The mass spectrum of heterocyst glycolipid and the corresponding structures are shown on the right. The mass spectrum of heterocyst glycolipid and the.

Slides:



Advertisements
Similar presentations
Figure 1.1 The observer in the truck sees the ball move in a vertical path when thrown upward. (b) The Earth observer views the path of the ball as a parabola.
Advertisements

2011 vs 2012 Z +  measurements Al Goshaw June 23, 2012.
22 kDa a-coixin gene cluster
Correlation between the ability of Novosphingobium strains from four different habitats to degrade aromatic and xenobiotic compounds. Correlation between.
Heatmap displaying consistent similarity-based OTU results based on SIMPER intragroup similarity analyses for the tissue, mucus, holobiont, and seawater.
مديريت موثر جلسات Running a Meeting that Works
The molecular network of the fungal molecule asperphenamate (m/z 507
Alignment of H-NS, H-NS2, and StpA amino acid sequences.
Characterized LuxR-associated and QS-regulated BGCs were identified in our screen. Characterized LuxR-associated and QS-regulated BGCs were identified.
(a) PCoA of the abundance of unique OTUs per sample from the 16S marker gene sequencing data from the AGP data repository (small spheres) and the San Diego.
Expression profiles of GAS virulence factors during planktonic and biofilm growth. Expression profiles of GAS virulence factors during planktonic and biofilm.
(a) Bifurcating tree generated from hierarchical clustering of OTUs based on mean pH. (a) Bifurcating tree generated from hierarchical clustering of OTUs.
Hierarchical cluster analysis of reproducible parent masses (MS) representative of produced SMs from oral in vitro-grown biofilm representing >100 bacterial.
Plots of the number of sequences [log (x + 1) scale] from bacterial OTUs in both PCR replicates (PCR1 and PCR2) of the 348 wild rodents analyzed in the.
Magnitude of mRNA fold change is best predictor of mRNA-to-protein correlation. Magnitude of mRNA fold change is best predictor of mRNA-to-protein correlation.
Gene content and order of the clade B-specific GT-rich gene cluster.
Golden Gate assembly of transposon delivery vectors from part vectors.
Transcription levels of metabolic pathways and genes in mother and infant pair 4 at time point 2. Transcription levels of metabolic pathways and genes.
Lack of phylogenetic conservatism of Bacillus anthracis plasmid copy number. Lack of phylogenetic conservatism of Bacillus anthracis plasmid copy number.
Correlation of mouse gene expression with bacterial gene expression.
Maximum-likelihood phylogenetic tree of norovirus genomes belonging to genogroup GI, with the norovirus GII reference genome as an outlier. Maximum-likelihood.
Genomes with Fe-S cluster assembly-related genes.
Parallel evolution of coding sequences above neutral expectation.
Comparison of the global transcriptomes of nine EPEC isolates.
Box plots of quality scores over positions in sequenced reads.
Relative abundances (percent) of genes that code for key enzymes involved in direct and indirect butyrate production during glucose fermentation at different.
Maximum-likelihood phylogeny of the household isolates from core SNPs
Locations of genes that exhibited decreased levels of distribution of the RpoZ-defective RNAP. The genes that showed decreased-level distribution of RpoZ-defective.
Example usage of mockrobiota MC resource for marker gene and metagenome sequencing pipelines. Example usage of mockrobiota MC resource for marker gene.
Distribution of microbial functions in urban waterways.
Maximum likelihood (ML) unrooted tree based on the full-length 16S rRNA genes (A) and 31 conserved single-copy genes (B) showing the phylogenetic position.
Proportion of 16S rRNA gene sequences in each category of phylogenetic novelty relative to cultures for each environment, by amplicons, metagenomes (without.
Field community comparisons via 16S and between sequencing runs.
16S rRNA gene survey reveals a moderate impact of formula-based B
Transcription of cellulolytic genes disaggregated by genome.
Individuals (dots) colored according to results of hierarchical clustering of copy number estimates (as described in Supplementary Text) for IGHV
Trends in metabolite predictability in terms of key gene contributors.
RNA abundance correlates with fitness.
The molecular network of a family of sesquiterpene lactones and the distribution of a representative molecule with an MS/MS spectrum match to alantolactone.
