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The Analysis of Crack Causation of Type CDZ 3150 KN Elevator Latch Shoulder Root

毛, 建设

In: Mechanical Engineering and Technology ; volume 08, issue 01, page 8-16 ; ISSN 2167-6631 2167-6623, 2019

academicJournal

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Role of Recipient Susceptibility Factors During Contact-Dependent Interbacterial Competition

Lin, Hsiao-Han ; Filloux, Alain ; et al.

2020

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Figure 7. Phylogenetic distribution of putative Cdz-like systems in bacteria. ; (A) Multiple sequence alignment used as the seed in an iterative computational search for Cdz-like systems (see Materials and methods). The presumed leader peptide of each sequence is indicated. Amino acid composition is represented with colors as follows: grey, hydrophobic; glycine, green; positively charged, red; negatively charged, blue. The location of the conserved glycine zipper region is indicated below the alignment. The Aβ peptide, which also contains a glycine zipper, is shown for comparison. The sequence logo generated from all 239 Cdz-like proteins identified is shown at the bottom. (B) Phylogenetic distribution of Cdz-like systems identified in UniProtKB. Each branch corresponds to a unique sequence. Numbers at the tips of collapsed branches indicate the number of strains for a given species harboring a Cdz-like system. Orange branches correspond to the Enterobacteriaceae. Predicted number of Cdz-like proteins is indicated based on the legend at the bottom left.

2017

unknown

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Figure 1. The cdz gene cluster is very highly expressed in stationary phase. ; (A) Genome-wide RNA-seq profiles of C. crescentus CB15N grown in rich medium to exponential (top) or stationary (bottom) phase. Expression levels (RPM) for both strands combined are plotted as a function of genomic position. A schematic of the cdz cluster is shown beneath the RNA-seq profiles. (B) RNA-seq profile of the cdz gene cluster in stationary phase. Each strand is shown separately. (C) Activity of a cdzC transcriptional reporter (YFP) as a function of culture density (for the corresponding growth curve, see Figure 1—figure supplement 1). Induction is reported relative to the level when OD600 = 0.025. Data points are mean of three independent cultures; error bars indicate standard deviation (S.D.). (D) Western blot analysis of epitope-tagged CdzC, CdzD, and CdzI in the cell pellets of supernatant taken from cultures at the OD600 values indicated. RpoA is a loading control.

2017

unknown

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CDZ-English Glossary

Napiorkowska, Lidia

In: A Grammar of the Christian Neo-Aramaic Dialect of Diyana-Zariwaw ; page 479-582 ; ISBN 9789004290327 9789004290334; (2015)

Online Buch

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Figure 4. Cdz-mediated killing requires cell-cell contact between a producer and an indicator. ; (A) Survival of a ∆cdzABCDI indicator when treated for 16 hr with live producer cells, producer culture supernatant, producer culture supernatant concentrated 2000X by trichloroacetic acid precipitation, producer culture supernatant concentrated 20X by centrifugation, producer cells that were boiled for 5 min, or producer cells treated with gentamicin. (B) Competitive index of ∆cdzABCDI indicator grown in co-culture with a wild-type producer or ∆cdzABCDI mock-producer using the split-well set-up shown (left). The membrane separating the two compartments had a pore size of 8 or 0.4 µm, as indicated. (C) Flow cytometry analysis of a 1:1 mixture in stationary phase of wt producer cells expressing Venus and ∆cdzABCDI indicator cells expressing TdTomato.

2017

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Figure 2. The cdz gene cluster encodes a two-peptide bacteriocin, secreted via a type I secretion system, and a small transmembrane immunity protein. ; (A) Co-culture competition of wild-type C. crescentus and ∆cdzABCDI in rich medium. Strains were mixed 1:1 in exponential phase and co-cultured, with CFUs of each strain measured up to 14 hr. (B) Experimental set-up for co-culture competitions in stationary phase and overview of competitive index calculation. (C–F) Competitions between the indicator and producer strains with the genotypes indicated schematically. Graphs show the competitive index of the indicator strain in each experiment. In each panel, data points represent the mean of at least three independent experiments; error bars indicate S.D. Induction of the Pvan promoter by vanillate is indicated by '+ van'.

