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AimsFeathers are keratin-rich byproducts of poultry processing, but those are often frequently abandoned as garbage and thus polluting the environment. Therefore, the study focused on the efficient biodegradation, bioactivity, and high-value application of feather keratin.Methods and resultsFeather-degrading bacteria were identified, and the degradation properties were characterized. DPPH (1,1-Diphenyl-2-picrylhydrazyl radical) and ABTS (2,2′-Azino-bis (3-ethylbenzthiazoline-6-sulfonic acid))radical scavenging assays, cytotoxicity assays, intracellular reactive oxygen scavenging assays, and cell migration assays were used to examine the biological activities of the feather keratin hydrolysis peptides (FKHPs). The results showed that we screened a feather-degrading strain of Bacillus licheniformis 8-4, which achieved complete degradation of 2% (w/v) feathers within 48 h. Notably, the feather fermentation broth was particularly high in FKHPs, which exhibited good DPPH and ABTS radical scavenging ability. Further studies revealed that FKHPs had both the ability to scavenge H2O2-induced ROS from HaCat cells and the ability to promote HaCat cell migration, while remaining non-toxic.ConclusionsThe effective feather-degrading ability of B. licheniformis 8-4 allowed for the fermentation of feather medium to yield active peptides that were both antioxidants and cell-migration enhancers.

A reliable method for simultaneous determination of four organic selenium species by HPLC-ICP-MS was developed and implemented in determining organic selenoamino acids (Se-AAs) in selenoproteins from Lactococcus lactis (L. lactis) NZ9000. The method consisted of liberating Se-AAs from selenoproteins using ultrasound-assisted protease hydrolysis, and quantitatively detecting Se-AA speciations by HPLC-ICP-MS. After optimizations of proteolysis conditions, chromatographic conditions and determination conditions, the established method could efficiently separate the four Se-AAs, including SeCys, SeCys2, SeMeCys and SeMet within 10 min. It presented high sensitivity with the limits of detection and quantitation in the range of 0.197∼0.240 μg∙L

X-ray differential phase contrast imaging technology can reveal the weakly absorbing fine structure which cannot be observed by the conventional X-ray absorption contrast imaging. Hence, it has potential applications in many fields such as medical science, and material science. But in the traditional X-ray grating differential phase contrast imaging system, the analyser grating is used as a spatial filter, and needs to be phase stepped, then multiple exposures are required for information extraction. Thus this leads to high-dose radiation exposure and low efficiency of X-ray utilization. All these disadvantages limit its application in various disciplines. In order to cope with the above issues, a new algorithm based on single-shot grating differential phase contrast imaging system without analyzer grating is proposed. In such a system the absorption, refraction and scattering information can be obtained from one projective image of the sample acquired by a high-resolution detector. The reliability of this new algorithm is confirmed by numerical simulation. Compared with the phase stepping algorithm, the proposed algorithm can provide very accurate and reliable information extraction results without requiring the grating period to match with detector pixel size. It facilitates the reduction of the radiation damage to sample. We emphasize that this method is highly compatible with the future X-ray phase contrast imaging clinical applications.