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海洋细菌 H5 中的类固醇降解和两种类固醇诱导酶。

Steroid degradation and two steroid-inducible enzymes in the marine bacterium H5.

机构信息

Institute of Toxicology and Pharmacology for Natural Scientists, University, Medical School Schleswig-Holstein, Kiel, Germany.

出版信息

Chem Biol Interact. 2011 May 30;191(1-3):89-94. doi: 10.1016/j.cbi.2011.01.027. Epub 2011 Jan 31.

Abstract

Natural and synthetic steroid hormones excreted into the environment are potentially threatening the population dynamics of all kinds of animals and public health. We have previously isolated a steroid degrading bacterial strain (H5) from the Baltic Sea, at Kiel, Germany. 16S-rRNA analysis showed that bacterial strain H5 belongs to the genus Vibrio, family Vibrionaceae and class Gamma-Proteobacteria. Bacterial strain H5 can degrade steroids such as testosterone and estrogens, which was shown in this study by determining the (3)H labeled steroid retaining in the bacterial H5 culture medium at incubation times of 5 h and 20 h. Since 3α-hydroxysteroid dehydrogenase/carbonyl reductase (3α-HSD/CR) is a key enzyme in adaptive steroid degradation in Comamonas testosteroni (C. testosteroni), in previous investigations, a meta-genomic system with the 3α-HSD/CR gene as a positive control was established. By this meta-genomic system, two estradiol inducible genes coding 3-ketosteroid-delta-1-dehydrogenase and carboxylesterase, respectively, which are involved in steroid degradation, were found in marine strain H5. In the present work, the 3-ketosteroid-delta-1-dehydrogenase and carboxylesterase genes were subcloned into plasmids pET38-12 and pET24-17, respectively. Overexpression in Escherichia coli (E. coli) strain BL21(DE3)pLysS cells resulted in corresponding proteins with an N-terminal His-tag sequence. After induction with isopropyl-β-D-thiogalactoside, 3-ketosteroid-delta-1-dehydrogenase and carboxylesterase were purified in one step using nickel-chelate chromatography. After protein determination, 3-ketosteroid-delta-1-dehydrogenase (0.48 mg/ml) and carboxylesterase (1.28 mg/ml) were used to prepare antibodies to determine steroid binding specificity in future research. In summary, we have shown that the marine strain H5 could metabolize steroids; have isolated two estradiol inducible genes from strain H5 chromosomal DNA, and purified the corresponding proteins for further research. The exact characterization and systematic classification of the marine steroid degrading bacterial strain H5 is envisaged. The strain might be used for the bioremediation of steroid contaminations in seawater.

摘要

天然和合成的甾体激素被排泄到环境中,可能会威胁到各种动物的种群动态和公共健康。我们之前从德国基尔的波罗的海分离到一株甾体降解细菌(H5)。16S-rRNA 分析表明,细菌株 H5 属于弧菌属、弧菌科和γ-变形菌纲。在这项研究中,通过测定 5 小时和 20 小时孵育时保留在细菌 H5 培养基中的(3)H 标记甾体,可以看出细菌株 H5 可以降解睾酮和雌激素等甾体。由于 3α-羟甾类脱氢酶/羰基还原酶(3α-HSD/CR)是康氏棒杆菌(Comamonas testosteroni,C. testosteroni)中适应性甾体降解的关键酶,在之前的研究中,建立了一个以 3α-HSD/CR 基因为阳性对照的元基因组系统。通过这个元基因组系统,在海洋菌株 H5 中发现了分别编码 3-酮甾体-Δ1-脱氢酶和羧酸酯酶的两个雌二醇诱导基因,这两种酶都参与了甾体的降解。在本工作中,3-酮甾体-Δ1-脱氢酶和羧酸酯酶基因分别亚克隆到质粒 pET38-12 和 pET24-17 中。在大肠杆菌(Escherichia coli)菌株 BL21(DE3)pLysS 细胞中的过表达导致相应的蛋白带有 N 端 His 标签序列。用异丙基-β-D-硫代半乳糖苷诱导后,3-酮甾体-Δ1-脱氢酶和羧酸酯酶可通过镍螯合层析一步纯化。蛋白定量后,用 0.48mg/ml 的 3-酮甾体-Δ1-脱氢酶和 1.28mg/ml 的羧酸酯酶制备抗体,用于在未来的研究中确定甾体结合特异性。总之,我们已经表明,海洋菌株 H5 可以代谢甾体;已经从 H5 染色体 DNA 中分离出两个雌二醇诱导基因,并对相应的蛋白进行了纯化,以便进一步研究。预计将对海洋甾体降解细菌株 H5 进行更准确的特征描述和系统分类。该菌株可能用于海水甾体污染的生物修复。

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