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AdpA,一种发育调节剂,可促进白色链霉菌中 ε-聚赖氨酸的生物合成。

AdpA, a developmental regulator, promotes ε-poly-L-lysine biosynthesis in Streptomyces albulus.

机构信息

Key Laboratory of Molecular Microbiology and Technology, Ministry of Education, College of Life Sciences, Nankai University, Tianjin, 300071, China.

Key Laboratory of Bioactive Materials, Ministry of Education, College of Life Sciences, Nankai University, Tianjin, 300071, China.

出版信息

Microb Cell Fact. 2022 Apr 9;21(1):60. doi: 10.1186/s12934-022-01785-6.

Abstract

BACKGROUND

AdpA is a global regulator of morphological differentiation and secondary metabolism in Streptomyces, but the regulatory roles of the Streptomyces AdpA family on the biosynthesis of the natural product ε-poly-L-lysine (ε-PL) remain unidentified, and few studies have focused on increasing the production of ε-PL by manipulating transcription factors in Streptomyces.

RESULTS

In this study, we revealed the regulatory roles of different AdpA homologs in ε-PL biosynthesis and morphological differentiation and effectively promoted ε-PL production and sporulation in Streptomyces albulus NK660 by heterologously expressing adpA from S. neyagawaensis NRRLB-3092 (adpA). First, we identified a novel AdpA homolog named AdpA in S. albulus NK660 and characterized its function as an activator of ε-PL biosynthesis and morphological differentiation. Subsequently, four heterologous AdpA homologs were selected to investigate their phylogenetic relationships and regulatory roles in S. albulus, and AdpA was demonstrated to have the strongest ability to promote both ε-PL production and sporulation among these five AdpA proteins. The ε-PL yield of S. albulus heterologously expressing adpA was approximately 3.6-fold higher than that of the control strain. Finally, we clarified the mechanism of AdpA in enhancing ε-PL biosynthesis and its effect on ε-PL polymerization degree using real-time quantitative PCR, microscale thermophoresis and MALDI-TOF-MS. AdpA was purified, and its seven direct targets, zwf, tal, pyk2, pta, ack, pepc and a transketolase gene (DC74_2409), were identified, suggesting that AdpA may cause the redistribution of metabolic flux in central metabolism pathways, which subsequently provides more carbon skeletons and ATP for ε-PL biosynthesis in S. albulus.

CONCLUSIONS

Here, we characterized the positive regulatory roles of Streptomyces AdpA homologs in ε-PL biosynthesis and their effects on morphological differentiation and reported for the first time that AdpA promotes ε-PL biosynthesis by affecting the transcription of its target genes in central metabolism pathways. These findings supply valuable insights into the regulatory roles of the Streptomyces AdpA family on ε-PL biosynthesis and morphological differentiation and suggest that AdpA may be an effective global regulator for enhanced production of ε-PL and other valuable secondary metabolites in Streptomyces.

摘要

背景

AdpA 是链霉菌形态分化和次生代谢的全局调控因子,但链霉菌 AdpA 家族在天然产物 ε-聚赖氨酸(ε-PL)生物合成中的调控作用尚不清楚,并且很少有研究集中在通过操纵链霉菌中的转录因子来增加 ε-PL 的产量。

结果

在本研究中,我们揭示了不同 AdpA 同源物在 ε-PL 生物合成和形态分化中的调控作用,并通过异源表达来自 S. neyagawaensis NRRLB-3092(adpA)的 adpA,有效地促进了链霉菌 albulus NK660 中 ε-PL 的生产和产孢。首先,我们在 S. albulus NK660 中鉴定了一个新的 AdpA 同源物,命名为 AdpA,并表征了其作为 ε-PL 生物合成和形态分化激活剂的功能。随后,选择了四个异源 AdpA 同源物来研究它们在 S. albulus 中的系统发育关系和调控作用,结果表明 AdpA 是这五个 AdpA 蛋白中促进 ε-PL 生产和产孢能力最强的。异源表达 adpA 的 S. albulus 的 ε-PL 产量比对照菌株高约 3.6 倍。最后,我们使用实时定量 PCR、微量热泳动和 MALDI-TOF-MS 阐明了 AdpA 增强 ε-PL 生物合成及其对 ε-PL 聚合度的影响的机制。纯化了 AdpA,并鉴定了其七个直接靶标,zwf、tal、pyk2、pta、ack、pepc 和一个转酮醇酶基因(DC74_2409),表明 AdpA 可能导致中心代谢途径中代谢通量的重新分配,从而为 S. albulus 中 ε-PL 生物合成提供更多的碳骨架和 ATP。

结论

本研究描述了链霉菌 AdpA 同源物在 ε-PL 生物合成中的正调控作用及其对形态分化的影响,并首次报道 AdpA 通过影响中心代谢途径中靶基因的转录来促进 ε-PL 生物合成。这些发现为链霉菌 AdpA 家族对 ε-PL 生物合成和形态分化的调控作用提供了有价值的见解,并表明 AdpA 可能是增强 ε-PL 和其他有价值的链霉菌次生代谢产物生产的有效全局调控因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34c0/8994273/2f9264854ecf/12934_2022_1785_Fig1_HTML.jpg

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