Bioleaching Mercury from Coal with Aspergillus flavus M-3.

This study focuses on the utilization of Aspergillus flavus(M-3) for the bioleaching mercury from coal, offering an alternative and environmentally to its clean utilization. The fungus was isolated from the soil near a high mercury coal mine in Lao Ying Shan (LYS), Guizhou. Utilizing direct mercury analysis, X-ray diffraction (XRD), and Fourier Transform-Infrared (FT-IR) analysis techniques, the transformation of mercury speciation, mineral components, and organic groups in the coal were analyzed before and after the bioleaching process. The findings of the study illustrated that the fungus M-3 exhibited a remarkable capacity for coal bioliquefaction and mercury leaching from LYS coal. Following a 15-day bioleaching process, a remarkable mercury leaching rate of 83.79% was achieved. Various forms of mercury speciation, including residue, organic matter, sulfide-bound, oxide-bound, exchangeable, and carbonate-bound forms, were released from the coal, with leaching rates ranging from 80.41% to 92.60%. XRD analysis indicated that the M-3 strain facilitated the dissolution of coal pyrite and the degradation of macromolecules, effectively loosening the coal structure. FT-IR analysis of raw and residual coal demonstrated the breakdown of the aromatic ring structure and introduced oxygen-containing functional groups by M-3. Overall, this study highlights the efficacy of bioliquefying coal using Aspergillus flavus (M-3) as a method for clean coal utilization while simultaneously bioleaching mercury.

Genome-wide evolutionary characterization and expression analyses of WRKY family genes in Brachypodium distachyon.

Members of plant WRKY gene family are ancient transcription factors that function in plant growth and development and respond to biotic and abiotic stresses. In our present study, we have investigated WRKY family genes in Brachypodium distachyon, a new model plant of family Poaceae. We identified a total of 86 WRKY genes from B. distachyon and explored their chromosomal distribution and evolution, domain alignment, promoter cis-elements, and expression profiles. Combining the analysis of phylogenetic tree of BdWRKY genes and the result of expression profiling, results showed that most of clustered gene pairs had higher similarities in the WRKY domain, suggesting that they might be functionally redundant. Neighbour-joining analysis of 301 WRKY domains from Oryza sativa, Arabidopsis thaliana, and B. distachyon suggested that BdWRKY domains are evolutionarily more closely related to O. sativa WRKY domains than those of A. thaliana. Moreover, tissue-specific expression profile of BdWRKY genes and their responses to phytohormones and several biotic or abiotic stresses were analysed by quantitative real-time PCR. The results showed that the expression of BdWRKY genes was rapidly regulated by stresses and phytohormones, and there was a strong correlation between promoter cis-elements and the phytohormones-induced BdWRKY gene expression.