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Vibralactone Biogenesis-Associated Analogues from Submerged Cultures of the Fungus Boreostereum vibrans.来自真菌振动拟层孔菌深层培养物的与振动内酯生物合成相关的类似物。
Nat Prod Bioprospect. 2018 Feb;8(1):37-45. doi: 10.1007/s13659-017-0147-5. Epub 2017 Dec 5.
2
RNAi-mediated down-regulation of a melanin polyketide synthase (pks1) gene in the fungus Slafractonia leguminicola.RNA干扰介导的豆科刺盘孢菌中黑色素聚酮合酶(pks1)基因的下调。
World J Microbiol Biotechnol. 2017 Sep 20;33(10):179. doi: 10.1007/s11274-017-2346-y.
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Secondary Metabolites from Higher Fungi.高等真菌的次生代谢产物
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Membrane fluidity is involved in the regulation of heat stress induced secondary metabolism in Ganoderma lucidum.膜流动性参与调控灵芝中热胁迫诱导的次生代谢。
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Biochemical and genetic basis of orsellinic acid biosynthesis and prenylation in a stereaceous basidiomycete.
Fungal Genet Biol. 2017 Jan;98:12-19. doi: 10.1016/j.fgb.2016.11.007. Epub 2016 Nov 27.
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Functional analysis of the role of glutathione peroxidase (GPx) in the ROS signaling pathway, hyphal branching and the regulation of ganoderic acid biosynthesis in Ganoderma lucidum.谷胱甘肽过氧化物酶(GPx)在灵芝活性氧信号通路、菌丝分支及灵芝酸生物合成调控中的作用的功能分析
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Vib-PT,一种参与 Vibralactone 生物合成的芳香基 prenyltransferase,来自.

Vib-PT, an Aromatic Prenyltransferase Involved in the Biosynthesis of Vibralactone from .

机构信息

State Key Laboratory for Conservation and Utilization of Bio-Resources in Yunnan and Key Laboratory for Microbial Resources of the Ministry of Education, Yunnan University, Kunming, People's Republic of China.

Department of Chemistry, University of Nebraska-Lincoln, Lincoln, Nebraska, USA.

出版信息

Appl Environ Microbiol. 2020 May 5;86(10). doi: 10.1128/AEM.02687-19.

DOI:10.1128/AEM.02687-19
PMID:32144102
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7205494/
Abstract

Vibralactone, a hybrid compound derived from phenols and a prenyl group, is a strong pancreatic lipase inhibitor with a rare fused bicyclic β-lactone skeleton. Recently, a researcher reported a vibralactone derivative (compound C1) that caused inhibition of pancreatic lipase with a half-maximal inhibitory concentration of 14 nM determined by structure-based optimization, suggesting a potential candidate as a new antiobesity treatment. In the present study, we sought to identify the main gene encoding prenyltransferase in , which is responsible for the prenylation of phenol leading to vibralactone synthesis. Two RNA silencing transformants of the identified gene () were obtained through -mediated transformation. Compared to wild-type strains, the transformants showed a decrease in expression ranging from 11.0 to 56.0% at 5, 10, and 15 days in reverse transcription-quantitative PCR analysis, along with a reduction in primary vibralactone production of 37 to 64% at 15 and 21 days, respectively, as determined using ultra-high-performance liquid chromatography-mass spectrometry analysis. A soluble and enzymatically active fusion Vib-PT protein was obtained by expressing in , and the enzyme's optimal reaction conditions and catalytic efficiency ( /) were determined. experiments established that Vib-PT catalyzed the -prenylation at C-3 of 4-hydroxy-benzaldehyde and the -prenylation at the 4-hydroxy of 4-hydroxy-benzenemethanol in the presence of dimethylallyl diphosphate. Moreover, Vib-PT shows promiscuity toward aromatic compounds and prenyl donors. Vibralactone is a lead compound with a novel skeleton structure that shows strong inhibitory activity against pancreatic lipase. Vibralactone is not encoded by the genome directly but rather is synthesized from phenol, followed by prenylation and other enzyme reactions. Here, we used an RNA silencing approach to identify and characterize a prenyltransferase in a basidiomycete species that is responsible for the synthesis of vibralactone. The identified gene, , was expressed in to obtain a soluble and enzymatically active fusion Vib-PT protein. characterization of the enzyme demonstrated the catalytic mechanism of prenylation and broad substrate range for different aromatic acceptors and prenyl donors. These characteristics highlight the possibility of Vib-PT to generate prenylated derivatives of aromatics and other compounds as improved bioactive agents or potential prodrugs.

摘要

振动内酯是一种源自酚类和异戊烯基的杂合化合物,是一种具有罕见稠合双环β-内酰胺骨架的强效胰腺脂肪酶抑制剂。最近,一位研究人员报道了一种振动内酯衍生物(化合物 C1),其通过基于结构的优化确定的胰腺脂肪酶抑制的半数最大抑制浓度为 14 nM,这表明它可能成为一种新的抗肥胖治疗候选药物。在本研究中,我们试图鉴定出负责酚类异戊烯基化导致振动内酯合成的 中编码异戊烯基转移酶的主要基因。通过介导的转化获得了两个鉴定基因()的 RNA 沉默转化体。与野生型菌株相比,转化体在反转录定量 PCR 分析中在 5、10 和 15 天的表达水平降低了 11.0%至 56.0%,同时在 15 和 21 天的初级振动内酯产量分别降低了 37%至 64%,这是通过超高效液相色谱-质谱分析确定的。通过在 中表达 获得了可溶性和酶活性融合 Vib-PT 蛋白,并确定了酶的最佳反应条件和催化效率( /)。实验确定 Vib-PT 在二甲基烯丙基二磷酸存在下催化 4-羟基苯甲醛的 C-3-异戊烯基化和 4-羟基苯甲醇的 4-羟基异戊烯基化。此外,Vib-PT 对芳香族化合物和异戊烯供体表现出混杂性。振动内酯是一种具有新型骨架结构的先导化合物,对胰腺脂肪酶表现出强烈的抑制活性。振动内酯不是直接由基因组编码的,而是由酚类合成的,然后进行异戊烯基化和其他酶反应。在这里,我们使用 RNA 沉默方法鉴定和表征了担子菌物种中负责振动内酯合成的异戊烯基转移酶。鉴定的基因 ,在 中表达以获得可溶性和酶活性融合 Vib-PT 蛋白。对酶的表征表明了异戊烯基化的催化机制和不同芳香受体和异戊烯供体的广泛底物范围。这些特征突出了 Vib-PT 生成芳香族化合物和其他化合物的异戊烯基化衍生物作为改进的生物活性试剂或潜在前药的可能性。