2017

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Figure 3—figure supplement 1. Control experiments for the microscopy-based analysis of Cdz-dependent killing. ; (A) Phase and epifluorescence microscopy of aliquots taken from a co-culture competition of a wild-type producer synthesizing YFP (green) and a ∆cdzCDI indicator synthesizing CFP (blue), with the viability stain propidium iodide (red). A merge of phase and all three fluorescence channels is shown at each time point. Cells staining blue and red are shown in magenta. (B) Same as panel A, but for a competition between two wild-type producers synthesizing CFP or YFP.

2017

unknown

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Supplementary file 1. Cdz-like peptides identified in UniprotKB.

2017

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Figure 7—figure supplement 1. Competitions between a wild-type or ∆cdzABCDI Caulobacter crescentus producer and the indicator species shown: ∆cdz Caulobacter crescentus, Caulobacter segnis, Brevundimonas subvibrioides, Asticcacaulis excentricus, Rhodobacter sphaeroides, Sinorhizobium meliloti, Agrobacterium tumefaciens, or E. coli. ; In each panel, data points represent the mean of at least three independent experiments; error bars indicate S.D. Tree on the left illustrates phylogenetic relationship between groups, branch lengths are not representative of phylogenetic distance.

2017

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Figure 7—figure supplement 1. CDZ inhibits SV replenishment during tonic transmission in WT neurons. ; (A) Plot of cumulative total tonic charge transfer vs time from WT and KO neurons, in the presence and absence of CDZ, during HFS. Data were fitted and analyzed as described in Figure 3C. (B) During tonic transmission, CDZ treatment reduced SV replenishment in WT neurons (1.88 ± 0.32 s−1 vs 3.95 ± 0.61 s−1 for controls), but had no effect on the already compromised replenishment rate in KO neurons (1.73 ± 0.34 s−1 vs 2.19 ± 0.22 s−1 for controls). The n values indicate the number of neurons, obtained from three independent litters of mice, used for these experiments. All data shown represent mean ± SEM. ***p

2014

unknown

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Figure 8. CDZ inhibits RRP recovery in WT neurons, phenocopying the KO. ; (A) Time course for the recovery of phasic release upon HFS; data were collected and analyzed as described in Figure 4A. The inset panel shows the expanded early phase of the plot. (B) CDZ slowed the time course of fast recovery of the RRP in WT neurons (1.35 ± 0.37 s vs 0.55 ± 0.17 s for control), phenocopying the KO neurons, which were not affected by CDZ (1.22 ± 0.36 s vs 1.32 ± 0.22 s for control). (C) The time course of slow recovery of the RRP was the same between WT and KO neurons with or without CDZ (WT: 16.02 ± 3.02 s vs 15.72 ± 2.85 s for controls; KO: 15.78 ± 2.5 s vs 14.13 ± 2.24 s for controls). (D) Typical responses to sequential (7 s) applications of sucrose to WT and KO neurons in 2 mM [Ca2+]o in the presence of CDZ. The upper diagram illustrates the protocol used (Δt = 7, 14, 21, 28 and 60 s). (E) Time course for the recovery of the RRP after depletion with hypertonic sucrose in 2 mM [Ca2+]o. Data were fitted with a single exponential function to calculate the recovery time constant (F). (F) CDZ increased the time constant for recovery of the RRP in WT neurons (20.69 ± 1.43 s vs 7.29 ± 1.05 s for controls), but had no effect on KO neurons (20.37 ± 2.1 s vs 18.03 ± 2.87 s for controls). The n values indicate the number of neurons, obtained from three independent litters of mice, used for these experiments. All data shown represent mean ±SEM. ***p

