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Separation and Evaluation of Anticancer Components from Myxococcus Macrosporus STXZ54 |
WEN Ye, TANG Shao-jun, XIAO Rong, HUANG Tong-long, LEI Liang-huan, DING Xue-zhi, XIA Li-qiu |
State Key Laboratory Breeding Base of Microbial Molecular Biology, College of Life Science, Hunan Normal University, Changsha, Province 410081, China |
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Abstract Myxobacteria are known to be the third category of bacteria, which produce metabolites of potential anticancer effects. Here the lab-stored Myxococcus macrosporus STXZ54 was cultured, and components of its supernatants were attained by ammonium sulfate or acetone precipitation. Cytotoxic effects of the sediments were evaluated through an in vitro method. Further, the unique protein, WGF5, was successfully separated by high performance liquid chromatography from the myxobacteria. Its inhibitory effects on cancer cells were also analyzed by MTT assay. Simultaneously, confocal microscopy was employed to observe the alterations of B16 subcellular structure after treatment by WGF5. The results demonstrated that WGF5 was a very stable protein under room temperature and could efficiently inhibit the growth of B16, Hela, MCF-7 and Hep-3B cancer cells. The IC50 of WGF5 after 48 h incubation with the cancer cells was 2.767 μg/ml, 2.204 μg/ml, 3.758 μg/ml and 3.073 μg/ml, respectively. Moreover, MTT assay and confocal microscopy observation found that WGF5 probably restrains the proliferation of the cancer cells through changing the cell morphology. Briefly, this study indicates that the WGF5 of Myxococcus macrosporus STXZ54 has an broad-spectrum anticancer effects and could be used for cancer therapy in the near future.
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Received: 29 May 2014
Published: 25 September 2014
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