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IDENTIFICATION OF AGAROLYTIC BACTERIA PDF

special ecological reason for the presence of agarolytic bacteria in fresh water but that Identification of Medical Bacteria, 2nd edn. Cam-. Endolytic β-agarase Aga2 was identified from Cellulophaga omnivescoria W5C. SJP92 was shown to retain almost 90% of agarolytic activity under Recently, thermostable agarases from marine bacteria Flammeovirga sp. Abstract: Agarolytic bacteria use agarase to utilize agar as sole source of carbon. It is usually observed in life sciences labs that lot of agar medium needs to be.

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Purification and properties of an extracellular agarase from Alteromonas sp. An overnight culture of isolated colonies was prepared in a medium of the same composition as that of medium A, except that the agar concentration was lowered to 0.

Numerical taxonomy of aerobic, gram-negative bacteria associated with oysters and surrounding seawater of the gaarolytic coast. Idwntification PMSF was added to a final concentration of 0. Hydrolysis of agar, alginic acid, carboxymethyl-cellulose, esculin, gelatin, and starch.

A Effect of pH on the activity of the purified agarase. The GenBank accession number for the small subunit of P. Guinea University bacteris Barcelona, Barcelona, Spain The single DNA band of approximately 1.

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Previous studies have shown that agar degradation can occur by two mechanisms that depend on the specificity of the cleaving enzymes. Strain N-1 and P. Agarase N-1 had a molecular mass of 33 kDa, as determined by a comparison with the mobility of protein standards Fig.

American Society for Microbiology; The release of proteases into the medium during the stationary phase was demonstrated utilizing Azocoll Calbiochem-Behring, La Jolla, Calif. Staining, morphology, and motility were determined as described by Cowan The enzyme was incubated in 50 mM sodium phosphate at pH 6. The highest level of agarase was reached during the stationary phase. B Effect of temperature on the stability of agarase from P.

The enzyme was concentrated with polyethylene glycol and dialyzed against buffer A. Strain N-1 was cultured in liquid medium containing 0.

Van Hofsteen B, Malmqvist M. Effects of pH and temperature on enzyme activity. Agar clearing, softening, and depressions around the colonies is characteristic for bacteria in groups 1 and 2.

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Purification and some properties of agarase from Pseudomonas sp. Van der Meulen H, Vedkamp H. Chromatography of agarase from P. The exception is Alteromonas sp. The oligosaccharides were detected by evaluation of the refractive index. Toffanin for the NMR technical support.

Isolation And Identification of agarolytic bacteria in Marin by Faizah Rahman on Prezi

Cloning and gene replacement mutagenesis of a Pseudomonas atlantica agarase gene. Enzymatic hydrolysis of agar: Sugano Y, Noma M. Int J Syst Bacteriol. Hydrolysis products of agar by agarase from P.

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The screening was carried out on agar plates in a medium containing 0. The rDNA sequence of strain N-1 was compared to sequences available from public databases. An overnight culture of isolated colonies of strain N-1 was prepared in the medium described above and used to inoculate 2 liters of fresh medium containing 0.

We describe here bactfria identification of a new agarolytic bacterial strain, P.