LYSOGENY IN A STRAIN OF XANTHOMONAS GAMPESTRIS

1963 ◽  
Vol 9 (6) ◽  
pp. 821-828 ◽  
Author(s):  
M. D. Sutton ◽  
C. Quadling
Keyword(s):  
Electron Microscope ◽  
Host Range ◽  
Mitomycin C ◽  
Xanthomonas Campestris ◽  
Temperate Phage ◽  
Nutrient Broth ◽  
Bacterial Strains ◽  
Phage Development ◽  
Before And After

Fourteen bacterial strains representing eight so-called species of phytopathogenic xanthomonads were tested for lysogeny both before and after treatments known to induce phage development in lysogenic bacteria. Only a single temperate phage, of restricted host range, was found. Evidence suggestive of defective lysogeny was found in a number of cases.Strain P165, Xanthomonas campestris, when treated with antibiotic Mitomycin C at a concentration of 0.1,ug/ml in nutrient broth, produced phage particles active on strain P12S, X. campestris. No other sensitive strains were found among the 81 tested, representing 22 species of Xanthomonas. This phage (P165/P125) produced small turbid plaques, 0.6 mm to 0.8 mm in diameter, with indefinite margins. Evidence for the lysogenization of P125 strain by this phage was found. Clear plaques were sometimes found in lawns of lysogenized cells of P12S. These were presumably derived from phage mutants with increased virulence. When examined under the electron microscope, the phage particles were semispherical, approximately 65 m/x in diameter with rudimentary tails.

An Electron Microscope Study of Interdiffusion and Compound Formation in Ta-Au Thin Films

1973 ◽  
Vol 31 ◽  
pp. 32-33 ◽  
Author(s):  
T. C. Tisone ◽  
S. Lau
Keyword(s):  
Electron Microscope ◽  
Electron Microscope Study ◽  
Thermally Grown Oxide ◽  
Ion Milling ◽  
Compound Formation ◽  
Technology Application ◽  
Transmission Electron ◽  
Before And After ◽  
Au Thin Films

In a study of the properties of a Ta-Au metallization system for thin film technology application, the interdiffusion between Ta(bcc)-Au, βTa-Au and Ta2M-Au films was studied. Considered here is a discussion of the use of the transmission electron microscope(TEM) in the identification of phases formed and characterization of the film microstructures before and after annealing.The films were deposited by sputtering onto silicon wafers with 5000 Å of thermally grown oxide. The film thicknesses were 2000 Å of Ta and 2000 Å of Au. Samples for TEM observation were prepared by ultrasonically cutting 3mm disks from the wafers. The disks were first chemically etched from the silicon side using a HNO3 :HF(19:5) solution followed by ion milling to perforation of the Au side.

scholarly journals Phenotypically and Genotypically Heterogeneous Strains of Pseudomonas syringae Associated With Alfalfa Leaf Spot Disease in Iran

Plant Disease ◽  
2019 ◽  
Vol 103 (12) ◽  
pp. 3199-3208 ◽  
Author(s):  
Maryam Ansari ◽  
S. Mohsen Taghavi ◽  
Sadegh Zarei ◽  
Soraya Mehrb-Moghadam ◽  
Hamzeh Mafakheri ◽  
...  
Keyword(s):  
Host Range ◽  
Pseudomonas Syringae ◽  
Leaf Spot ◽  
Phylogenetic Analyses ◽  
Housekeeping Genes ◽  
Pcr Primers ◽  
Phylogenetic Position ◽  
Leaf Spot Disease ◽  
Bacterial Strains ◽  
Alfalfa Leaf

In this study, we provide a polyphasic characterization of 18 Pseudomonas spp. strains associated with alfalfa leaf spot symptoms in Iran. All of the strains were pathogenic on alfalfa, although the aggressiveness and symptomology varied among the strains. All strains but one were pathogenic on broad bean, cucumber, honeydew, and zucchini, whereas only a fraction of the strains were pathogenic on sugar beet, tomato, and wheat. Syringomycin biosynthesis genes (syrB1 and syrP) were detected using the corresponding PCR primers in all of the strains isolated from alfalfa. Phylogenetic analyses using the sequences of four housekeeping genes (gapA, gltA, gyrB, and rpoD) revealed that all of the strains except one (Als34) belong to phylogroup 2b of P. syringae sensu lato, whereas strain Als34 placed within phylogroup 1 close to the type strain of P. syringae pv. apii. Among the phylogroup 2b strains, nine strains were phylogenetically close to the P. syringae pv. aptata clade, whereas the remainder were scattered among P. syringae pv. atrofaciens and P. syringae pv. syringae strains. Pathogenicity and host range assays of the bacterial strains evaluated in this study on a set of taxonomically diverse plant species did not allow us to assign a “pathovar” status to the alfalfa strains. However, these results provide novel insight into the host range and phylogenetic position of the alfalfa-pathogenic members of P. syringae sensu lato, and they reveal that phenotypically and genotypically heterogeneous strains of the pathogen cause bacterial leaf spot of alfalfa.

