首页> 外文会议>International Conference on Advances in Energy and Environmental Science >Characterization of putative a (1,3)-β-D-glucan (curdlan) synthase for a low molecular weight curdlan biosynthesis from Agrobacterium sp. M503
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Characterization of putative a (1,3)-β-D-glucan (curdlan) synthase for a low molecular weight curdlan biosynthesis from Agrobacterium sp. M503

机译:从Agrobacterium sp的低分子量Curdlan生物合成诱发A(1,3)-β-D-葡聚糖(Curdlan)合酶的表征。 M503.

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A β-(1,3)-D-glucan (curdlan) synthase gene for a low molecular weight curdlan biosynthesis, crdS_(Ag), from Agrobacterium sp. M503 was cloned and its encoding protein was characterized by several online protein analysis softwares. The crdS_(Ag) consists of 1965-base-pairs Open Reading Frame (ORF) encoding a protein with molecular weight approximate 73.5 kDa, which contains the conserved domain of CESA-CelA_like belonging to glycosyltransferase family 2 (GT2). Moreover, CrdS_(Ag) was a membrane protein with seven hydrophobic transmembrance domains. The second structure analysis indicated it was composed of 43.12% α-helix, 17.89% β-sheet, and 38.99% random coil structure. These data will lay a foundation to clarify the biosynthesis mechanism of the low molecular weight curdlan.
机译:β-(1,3)-D-葡聚糖(Curdlan)合成酶基因,用于低分子量Curdlan生物合成,CRDS_(AG),来自Agrobacterium sp。 克隆M503,其编码蛋白质的特征在于几种在线蛋白质分析软件。 CRDS_(AG)由1965-碱基对的开放阅读框(ORF)组成,所述蛋白质重量近似73.5kDa,其含有属于糖基转移酶的CESA-CELA_LIKE的保守结构域(GT2)。 此外,CRDS_(AG)是一种膜蛋白,具有七种疏水性跨膜域。 第二结构分析表明它由43.12%的α-螺旋,17.89%β-薄片和38.99%的随机线圈结构组成。 这些数据将奠定基础,以阐明低分子量凝乳兰的生物合成机制。

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