氧化亚铁硫杆菌固定化技术研究

在生物脱硫过程中 ,以H - 2软性填料作为氧化亚铁硫杆菌 (Thiobacillusferrooxidans)的固定化载体 ,构建了固定床生化反应器。考察了不同稀释率固定下床生化反应器氧化Fe2 + 的情况 ,在通气量为 330L/h ,稀释率为 0 6h-1条件下 ,Fe2 + 最大氧化速率达 7 6 7g[Fe2 + ]/L·h。该反应器连续运行 10 0d,固定化细胞稳定性良好     

氧化亚铁硫杆菌分离复壮及固定化的研究

用稀释涂布平板法从已退化的氧化亚铁硫杆菌（Thiobacillus ferrooxidans）菌液中分离出氧化活性较高、生命力强的氧化亚铁硫杆菌T1。以H2软性填料作为氧化亚铁硫杆菌的固定化载体,构建了固定床生物反应器。考察了固定床生物反应器氧化Fe2+的情况：Fe2+最大氧化速率达7.67g/(L·h)。并对固定床生物反应器运行过程中在载体表面形成的沉淀物进行了研究,通过X衍射证明此沉淀物为黄钾铁矾［Kfe3(SO4)2(OH)6］。     

氧化亚铁硫杆菌生物冶金的新进展

综述了Thiobacillus ferrooxidans生物冶金的催化作用机制,能量变化,细胞外多聚物和基底金属在浸出过程中的作用和影响,以及温度,矿物的大小,空气分离器,pH,细菌载体的影响。     

海藻酸钙包埋氧化亚铁硫杆菌的固定化研究

采用非稳态法测定FeSO4在包埋和未包埋氧化亚铁硫杆菌的凝胶中的有效扩散系数。结果表明,FeSO4在凝胶中的有效扩散系数De随着海藻酸钠浓度的升高而降低,当海藻酸钠浓度为2%时最优;凝胶剂CaCl2的浓度对扩散系数的影响较小。包埋的氧化亚铁硫杆菌在10h达到增殖平衡,而FeSO4在包埋细菌的凝胶内扩散系数明显减少。     

氧化亚铁硫杆菌对金属铜的加工

材料加工的传统技术包括物理方法和化学方法。当今 ,生物技术已进入各个领域 ,也渗透到材料加工领域。因此 ,材料加工技术也包括生物方法。根据加工工件体积变化 ,生物方法加工分为生物去除加工 (Ｒｅｍｏｖａｌ)、生物沉积加工 (Ａｄｄｉｔｉｏｎ)和生物成形加工 (Ｄｅｆｏｒｍａｔｉｏｎ)。研究生物加工方法的最早报导是 1 993年日本冈山大学宇野义幸等人[1～ 3] ,证实了细菌对纯铁、纯铜去除加工的可能性以及附加电场的作用。国内的研究工作进一步证实了生物加工能力 ,并加工出微小齿轮[4～5] 。本文报导氧化亚铁硫杆菌 (Ｔｈｉｏｂａｃ…     

氧化亚铁硫杆菌培养过程中沉淀的研究

为了减少氧化亚铁硫杆菌培养过程中产生的沉淀,对氧化亚铁硫杆菌培养过程中产生的沉淀物进行了研究,确定了在pH为1．5,K2HPO4用量为0．25g/l,KH2PO4为0．195g/l时菌体可以保持其最高氧化活性,同时产生最少量沉淀物的培养条件,并发现沉淀物对菌体的生长和氧化Fe^2 没有影响。利用饥饿状态的氧化亚铁硫杆菌证明了菌体在一定条件下可以利用黄铁钒沉淀中的部分离子进行生长繁殖。     

氧化亚铁硫杆菌的诱变机理研究

目的：通过物理诱变提高氧化亚铁硫杆菌（T.f）的活性。方法：利用紫外线对高氧化亚铁硫杆菌进行诱变,对比紫外线辐照120s、240s和300s后培养的氧化亚铁硫杆菌的活性,得到最佳的辐照时间。结果：紫外线诱变氧化亚铁硫杆菌的最佳时间为240s,超过该值后T.f菌很难培养。结论：经过240s的紫外线辐照后,利用Leathen培养基培养的氧化亚铁硫杆菌与对照组相比,浓度为对照组的1.21倍,pH值低0.28,氧化还原电位的绝对值比值为1.13,在同样时间条件下,培养液中Fe2＋浓度的曲线变化斜率分别为0.683和0.236。     