scholarly journals Mitomycin C Inhibits Esophageal Fibrosis by Regulating Cell Apoptosis and Autophagy via lncRNA-ATB and miR-200b

2021 ◽  
Vol 8 ◽  
Author(s):  
Yin Zhang ◽  
Qinge Wang ◽  
Yuping Xu ◽  
Jing Sun ◽  
Yanbo Ding ◽  
...  
Keyword(s):  
Electron Microscope ◽  
Mitomycin C ◽  
Cell Apoptosis ◽  
Optimal Dose ◽  
The Other ◽  
Fibroblast Cells ◽  
Transmission Electron ◽  
Esophageal Strictures ◽  
Related Proteins

Benign esophageal strictures (BESs) frequently results from esophageal fibrosis. The transformation of fibroblasts into fibrocyte is an important cause of fibrosis. The treatment of fibrosis is challenging. Some previous studies have indicated the antifibrotic effect of mitomycin C (MMC). However, the mechanism of action of MMC and its optimal dose for treatment remains unclear. In the present study, the role of MMC in fighting fibrosis and its mechanism was investigated. Human esophageal fibroblast cells (HEFs)were treated without or with MMC, at 2, 5, 10 μg/ml, combining with mimic lncRNA-ATB, miR-200b inhibitor, rapamycin (RAPA), and 3-Methyladenine (3-MA). The cell viability, and cell apoptosis were evaluated. In addition, expression of apoptosis related proteins (caspase8 and caspase3), autophagy related proteins (LC3II and ATG5) and fibrosis related proteins (α-SMA collagen-1 and TGF-β) were also evaluated. Furthermore, autophagosome was observed by transmission electron microscope. Results showed that the expression of lncRNA-ATB was down-regulated and miR-200b was up-regulated after treated with MMC. And MMC induced cell apoptosis and inhibited cell autophagy. On the other hand, RAPA, mimic lncRNA-ATB and miR-200b inhibitor reduced fibrogenic effect of MMC on HEFs. Collectively, this study suggests that MMC inhibited esophageal fibrosis by regulating cell apoptosis and autophagy via downregulating lncRNA-ATB and upregulating miR-200b.

scholarly journals Blue light is a universal tactic signal forEscherichia coli

2017 ◽  
Author(s):  
Tatyana Perlova ◽  
Martin Gruebele ◽  
Yann R. Chemla
Keyword(s):  
Blue Light ◽  
Light Exposure ◽  
Biological Significance ◽  
Proton Motive Force ◽  
Motive Force ◽  
Swimming Velocity ◽  
Bacterial Strains ◽  
E Coli ◽  
Before And After ◽  
Swimming Bacteria

AbstractBlue light has been shown to elicit a tumbling response inE. coli, a non-phototrophic bacterium. The exact mechanism of this phototactic response is still unknown, and its biological significance remains unclear. Here, we quantify phototaxis inE. coliby analyzing single-cell trajectories in populations of free-swimming bacteria before and after light exposure. Bacterial strains expressing only one type of chemoreceptor reveal that all fiveE. colireceptors - Aer, Tar, Tsr, Tap and Trg - are capable of mediating a response to light. In particular, light exposure elicits a running response in Tap-only strain, the opposite of the tumbling response observed for all other strains. Light therefore emerges as a universal stimulus for allE. colichemoreceptors. We also show that blue light exposure causes a reversible decrease in swimming velocity, a proxy for proton motive force. We hypothesize that rather than sensing light directly, chemoreceptors sense light-induced perturbations in proton motive force.ImportanceOur findings provide new insights on the mechanism ofE. coliphototaxis, showing that all five chemoreceptor types respond to light and that their interactions play an important role in cell behavior. Our results also open up new avenues for examining and manipulatingE. colitaxis. Since light is a universal stimulus, it may provide a way to quantify interactions between different types of receptors. Since light is easier to control spatially and temporally than chemicals, it may be used to study swimming behavior in complex environments. Since phototaxis can cause migration ofE. colibacteria in light gradients, light may be used to control bacterial density for studying density-dependent processes in bacteria.

scholarly journals A rapidly-dissolving silica-silver bioactive glass for cariostatic applications

2021 ◽  
Author(s):  
Saad Arshad
Keyword(s):  
Oral Cavity ◽  
Antibacterial Effect ◽  
Surface Hardness ◽  
Tris Buffer ◽  
Bacterial Strains ◽  
Buffer Solution ◽  
Solution Ph ◽  
Before And After ◽  
Knoop Microhardness ◽  
Tris Buffer Solution

