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논문 기본 정보

자료유형
학술저널
저자정보
Tsevelkhoroloo Maral (Department of Bioscience and Bioinformatics Myongji University Yongin 17058 Republic of Korea) Xiaoqiang Li (Department of Bioscience and Bioinformatics Myongji University Yongin 17058 Republic of KoreaGeneNe) Jin Xue-Mei (Department of Bioscience and Bioinformatics Myongji University Yongin 17058 Republic of KoreaCharac) Shin Jung-Ho (R&D Health & Bioscience DuPont-IFF Wilmington 19898 DE USA) 이창로 (명지대학교) Kang Yup (Institute for Medical Sciences Ajou University School of Medicine Suwon 16499 Republic of Korea) 홍순광 (명지대학교)
저널정보
한국미생물생명공학회 Journal of Microbiology and Biotechnology Journal of Microbiology and Biotechnology 제32권 제9호
발행연도
2022.9
수록면
1,134 - 1,145 (12page)
DOI
10.4014/jmb.2205.07050

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SCO6993 (606 amino acids) in Streptomyces coelicolor belongs to the large ATP-binding regulators of the LuxR family regulators having one DNA-binding motif. Our previous findings predicted that SCO6993 may suppress the production of pigmented antibiotics, actinorhodin, and undecylprodigiosin, in S. coelicolor, resulting in the characterization of its properties at the molecular level. SCO6993-disruptant, S. coelicolor ΔSCO6993 produced excess pigments in R2YE plates as early as the third day of culture and showed 9.0-fold and 1.8-fold increased production of actinorhodin and undecylprodigiosin in R2YE broth, respectively, compared with that by the wild strain and S. coelicolor ΔSCO6993/SCO6993+. Real-time polymerase chain reaction analysis showed that the transcription of actA and actII-ORF4 in the actinorhodin biosynthetic gene cluster and that of redD and redQ in the undecylprodigiosin biosynthetic gene cluster were significantly increased by SCO6993-disruptant. Electrophoretic mobility shift assay and DNase footprinting analysis confirmed that SCO6993 protein could bind only to the promoters of pathway-specific transcriptional activator genes, actII-ORF4 and redD, and a specific palindromic sequence is essential for SCO6993 binding. Moreover, SCO6993 bound to two palindromic sequences on its promoter region. These results indicate that SCO6993 suppresses the expression of other biosynthetic genes in the cluster by repressing the transcription of actII-ORF4 and redD and consequently negatively regulating antibiotic production.

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