Frozen prepared microbiological culture media

1973 ◽  
Vol 49 (2-3) ◽  
pp. 137-139
Author(s):  
Bernard Witlin
2009 ◽  
Vol 25 ◽  
pp. S232-S233 ◽  
Author(s):  
K.F. Fernandes ◽  
K.A. Batista ◽  
I.T.N. Campos ◽  
L.A. Bataus

1944 ◽  
Vol 47 (3) ◽  
pp. 293-299 ◽  
Author(s):  
J. L. Stokes ◽  
Marion Gunness ◽  
J. W. Foster

Science ◽  
1951 ◽  
Vol 113 (2935) ◽  
pp. 359-359
Author(s):  
G. H. Warren ◽  
J. G. Durso

2018 ◽  
Vol 14 (4) ◽  
Author(s):  
Liguo Zhang ◽  
Jinhua Du ◽  
Yang Jiang

Abstract Commercial agar used in microbiological culture has a disadvantage of impurity and opacity. This work aimed to provide an alternative gelling agent to agar and the function of low acyl gellan gum in microbiological culture media was studied. The results showed the texture and water activity of GYGs (glucose-YNB medium containing low acyl gellan gum at different concentrations of 0.3%, 0.6%, 0.9%, 1.2%, 1.5%) were suitable for cultivation of Saccharomyces yeasts. The gelling temperature of GYGs was enhanced with the increased concentration of low acyl gellan gum, while clarity of medium and colony diameter decreased. Scanning electron microscope showed that GYG09 (glucose-YNB medium containing 0.9% low acyl gellan gum) possessed homogeneous porous structures, which was superior to GYA20 with respect to higher clarity and lower dosage of gelling agent when surface plating method was used; however, GYG09 was not suitable for pour plating method.


2020 ◽  
Vol 40 (2) ◽  
pp. 82-87
Author(s):  
Anelise Salina ◽  
Jorge Timenetsky ◽  
Maysa S. Barbosa ◽  
Cristiane M. Azevedo ◽  
Helio Langoni

ABSTRACT: The genus Mycoplasma includes more than 200 bacterial species that cause disease in animals. It is responsible for causing mastitis in bovines and may be related to other manifestations, such as arthritis and pneumonia in calves and heifers. The present study aimed to detect Mycoplasma bovis isolated from milk samples of bovine clinical mastitis, and to compare the isolation rates in two culture media: Hayflick and SP4. An initial screening was performed in order to detect the presence of the class Mollicutes in 1166 milk samples from clinical mastitis by the conventional Polymerase Chain Reaction (PCR) technique. According to the 1166 milk samples evaluated, 8.6% (100/1166) were positive to class Mollicutes. Regarding molecular analyses, 1.1% (13/1166) of conventional PCR for positive M. bovis was obtained and 0.9% (11/1166) in real-time PCR. The results of the microbiological culture of the 100 samples previously screened demonstrated that 6% (6/100) of colony growth have been developed when using the Hayflick medium, and 11% (11/100) when using the SP4 medium (including the positive on Hayflick medium). Concerning the 11 isolates obtained in the microbiological culture, conventional PCR confirmed M. bovis in nine of them, and two cultures were negative. In the phylogenetic analysis of the isolates, all of them were grouped in M. bovis and M. agalactiae clusters. The results confirmed the importance of the presence of M. bovis in the etiology of bovine clinical mastitis and reinforced the need for further studies to elucidate other Mycoplasma species that may be involved in bovine clinical mastitis in Brazil.


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