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首页> 外文期刊>Applied Microbiology and Biotechnology >Quorum-sensing antagonist (5Z)-4-bromo-5-(bromomethylene)-3-butyl-2(5H)-furanone influences siderophore biosynthesis in Pseudomonas putida and Pseudomonas aeruginosa
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Quorum-sensing antagonist (5Z)-4-bromo-5-(bromomethylene)-3-butyl-2(5H)-furanone influences siderophore biosynthesis in Pseudomonas putida and Pseudomonas aeruginosa

机译:仲裁感应拮抗剂(5Z)-4-溴-5-(溴亚甲基)-3-丁基-2(5H)-呋喃酮影响恶臭假单胞菌和铜绿假单胞菌的铁载体生物合成

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摘要

Siderophore synthesis of Pseudomonas putida F1 was found to be regulated by quorum sensing since normalized siderophore production (per cell) increased 4.2-fold with cell density after the cells entered middle exponential phase; similarly, normalized siderophore concentrations in Pseudomonas aeruginosa JB2 increased 28-fold, and a 5.5-fold increase was seen for P. aeruginosa PAO1. Further evidence of the link between quorum sensing and siderophore synthesis of P. putida F1 was that the quorum-sensing-disrupter (5Z)-4-bromo-5-(bromomethylene)-3-butyl-2(5H)-furanone (furanone) from the marine red alga Delisea pulchra was found to inhibit the formation of the siderophore produced by P. putida F1 in a concentration-dependent manner, with 57% siderophore synthesis repressed by 100 μg/ml furanone. In contrast, this furanone did not affect the siderophore synthesis of Burkholderia cepacia G4 at 20–40 μg/ml, and stimulated siderophore synthesis of P. aeruginosa JB2 2.5- to 3.7-fold at 20–100 μg/ml. Similarly, 100 μg/ml furanone stimulated siderophore synthesis in P. aeruginosa PAO1 about 3.5-fold. The furanone appears to interact with the quorum-sensing machinery of P. aeruginosa PAO1 since it stimulates less siderophore synthesis in the P. aeruginosa qscR quorum-sensing mutant (QscR is a negative regulator of LasI, an acylated homoserine lactone synthase).
机译:发现恶臭假单胞菌F1的铁载体合成受群体感应调控,因为在细胞进入中间指数期后,标准化的铁载体产量(每细胞)随细胞密度的增加增加了4.2倍。同样,铜绿假单胞菌JB2中的标准化铁载体浓度增加了28倍,而铜绿假单胞菌PAO1则增加了5.5倍。恶臭假单胞菌F1群体感应与铁载体合成之间联系的进一步证据是群体感应破坏者(5Z)-4-溴-5-(溴亚甲基)-3-丁基-2(5H)-呋喃酮(呋喃酮) )发现来自海洋红藻的Delisea pulchra以浓度依赖的方式抑制恶臭假单胞菌F1产生的铁载体的形成,其中100%g / ml呋喃酮抑制了57%的铁载体合成。相比之下,该呋喃酮在20–40μg/ ml时不影响洋葱伯克霍尔德菌G4的铁载体合成,而在20–100μg/ ml时刺激铜绿假单胞菌JB2的铁载体合成为2.5- 3.7倍。同样,100μg/ ml呋喃酮可刺激铜绿假单胞菌PAO1中的铁载体合成约3.5倍。呋喃酮似乎与铜绿假单胞菌PAO1的群体感应机制相互作用,因为它刺激了铜绿假单胞菌qscR群体感应突变体(QscR是LasI(一种酰化的高丝氨酸内酯合酶)的负调控子)中较少的铁载体合成。

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  • 来源
    《Applied Microbiology and Biotechnology》 |2005年第6期|689-695|共7页
  • 作者单位

    Departments of Chemical Engineering and Molecular Cell Biology University of ConnecticutChemical and Biomolecular Engineering Cornell University;

    Departments of Chemical Engineering and Molecular Cell Biology University of Connecticut;

    Departments of Chemical Engineering and Molecular Cell Biology University of Connecticut;

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