Evaluation of the Lignite Biotransformation Capacity of Fusarium sp. NF01 Cultured on Different Growth Substrates
Screening and studying the lignite solubilization/degradation capacities of indigenous microorganisms are key to exploring the in-situ biotransformation of lignite. Here, a fungus was isolated from in-situ lignite samples and identified as Fusarium sp. NF01. This isolate was then cultured on four different carbon sources to evaluate its lignite transformation capacity. When cultured on a solid agar medium containing sodium gluconate or sodium glutamate, Fusarium sp. NF01 completely liquefied 0.5 g of lignite within six days, and when cultured in a liquid medium containing sodium gluconate, the weight of lignite decreased by 28.4% within seven days. Elemental analysis showed that the lignite biodegradation rate was inversely proportional to the C/O ratio of the residual lignite samples. Additionally, a 5.9% biodesulfurization rate was achieved when Fusarium sp. NF01 was cultured in the presence of sodium gluconate. Finally, Fourier-transform infrared analysis of the residual lignite samples revealed relatively weak signal intensities of the signature peaks representing the following: aromatic ring side chains; ether, ester, and alcohol bonds; aromatic ring carbon-carbon double bonds; and aliphatic methyl and methylene. The results showed that Fusarium sp. NF01 can degrade lignite in a carbon-dependent manner and could be thus used for the bioconversion of subsurface coalbeds.