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首页> 外文期刊>Archives of microbiology >Glycine betaine aldehyde dehydrogenase from Bacillus subtilis: characterization of an enzyme required for the synthesis of the osmoprotectant glycine betaine
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Glycine betaine aldehyde dehydrogenase from Bacillus subtilis: characterization of an enzyme required for the synthesis of the osmoprotectant glycine betaine

机译:枯草芽孢杆菌的甘氨酸甜菜碱醛脱氢酶:表征渗透保护剂甘氨酸甜菜碱的合成所需的酶

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Production of the compatible solute glycine betaine from its precursors choline or glycine betaine aldehyde confers a considerable level of tolerance against high osmolarity stress to the soil bacterium Bacillus subtilis, The glycine betaine aldehyde dehydrogenase GbsA is an integral part of the osmoregulatory glycine betaine synthesis pathway, We strongly overproduced this enzyme in an Escherichia coli strain that expressed a plasmid-encoded gbsA gene under T7 phi 10 control, The recombinant GbsA protein was purified 23-fold to apparent homogeneity by fractionated ammonium sulfate precipitation, ion-exchange chromatography on Q-Sepharose, and subsequent hydrophobic interaction chromatography on phenyl-Sepharose, Molecular sieving through Superose 12 and sedimentation centrifugation through a glycerol gradient suggested that the native enzyme is a homodimer with 53.7-kDa subunits. The enzyme was specific for glycine betaine aldehyde and could use both NAD(+) and NADP(+) as cofactors, but NAD(+) was strongly preferred. A kinetic analysis of the GbsA-mediated oxidation of glycine betaine aldehyde to glycine betaine revealed K-m values of 125 mu M and 143 mu M for its substrates glycine betaine aldehyde and NAD(+), respectively. Low concentrations of salts stimulated the GbsA activity, and the enzyme was highly tolerant of high ionic conditions, Even in the presence of 2.4 M KCl, 88% of the initial enzymatic activity was maintained. B, subtilis synthesizes high levels of proline when grown at high osmolarity, and the presence of this amino acid strongly stimulated the GbsA activity in vitro. The enzyme was stimulated by moderate concentrations of glycine betaine, and its activity was highly tolerant against molar concentrations of this osmolyte. The high salt tolerance and its resistance to its own reaction product are essential features of the GbsA enzyme and ensure that B. subtilis can produce high levels of the compatible solute glycine betaine under conditions of high osmolarity stress.
机译:由其前体胆碱或甘氨酸甜菜碱醛生产兼容的溶质甘氨酸甜菜碱,赋予了对土壤细菌枯草芽孢杆菌高渗透压胁迫的相当高的耐受性。甘氨酸甜菜碱醛脱氢酶GbsA是渗透调节甘氨酸甜菜碱合成途径不可或缺的一部分,我们在大肠杆菌菌株中强烈过量生产了这种酶,该菌株在T7 phi 10的控制下表达了质粒编码的gbsA基因。重组GbsA蛋白通过分级分离的硫酸铵沉淀,Q-Sepharose上的离子交换色谱法纯化了23倍,达到表观同质性。 ,以及随后在苯基-琼脂糖上的疏水相互作用色谱,通过Superose 12进行分子筛和通过甘油梯度进行沉降离心,表明该天然酶是具有53.7-kDa亚基的同型二聚体。该酶对甘氨酸甜菜碱醛具有特异性,可以同时使用NAD(+)和NADP(+)作为辅因子,但强烈建议使用NAD(+)。对GbsA介导的甘氨酸甜菜碱醛氧化为甘氨酸甜菜碱的动力学分析表明,其底物甘氨酸甜菜碱醛和NAD(+)的K-m值分别为125μM和143μM。低浓度的盐刺激了GbsA活性,并且该酶对高离子条件具有高度的耐受性。即使在存在2.4 M KCl的情况下,仍保持了88%的初始酶活性。 B,枯草杆菌在高渗透压下生长时会合成高水平的脯氨酸,并且这种氨基酸的存在强烈刺激了GbsA的体外活性。该酶被中等浓度的甘氨酸甜菜碱刺激,并且其活性对这种渗透液的摩尔浓度高度耐受。高耐盐性及其对自身反应产物的抗性是GbsA酶的基本特征,可确保枯草芽孢杆菌在高渗透压胁迫下可产生高水平的相容性溶质甘氨酸甜菜碱。

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