h i g h l i g h t sA predictive model for log K OA of PCBs was developed based on △G OA . The optimal combination of theoretical method and basis-set was HF/MIDI!6D. The model was improved after taking the dimer formation into account. Log K OA values of PCBs at different ambient temperatures were predicted.

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The excellent properties of micro-nano materials and structures have attracted extensive attention especially in wastewater treatment. Based on this, magnetic multi-walled carbon nanotubes (MMWCNTs) have been prepared and used for the sorptive removal of five typical cationic dyes from aqueous solutions in the present study. Effects of several operational and environmental factors were investigated carefully, including initial pH values, common ions, contact time and temperature. The kinetics processes were well fitted by the pseudo-second-order kinetic model. The maximum adsorption capacities on MMWCNTs at 298.15 K for malachite green oxalate, auramine O, neutral red, crystal violet and rhodamine B were 442.2, 295.2, 183.4, 165.3 and 143.0 mg g−1, respectively. Differences in the size, structure and properties of these dyes led to the difference of adsorption amounts. ΔG0 were all negative within the temperature range tested, which meant the adsorption processes were spontaneous nature. Moreover, the adsorption processes of targeted dyes, except auramine O, were exothermic and entropy decreasing. The regeneration studies indicated that the MMWCNTs showed high reusability and the removal efficiencies can be achieved above 75% after four consecutive cycles. For the adsorption mechanism, electrostatic interaction, hydrogen bonds, π-π interaction together with hydrophobic interaction, could coexist during the adsorption process.

Leukemia is an aberrant hyper-proliferation of immature blood cells that do not form solid tumors. The transcriptomes of microRNAs (miRNAs) of leukemia have been intensively explored. However, miRNA editing of leukemia has not been extensively studied. To identify miRNA editing patterns and explore their functional relevance in leukemia, we analyzed 200 small RNA sequencing profiles of three subtypes of leukemia and identified hundreds of miRNA editing sites in three subtypes of leukemia. Then, we compared the editing levels of identified miRNA editing sites in leukemia and normal controls. Many miRNAs were differential edited in different subtypes of leukemia. We also found the editing levels of 3′-A editing sites of hsa-mir-21-5p and hsa-mir-155-5p decreased in chronic lymphocytic leukemia patients with radiation treatments. By integrating PAR-CLIP sequencing profiles, we predicted the targets of original and edited miRNAs. One of the edited miRNA, hsa-let-7b_5c, with an additional cytosine at 5′ end of hsa-let-7b-5p, potentially targeted VBP1 and CTDSP1. CTDSP1 was significantly downregulated in T-ALL compared to normal controls, which might be originated from the hyperediting of hsa-let-7b-5p in T-ALL. Our study provides a comprehensive view of miRNA editing in three different subtypes of leukemia.

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