Marine Drugs | |
Harnessing the Potential of Halogenated Natural Product Biosynthesis by Mangrove-Derived Actinomycetes | |
Xue-Gong Li2  Xiao-Min Tang1  Jing Xiao1  Guang-Hui Ma1  Li Xu1  Shu-Jie Xie1  Min-Juan Xu4  Xiang Xiao3  | |
[1] Key Laboratory of Marine Biogenetic Resources, The Third Institute of Oceanography, State Oceanic Administration, Xiamen 361005, China; E-Mails:;College of Marine Life Sciences, Ocean University of China, Qingdao 266003, China; E-Mail:;State Key Laboratory of Microbial Metabolism and School of Life Science & Biotechnology, State Key Laboratory of Ocean Engineering, Shanghai Jiao Tong University, Shanghai 200240, China; E-Mail:;Ministry of Education Key Laboratory of Systems Biomedicine, Shanghai Center for Systems Biomedicine, Shanghai Jiao Tong University, Shanghai 200240, China | |
关键词: mangrove-derived actinomycetes; genome mining; halogenase; enduracidin; ansamycin; | |
DOI : 10.3390/md11103875 | |
来源: mdpi | |
【 摘 要 】
Mangrove-derived actinomycetes are promising sources of bioactive natural products. In this study, using homologous screening of the biosynthetic genes and anti-microorganism/tumor assaying, 163 strains of actinomycetes isolated from mangrove sediments were investigated for their potential to produce halogenated metabolites. The FADH2-dependent halogenase genes, identified in PCR-screening, were clustered in distinct clades in the phylogenetic analysis. The coexistence of either polyketide synthase (PKS) or nonribosomal peptide synthetase (NRPS) as the backbone synthetases in the strains harboring the halogenase indicated that these strains had the potential to produce structurally diversified antibiotics. As a validation, a new enduracidin producer,
【 授权许可】
CC BY
© 2013 by the authors; licensee MDPI, Basel, Switzerland.
【 预 览 】
Files | Size | Format | View |
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RO202003190032654ZK.pdf | 509KB | download |