Abstract
Bacterial metabolism plays an important role on the formation and exploitation of oil shale, and the cost-efficient and environmentally friendly disposal are of great significance for shale oil sustainable development. In the present study, a promising nitrate reducing bacterium was isolated from shale oil in the Ordos Basin with a superior ability to degrade long-chain alkane and produce biosurfactant, which was identified as Stenotrophomonas maltophilia designated strain WGB211 based on morphological and biochemical characteristics as well as 16 S rRNA sequence analysis. The WGB211 degraded a wide range of medium-long length n-alkanes and exhibited highly efficient in 32 C’s n-alkane degradation of over 73% removal rate within 7 days at 31 °C, pH 6.4 and 230 mg/L 32 C’s n-alkane under response surface methodology (RSM) predicted conditions. The biosurfactant product was identified as a mixture of lipopeptides and glycolipids through Fourier transform infrared spectroscopy (FT-IR). The whole genomic analysis showed that strain WGB211 contained a chromosome of 4913676 bp and 4472 protein-coding genes by Illumina NovaSeq. A great number of genes and enzymes related to alkane degradation, such as flavin-binding protein AlmA1 and AlmA2, and long-chain alkane hydroxylase LadA, were identified based on gene annotation. RT-qPCR analysis showed that a dissimilarity of gene expression could be induced by 32 C's n-alkane. This study suggests that S. maltophilia WGB211 could be a potential species for exploitation of oil shale and its genome analysis is valuable for insight into the molecular basis of bioremediation.
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