In this study, bioactive glasses were designed for the purposes of reducing the incidence of dental caries and lesion formation by supplying the teeth with therapeutic ions which may support remineralization and provide an antibacterial effect against oral cavity bacteria. Three glasses were synthesised through the melt quench method: Si-Control (SiO2-CaO-P2O5-Na2O), Si-02 and Si-05, where 0.2% and 0.5% Ag2O were substituted, respectively, for SiO2 in the control glass. The glasses were then ground, characterized and dissolved in tris buffer solution (pH=7.30) for 6, 12 and 24 hours, with the pH rise of the solution being recorded (7.48 for Si-Control, and 7.66 for both Si-02 and Si-05 after 24 hours) and the ions that were released into the tris buffer solution quantified. Samples of each glass were subsequently embedded into non-fluoridated toothpaste and samples of the paste were used to brush resin-mounted lamb molars after a 1.0M HCl overnight demineralization challenge. Knoop microhardness measurements were recorded before and after brushing to determine the presence of remineralization on the surface of the teeth (Percent Surface Hardness Loss of 37%, 35% and 34% for Si-Control, Si-02 and Si-05 respectively after 24 hours). Four oral cavity bacterial strains were isolated through swabs of the inner cheek, gums and teeth surfaces of three volunteers, and placed on agar discs. 0.5g of each glass were placed onto the discs and the resultant inhibition zones were measured after 6, 12 and 24 hours. Si-05 consistently performed better than Si-02 on all strains and timeframes, while Si-Control exhibited no antibacterial effect at any time point.

scholarly journals A rapidly-dissolving silica-silver bioactive glass for cariostatic applications

2021 ◽  
Author(s):  
Saad Arshad
Keyword(s):  
Oral Cavity ◽  
Antibacterial Effect ◽  
Surface Hardness ◽  
Tris Buffer ◽  
Bacterial Strains ◽  
Buffer Solution ◽  
Solution Ph ◽  
Before And After ◽  
Knoop Microhardness ◽  
Tris Buffer Solution

In this study, bioactive glasses were designed for the purposes of reducing the incidence of dental caries and lesion formation by supplying the teeth with therapeutic ions which may support remineralization and provide an antibacterial effect against oral cavity bacteria. Three glasses were synthesised through the melt quench method: Si-Control (SiO2-CaO-P2O5-Na2O), Si-02 and Si-05, where 0.2% and 0.5% Ag2O were substituted, respectively, for SiO2 in the control glass. The glasses were then ground, characterized and dissolved in tris buffer solution (pH=7.30) for 6, 12 and 24 hours, with the pH rise of the solution being recorded (7.48 for Si-Control, and 7.66 for both Si-02 and Si-05 after 24 hours) and the ions that were released into the tris buffer solution quantified. Samples of each glass were subsequently embedded into non-fluoridated toothpaste and samples of the paste were used to brush resin-mounted lamb molars after a 1.0M HCl overnight demineralization challenge. Knoop microhardness measurements were recorded before and after brushing to determine the presence of remineralization on the surface of the teeth (Percent Surface Hardness Loss of 37%, 35% and 34% for Si-Control, Si-02 and Si-05 respectively after 24 hours). Four oral cavity bacterial strains were isolated through swabs of the inner cheek, gums and teeth surfaces of three volunteers, and placed on agar discs. 0.5g of each glass were placed onto the discs and the resultant inhibition zones were measured after 6, 12 and 24 hours. Si-05 consistently performed better than Si-02 on all strains and timeframes, while Si-Control exhibited no antibacterial effect at any time point.

scholarly journals Differential Pathogenicity of Xanthomonas campestris pv. phaseoli and X. fuscans subsp. fuscans Strains on Bean Genotypes with Common Blight Resistance

Plant Disease ◽  
2008 ◽  
Vol 92 (4) ◽  
pp. 546-554 ◽  
Author(s):  
N. Mutlu ◽  
A. K. Vidaver ◽  
D. P. Coyne ◽  
J. R. Steadman ◽  
P. A. Lambrecht ◽  
...  
Keyword(s):  
Common Bean ◽  
Bacterial Blight ◽  
Xanthomonas Campestris ◽  
South American ◽  
Bacterial Strains ◽  
Genetic Changes ◽  
Germplasm Screening ◽  
Lack Of Information ◽  
Pathogenic Variation ◽  
The Common

