Chavagnat F, Duez C, Guinand M, Potin P, Barbeyron T, Henrissat B, Wallach J, Ghuysen J M
Laboratoire de Biochimie Analytique et Synthèse Bioorganique, Université Claude Bernard, Villeurbanne, France.
Biochem J. 1996 Oct 15;319 ( Pt 2)(Pt 2):575-83. doi: 10.1042/bj3190575.
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.
利用一系列聚合酶链式反应(PCR)技术,已在大肠杆菌中克隆了褐藻胶弧菌(Pseudomonas alginovora)的一个名为aly的基因,并对其进行了测序。它编码一种210个氨基酸的藻酸盐裂解酶(EC 4.2.2.3),即Aly,其形式为一个233个氨基酸的前体。在避免形成包涵体的条件下,褐藻胶弧菌Aly已在大肠杆菌中过量表达,其C末端融合了一个His标签序列。带有His标签的褐藻胶弧菌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解酶的特异性。它可以通过在Ni(2+)-次氮基三乙酸树脂上进行亲和层析一步纯化。每升培养物的酶产量为5毫克。与野生型褐藻胶弧菌的产量水平相比,扩增倍数为12.5。已知一级结构的六种藻酸盐裂解酶分为三个不同的类别,其中一类包括褐藻胶弧菌Aly和肺炎克雷伯菌(Klebsiella pneumoniae)Aly这一对。