Characterization of differentially expressed genes based on their COG classification. Characterization of differentially expressed genes based on their.
Single-cell phenotyping with Traitar.
Sequence similarity network of 436 TonB-dependent transporters from 153 different Roseobacter genomes. Sequence similarity network of 436 TonB-dependent.
Linear schematic of the basic quality control procedure for marker gene (microbiome) data. Linear schematic of the basic quality control procedure for.
Putative sources of interphylum horizontal gene transfer in the M
Box plots displaying the median, minimum, maximum, and first and third quartiles of the percentage of the 25 members of the core microbiome detected in.
Distribution of ARGs in RefSoil genomes and plasmids.
Strong parallelism in mutated genes defines adaptations to the environment of CF patient lungs. Strong parallelism in mutated genes defines adaptations.
MLST analysis of Bacillus strains of this study and related species of the B. cereus sensu lato group. MLST analysis of Bacillus strains of this study.
(a) Molecular network clusters of pheophytin and procyanidin and their related metabolites. (a) Molecular network clusters of pheophytin and procyanidin.
Comparison of species and function profiles with ultradeep sequencing data. Comparison of species and function profiles with ultradeep sequencing data.
The MS/MS spectra and MALDI IMS distributions of mannitol and the corresponding polysaccharide containing mannitol are shown. The MS/MS spectra and MALDI.
Sequence variation of 16S rRNA gene primer-binding sites.
Fig. 1. Microarray analyses of genes whose expression is regulated by innervation during synaptogenesis.(A) Schematic drawings of the experimental design.
Most mutations were nonsynonymous, especially at the nodes of new clades, with affected genes encoding regulatory functions, lipid metabolism, and envelope.
Expression of selected genes in the ΔSMcomS strain in response to increasing concentrations of XIP. RT-PCR analysis of gene expression was performed in.
Fig. 8. Expression of other genomic-clustered Chrn subunits in the mesodiencephalon.(A) Schematic representation illustrating the assembly of the Chrnb4,
The distribution of fungal molecules PF1140, asperphenamate, and alantolactone (A) and cyanobacterial molecules (chlorophyll and heterocyst glycolipid)
Expression of selected intergenic regions in response to increasing concentrations of XIP. qRT-PCR analysis of gene expression was performed with strain.
Run time performance for all benchmarked software.
Enrichment of KEGG pathways in microbial genes in different samples.
ITS rRNA gene locus. ITS rRNA gene locus. Schematic of the eukaryotic ribosomal gene cluster. The SILVA database contains sequences of the 18S gene, while.
Comparison of gut microbiota alpha diversity in different preservatives based on 16S rRNA gene V3-V4 amplicon sequencing. Comparison of gut microbiota.
Nine examples of MCXC MMCGs which were not also selected as MCXC BCGs
KEGG categories of host DEGs (up- and downregulated genes) enriched at selected points after φAbp1 infection. KEGG categories of host DEGs (up- and downregulated.
P-network of 2,616 prokaryote genomes based on chromosomal sequences with rRNA genes removed. P-network of 2,616 prokaryote genomes based on chromosomal.
K-means clusters of T. elongatus and M
Fig. 4 The three DBT cycles involved in building syn3.0.
Driver pathways and key genes in OSCC
ChIP-chip analysis of wild-type (WT) and RpoZ-defective mutant RNAP
Relative abundance and expression of the 10 most abundant MAGs in the bioreactor at day 96. Relative abundance and expression of the 10 most abundant MAGs.
Presentation transcript:

The mass spectrum of heterocyst glycolipid and the corresponding structures are shown on the right. The mass spectrum of heterocyst glycolipid and the corresponding structures are shown on the right. The cyanobacterial heterocyst glycolipid colocalizes with the cyanobacterial chlorophyll (Fig. 5 and 8B). The heterocyst biosynthetic gene cluster was identified by running antiSMASH on the metaSPAde assembly of the short-read data set. The gene cluster identified by using antiSMASH is shown as the query sequence, and the gene cluster previously deposited in antiSMASH corresponds to the gene cluster named BGC0000869_c1. Neha Garg et al. mSystems 2016; doi:10.1128/mSystems.00139-16