Abstract | BACKGROUND: RESULTS: In this study, RNA-sequencing ( RNA-seq) technology was employed for investigation of the genome-wide differential gene expression in U32 cultured with or without nitrate supplementation. In the presence of nitrate, U32 maintained a high transcriptional level of genes both located in the rifamycin biosynthetic cluster and involved in the biosynthesis of rifamycin precursors, including 3-amino-5-dihydroxybenzoic acid, malonyl-CoA and (S)- methylmalonyl-CoA. However, when nitrate was omitted from the medium, the transcription of these genes declined sharply during the transition from the mid-logarithmic phase to the early stationary phase. With these understandings, one may easily propose that nitrate stimulates the rifamycin SV production through increasing both the precursors supply and the enzymes for rifamycin biosynthesis. CONCLUSION: It is the first time to thoroughly illustrate the mechanism of the nitrate-mediated stimulation of rifamycin production at the transcriptional level, which may facilitate improvement of the industrial production of rifamycin SV, e.g. through optimizing the global rifamycin biosynthetic pathways on the basis of RNA-seq data.
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Authors | Zhi Hui Shao, Shuang Xi Ren, Xin Qiang Liu, Jian Xu, Han Yan, Guo Ping Zhao, Jin Wang |
Journal | Microbial cell factories
(Microb Cell Fact)
Vol. 14
Pg. 75
(Jun 04 2015)
ISSN: 1475-2859 [Electronic] England |
PMID | 26041361
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Nitrates
- Rifamycins
- RNA
- rifamycin SV
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Topics |
- Actinomycetales
(enzymology, genetics, metabolism)
- Nitrates
(metabolism)
- RNA
(metabolism)
- Rifamycins
- Transcriptome
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