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Cloning, sequencing and overexpression in Escherichia coli of the alginate lyase-encoding aly gene of Pseudomonas alginovora: identification of three classes of alginate lyases

机译:编码海藻假单胞菌海藻酸裂解酶aly基因的大肠杆菌的克隆,测序和过表达:鉴定三类海藻酸裂解酶

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摘要

A gene of Pseudomonas alginovora, called aly, has been cloned in Escherichia coli using a battery of PCR techniques and sequenced. It encodes a 210-amino-acid alginate lyase (EC 4.2.2.3), Aly, in the form of a 233-amino-acid precursor. P. alginovora Aly has been overproduced in E. coli with a His-tag sequence fused at the C-terminal end under conditions in which the formation of inclusion bodies is avoided. His-tagged P. alginovora Aly has the same enzymic properties as the wild-type enzyme and has the specificity of a mannuronate lyase. It can be purified in a one-step procedure by affinity chromatography on Ni(2+)-nitriloacetate resin. The yield is of 5 mg of enzyme per litre of culture. The amplification factor is 12.5 compared with the level of production by wild-type P. alginovora. The six alginate lyases of known primary structure fall into three distinct classes, one of which comprises the pair P. alginovora Aly and Klebsiella pneumoniae Aly.
机译:利用一系列PCR技术,已在大肠杆菌中克隆了一种名为ally的假单胞菌假单胞菌基因,并进行了测序。它以233个氨基酸的前体形式编码一个210个氨基酸的藻酸裂解酶(EC 4.2.2.3)。在避免包涵体形成的条件下,已在大肠杆菌中过量生产了带有在C末端融合的His标签序列的海藻假单胞菌Aly。具有组氨酸标签的褐藻假单胞菌Aly具有与野生型酶相同的酶学性质,并且具有甘露糖醛酸裂合酶的特异性。可以通过亲和色谱法在Ni(2 +)-亚硝基乙酸树脂上一步纯化。每升培养物中酶的产量为5 mg。与野生型P. alginovora的生产水平相比,扩增因子为12.5。已知一级结构的六种藻酸盐裂解酶分为三类,其中一类包括成对的P. alginovora Aly和肺炎克雷伯菌。

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