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DBT desulfurization by decorating Rhodococcus erythropolis IGTS8 using magnetic Fe3O4 nanoparticles in a bioreactor

机译:通过在生物反应器中使用磁性Fe3O4纳米粒子装饰红球菌IGTS8来装饰DBT脱硫

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摘要

Today, crude oil is an important source of energy and environmental contamination due to the continued use of petroleum products is a matter or urgent concern. In this work, two technological platforms, namely, the use of a robust desulfurizing bacteria and the use of nanotechnology to decorate the surface of the bacteria with nanoparticles (NP), were combined to enhance biodesulfurization (BDS). BDS is an ecologically friendly method for desulfurizing petroleum products while avoiding damage to the hydrocarbons due to the high temperatures normally associated with physical desulfurization methods. First, a bacterium known to be a good organism for desulfurization ( IGTS8) was employed in cell culture to remove a recalcitrant sulfur molecule from a common sulfur‐containing compound found in crude petroleum products (dibenzothiophene). 2‐Hydroxybiphenyl (2‐HBP) produced as a consequence of the BDS of dibenzothiophene was determined using Gibbs’ assay. The synthesized NP were characterized by field emission scanning electron microscope, transmission electron microscopy, Fourier transform infrared spectroscopy, X‐ray diffraction spectroscopy, and vibrating sample magnetometer. The field emission scanning electron microscope and transmission electron microscopy images showed the size of the NP is 7–8 nm. The decorated cells had a long lag phase, but the growth continued until 148 h (at OD = 3.408) while the noncoated bacteria grow until 96 h before entering the stationary phase at OD = 2.547. Gibbs’ assay results showed that production of 2‐HBP by decorated cells was 0.210 mM at = 148 h, while 2‐HBP production by nondecorated cells was 0.182 mM at = 96 h. Finally, the experiments were repeated in a fermenter.
机译:如今,由于持续使用石油产品,原油已成为能源和环境污染的重要来源,这已成为人们关注或迫切关注的问题。在这项工作中,结合了两个技术平台,即使用强大的脱硫细菌和使用纳米技术用纳米颗粒(NP)装饰细菌表面,以增强生物脱硫(BDS)。 BDS是一种对石油产品进行脱硫的生态友好方法,同时避免了通常与物理脱硫方法相关的高温导致的碳氢化合物损坏。首先,在细胞培养中使用一种已知是脱硫良好生物的细菌(IGTS8)从原油产品(二苯并噻吩)中常见的含硫化合物中去除顽固性硫分子。使用吉布斯测定法确定了由于二苯并噻吩的BDS产生的2-羟基联苯(2-HBP)。通过场发射扫描电子显微镜,透射电子显微镜,傅立叶变换红外光谱,X射线衍射光谱和振动样品磁力计对合成的NP进行表征。场发射扫描电子显微镜和透射电子显微镜图像显示NP的大小为7-8 nm。装饰的细胞具有较长的滞后阶段,但生长持续到148 h(OD = 3.408),而未覆盖的细菌生长直到96 h,然后进入OD = 2.547的固定相。 Gibbs的化验结果显示,经过修饰的细胞在148 h时产生2-HBP的量为0.210 mM,而未经修饰的细胞在= 96 h时产生的2-HBP的量为0.182 mM。最后,在发酵罐中重复实验。

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