Filipe Smith Buarque, Júlio Cesar Soares Sales, Lívia Cabral Lobo, Erika Christina Ashton Nunes Chrisman, Bernardo Dias Ribeiro, Maria Alice Zarur Coelho
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引用次数: 0
Abstract
Heavy crude oil reserves are characterized by their high viscosity and density, largely due to significant quantities of asphaltenes. The removal of asphaltene precipitates from oil industry installations is crucial, as they can contaminate catalysts and obstruct pipelines. Therefore, this study aimed to bio-transform heavy oil asphaltenes into smaller molecules using the yeast Yarrowia lipolytica, known for its ability to efficiently degrade hydrophobic substrates. For this purpose, asphaltenes were extracted from crude oil samples, and yeast growth was assessed in a mineral medium containing 2, 5, or 10 g L-1 of asphaltenes. After 168 h of incubation, liquid-liquid extraction was conducted on samples from the Yarrowia lipolytica growth medium using chloroform. The extracted fractions were then quantified by gas chromatography. The results indicated that the yeast could utilize the asphaltenes as a carbon source for growth, though there was a delay in growth compared to the control (glucose as the carbon source), with a maximum biomass concentration of 2.26 g L-1 achieved at 144 h. From the experimental design, it was determined that a higher concentration of aromatic compounds was achieved under the conditions of 115 rpm, 2 g L-1 of asphaltenes, and 0.5 g L-1 of cell inoculum. Conversely, to obtain a higher concentration of saturated compounds, the optimal conditions were 160 rpm, 5 g L-1 of asphaltenes, and 1.0 g L-1 of cell inoculum. Molecular docking results indicated that asphaltenes have a high affinity for cytochrome P450, laccase, and Lip2, with interactions observed with their catalytic triads, suggesting a significant role for these enzymes in asphaltene bioconversion.
重质原油储量的特点是其高粘度和密度,主要是由于大量的沥青质。从石油工业设施中清除沥青质沉淀物至关重要,因为它们会污染催化剂并堵塞管道。因此,本研究旨在利用酵母脂解耶氏酵母将重油沥青烯生物转化为更小的分子,耶氏酵母以其有效降解疏水底物的能力而闻名。为此,从原油样品中提取沥青质,并在含有2、5或10 g L-1沥青质的矿物培养基中评估酵母的生长情况。孵育168 h后,用氯仿对多脂耶氏菌生长培养基中的样品进行液液萃取。然后用气相色谱法对提取的组分进行定量。结果表明,酵母可以利用沥青质作为碳源进行生长,尽管与对照(葡萄糖作为碳源)相比,生长有所延迟,但在144 h时可达到2.26 g L-1的最大生物量浓度。从实验设计中可以确定,在115 rpm, 2 g L-1沥青质和0.5 g L-1细胞接种的条件下,可获得更高浓度的芳香族化合物。相反,为了获得更高浓度的饱和化合物,最佳条件是160 rpm, 5 g L-1沥青质,1.0 g L-1细胞接种量。分子对接结果表明,沥青质与细胞色素P450、漆酶和Lip2具有高亲和力,并与它们的催化三联体相互作用,表明这些酶在沥青质生物转化中起着重要作用。
期刊介绍:
Bioprocess and Biosystems Engineering provides an international peer-reviewed forum to facilitate the discussion between engineering and biological science to find efficient solutions in the development and improvement of bioprocesses. The aim of the journal is to focus more attention on the multidisciplinary approaches for integrative bioprocess design. Of special interest are the rational manipulation of biosystems through metabolic engineering techniques to provide new biocatalysts as well as the model based design of bioprocesses (up-stream processing, bioreactor operation and downstream processing) that will lead to new and sustainable production processes.
Contributions are targeted at new approaches for rational and evolutive design of cellular systems by taking into account the environment and constraints of technical production processes, integration of recombinant technology and process design, as well as new hybrid intersections such as bioinformatics and process systems engineering. Manuscripts concerning the design, simulation, experimental validation, control, and economic as well as ecological evaluation of novel processes using biosystems or parts thereof (e.g., enzymes, microorganisms, mammalian cells, plant cells, or tissue), their related products, or technical devices are also encouraged.
The Editors will consider papers for publication based on novelty, their impact on biotechnological production and their contribution to the advancement of bioprocess and biosystems engineering science. Submission of papers dealing with routine aspects of bioprocess engineering (e.g., routine application of established methodologies, and description of established equipment) are discouraged.