| 论文题目: | Disruption of rimP, encoding a ribosome assembly cofactor, widely enhances production of several distinct antibiotics by affecting the translational efficiency and fidelity of Streptomyces |
|---|---|
| 作者: | Pan Yuanyuan#, Lu Cheng#, Jiang Linjuan, Liu Gang*, Tan Huarong* |
| 联系作者: | Liu Gang*, Tan Huarong* |
| 刊物名称: | Microbial Cell Factories |
| 期: | |
| 卷: | 12 |
| 页: | 56 |
| 年份: | 2013 |
| 影响因子: | 4.100 |
| 论文下载: | http://www.microbialcellfactories.com/content/12/1/65/abstract |
| 摘要: | Background
Ribosome assembly cofactor RimP is one of the auxiliary proteins required for maturation of the 30S subunit in Escherichia coli. Although RimP in protein synthesis is important, its role in secondary metabolites biosynthesis has not been reported so far. Considering the close relationship between protein synthesis and the production of secondary metabolites, the function of ribosome assembly cofactor RimP on antibiotics production was studied in Streptomyces coelicolor and Streptomyces venezuelae.
Results
In this study, the rimP homologue rimP-SC was identified and cloned from Streptomyces coelicolor. Disruption of rimP-SC led to enhanced production of actinorhodin and calcium-dependent antibiotics by promoting the transcription of actII-ORF4 and cdaR. Further experiments demonstrated that MetK was one of the reasons for the increment of antibiotics production. In addition, rimP-SC disruption mutant could be used as a host to produce more peptidyl nucleoside antibiotics (polyoxin or nikkomycin) than the wild-type strain. Likewise, disruption of rimP-SV of Streptomyces venezuelae also significantly stimulated jadomycin production, suggesting that enhanced antibiotics production might be widespread in many other Streptomyces species.
Conclusion
These results established an important relationship between ribosome assembly cofactor and secondary metabolites biosynthesis and provided an approach for yield improvement of secondary metabolites in Streptomyces. |
京公网安备 11010502044263号