is more toxic to Aedes albopictus and Anopheles gambiae than to Culex pipiens. Whole-genome sequencing and crystal analysis revealed that H3 can produce 11 novel Cry proteins, 8 of which are assembled in genes with an orf1-gap-orf2 organization, where orf2 is a potential Cry4-type crystallization domain. Moreover, pH3-180, the toxin-carrying plasmid, holds a wide repertoire of mobile genetic elements that amount to ca. 22% of its size., including novel insertion sequences and class II transposable elements. Two other large plasmids present in H3 carry genetic determinants for the production of many interesting molecules—such as chitinase, cellulase, and bacitracin—that may add up to H3 bioactive properties. This paper therefore reports a novel mosquitocidal Bacillus thuringiensis strain with unusual Cry toxin genes in a rich mobile DNA environment

    Spatio-temporal evolution of sporulation in Bacillus thuringiensis biofilm

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    Bacillus thuringiensis can produce a floating biofilm which includes two parts: a ring and a pellicle. The ring is a thick structure which sticks to the culture container, while the pellicle extends over the whole liquid surface and joins the ring. We have followed over time, from 16 to 96 h, sporulation in the two biofilm parts. Sporulation was followed in situ in 48-wells polystyrene microtiterplates with a fluorescence binocular stereomicroscope and a spoIID-yfp transcriptional fusion. Sporulation took place much earlier in the ring than in the pellicle. In 20 h-aged biofilms, spoIID was expressed only in the ring, which could be seen as a green fluorescent circle surrounding the non-fluorescent pellicle. However, after 48 h of culture, the pellicle started to express spoIID in specific area corresponding to protrusions, and after 96 h both the ring and the whole pellicle expressed spoIID. Spore counts and microscopy observations of the ring and the pellicle harvested separately confirmed these results and revealed that sporulation occured 24 h-later in the pellicle comparatively to the ring, although both structures contained nearly 100% spores after 96 h of culture. We hypothesize that two mechanisms, due to microenvironments in the biofilm, can explain this difference. First, the ring experiences a decreased concentration of nutrients earlier than the pellicle, because of a lower exchange area with the culture medium. An second, the ring is exposed to partial dryness. Both reasons could speed up sporulation in this biofilm structure. Our results also suggest that spores in the biofilm display a phenotypic heterogeneity. These observations might be of particular significance for the food industry, since the biofilm part sticking to container walls the ring is likely to contain spores and will therefore resist both to washing and to cleaning procedures, and will be able to restart a new biofilm when food production has resumed
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