首页> 美国卫生研究院文献>Antimicrobial Agents and Chemotherapy >Novel Cyclic Lipodepsipeptide from Pseudomonas syringae pv. lachrymans Strain 508 and Syringopeptin Antimicrobial Activities
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Novel Cyclic Lipodepsipeptide from Pseudomonas syringae pv. lachrymans Strain 508 and Syringopeptin Antimicrobial Activities

机译:丁香假单胞菌PV的新型环状脂肽肽。 lachrymans菌株508和Syringopeptin抗菌活性

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摘要

The syringopeptins are a group of antimicrobial cyclic lipodepsipeptides produced by several plant-associated pseudomonads. A novel syringopeptin, SP508, was shown to be produced as two homologs (A and B) by Pseudomonas syringae pv. lachrymans strain 508 from apple and to structurally resemble syringopeptin SP22. SP508 differed from SP22 and other syringopeptins by having three instead of four α,β-unsaturated amino acids and a longer β-hydroxy acyl chain. Both SP508 and SP22 displayed growth-inhibitory activities against Mycobacterium smegmatis, other gram-positive bacteria, and yeasts but not against gram-negative bacteria. Structure-activity analyses of the SP508 and SP22 homologs indicated chemical structural features that lead to enhanced antimycobacterial activity by these pseudomonad cyclic lipodepsipeptides.
机译:丁香脂肽是一组由几种植物相关的假单胞菌产生的抗微生物环脂肽。新型假单胞菌素SP508被显示为丁香假单胞菌PV的两个同源物(A和B)。苹果的lachrymans菌株508,在结构上类似于syringopeptin SP22。 SP508与SP22和其他syringopepteptins的区别在于,具有三个而不是四个α,β-不饱和氨基酸和一个更长的β-羟基酰基链。 SP508和SP22均显示出对耻垢分枝杆菌,其他革兰氏阳性菌和酵母菌的生长抑制活性,但对革兰氏阴性菌却无抑制作用。 SP508和SP22同源物的结构活性分析表明,化学结构特征可导致这些假单环环状脂肽肽增强抗分枝杆菌活性。

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