The largest database of trusted experimental protocols

19 protocols using dm1000 photonic microscope

1

Characterization of Bacillus andreraoultii

Check if the same lab product or an alternative is used in the 5 most similar protocols
Bacillus andreraoultii strain SIT1T was observed, after negative colouration, using a Morgani 268D (Philips, Amsterdam, The Netherlands) transmission electron microscope at an operating voltage of 60 kV. The Gram colouration was performed using Color Gram 2 Kit (bioMérieux) and observed by using the DM1000 photonic microscope (Leica Microsystems, Wetzlar, Germany) with a 100× oil-immersion objective lens. The sporulation test was done doing a thermic shock (80°C during 30 minutes). To evaluate the motility of Bacillus andreraoultii, fresh colonies were observed between blades and slats using a DM1000 photonic microscope (Leica) with a 40× objective lens.
API ZYM, API 20 NE and API 50 CH (bioMérieux) gallery systems were used to perform biochemical assays. Oxidase (Becton Dickinson, Franklin Lakes, NJ, USA) and catalase assays (bioMérieux) were done separately. The antibiotic susceptibility was tested using SirScan Discs antibiotics (i2a, Montpellier, France).
+ Open protocol
+ Expand
2

Biochemical Profiling and Microscopy of Marseille-P3135

Check if the same lab product or an alternative is used in the 5 most similar protocols
In order to biochemically describe strain Marseille‐P3135; different API tests (ZYM, 20A and 50CH, bioMérieux) were used. Sporulation ability of this bacterium was tested by exposing a bacterial suspension for 10 min to a thermal shock at 80°C, and then cultured on COS media. Moreover, the motility of the strain was detected using a DM1000 photonic microscope (Leica Microsystems, Nanterre, France) under a 100× objective lens. Also, a bacterial suspension was fixed with a solution of 2.5% glutaraldehyde in 0.1 mol/L cacodylate buffer for more than 1 hr at 4°C for observation under the Morgagni 268D (Philips) transmission electron microscope. Finally, Gram staining results and images were obtained by DM1000 photonic microscope (Leica Microsystems) using a 100× oil‐immersion objective lens.
+ Open protocol
+ Expand
3

Characterization of Strain SN6 Bacterium

Check if the same lab product or an alternative is used in the 5 most similar protocols
Strain SN6 was isolated at first under microaerophilic conditions (CampyGen) at 37°C for 48 hours on Columbia medium supplemented with 5% sheep's blood (COS) agar (bioMérieux) and we also tested its growth under aerobic and anaerobic conditions generated by AnaeroGen (bioMérieux). The minimum and maximum growth temperature ranges (28°C, 37°C, 45°C, 55°C) were determined as well as maximum salinity levels (0–5, 50–75, 100 g/L NaCl). The ability of the strain to grow on media with different pH was also tested. The colonies appeared on day 3 after culture on Columbia agar, and their diameter was measured. Cell morphology, Gram staining and motility were observed in fresh colonies using a DM1000 photonic microscope (Leica Microsystems, Nanterre, France) with a 40 × objective lens. Sporulation was tested by thermal shock, which consists of exposing the bacterium to a temperature of 60°C for 20 minutes and then watching its growth after 48 hours. Negative staining was carried out with detection Formvar-coated grids placed on a drop of 40 μL of bacterial suspension (after an overnight fixation in glutaraldehyde 2.5%) and incubated at 37°C for 30 minutes, followed by a 10-second incubation in 1% ammonium molybdate. The grids were dried on blotting paper and finally observed using a Tecnai G20 transmission electron microscope (FEI Company, Limeil-Brévannes, France).
+ Open protocol
+ Expand
4

Comprehensive Characterization of Bacterial Strain

Check if the same lab product or an alternative is used in the 5 most similar protocols
Gram staining and motility were observed from fresh colonies between blades and slats using a DM1000 photonic microscope (Leica Microsystems, Nanterre, France) with a 40 × objective lens [16] (link). Spore formation was determined by thermal shock (80°C for 20 minutes) and observed under a microscope. Negative staining was carried out with detection formvar-coated grids placed on a drop of 40 μL of bacterial suspension and incubated at 37°C for 30 minutes, followed by a 10-second incubation in 1% ammonium molybdate. The grids were dried on blotting paper and then observed with a Tecnai G20 transmission electron microscope (FEI Company, Limeil-Brévannes, France). We studied the biochemical characteristics of this strain using API 20NE, API ZYM and API 50CH strips according to the manufacturer's instructions (bioMérieux). Oxidase and catalase reactions were determined using a BBL DrySlide (Becton, Le Pont de Claix, France) according to the manufacturer's instructions. The antimicrobial activity test was performed using the disc diffusion method (i2a, Montpellier, France) [17] (link) on Mueller-Hinton agar in a petri dish (bioMérieux).
+ Open protocol
+ Expand
5