2014

unknown

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Figure 7. Syt 7 cooperates with CaM to regulate Ca2+-dependent SV replenishment. ; (A) Immobilized CaM efficiently pulled-down the C2AB domain of syt 7, but not syt 1, 2, 4, 9 or 10, in the presence, but not the absence, of Ca2+; the syt 7 4D/N mutant failed to bind. E, 2 mM EGTA; Ca, 1 mM free Ca2+. Spaces between gels indicate samples that were run separately. Input corresponds to 25% of the starting material; 50% of the bound material was loaded per lane; no binding was observed when CaM was omitted from the beads (data not shown). (B) Mg2+ fails to promote binding of syt 7 C2AB to CaM. E, 2 mM EGTA; Ca, 1 mM free Ca2+; Mg, 1 mM free Mg2+. Gels were loaded as in panel A. (C) Representative EPSCs traces (20 Hz/2.5 s) recorded from WT (black) and KO (red) neurons in the presence of CDZ. (D) Plot of cumulative total phasic release charge vs time in the presence of CDZ. Data were analyzed as described in Figure 3C. (E) The size of the RRP was the same among all groups (in control: WT: 38.70 ± 4.78 pC; KO: 33.49 ± 2.48 pC; in CDZ treated neurons: WT: 36.85 ± 5.35 pC; KO: 34.77 ± 6.74 pC). (F) CDZ treatment reduced SV replenishment in WT neurons (0.24 ± 0.04 s−1 vs 0.52 ± 0.06 s−1 for controls), but had no effect on KO neurons (0.21 ± 0.05 s−1 vs 0.26 ± 0.03 s−1 for controls). The n values indicate the number of neurons, obtained from three independent litters of mice, used for these experiments. All data shown represent mean ± SEM. ***p

2014

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Figure 8—figure supplement 2. CDZ does not compete with syt 7 for binding to CaM. ; The cytoplasmic domains of syt 7 (syt 7 C2AB) and different concentrations of CDZ were simultaneously incubated with immobilized CaM for 2 hr at 37°C in the presence and absence of Ca2+. CDZ had no effect on Ca2+-dependent binding of syt 7 to CaM. E, 2 mM EGTA; Ca, 1 mM free Ca2+.

2014

unknown

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Figure 8—figure supplement 1. CDZ impairs recovery of tonic transmission in WT neurons. ; (A) Time course of recovery of tonic transmission. Data were fitted and analyzed as described in Figure 4A. Upper diagram describes the stimulation protocol (Δt = 0.5, 1, 3, 5, 9, 17, 33 and 65 s). Inset: expanded view of the initial section of the plot. (B) CDZ slowed the fast recovery component during tonic transmission in WT neurons (1.34 ± 0.35 s vs 0.54 ± 0.05 s for controls), but had no effect on KO neurons (1.18 ± 0.24 s vs 1.20 ± 0.24 s for controls). (C) The slow recovery time constant was the same between WT and KO neurons, with or without CDZ (WT: 17.32 ± 2.64 s vs 18.52 ± 2.43 s for controls; KO: 15.83 ± 3.13 s vs 17.43 ± 3.39 s for controls). The n values indicate the number of neurons, obtained from three independent litters of mice, used for these experiments. All data shown represent mean ± SEM. ***p

2014

unknown

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МОРФОЛОГИЧЕСКОЕ ИССЛЕДОВАНИЕ ВНУТРЕННИХ ОРГАНОВ И ТКАНЕЙ ЖИВОТНЫХ ПОД ВЛИЯНИЕМ СУБСТАНЦИИ КДЗ В УСЛОВИЯХ ХРОНИЧЕСКОЙ ТОКСИЧНОСТИ

КАМЧИБЕКОВА, ЧОЛПОН

2016

academicJournal

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Sino-German Center for Research - Promotion[CDZ 1080]

2018

unknown

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A 2 × 2048 Pixel Bilinear CCD Array for Spectroscopy (TH 7832 CDZ)

Coutures, J.L. ; Boucharlat, G.

In: Photo-Electronic Image Devices - Proceedings of the Ninth Symposium ; Advances in Electronics and Electron Physics ; page 173-179 ; ISSN 0065-2539; (1988)

Buch

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Grokster and Beyond: Secondary Liability for Copyright Infringement During Live Musical Performances

Holt, Kathryn Dailey

In: Journal of Intellectual Property Law, 2016

academicJournal

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For Viable and Sustainable Paddy Production in Cauvery Delta Zone, Tamil Nadu, India ...

Radhakrishnan, Gopinath ; Kumar, Aparajay ; et al.

2023

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