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Native granule associated short chain length polyhydroxyalkanoate synthase from a marine derived Bacillus sp NQ-11/A2

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dc.contributor.author Prabhu, N.N.
dc.contributor.author Santimano, M.C.
dc.contributor.author Mavinkurve, S.
dc.contributor.author Bhosle, S.
dc.contributor.author Garg, S.
dc.date.accessioned 2015-06-04T02:52:36Z
dc.date.available 2015-06-04T02:52:36Z
dc.date.issued 2010
dc.identifier.citation Antonie Van Leeuwenhoek. 97(1); 2010; 41-50. en_US
dc.identifier.uri http://dx.doi.org/10.1007/s10482-009-9386-8
dc.identifier.uri http://irgu.unigoa.ac.in/drs/handle/unigoa/2488
dc.description.abstract A rapidly growing marine derived Bacillus sp.strain NQ-11/A2, identified as Bacillus megaterium, accumulated 61 percent polyhydroxyalkanoate by weight. Diverse carbon sources served as substrates for the accumulation of short chain length polyhydroxyalkanoate. Three to nine granules either single or attached as buds could be isolated intact from each cell. Maximum activity of polyhydroxyalkanoate synthase was associated with the granules. Granule-bound polyhydroxyalkanoate synthase had a K(m) of 7.1 x 10(-5) M for DL-beta-hydroxybutyryl-CoA. Temperature and pH optima for maximum activity were 30 degrees C and 7.0, respectively. Sodium ions were required for granule-bound polyhydroxyalkanoate synthase activity and inhibited by potassium. Granule-bound polyhydroxyalkanoate synthase was apparently covalently bound to the polyhydroxyalkanoate-core of the granules and affected by the chaotropic reagent urea. Detergents inhibited the granule-bound polyhydroxyalkanoate synthase drastically whilst glycerol and bovine serum albumin stabilized the synthase. en_US
dc.publisher Springer Verlag (Germany) en_US
dc.subject Microbiology en_US
dc.title Native granule associated short chain length polyhydroxyalkanoate synthase from a marine derived Bacillus sp NQ-11/A2 en_US
dc.type Journal article en_US
dc.identifier.impf y


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