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絮凝基因的克隆及其絮凝机理分析
摘要点击 1505  全文点击 2307  投稿时间:2007-01-22  修订日期:2007-03-06
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中文关键词  絮凝基因  原子力显微镜  Zeta(ξ)电位  微观形貌
英文关键词  flocculent gene  AFM  Zeta-potential  microtopography
作者单位
常玉广 哈尔滨工业大学市政环境工程学院哈尔滨150090 
马放 哈尔滨工业大学市政环境工程学院哈尔滨150090 
郭静波 哈尔滨工业大学市政环境工程学院哈尔滨150090 
任南琪 哈尔滨工业大学市政环境工程学院哈尔滨150090 
中文摘要
      分离到1株具有强絮凝特性的芽孢杆菌Bacillus sp. F2,絮凝率达84%,并构建絮凝基因组文库.以絮凝菌F2为实验材料,提取基因组总DNA,经限制性内切酶Sau3AI部分酶切后,与用限制性内切酶BamHI完全酶切的载体PUC19DNA连接,并转化到感受态细胞JM109中.然后将其涂布于含氨苄青霉素的LB培养基上,过夜培养后,经蓝白斑筛选,构建了絮凝基因组文库,该文库包含3.5×104个重组子,经测定文库滴度为3.5×105 pfu/mL.从文库中筛选而获得1株表达絮凝活性的大肠杆菌阳性克隆子FC2.序列分析得出该克隆序列为新的絮凝基因.絮凝试验测定FC2的絮凝率为90%,稍高于原絮凝菌F2,高于受体菌JM109(6.9%).红外光谱分析证明FC2的絮凝有效成分与F2一致,说明FC2絮凝性状遗传于原絮凝菌F2.采用轻敲模式下的原子力显微镜成像技术、Zeta(ξ)电位测定对加入絮凝剂FC2与加入絮凝剂F2、不加入絮凝剂的絮凝微观形貌进行了测定.原子力显微成像显示,加入克隆菌FC2发酵液的高岭土悬浮液(5‰的高岭土水溶液)形成的絮凝体出现较大而且紧密的球形颗粒结构,且表面积粗糙,凹凸程度大,具有大的比表面积和吸附液体悬浮颗粒的能力.向高岭土悬浮液中加入克隆菌FC2发酵液后,絮凝颗粒由不定形且松散的结构转变为密集分布、水平尺寸均匀的球形结构,表明克隆菌FC2发酵液中的凝集素容易以高岭土悬浮颗粒为中心吸附在其表面,而且絮凝试验中絮凝率达90%,从更直观上进一步证实了克隆菌FC2发酵液的除污染效能.Zeta(ξ)电位测定结果表明,离子键作用强度不同,致使絮凝形态存在着差异,为研究生物絮凝剂的絮凝机理提供了有力的依据.
英文摘要
      One strain, named as Bacillus sp. F2, of which flocculent ability can reach 84%, was separated. Flocculent genomic library was constructed. The total genomic DNA of F2 was extracted. It was partly digested by restriction enzyme Sau3AI and then was connected with carrier PUC19DNA which was totally digested by restriction enzyme BamHI and further was converted to competent cells JM109.These cells were smeared on the ampicillin substrate. After one night culture, we selected them by white-blue spot screening and constructed the flocculent genomic library. The library included 3.5×104 recons and the titre was 3.5×105 dpfu/mL. strain of Escherichia coli. positive clone FC2, which could express flocculent activity, was acquired after selection. Flocculent tests showed that the flocculent efficiency of FC2 was 90%, which was slightly higher than the original flocculent bacterium F2 and greatly higher than the competent cell JM109 (6.9%). It demonstrated that FC2's flocculent characteristic inherited from the original flocculent bacterium F2. By adopting the tapping mode AFM and Zeta-potential test, the flocculent microtopography of FC2, F2 and pure kaolin suspending solution was identified. The AFM study revealed that, compared to the kaolin suspending solution with and without F2's fermented liquid, the kaolin suspending solution which has cloning bacterium FC2's fermented liquid had larger flocculent gel and more compact spherical structure, and the surface was rough with high degree concave and convex, and had large specific surface area and strong adsorption ability to the suspending particles in the solution. After adding the fermented solution of cloning bacterium FC2 into kaolin suspending solution, the amorphous and incompact flocculent particles transformed into spherical structure which was compact and had even horizontal dimension, which indicated that the agglutinin in FC2's fermented liquid could easily take kaolin suspending particles as its adsorption core and adsorbed on its surface and the flocculent efficiency was about 90%, which gave further confirmation to the great pollution removal capability of FC2's fermented liquid. The results of Zeta-potential test illustrated that the intensity of electrovalent bond was different, resulting in various flocculent morphology, which provided significant evidences for studying flocculent mechanisms of biofloculant.

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