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Comparative Proteomic Analysis of saccharopolyspora spinosa SP06081 and PR2 strains reveals the differentially expressed proteins correlated with the increase of spinosad yield

机译:糖多孢菌SP06081和PR2菌株的比较蛋白质组学分析显示差异表达的蛋白质与多杀菌素产量的增加有关

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Background Saccharopolyspora spinosa produces the environment-friendly biopesticide spinosad, a mixture of two polyketide-derived macrolide active ingredients called spinosyns A and D. Therefore considerable interest is in the improvement of spinosad production because of its low yield in wild-type S. spinosa. Recently, a spinosad-hyperproducing PR2 strain with stable heredity was obtained from protoplast regeneration of the wild-type S. spinosa SP06081 strain. A comparative proteomic analysis was performed on the two strains during the first rapid growth phase (RG1) in seed medium (SM) by using label-free quantitative proteomics to investigate the underlying mechanism leading to the enhancement of spinosad yield. Results In total, 224 proteins from the SP06081 strain and 204 proteins from the PR2 strain were unambiguously identified by liquid chromatography-tandem mass spectrometry analysis, sharing 140 proteins. A total of 12 proteins directly related to spinosad biosynthesis were identified from the two strains in RG1. Comparative analysis of the shared proteins revealed that approximately 31% of them changed their abundance significantly and fell in all of the functional groups, such as tricarboxylic acid cycles, glycolysis, biosynthetic processes, catabolic processes, transcription, translation, oxidation and reduction. Several key enzymes involved in the synthesis of primary metabolic intermediates used as precursors for spinosad production, energy supply, polyketide chain assembly, deoxysugar methylation, and antioxidative stress were differentially expressed in the same pattern of facilitating spinosad production by the PR2 strain. Real-time reverse transcriptase polymerase chain reaction analysis revealed that four of five selected genes showed a positive correlation between changes at the translational and transcriptional expression level, which further confirmed the proteomic analysis. Conclusions The present study is the first comprehensive and comparative proteome analysis of S. spinosa strains. Our results highlight the differentially expressed proteins between the two S. spinosa strains and provide some clues to understand the molecular and metabolic mechanisms that could lead to the increased spinosad production yield.
机译:背景棘孢糖质多孢菌(Saccharopolyspora spinosa)生产环境友好型生物农药多杀菌素(spinosad),这是两种聚酮化合物衍生的大环内酯活性成分称为多杀菌素A和D的混合物。因此,由于在野生型多杀葡萄球菌中产量低,人们对提高多杀菌素的生产具有相当大的兴趣。最近,从野生型刺糖多孢菌SP06081菌株的原生质体再生中获得了具有稳定遗传的多刺多孢素高产PR2菌株。通过使用无标记的定量蛋白质组学研究了导致多杀菌素产量提高的潜在机理,在种子培养基(SM)的第一个快速生长阶段(RG1)期间对这两个菌株进行了比较蛋白质组学分析。结果液相色谱-串联质谱分析共鉴定出SP06081菌株中的224种蛋白质和PR2菌株中的204种蛋白质,共有140种蛋白质。从RG1的两个菌株中鉴定出总共12个与多杀菌素生物合成直接相关的蛋白质。共享蛋白的比较分析表明,其中约31%的蛋白显着改变了其丰度,并落在所有功能基团中,例如三羧酸循环,糖酵解,生物合成过程,分解代谢过程,转录,翻译,氧化和还原。几种主要的代谢中间体的合成中涉及的几种关键酶被用作多杀菌素生产,能量供应,聚酮化合物链组装,脱氧糖甲基化和抗氧化应激的前体,它们以相同的模式差异表达,以促进PR2菌株产生多杀菌素。实时逆转录酶聚合酶链反应分析表明,五个选定的基因中有四个在翻译和转录表达水平的变化之间呈正相关,这进一步证实了蛋白质组学分析。结论本研究是棘刺葡萄球菌菌株的首次综合和比较蛋白质组分析。我们的结果突出了两个棘孢链霉菌菌株之间差异表达的蛋白质,并提供了一些线索来了解可能导致棘藻类产量增加的分子和代谢机制。

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