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Characterization of alginate lyase gene using a metagenomic library constructed from the gut microflora of abalone
Authors:Su-Jung Sim  Keun Sik Baik  Seong Chan Park  Han Na Choe  Chi Nam Seong  Tai-Sun Shin  Hee Chul Woo  Jeong-Yong Cho  Duwoon Kim
Affiliation:(1) Department of Food Science and Technology and Functional Food Research Center, Chonnam National University, Gwangju, 500-757, Republic of Korea;(2) Department of Biology, Sunchon National University, Suncheon, 540-742, Jeonnam, Republic of Korea;(3) Department of Food Science and Nutrition, Chonnam National University, Yeosu, 550-757, Republic of Korea;(4) Department of Chemical Engineering, Pukyung National University, Busan, 608-739, Republic of Korea;
Abstract:A metagenomic fosmid library was constructed using a genomic DNA mixture extracted from the gut microflora of abalone. The library gave an alginate lyase positive clone (AlyDW) harboring a 31.7-kbp insert. The AlyDW insert consisted of 22 open reading frames (ORFs). The deduced amino acid sequences of ORFs 11–13 were similar to those of known alginate lyase genes, which are found adjacent in the genome of Klebsiella pneumoniae subsp. aerogenes, Vibrio splendidus, and Vibrio sp. belonging to the phylum Gammaproteobacteria. Among the three recombinant proteins expressed from the three ORFs, alginate lyase activity was only observed in the recombinant protein (AlyDW11) coded by ORF 11. The expressed protein (AlyDW11) had the highest alginate lyase activity at pH 7.0 and 45°C in the presence of 1 mM AgNO3. The alginate lyase activity of ORF 11 was confirmed to be endolytic by thin-layer chromatography. AlyDW11 preferred poly(β-d-mannuronate) as a substrate over poly(α-l-guluronate). AlyDW11 contained three highly conserved regions, RSEL, QIH, and YFKAGVYNQ, which may act to stabilize the three-dimensional conformation and function of the alginate lyase.
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