The impact of immersed liquid circulation on anaerobic digestion of rice straw bale and methane generation improvement.

Immersed liquid circulation is assumed to improve solid-state anaerobic digestion (SS-AD) with digestate flow convection on the surface of solid-state bed (SSB), which depends on SSB concentration and circulation rate (CR). In this study, the impact of CR on rice straw SS-AD was investigated within a 30 L pilot digester. Results showed that SSB threshold concentration for efficient biogas conversion was 10%-12% TS, achieving the methane yield of 185.3 mL/g VS. Within the threshold, methane production progress and VFAs release could be enhanced simultaneously by rational CR increasing, but no significant methane yield improvement was observed; above, the rapid and stable biogas generation could be acquired with a competitive methane yield of 174.7 mL/g VS (150% CR). No matter within or above the threshold, efficient lingo-cellulosic degradation was always accompanied by the moderate CR for effective methane generation. SSB was proposed to be above threshold for industrial application.

IRGM1 enhances B16 melanoma cell metastasis through PI3K-Rac1 mediated epithelial mesenchymal transition.

Melanoma is one of the most aggressive skin cancers and is well known for its high metastatic rate. Studies have shown that epithelial mesenchymal transition (EMT) is essential for melanoma cell metastasis. However, the molecular mechanisms underlying EMT are still not fully understood. We have shown that IRGM1, a member of immunity-related GTPase family that regulates immune cell motility, is highly expressed by melanoma cells. The current study aimed to explore whether and how IRGM1 may regulate melanoma cell metastasis. To test this, we modified IRGM1 expression in B16 melanoma cells. We found that over-expression of IRGM1 substantially enhanced pulmonary metastasis in vivo. In keeping with that, knocking-in IRGM1 strongly enhanced while knocking-down IRGM1 impaired B16 cell migration and invasion ability in vitro. Interestingly, we observed that IRGM1 enhanced F-actin polymerization and triggers epithelial mesenchymal transition (EMT) through a mechanism involved in PIK3CA mediated Rac1 activation. Together, these data reveals a novel molecular mechanism that involved in melanoma metastasis.