Regulatory orchestration of FK506 biosynthesis in Streptomyces tsukubaensis NRRL 18488 revealed through systematic analysis

<i>Streptomyces tsukubaensis</i> NRRL 18488, the primary producer of the immunosuppressant FK506, was analyzed to elucidate regulatory features of secondary metabolism. Completion of its 7.9-Mb linear genome enabled accurate re-annotation of the FK506 biosynthetic gene cluster (BGC). Transcriptome analysis during BGC activation revealed major transcriptional shifts from primary to secondary metabolism, especially in genes involved in FK506 biosynthesis and lysine metabolism. Primary transcriptome mapping identified 1,225 transcription units and uncovered post-transcriptional regulation of allylmalonyl-CoA production, a key FK506 precursor. Ribosome profiling demonstrated that AT-rich codons reduce translational efficiency in <i>S. tsukubaensis</i>, with pronounced ribosome pausing at the TTA codon within the FK506 BGC. Substituting this codon relieved pausing and improved FK506 production. Together, these integrative genomic, transcriptomic, and translatomic analyses highlight how multi-level regulatory mechanisms shape secondary metabolism in <i>Streptomyces</i>. This work offers insights into metabolic control that could inform future efforts in strain improvement for efficient natural products production.

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Journal
iScience
Published
2025-05-19
DOI
https://doi.org/10.1016/j.isci.2025.112698
Citations
2
Primary Topic
RNA and protein synthesis mechanisms
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article
Field-Weighted Citation Impact
1.61

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article

Regulatory orchestration of FK506 biosynthesis in Streptomyces tsukubaensis NRRL 18488 revealed through systematic analysis

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2 citations
iScience
RNA and protein synthesis mechanisms
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article

Regulatory orchestration of FK506 biosynthesis in Streptomyces tsukubaensis NRRL 18488 revealed through systematic analysis

Jay D. Keasling, Soonkyu Hwang, Suhyung Cho, Woori Kim, Namil Lee, Yong‐Jae Lee, Qingyun Dan, Bernhard Ø. Palsson, Yeo Joon Yoon, Gahyeon Kim, Hyeseong Kim, Byung‐Kwan Cho, Ji Hun Kim, Matthias Schmidt
article en
2 citations

Abstract

<i>Streptomyces tsukubaensis</i> NRRL 18488, the primary producer of the immunosuppressant FK506, was analyzed to elucidate regulatory features of secondary metabolism. Completion of its 7.9-Mb linear genome enabled accurate re-annotation of the FK506 biosynthetic gene cluster (BGC). Transcriptome analysis during BGC activation revealed major transcriptional shifts from primary to secondary metabolism, especially in genes involved in FK506 biosynthesis and lysine metabolism. Primary transcriptome mapping identified 1,225 transcription units and uncovered post-transcriptional regulation of allylmalonyl-CoA production, a key FK506 precursor. Ribosome profiling demonstrated that AT-rich codons reduce translational efficiency in <i>S. tsukubaensis</i>, with pronounced ribosome pausing at the TTA codon within the FK506 BGC. Substituting this codon relieved pausing and improved FK506 production. Together, these integrative genomic, transcriptomic, and translatomic analyses highlight how multi-level regulatory mechanisms shape secondary metabolism in <i>Streptomyces</i>. This work offers insights into metabolic control that could inform future efforts in strain improvement for efficient natural products production.

iScienceVol. 28(6)
QB3 (US), Seoul National University (KR), Lawrence Berkeley National Laboratory (US), Korea Advanced Institute of Science and Technology (KR), Novo Nordisk Foundation (DK), University of California San Diego (US), Joint BioEnergy Institute (US), University of California, Berkeley (US), Technical University of Denmark (DK)
National Research Foundation of Korea, Novo Nordisk Fonden, Ministry of Science and ICT, South Korea, Office of Science, University of California, San Diego
Zero hunger
Openalex Percentile: Top 17%
RNA and protein synthesis mechanisms
1.61
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