Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5038
Title: Extracellular beta-agarase LSL-1 producing neoagarobiose from a newly isolated agar-liquefying soil bacterium, Acinetobacter sp., AG LSL-1
Authors: Lakshmikanth M
Manohar S
Souche Y
Lalitha J.
Keywords: Acinetobacter sp.
Activity staining
AG LSL-1
Agar
Agarase LSL-1
Native-PAGE
Neoagarobiose
Issue Date: 2006
Citation: World Journal of Microbiology and Biotechnology , Vol. 22 , 10 , p. 1087 - 1094
Abstract: An agar-liquefying Acinetobacter species capable of utilizing agar as sole source of carbon and energy was isolated from soil samples and the culture conditions were standardized for the maximal production of extracellular agarase. The bacterium was capable of liquefying an agar-plate within 3 days of incubation and produced extracellular agarase within a short period of time (16-18 h) when grown in defined mineral salts medium. Bacterium grew in the pH range 4.0-9.0, optimal at pH 7.0; temperature 25-40°C and optimal at 37°C. The agarase secreted by the Acinetobacter strain was inducible by agar and not repressed by other simple sugars when supplemented along with agar in the medium. The bacterium did not require NaCl for growth or production of agarase. The bacterium did not utilize other polysaccharides like ?-carrageenan, alginate, cellulose, and CMC. The activity staining of partially purified agarase preparations after native-PAGE and SDS PAGE revealed the presence of a single zone of clearance corresponding to the molecular weight 100 kDa, suggesting that it is a monomer. Neoagarobiose was the end product of agarose hydrolysis by this enzyme. The agarase was an endo-type glycosidase and belongs to Group-III ?-agarase family. © 2006 Springer Science+Business Media B.V.
URI: 10.1007/s11274-006-9147-z
http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5038
Appears in Collections:1. Journal Articles

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