15,889 research outputs found

    Changes in microbial (Bacteria and Archaea) plankton community structure after artificial dispersal in grazer-free microcosms

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    Microbes are considered to have a global distribution due to their high dispersal capabilities. However, our knowledge of the way geographically distant microbial communities assemble after dispersal in a new environment is limited. In this study, we examined whether communities would converge because similar taxa would be selected under the same environmental conditions, or would diverge because of initial community composition, after artificial dispersal. To this aim, a microcosm experiment was performed, in which the temporal changes in the composition and diversity of different prokaryoplankton assemblages from three distant geographic coastal areas (Banyuls-sur-Mer in northwest Mediterranean Sea, Pagasitikos Gulf in northeast Mediterranean and Woods Hole, MA, USA in the northwest Atlantic), were studied. Diversity was investigated using amplicon pyrosequencing of the V1-V3 hypervariable regions of the 16S rRNA. The three assemblages were grown separately in particle free and autoclaved Banyuls-sur-mer seawater at 18 °C in the dark. We found that the variability of prokaryoplankton community diversity (expressed as richness, evenness and dominance) as well as the composition were driven by patterns observed in Bacteria. Regarding community composition, similarities were found between treatments at family level. However, at the OTU level microbial communities from the three different original locations diverge rather than converge during incubation. It is suggested that slight differences in the composition of the initial prokaryoplankton communities, resulted in separate clusters the following days even when growth took place under identical abiotic conditions

    On subset seeds for protein alignment

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    We apply the concept of subset seeds proposed in [1] to similarity search in protein sequences. The main question studied is the design of efficient seed alphabets to construct seeds with optimal sensitivity/selectivity trade-offs. We propose several different design methods and use them to construct several alphabets. We then perform a comparative analysis of seeds built over those alphabets and compare them with the standard BLASTP seeding method [2], [3], as well as with the family of vector seeds proposed in [4]. While the formalism of subset seeds is less expressive (but less costly to implement) than the cumulative principle used in BLASTP and vector seeds, our seeds show a similar or even better performance than BLASTP on Bernoulli models of proteins compatible with the common BLOSUM62 matrix. Finally, we perform a large-scale benchmarking of our seeds against several main databases of protein alignments. Here again, the results show a comparable or better performance of our seeds vs. BLASTP.Comment: IEEE/ACM Transactions on Computational Biology and Bioinformatics (2009

    Bioaugmentation For Recovery of Anaerobic Digesters Subjected to Organic Overload

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    Anaerobic digester upset due to organic overload is common and methods to reduce recovery time would be beneficial. One potential method is bioaugmentation, the addition of an external culture for performance improvement. Methanogenic community structure differs from digester to digester and there may exist a relation between specific methanogenic activity (SMA) and microbial community composition. The research presented herein tested whether there is a relationship between SMA and community structure. Also, the effectiveness of bioaugmentation was tested by hypothesizing that bioaugmenting with a methanogenic, propionate-degrading culture acclimated to small oxygen doses will help rapid recovery of organically overloaded digesters. Fourteen different anaerobic cultures were tested for SMA and microbial community using the mcrA gene and DGGE to establish a relationship between SMA and community structure. The culture with the highest SMA was enriched by feeding 0.17g propionate/L-day and different oxygen doses. The enrichment cultures were used to bioaugment organically overloaded anaerobic digesters. Microbial communities present in bioaugmented, non-bioaugmented and undisturbed control digesters as well as the bioaugmentation culture were analyzed using 16S rDNA. A statistically significant relationship between SMA and community structure could not be established, highlighting the difficulty in establishing activity/community structure relationships. However, the results indicated that there was a relation between SMA and methanogenic community compositions studied. Enriching a culture for 25mgO2/L-day increased its SMA by 29.7%, but higher oxygen doses yielded lower SMA values. Bioaugmentation with this enrichment culture reduced the time required for upset digester effluent to decrease below 1000mgSCOD/L by 114 days (11.4 SRTs) and the time required to reach 25mLCH4/day by 37 days (3.7 SRTs) respectively. Bioaugmented digesters consistently produced lower effluent SCOD and more methane than non-bioaugmented digesters. Bioaugmentation is a promising approach for speeding up recovery of organically overloaded digesters. Bacterial and archaeal communities of the bioaugmented and undisturbed control digesters had similar phylogenetic tree structures (p\u3e0.3), whereas the tree structures of non-bioaugmented and undisturbed control digesters differed significantly (pMethanospirillum hungatei may have caused better performance of bioaugmented digesters

    Universal Global Imprints of Genome Growth and Evolution – Equivalent Length and Cumulative Mutation Density

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    BACKGROUND: Segmental duplication is widely held to be an important mode of genome growth and evolution. Yet how this would affect the global structure of genomes has been little discussed. METHODS/PRINCIPAL FINDINGS: Here, we show that equivalent length, or L(e), a quantity determined by the variance of fluctuating part of the distribution of the k-mer frequencies in a genome, characterizes the latter's global structure. We computed the L(e)s of 865 complete chromosomes and found that they have nearly universal but (k-dependent) values. The differences among the L(e) of a chromosome and those of its coding and non-coding parts were found to be slight. CONCLUSIONS: We verified that these non-trivial results are natural consequences of a genome growth model characterized by random segmental duplication and random point mutation, but not of any model whose dominant growth mechanism is not segmental duplication. Our study also indicates that genomes have a nearly universal cumulative "point" mutation density of about 0.73 mutations per site that is compatible with the relatively low mutation rates of (1-5) x 10(-3)/site/Mya previously determined by sequence comparison for the human and E. coli genomes
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