Both the common bacterial blight (CBB) pathogen (Xanthomonas campestris pv. phaseoli) and X. fuscans subsp. fuscans, agent of fuscous blight, cause indistinguishable symptoms in common bean, Phaseolus vulgaris. Yield losses can exceed 40%. Lack of information about the specificity between X. campestris pv. phaseoli strains and major quantitative trait loci (QTL) or alleles conferring resistance makes the task of identifying genetic changes in host–pathogen interactions and the grouping of bacterial strains difficult. This, in turn, affects the choice of pathogen isolates used for germplasm screening and complicates breeding for CBB resistance. Common bean host genotypes carrying various sources and levels of resistance to CBB were screened with 69 X. campestris pv. phaseoli and 15 X. fuscans subsp. fuscans strains from around the world. Differential pathogenicity of the CBB pathogen was identified on the 12 selected bean genotypes. The X. fuscans subsp. fuscans strains showed greater pathogenicity than X. campestris pv. phaseoli strains having the same origin. African strains were most pathogenic. The largest variation in pathogenicity came from X. campestris pv. phaseoli strains that originated in Caribbean and South American countries. Pathogenic variation was greater within X. campestris pv. phaseoli than within X. fuscans subsp. fuscans strains. Implications for breeding for CBB resistance are discussed.

scholarly journals Grinding Test on Tremolite with Fibrous and Prismatic Habit

Fibers ◽  
2019 ◽  
Vol 7 (6) ◽  
pp. 52 ◽  
Author(s):  
Oliviero Baietto ◽  
Mariangela Diano ◽  
Giovanna Zanetti ◽  
Paola Marini
Keyword(s):  
Electron Microscope ◽  
Phase Contrast ◽  
Health And Safety ◽  
Optical Microscope ◽  
Diameter Ratio ◽  
Grinding Process ◽  
Identification Procedure ◽  
Dimensional Parameter ◽  
Before And After ◽  
Scanning Electron

The main objective of this work is the evaluation of the morphology change in tremolite particles before and after a grinding process. The crushing action simulates anthropic alteration of the rock, such as excavation in rocks containing tremolite during a tunneling operation. The crystallization habit of these amphibolic minerals can exert hazardous effects on humans. The investigated amphibolic minerals are four tremolite samples, from the Piedmont and Aosta Valley regions, with different crystallization habits. The habits can be described as asbestiform (fibrous) for longer and thinner fibers and non-asbestiform (prismatic) for prismatic fragments, also known as “cleavage” fragments. In order to identify the morphological variation before and after the grinding, both a phase contrast optical microscope (PCOM) and a scanning electron microscope (SEM) were used. The identification procedure for fibrous and prismatic elements is related to a dimensional parameter (length–diameter ratio) defined by the Health and Safety Executive. The results highlight how mineral comminution leads to a rise of prismatic fragments and, therefore, to a potentially safer situation for worker and inhabitants.

scholarly journals Blue Light Is a Universal Signal forEscherichia coliChemoreceptors

2019 ◽  
Vol 201 (11) ◽  
Author(s):  
Tatyana Perlova ◽  
Martin Gruebele ◽  
Yann R. Chemla
Keyword(s):  
Blue Light ◽  
Light Exposure ◽  
Proton Motive Force ◽  
Motive Force ◽  
Swimming Velocity ◽  
Bacterial Strains ◽  
Content Type ◽  
E Coli ◽  
Before And After ◽  
Swimming Bacteria

ABSTRACTBlue light has been shown to elicit a tumbling response inEscherichia coli, a nonphototrophic bacterium. The exact mechanism of this phototactic response is still unknown. Here, we quantify phototaxis inE. coliby analyzing single-cell trajectories in populations of free-swimming bacteria before and after light exposure. Bacterial strains expressing only one type of chemoreceptor reveal that all fiveE. colireceptors (Aer, Tar, Tsr, Tap, and Trg) are capable of mediating responses to light. In particular, light exposure elicits a running response in the Tap-only strain, the opposite of the tumbling responses observed for all other strains. Therefore, light emerges as a universal stimulus for allE. colichemoreceptors. We also show that blue light exposure causes a reversible decrease in swimming velocity, a proxy for proton motive force. This result is consistent with a previously proposed hypothesis that, rather than sensing light directly, chemoreceptors sense light-induced perturbations in proton motive force, although other factors are also likely to contribute.IMPORTANCEOur findings provide new insights into the mechanism ofE. coliphototaxis, showing that all five chemoreceptor types respond to light and their interactions play an important role in cell behavior. Our results also open up new avenues for examining and manipulatingE. colitaxis. Since light is a universal stimulus, it may provide a way to quantify interactions among different types of receptors. Because light is easier to control spatially and temporally than chemicals, it may be used to study swimming behavior in complex environments. Since phototaxis can cause migration ofE. colibacteria in light gradients, light may be used to control bacterial density for studying density-dependent processes in bacteria.

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