首页> 美国卫生研究院文献>Journal of Bacteriology >Cloning and Expression of Three New Azotobacter vinelandii Genes Closely Related to a Previously Described Gene Family Encoding Mannuronan C-5-Epimerases
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Cloning and Expression of Three New Azotobacter vinelandii Genes Closely Related to a Previously Described Gene Family Encoding Mannuronan C-5-Epimerases

机译:与以前描述的编码Mannuronan C-5-Epimerases的基因家族密切相关的三个新的固氮酵母新基因的克隆和表达

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摘要

The cloning and expression of a family of five modular-type mannuronan C-5-epimerase genes from Azotobacter vinelandii (algE1 to -5) has previously been reported. The corresponding proteins catalyze the Ca2+-dependent polymer-level epimerization of β-d-mannuronic acid to α-l-guluronic acid (G) in the commercially important polysaccharide alginate. Here we report the identification of three additional structurally similar genes, designated algE6, algE7, and algY. All three genes were sequenced and expressed in Escherichia coli. AlgE6 introduced contiguous stretches of G residues into its substrate (G blocks), while AlgE7 acted as both an epimerase and a lyase. The epimerase activity of AlgE7 leads to formation of alginates with both single G residues and G blocks. AlgY did not display epimerase activity, but a hybrid gene in which the 5′-terminal part was exchanged with the corresponding region in algE4 expressed an active epimerase. Southern blot analysis of genomic A. vinelandii DNA, using the 5′ part of algE2 as a probe, indicated that all hybridization signals originated from algE1 to -5 or the three new genes reported here.
机译:先前已经报道了来自葡萄固氮菌的五个模块型甘露糖醛酸C-5-表异构酶基因的家族的克隆和表达(algE1至-5)。在商业上重要的藻酸盐藻酸盐中,相应的蛋白质催化β-d-甘露糖醛酸对Ca 2 + 的聚合物水平的差向异构化为α-1-古洛糖醛酸(G)。在这里,我们报告鉴定三个另外的结构相似的基因,命名为algE6,algE7和algY。对这三个基因进行测序并在大肠杆菌中表达。 AlgE6在其底物(G块)中引入了连续的G残基片段,而AlgE7既充当了差向异构酶又是裂解酶。 AlgE7的差向异构酶活性导致形成具有单个G残基和G嵌段的藻酸盐。 AlgY没有显示差向异构酶活性,但是其中5'-末端部分与algE4中的相应区域交换的杂合基因表达了活性差向异构酶。使用algE2的5'部分作为探针对基因组酿酒酵母DNA的Southern印迹分析表明,所有杂交信号均源自algE1至-5或此处报道的三个新基因。

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