氧化亚铁硫杆菌氧化亚硫酸盐的动力学研究

实验用Ms培养基,利用去除铁离子的氧化亚铁硫杆菌(Thiobacillus ferrooxidans)进行了细菌亚硫酸盐的生长代谢研究。实验结果表明氧化亚铁硫杆菌对亚硫酸根具有一定的氧化能力。用Origin 7.0对实验数据进行拟合处理,表明了氧化亚铁硫杆菌催化氧化亚硫酸盐的动力学方程符合Hill方程。氧化亚铁硫杆菌催化氧化亚硫酸盐是一个底物抑制的细胞反应,其KS值随pH值和底物浓度的改变而变化。pH值对反应有很大的影响,pH值越接近中性KS就越小,反应速率就越大。     

氧化亚铁硫杆菌胞外多聚物在生物浸出中的作用

氧化亚铁硫杆菌(Thiobacillus ferrooxidans,T.f)是一种重要的浸矿微生物。它与矿物的界面作用机理是复杂的,涉及物理化学的和生物化学的参数。本文运用电镜细胞化学方法对氧化亚铁硫杆菌(Thiobacillus ferrooxidans)的胞外多聚物(EPS)的脂类、多糖、蛋白质等生物大分子以及铁离子进行了研究,并探讨了EPS与吸附、生物膜形成的关系以及生物膜在浸矿过程中的作用。     

Bio-oxidation of iron using Thiobacillus ferrooxidans

The effects of pH, ferrous and ferric ion concentrations on iron oxidation by Thiobacillus ferrooxidans were examined. The initial temperature and bacterial concentration were maintained at 37°C and 2±1×104cells/ml, respectively. The iron oxidation rate increased with increased initial ferrous iron concentration to 4g/l and thereafter decreased. The presence of iron(III) showed a negative effect on the bacterial iron oxidation rate. The increase of pH also showed an increase in the oxidation rate up to pH 1.75. The oxidation rate followed first order kinetics for the parameters studied. A rate equation has been developed.     

Chemotaxis of chemolithotrophic Thiobacillus ferrooxidans toward thiosulfate

Abstract The chemotactic response of Thiobacillus ferrooxidans toward thiosulfate was observed. The traditional assay technique was modified by direct microscopic enumeration of cells which moved into the attractant solution. The optimum concentration shown by thiosulfate-grown cells, tetrathionate-grown cells as well as iron-grown cells was 10³ times the optimum concentration shown by cells grown on elemental sulfur. Iron-grown cells which lack thiosulfate-oxidizing activity showed increased accumulation at optimum concentration as compared to cells grown on elemental sulfur and other reduced sulfur compounds. This indicated the constitutive nature of chemotaxis by T. ferrooxidans toward thiosulfate.     

Influence of lipopolysaccharides on the attachment of Thiobacillus ferrooxidans to minerals

The loss of part of the lipopolysaccharides (LPS) of the outer membrane of T. ferrooxidans negatively influenced the attachment of the bacteria to minerals and the bioleaching process. LPS previously extracted from T. ferrooxidans and which had come into contact with pyrite inhibited the attachment of cells to minerals and also negatively affected the bioleaching. These results suggest that LPS play an important role in the attachment of the microorganisms and therefore, its presence or absence could affect the bioleaching process.     

Thermal characterization of different isolates of Thiobacillus ferrooxidans

Abstract Ten different isolates of Thiobacillus ferrooxidans were characterized with respect to temperature in the range 2–35°C. Four of the ten strains oxidized ferrous iron exponentially over the entire range of incubation temperatures, including the lowest temperature tested (2°C), and were therefore characterized as psychrotrophic. Jarosite production was substantially reduced at temperatures less than 10°C and was not observed at 2°C. Energy of activation values were in the range 75.2–96.6 kJ/mol°C and indicated that iron oxidation at low temperatures was governed by both a chemical and a physical control.     

The reductive reactions of Thiobacillus ferrooxidans on sulphur and selenium

Abstract An investigation into the sulphur oxidation of iron grown Thiobacillus ferrooxidans is reported. A new mechanism for sulphur catabolism in this obligate acidophile, involving the initial reduction of the substrate, is proposed. Evidence to support substrate reduction comes from the evolution of H₂S in both aerobic and anaerobic conditions (O₂ and Fe³⁺ acting as terminal electron acceptors, respectively) and a accurate trapping method of detection is described. Levels of sulphur reduction are such that a role in the full catabolism of sulphur can be envisaged. In addition, red selenium reduction was investigated and the bioenergetic implications for both substrates are discussed.     

Dissolution of sulphur particles by Thiobacillus ferrooxidans: substrate for unattached cells

The growth of Thiobacillus ferrooxidans on sulphur is known to proceed through the attachment of cells to the sulphur particles. Experiments, However, show that the cells in the liquid phase, which are not attached to the sulphur particles, also grow. It has been shown through the use of a two-compartment membrane reactor that this increase is partially due to the release of ions, corresponding to partially oxidized of sulphur, into the solution by the attached cells. The main soluble ion has been found to the thiosulphate, but traces of sulphite have also been detected. (c) 1993 John Wiley & Sons, Inc.