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논문 기본 정보

자료유형
학술저널
저자정보
Chan Mooi Kwai (Universiti Sains Malaysia) Wai Wen Xuan (Universiti Sains Malaysia) Ang Ruo Ping (Universiti Sains Malaysia) Chew Ai Lan (Universiti Sains Malaysia) Khoo Boon Yin (Universiti Sains Malaysia)
저널정보
한국미생물학회 미생물학회지 미생물학회지 제56권 제1호
발행연도
2020.3
수록면
44 - 53 (10page)

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초록· 키워드

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The expression of in-house DNA topoisomerase I (Topo1) was optimized in order to develop a gel-based DNA relaxation assay for the screening of potential bioactive compounds. Results showed that nearly 4-fold increment in total protein level was achieved in the culture supernatant with 1.0% (v/v) methanol feeding every 24 h and cultivated for 72 h at 28℃. Crude recombinant TopoI was shown to relax the supercoiled plasmid DNA completely in the developed gel-based assay and reactions were not affected by DMSO addition and the features on electrophoresed gel could be improved by chloroform: isoamylalcohol extraction. The recombinant protein was then purified and the enzymatic activity of the recombinant TopoI in the crude and purified culture supernatant was studied and compared with a commercial TopoI. DNA relaxation assay showed that the purified recombinant TopoI is a more reliable source with an activity of approximately 20~30 U/μl. The developed assay was finally evaluated by determining the inhibitory effects of flavonoids and positive control Camptothecin on the recombinant TopoI catalytic activity. The efficiency of the gel-based assay using purified recombinant TopoI was further evaluated against a cell-based cytotoxicity assay in which the inhibitory effects on cell growth by the flavonoids and Camptothecin were assessed. The similar inhibitory trends shown by both assays demonstrated that potential inhibitors can be preliminarily screened using a gel-based assay prior to identification of the inhibitors using a cell-based assay to detect the DNA intercalating agents that interrupt the TopoI catalytic activity.

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Materials and Methods
Results
Discussion
Conclusion
References

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