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Label free quantitative analysis of Alicyclobacillus acidoterrestris spore germination subjected to low ambient pH

机译:环境低pH条件下酸环脂环酸芽孢杆菌萌发的无标记定量分析

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Inhibition of spore germination or sterilization after induction of spore germination would effectively control low pH food spoilage caused by Alicyclobacillus acidoterrestris spores. However, the characteristics and mechanisms of A. acidoterrestris spore germination in low ambient pH remains poorly understood. In this study, the germination rate of A. acidoterrestris spores at different ambient pH conditions was determined, and subsequently the proteomic profiles of A. acidoterrestris in spore germination were analysed by label-free quantification, in which the specific metabolic pathways involved were identified and key functional proteins were screened and validated using RT-qPCR (real time quantitative PCR). The suitable ambient pH value for the spore germination of A. acidoterrestris ranged from 3.0 to 5.0 with the optimum pH of 4.0. According to the LC-ESI-MS/MS (liquid chromatography electrospray ionization tandem mass spectrometry) analysis, 98 proteins of geminated spores of A. acidoterrestris incubated for 2 h at pH 3.0 were changed significantly in comparison to non-germinated spores, the expression of 20 proteins were up-regulated and that of 78 proteins down-regulated respectively. Those differential expressed proteins were mainly involved in cell wall hydrolysis, cell morphological changes, protein synthesis and folding, perception of external stimuli and signal transduction etc., and we observed that germination receptor D (GerD), cell wall hydrolase, transpeptidase, peptidase Si and two-component regulatory system phoR were significantly up-regulated, but hydrolase NlpC/P60, peptidoglycan glycosyltransferase, spore coat proteins CotX, CotJB and the Lrp/AsnC (leucine-responsive regulatory protein/asparagine synthase C products) protein were significantly down-regulated in the experiment, which implied the important roles of identified proteins during the spore germination. Furthermore, the pathway analysis showed the possible involvement of differentially expressed proteins in the p-lactam resistance, ribosome, biosynthesis of secondary metabolites, pyruvate metabolism, two-component system and other metabolic pathways, which indicated that synthesis and hydrolysis of cell wall, intracellular substance synthesis, energy generation and signal transduction were likely associated with the initiation of spore germination and restoration of vegetative growth. In conclusion, the quantitative proteomic landscape of A. acidoterrestris spores could provide the theoretic and experimental evidences for the hazard control of A. acidoterrestris spores in the thermal pasteurization process of acidic beverages industry.
机译:诱导孢子萌发后抑制孢子萌发或灭菌将有效控制由酸热脂环酸杆菌引起的低pH值食物腐败。但是,在较低的环境pH中,酸曲霉孢子萌发的特征和机理仍然知之甚少。在这项研究中,确定了在不同环境pH条件下酸曲霉孢子的萌发率,然后通过无标记定量分析了酸曲霉在孢子萌发中的蛋白质组学特征,从而确定了涉及的具体代谢途径并使用RT-qPCR(实时定量PCR)筛选并验证了关键功能蛋白。酸曲霉孢子萌发的合适环境pH值为3.0至5.0,最佳pH为4.0。根据LC-ESI-MS / MS(液相色谱电喷雾串联电离质谱)分析,在pH 3.0下温育2 h的嗜酸拟南芥萌发孢子的98种蛋白质与未萌发的孢子相比发生了显着变化。分别有20种蛋白被上调和78种蛋白被下调。这些差异表达的蛋白质主要参与细胞壁水解,细胞形态变化,蛋白质合成和折叠,外界刺激的感知和信号转导等,并且我们观察到萌发受体D(GerD),细胞壁水解酶,转肽酶,肽酶Si和两组分调节系统phoR显着上调,但是水解酶NlpC / P60,肽聚糖糖基转移酶,孢子外壳蛋白CotX,CotJB和Lrp / AsnC(亮氨酸反应性调节蛋白/天冬酰胺合成酶C产物)显着下调。在实验中进行了调控,这暗示了鉴定出的蛋白质在孢子萌发过程中的重要作用。此外,该途径分析表明差异表达的蛋白可能参与了对内酰胺的抗性,核糖体,次生代谢产物的生物合成,丙酮酸代谢,二组分系统和其他代谢途径,这表明细胞壁,细胞内的合成和水解物质合成,能量产生和信号转导可能与孢子萌发的开始和营养生长的恢复有关。综上所述,酸质假单胞菌孢子的定量蛋白质组学格局可为酸性饮料工业热巴氏灭菌过程中的危害性控制提供理论和实验依据。

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