Biochemical Characterization of K. gabonensis

Check if the same lab product or an alternative is used in the 5 most similar protocols
API ZYM, API 20A and API 50CH (bioMérieux) gallery systems were used to perform biochemical assays. The sporulation test was done with a thermic shock (80°C during 10 minutes). To evaluate the motility of K. gabonensis strain GM4, fresh colonies were observed between blades and slats using a DM1000 photonic microscope (Leica Microsystems, Nanterre, France) with a 40× objective lens.
+ Open protocol
+ Expand
6

Morphological Characterization of Bacterial Strain

Check if the same lab product or an alternative is used in the 5 most similar protocols
To observe the cell morphology, transmission electron microscopy of the strain was performed using a Tecnai G20 Cryo (FEI company, Limeil‐Brevannes, France) at an operating voltage of 60 Kv after negative staining. Gram staining was performed and observed using a photonic microscope Leica DM2500 (Leica Microsystems, Nanterre, France) with a 100X oil‐immersion objective (Atlas & Snyder, 2011). The motility of the strain was assessed by the Hanging Drop method. The slide was examined using a DM1000 photonic microscope (Leica Microsystems) at 40×. Sporulation was tested following a thermic shock at 80°C during 20 min, and the endospore formation was visualized using a Tecnai G20 Cryo transmission electron microscope (FEI company, Limeil‐Brevannes, France) at an operating voltage of 60 Kv after negative staining.
+ Open protocol
+ Expand
7

Microscopy and Motility Analysis of G. massiliensis

Check if the same lab product or an alternative is used in the 5 most similar protocols
To observe G. massiliensis strain Awa-1T morphology, transmission electron microscopy was performed after negative staining, using a Tecnai G20 (FEI Company, Limeil-Brevannes, France) at an operating voltage of 60 KV. The gram staining was performed and observed using a photonic microscope Leica DM2500 (Leica Microsystems, Nanterre, France) with a 100X oil-immersion objective. Motility testing was performed by observation of a fresh colony between the blades and slats using DM1000 photonic microscope (Leica Microsystems) at 40x. For the sporulation test, our strain was grown on Chapman agar (Oxoid, Dardilly, France) for 1 week, followed by gram staining and observation for the presence or absence of spores on colonies under the microscope.
+ Open protocol
+ Expand
8

Gram Staining and TEM Imaging of G. massiliensis

Check if the same lab product or an alternative is used in the 5 most similar protocols
G. massiliensis strain GM3 was observed after negative coloration using a Tecnai G20 (FEI, Limeil-Brevannes, France) transmission electron microscope at an operating voltage of 60 kV. Gram coloration was performed using a Color Gram 2 Kit (bioMérieux). This coloration was observed by using the DM1000 photonic microscope (Leica Microsystems) with a 100× oil-immersion objective lens.
+ Open protocol
+ Expand
9

Morphological Analysis of K. gabonensis GM4

Check if the same lab product or an alternative is used in the 5 most similar protocols
Images of K. gabonensis strain GM4 were obtained using a Tecnai G20 transmission electron microscope (FEI, Limeil-Brevannes, France) at an operating voltage of 60 kV. Gram staining was observed using a DM1000 photonic microscope (Leica Microsystems) with a 100× oil-immersion objective lens.
+ Open protocol
+ Expand
10

Comprehensive Bacterial Characterization

Check if the same lab product or an alternative is used in the 5 most similar protocols
The API 20A, API ZYM and API 50CH strips (bioMérieux) were used to biochemically characterize strain Marseille-P3237. Sporulation ability was tested after exposing a bacterial suspension to a thermic shock at 80°C for 10 min. Motility was evaluated using a DM1000 photonic microscope (Leica Microsystems, Nanterre, France) with a 1000× magnification. Cell morphology was observed using electron microscopy and the following protocol. Bacteria were fixed with 2.5% glutaraldehyde in 0.1 m cacodylate buffer for at least 1 h at 4°C. Then, a drop of cell suspension was deposited for approximately 5 min on glow-discharged formvar carbon film on 400-mesh nickel grids (FCF400-Ni, EMS). The grids were dried on blotting paper and cells were negatively stained for 10 seconds with a solution of 1% ammonium molybdate in filtered water at room temperature. Electron micrographs were acquired with a Tecnai G20 Cryo (FEI) transmission electron microscope operated at 200 keV.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!