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Biotechnological production and application of the antibiotic pimaricin: biosynthesis and its regulation.抗生素匹马霉素的生物技术生产与应用:生物合成及其调控
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四级调控基因控制多烯类抗生素棘白菌素在 FR-008 株中的产生。

A Hierarchical Network of Four Regulatory Genes Controlling Production of the Polyene Antibiotic Candicidin in sp. Strain FR-008.

机构信息

The State Key Laboratory of Microbial Technology, Shandong University, Qingdao, China.

Shandong Medicinal Biotechnology Center, Shandong Academy of Medical Sciences, Jinan, China.

出版信息

Appl Environ Microbiol. 2020 Apr 17;86(9). doi: 10.1128/AEM.00055-20.

DOI:10.1128/AEM.00055-20
PMID:32086301
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7170484/
Abstract

The four regulatory genes to in sp. strain FR-008 form a genetic arrangement that is widely distributed in macrolide-producing bacteria. Our previous work has demonstrated that and are critical for production of the polyene antibiotic candicidin. In this study, we further characterized the roles of the other two regulatory genes, and , focusing on the relationship between these four regulatory genes. Disruption of a single or multiple regulatory genes did not affect bacterial growth, but transcription of genes in the candicidin biosynthetic gene cluster decreased, and candicidin production was abolished, indicating a critical role for each of the four regulatory genes, including and , in candicidin biosynthesis. We found that to , although differentially expressed throughout the growth phase, displayed similar temporal expression patterns, with an abrupt increase in the early exponential phase, coincident with initial detection of antibiotic production in the same phase. Our data suggest that the four regulatory genes to have various degrees of control over structural genes in the biosynthetic cluster under the conditions examined. Extensive transcriptional analysis indicated that complex regulation exists between these four regulatory genes, forming a regulatory network, with and functioning at a lower level. Comprehensive cross-complementation analysis indicates that functional complementation is restricted among the four regulators and unidirectional, with complementing the loss of or - and complementing loss of Our study provides more insights into the roles of, and the regulatory network formed by, these four regulatory genes controlling production of an important pharmaceutical compound. The regulation of antibiotic biosynthesis by species is complex, especially for biosynthetic gene clusters with multiple regulatory genes. The biosynthetic gene cluster for the polyene antibiotic candicidin contains four consecutive regulatory genes, which encode regulatory proteins from different families and which form a subcluster within the larger biosynthetic gene cluster in sp. FR-008. Syntenic arrangements of these regulatory genes are widely distributed in polyene gene clusters, such as the amphotericin and nystatin gene clusters, suggesting a conserved regulatory mechanism controlling production of these clinically important medicines. However, the relationships between these multiple regulatory genes are unknown. In this study, we determined that each of these four regulatory genes is critical for candicidin production. Additionally, using transcriptional analyses, bioassays, high-performance liquid chromatography (HPLC) analysis, and genetic cross-complementation, we showed that FscR1 to FscR4 comprise a hierarchical regulatory network that controls candicidin production and is likely representative of how expression of other polyene biosynthetic gene clusters is controlled.

摘要

四个调控基因 to 在 sp. strain FR-008 中形成了一种广泛分布于产生大环内酯类抗生素的细菌中的遗传排列。我们之前的工作表明和是产生多烯抗生素坎地西丁的关键。在这项研究中,我们进一步研究了另外两个调控基因和的作用,重点是这四个调控基因之间的关系。单个或多个调控基因的缺失并不影响细菌的生长,但坎地西丁生物合成基因簇中的基因转录减少,坎地西丁的产量被消除,这表明这四个调控基因,包括和,在坎地西丁生物合成中都起着关键作用。我们发现,尽管在整个生长阶段都有差异表达,但和表现出相似的时间表达模式,在早期指数期突然增加,与同一阶段抗生素产生的初始检测相吻合。我们的数据表明,在研究条件下,这四个调控基因 to 对生物合成簇中的结构基因有不同程度的控制。广泛的转录分析表明,这四个调控基因之间存在着复杂的调节关系,形成了一个调节网络,和在较低水平起作用。全面的交叉互补分析表明,这四个调控因子之间存在功能互补,而且是单向的,互补了的缺失或-和的缺失互补了的缺失。我们的研究提供了更多关于这四个调控基因在控制重要药物化合物产生中的作用和调控网络的见解。物种抗生素生物合成的调控是复杂的,特别是对于具有多个调控基因的生物合成基因簇。多烯抗生素坎地西丁的生物合成基因簇包含四个连续的调控基因,它们编码来自不同家族的调节蛋白,并在 sp. FR-008 中的较大生物合成基因簇内形成一个亚簇。这些调控基因的同线性排列广泛分布于多烯基因簇中,如两性霉素和制霉菌素基因簇,这表明存在一种保守的调控机制来控制这些临床上重要的药物的产生。然而,这些多个调控基因之间的关系尚不清楚。在这项研究中,我们确定了这四个调控基因中的每一个都对坎地西丁的产生至关重要。此外,我们通过转录分析、生物测定、高效液相色谱(HPLC)分析和遗传交叉互补实验,表明 FscR1 到 FscR4 构成了一个层次化的调控网络,控制着坎地西丁的产生,这可能代表了其他多烯生物合成基因簇的表达是如何被控制的。