scholarly journals Determination of Bacterial Cell Number to Differentiate Campylobacter jejuni from C. coli by the Simple Hippurate Hydrolysis Test

2012 ◽  
Vol 2 (9) ◽  
Author(s):  
Miyuki Fujioka ◽  
Yoshimitsu Otomo
1994 ◽  
Vol 72 (7) ◽  
pp. 1211-1216 ◽  
Author(s):  
Loredana Stabili ◽  
Calogero Canicattì

Seminal plasma from Paracentrotus lividus exerted an inhibitory action on the growth of bacterial colonies. The antibacterial reaction took 30 min to reach full expression and depended on both the dose of seminal plasma and the bacterial cell number. Heating at 56 °C for 60 min did not lower the antibacterial power of the seminal plasma. Morphological examination of bacteria treated with seminal plasma revealed a conspicuous alteration of their surface and suggested a lytic mode of action for the antibacterial factor(s). Lysozyme could be involved in this process. In fact, inhibition of bacterial growth strongly decreased when this hydrolase was inactivated by heating at a basic pH.


Minerals ◽  
2019 ◽  
Vol 9 (5) ◽  
pp. 274 ◽  
Author(s):  
San Yee Khaing ◽  
Yuichi Sugai ◽  
Kyuro Sasaki ◽  
Myo Min Tun

Iodide-oxidizing bacteria (IOB) oxidize iodide into iodine and triiodide which can be utilized for gold dissolution. IOB can be therefore useful for gold leaching. This study examined the impact of incubation conditions such as concentration of the nutrient and iodide, initial bacterial cell number, incubation temperature, and shaking condition on the performance of the gold dissolution through the experiments incubating IOB in the culture medium containing the marine broth, potassium iodide and gold ore. The minimum necessary concentration of marine broth and potassium iodide for the complete gold dissolution were determined to be 18.7 g/L and 10.9 g/L respectively. The initial bacterial cell number had no effect on gold dissolution when it was 1 × 104 cells/mL or higher. Gold leaching with IOB should be operated under a temperature range of 30–35 °C, which was the optimal temperature range for IOB. The bacterial growth rate under shaking conditions was three times faster than that under static conditions. Shaking incubation effectively shortened the contact time compared to the static incubation. According to the pH and redox potential of the culture solution, the stable gold complex in the culture solution of this study could be designated as gold (I) diiodide.


Author(s):  
Golnar Rahimzadeh ◽  
Mohammad Sadegh Rezai

Nosocomial infections can be transmitted by contaminated hospital surfaces with resistant pathogens. conventional sanitations are not efficiently contributing to removing resistant pathogens. Bacteriophages suggest as decontaminating agents, safe, their selective ability to kill specific bacteria. This work aimed to assess the efficiency of a phage in removing Pseudomonas aeruginosa from different hard surfaces. The decontamination ability of phages w was tested in vitro against Pseudomonas aeruginosa strain. Cystoviridae Phages with titer (2 × 1012 PFU/mL) can efficiently reduce viable bacterial cells on contaminated surfaces. The treated surfaces with alcohol 70% and phage showed an evident drop of bacterial cell number from 1 h to 24 h. These results suggest that bacteriophages are biocontrol agents removing nosocomial infection pathogens transmitted by contaminated surfaces in the hospital environment.


2018 ◽  
Vol 12 (2) ◽  
pp. 88-91 ◽  
Author(s):  
Masaki Ishii ◽  
Yasuhiko Matsumoto ◽  
Kazuhisa Sekimizu

Biomaterials ◽  
2003 ◽  
Vol 24 (1) ◽  
pp. 27-34 ◽  
Author(s):  
Sarah J. Dexter ◽  
Miguel Cámara ◽  
Martyn Davies ◽  
Kevin M. Shakesheff

1991 ◽  
Vol 57 (2) ◽  
pp. 281-285 ◽  
Author(s):  
Masakazu Hoshi ◽  
Hideaki Nishi ◽  
Tetsuhito Hayashi ◽  
Masayo Okuzumi ◽  
Etsuo Watanabe

2012 ◽  
Vol 421 (2) ◽  
pp. 428-432 ◽  
Author(s):  
Shiro Yamashoji ◽  
Naoko Yoshikawa ◽  
Masayuki Kirihara ◽  
Toshihiro Tsuneyoshi
Keyword(s):  

2019 ◽  
Author(s):  
Natalie S. Al-Otaibi ◽  
Aidan J. Taylor ◽  
Daniel P. Farrell ◽  
Svetomir B. Tzokov ◽  
Frank DiMaio ◽  
...  

AbstractThe bacterial flagellum is a remarkable molecular motor, present at the surface of many bacteria, whose primary function is to allow motility through the rotation of a long filament protruding from the bacterial cell. A cap complex, consisting of an oligomeric assembly of the protein FliD, is localized at the tip of the flagellum, and is essential for filament assembly, as well as adherence to surfaces in some bacteria. However, the structure of the intact cap complex, and the molecular basis for its interaction with the filament, remains elusive. Here we report the cryo-EM structure of the Campylobacter jejuni cap complex. This structure reveals that FliD is pentameric, with the N-terminal region of the protomer forming an unexpected extensive set of contacts across several subunits, that contribute to FliD oligomerization. We also demonstrate that the native C. jejuni flagellum filament is 11-stranded and propose a molecular model for the filament-cap interaction.


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