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联合转录组和泛基因组分析指导代谢改良以提高天蚕菌素的产量。

Combined transcriptomic and pangenomic analyses guide metabolic amelioration to enhance tiancimycins production.

机构信息

Xiangya International Academy of Translational Medicine, Central South University, Yuelu District, Tongzipo Road, #172, Changsha, 410013, Hunan, China.

Hunan Engineering Research Center of Combinatorial Biosynthesis and Natural Product Drug Discovery, National Engineering Research Center of Combinatorial Biosynthesis for Drug Discovery, Changsha, 410013, Hunan, China.

出版信息

Appl Microbiol Biotechnol. 2024 Dec;108(1):18. doi: 10.1007/s00253-023-12937-y. Epub 2024 Jan 3.

Abstract

Exploration of high-yield mechanism is important for further titer improvement of valuable antibiotics, but how to achieve this goal is challenging. Tiancimycins (TNMs) are anthraquinone-fused enediynes with promising drug development potentials, but their prospective applications are limited by low titers. This work aimed to explore the intrinsic high-yield mechanism in previously obtained TNMs high-producing strain Streptomyces sp. CB03234-S for the further titer amelioration of TNMs. First, the typical ribosomal RpsL(K43N) mutation in CB03234-S was validated to be merely responsible for the streptomycin resistance but not the titer improvement of TNMs. Subsequently, the combined transcriptomic, pan-genomic and KEGG analyses revealed that the significant changes in the carbon and amino acid metabolisms could reinforce the metabolic fluxes of key CoA precursors, and thus prompted the overproduction of TNMs in CB03234-S. Moreover, fatty acid metabolism was considered to exert adverse effects on the biosynthesis of TNMs by shunting and reducing the accumulation of CoA precursors. Therefore, different combinations of relevant genes were respectively overexpressed in CB03234-S to strengthen fatty acid degradation. The resulting mutants all showed the enhanced production of TNMs. Among them, the overexpression of fadD, a key gene responsible for the first step of fatty acid degradation, achieved the highest 21.7 ± 1.1 mg/L TNMs with a 63.2% titer improvement. Our studies suggested that comprehensive bioinformatic analyses are effective to explore metabolic changes and guide rational metabolic reconstitution for further titer improvement of target products. KEY POINTS: • Comprehensive bioinformatic analyses effectively reveal primary metabolic changes. • Primary metabolic changes cause precursor enrichment to enhance TNMs production. • Strengthening of fatty acid degradation further improves the titer of TNMs.

摘要

探索高产机制对于进一步提高有价值抗生素的效价非常重要,但如何实现这一目标具有挑战性。天蚕菌素(TNMs)是具有有前途的药物开发潜力的蒽醌融合烯二炔,但由于效价低,其应用前景受到限制。本工作旨在探索先前获得的 TNMs 高产菌株链霉菌 sp.CB03234-S 中的内在高产机制,以进一步提高 TNMs 的效价。首先,验证了 CB03234-S 中的典型核糖体 RpsL(K43N)突变仅负责链霉素抗性,而不负责 TNMs 的效价提高。随后,联合转录组、泛基因组和 KEGG 分析表明,碳和氨基酸代谢的显著变化可以增强关键 CoA 前体的代谢通量,从而促使 CB03234-S 中 TNMs 的过度产生。此外,脂肪酸代谢被认为通过分流和减少 CoA 前体的积累对 TNMs 的生物合成产生不利影响。因此,分别在 CB03234-S 中过表达相关基因的不同组合以加强脂肪酸降解。所得突变体均表现出 TNMs 产量的提高。其中,负责脂肪酸降解第一步的关键基因 fadD 的过表达使 TNMs 的产量达到最高 21.7±1.1mg/L,效价提高了 63.2%。我们的研究表明,全面的生物信息学分析可有效探索代谢变化并指导合理的代谢重构,以进一步提高目标产物的效价。要点:•全面的生物信息学分析有效地揭示了主要的代谢变化。•主要代谢变化导致前体富集以增强 TNMs 的产量。•加强脂肪酸降解进一步提高了 TNMs 的效价。

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