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.

Author: Akisho Faegrel
Country: Iran
Language: English (Spanish)
Genre: Travel
Published (Last): 14 October 2011
Pages: 351
PDF File Size: 6.55 Mb
ePub File Size: 12.77 Mb
ISBN: 802-3-80240-910-4
Downloads: 38194
Price: Free* [*Free Regsitration Required]
Uploader: Tygodal

As shown by the HPLC profile, the purified enzyme from strain N-1 hydrolyzed agar to give two main oligosaccharide products Fig. The activity was determined at a pH between 3.

In the presence of agar, glucose or galactose sgarolytic not affect the production of agarase in this strain data not shown. Previous results on the purification and characterization of an extracellular agarase from the agar-liquefying strain Alteromonas sp. Enzymatic hydrolysis of agar: Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Percentages are indicated by bootstraps replicates for neighbor-joining analysis; replicates for parsimony. At this step the enzyme eluted in the flowthrough, indicating that the strong binding seen at the beginning of the purification could be mediated by an unidentified extracellular component of this strain or by an agar-derived product that is separated during the gel filtration step.

  KALPASAR PROJECT PDF

The pH profile of agarase from strain N-1 was bell shaped, with a maximum at pH 7.

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

Effect of salt concentration on enzyme activity. Purification and characterization of a new agarase from a marine bacterium, Vibrio sp. Van der Meulen H, Vedkamp H. The type of flagellum was determined by negative staining with uranyl acetate and electron microscopy as described by Cole and Popkin Proteins were stained with Coomassie brilliant blue R We describe here the characterization of a new agarolytic bacterium isolated from the southern Chilean coast.

The isolation and characterization of agarolytic bacteria from a lowland river. Other biochemical and physiological tests were carried out essentially as described by Stolp and Gadkari 38 and Stanier et al.

Cell growth and activity measurements. Effect of carbon sources on bacterial growth and agarase production. In solid agar, this isolate produced a diffusible agarase that caused agar softening around the colonies.

The sequence of the 16S rDNA of strain N-1 was aligned with the sequences of a number of Pseudoalteromonas strains available and was analyzed essentially as described by Gauthier et al. Stolp H, Bacyeria D.

Manual of methods identificatikn general microbiology. Numerical taxonomy of aerobic, gram-negative bacteria associated with oysters and surrounding seawater of the mediterranean coast. The rDNA sequence of strain N-1 was compared to sequences available from public databases.

  8279 MICROPROCESSOR PDF

The highest level of agarase was reached during the stationary phase.

There was a problem providing the content you requested

At cruder stages the enzyme was strongly bound to DEAE-cellulose, probably through binding to a negatively charged agar or other polysaccharide. Cleavage of the polysaccharide chains causes agar softening and allows faster evaporation of water, leading to the formation of depressions.

A Effect of pH on the activity of the purified agarase. B Oligosaccharides released by agarase. Strain N-1 was isolated from decomposing algae in Niebla Valdivia, Chile. Guinea University of Barcelona, Barcelona, Spain Isolation and characterization of Cytophaga flevensis sp.

Agar, a polysaccharide present in the cell walls of some red algae, can be degraded by several bacterial strains from marine environments and other sources.

DNA base composition of Rickettsia tsutsugamushi determined by reversed-phase high-performance liquid chromatography. Phylogenetic analysis and assessment of the genera VibrioPhotobacteriumand Plesiomonas deduced from small-subunit rRNA sequences. At longer incubation times, the colonies produced a red-brown diffusible idenitfication.