Enhanced biodesulfurization of recalcitrant organosulfur compounds by a newly identified Gordonia alkanivorans JT-2 in the presence of mycolic acid

IF 3.7 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Maosheng Yin , Shuiquan Chen , Meng Zang , Lin Li , Chaocheng Zhao , Xiuxia Zhang
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引用次数: 0

Abstract

With the increasing stringency of global regulations on the sulfur content of petroleum products, the development of efficient desulfurization technologies has become imperative. While biodesulfurization offers an eco-friendly alternative to hydrodesulfurization, its industrial adoption remains hindered by (i) poor degradation of alkylated DBTs/BTs and (ii) inefficient oil-water phase mass transfer. In this study, we identified a novel strain, Gordonia alkanivorans JT-2, demonstrating enhanced biodesulfurization performance, attributed to its production of mycolic acid, which improves hydrophobicity and mass transfer efficiency. Genomic analysis revealed key desulfurization genes (dszA, dszB, dszC, and dszD) and mycolic acid biosynthesis genes (fas, pks13, kasAB, fabD, and fadD32). Biodesulfurization experiments showed significant sulfur removal, reducing sulfur content in model oil to 35.7 ± 5.9 mg/L (DBT), 55.2 ± 7.9 mg/L (4-MDBT), 63.1 ± 5.7 mg/L (3-MBT), and 73.7 ± 3.8 mg/L (4,6-DMDBT) within 5 days. Protein interaction network analysis further illustrated the interplay between lipid biosynthesis and sulfur metabolism, underscoring the metabolic adaptability of strain JT-2. This work addresses a critical limitation in existing biodesulfurization technologies by improving mass transfer efficiency and broadening substrate range, positioning G. alkanivorans JT-2 as a promising candidate for industrial biodesulfurization applications.
在霉菌酸存在下,新鉴定的烷化戈登菌JT-2增强了难固定性有机硫化合物的生物脱硫作用
随着全球对石油产品含硫量法规的日益严格,开发高效脱硫技术已势在必行。虽然生物脱硫是一种环保的加氢脱硫替代方法,但其工业应用仍然受到以下因素的阻碍:(1)烷基化dbt / bt的降解能力差;(2)油水相传质效率低。在这项研究中,我们鉴定了一种新的菌株,Gordonia alkanivorans JT-2,由于其生产霉菌酸,提高了疏水性和传质效率,表现出增强的生物脱硫性能。基因组分析显示了关键的脱硫基因(dszA、dszB、dszC和dszD)和霉菌酸生物合成基因(fas、pks13、kasAB、fabD和fadD32)。Biodesulfurization实验显示重要的硫去除,减少模型油中硫含量 35.7±5.9  mg / L(印度生物技术部),55.2 ±7.9  mg / L (4-MDBT), 63.1 ±5.7  mg / L (3-MBT)和73.7 ±3.8  mg / L (4 6-DMDBT) 5天内。蛋白质相互作用网络分析进一步说明了脂质生物合成与硫代谢之间的相互作用,强调了菌株JT-2的代谢适应性。这项工作通过提高传质效率和扩大底物范围,解决了现有生物脱硫技术的一个关键限制,将G. alkanivorans JT-2定位为工业生物脱硫应用的有前途的候选物。
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来源期刊
Biochemical Engineering Journal
Biochemical Engineering Journal 工程技术-工程:化工
CiteScore
7.10
自引率
5.10%
发文量
380
审稿时长
34 days
期刊介绍: The Biochemical Engineering Journal aims to promote progress in the crucial chemical engineering aspects of the development of biological processes associated with everything from raw materials preparation to product recovery relevant to industries as diverse as medical/healthcare, industrial biotechnology, and environmental biotechnology. The Journal welcomes full length original research papers, short communications, and review papers* in the following research fields: Biocatalysis (enzyme or microbial) and biotransformations, including immobilized biocatalyst preparation and kinetics Biosensors and Biodevices including biofabrication and novel fuel cell development Bioseparations including scale-up and protein refolding/renaturation Environmental Bioengineering including bioconversion, bioremediation, and microbial fuel cells Bioreactor Systems including characterization, optimization and scale-up Bioresources and Biorefinery Engineering including biomass conversion, biofuels, bioenergy, and optimization Industrial Biotechnology including specialty chemicals, platform chemicals and neutraceuticals Biomaterials and Tissue Engineering including bioartificial organs, cell encapsulation, and controlled release Cell Culture Engineering (plant, animal or insect cells) including viral vectors, monoclonal antibodies, recombinant proteins, vaccines, and secondary metabolites Cell Therapies and Stem Cells including pluripotent, mesenchymal and hematopoietic stem cells; immunotherapies; tissue-specific differentiation; and cryopreservation Metabolic Engineering, Systems and Synthetic Biology including OMICS, bioinformatics, in silico biology, and metabolic flux analysis Protein Engineering including enzyme engineering and directed evolution.
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