PurR家族转录调节因子促进糖多孢子虫(Saccharopolyspora pogona)产生丁烯基旋蛋白

IF 3.9 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Applied Microbiology and Biotechnology Pub Date : 2025-01-21 DOI:10.1007/s00253-024-13390-1
Xinying Li, Jingnan Wang, Chang Su, Chao Guo, Zhouqin Xu, Kehui Wang, Jian Pang, Bo Lv, Chao Wang, Chun Li
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引用次数: 0

摘要

Butenyl-spinosyn是一种广谱、高效的生物杀虫剂,是从Saccharopolyspora pogona中提取的。然而,影响丁烯基- spinsyn合成的调控机制尚未完全阐明,阻碍了产量的提高。通过钴-60 γ射线诱变获得高产菌株S. pogona H2,其产量是野生型菌株S. pogona ASAGF58的2.7倍。通过比较S. pogona ASAGF58和H2的转录组学分析,阐明了利用更多的前体和能量合成丁烯基- spinsyn的高产机制。幸运的是,PurR家族转录调控因子TF00350被发现。TF00350过表达菌株RS00350诱导其形态分化和butenyl-spinosyn产量,最终使butenyl-spinosyn产量增加5.5倍(141.5±1.03 mg/L)。通过转录组学分析发现,嘌呤代谢途径相关基因大部分下调,丁烯基-spinosyn生物合成基因通过增加c-di-GMP浓度和降低c-di-AMP浓度而上调。这些结果为进一步挖掘关键调控因子和提高丁烯基- spinsyn的产量提供了有价值的见解。•通过60Co γ射线诱变获得了一株高产菌株。•转录组学鉴定出阳性调节因子TF00350,使丁烯基- spinsyn的产量增加5.5倍。•TF00350通过第二信使调节丁烯基- spinsyn的产生。
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The PurR family transcriptional regulator promotes butenyl-spinosyn production in Saccharopolyspora pogona

Butenyl-spinosyn, derived from Saccharopolyspora pogona, is a broad-spectrum and effective bioinsecticide. However, the regulatory mechanism affecting butenyl-spinosyn synthesis has not been fully elucidated, which hindered the improvement of production. Here, a high-production strain S. pogona H2 was generated by Cobalt-60 γ-ray mutagenesis, which showed a 2.7-fold increase in production compared to the wild-type strain S. pogona ASAGF58. A comparative transcriptomic analysis between S. pogona ASAGF58 and H2 was performed to elucidate the high-production mechanism that more precursors and energy were used to synthesize of butenyl-spinosyn. Fortunately, a PurR family transcriptional regulator TF00350 was discovered. TF00350 overexpression strain RS00350 induced morphological differentiation and butenyl-spinosyn production, ultimately leading to a 5.5-fold increase in butenyl-spinosyn production (141.5 ± 1.03 mg/L). Through transcriptomics analysis, most genes related to purine metabolism pathway were downregulated, and the butenyl-spinosyn biosynthesis gene was upregulated by increasing the concentration of c-di-GMP and decreasing the concentration of c-di-AMP. These results provide valuable insights for further mining key regulators and improving butenyl-spinosyn production.

A high production strain of S. pogona H2 was obtained by 60Co γ-ray mutagenesis.

Positive regulator TF00350 identified by transcriptomics, increasing butenyl-spinosyn production by 5.5-fold.

TF00350 regulated of butenyl-spinosyn production by second messengers.

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来源期刊
Applied Microbiology and Biotechnology
Applied Microbiology and Biotechnology 工程技术-生物工程与应用微生物
CiteScore
10.00
自引率
4.00%
发文量
535
审稿时长
2 months
期刊介绍: Applied Microbiology and Biotechnology focusses on prokaryotic or eukaryotic cells, relevant enzymes and proteins; applied genetics and molecular biotechnology; genomics and proteomics; applied microbial and cell physiology; environmental biotechnology; process and products and more. The journal welcomes full-length papers and mini-reviews of new and emerging products, processes and technologies.
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