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长时间冷冻复苏过程中的比较蛋白质组学和形态学变化分析

Comparative Proteomic and Morphological Change Analyses of During Resuscitation From Prolonged Freezing.

作者信息

Suo Biao, Yang Hua, Wang Yuexia, Lv Haipeng, Li Zhen, Xu Chao, Ai Zhilu

机构信息

College of Food Science and Technology, Henan Agricultural University, Zhengzhou, China.

Key Laboratory of Staple Grain Processing, Ministry of Agriculture, Zhengzhou, China.

出版信息

Front Microbiol. 2018 May 3;9:866. doi: 10.3389/fmicb.2018.00866. eCollection 2018.

Abstract

When frozen, survives in a sublethally injured state. However, can recover at a suitable temperature, which poses a threat to food safety. To elucidate the resuscitation mechanism of freezing survived , we used cells stored at -18°C for 90 days as controls. After resuscitating the survived cells at 37°C, the viable cell numbers were determined on tryptic soy agar with 0.6% yeast extract (TSAYE), and the non-injured-cell numbers were determined on TSAYE supplemented with 10% NaCl. The results showed that the total viable cell number did not increase within the first 3 h of resuscitation, but the osmotic regulation ability of freezing survived cells gradually recovered to the level of healthy cells, which was evidenced by the lack of difference between the two samples seen by differential cell enumeration. Scanning electron microscopy (SEM) showed that, compared to late exponential stage cells, some frozen survived cells underwent splitting and cell lysis due to deep distortion and membrane rupture. Transmission electron microscopy (TEM) showed that, in most of the frozen survived cells, the nucleoids (low electronic density area) were loose, and the cytoplasmic matrices (high electronic density area) were sparse. Additionally, a gap was seen to form between the cytoplasmic membranes and the cell walls in the frozen survived cells. The morphological changes were restored when the survived cells were resuscitated at 37°C. We also analyzed the differential proteome after resuscitation using non-labeled high-performance liquid chromatography-mass spectrometry (HPLC-MS). The results showed that, compared with freezing survived cells, the cells resuscitated for 1 h had 45 upregulated and 73 downregulated proteins. The differentially expressed proteins were functionally categorized by gene ontology enrichment, KEGG pathway, and STRING analyses. Cell membrane synthesis-related proteins, oxidative stress resistance-related proteins, metabolism-related proteins, and virulence factors exhibited distinct expression patterns during resuscitation. These findings have implications in the understanding of the resuscitation mechanism of freezing survived , which may facilitate the development of novel technologies for improved detection and control of foodborne pathogens in frozen food.

摘要

冷冻时,[某种微生物]以亚致死损伤状态存活。然而,[该微生物]能在适宜温度下复苏,这对食品安全构成威胁。为阐明冷冻存活的[某种微生物]的复苏机制,我们将在-18°C储存90天的细胞用作对照。在37°C复苏存活细胞后,在含有0.6%酵母提取物的胰蛋白胨大豆琼脂(TSAYE)上测定活细胞数,在添加10% NaCl的TSAYE上测定未损伤细胞数。结果表明,复苏的前3小时内总活细胞数未增加,但冷冻存活细胞的渗透调节能力逐渐恢复到健康细胞水平,这通过差异细胞计数显示的两个样本之间无差异得以证明。扫描电子显微镜(SEM)显示,与指数生长后期细胞相比,一些冷冻存活细胞因深度变形和膜破裂而发生分裂和细胞裂解。透射电子显微镜(TEM)显示,在大多数冷冻存活细胞中,类核(低电子密度区域)松散,细胞质基质(高电子密度区域)稀疏。此外,在冷冻存活细胞的细胞质膜和细胞壁之间可见形成间隙。当存活细胞在37°C复苏时,形态变化得以恢复。我们还使用非标记高效液相色谱-质谱联用(HPLC-MS)分析了复苏后的差异蛋白质组。结果表明,与冷冻存活的[某种微生物]细胞相比,复苏1小时的细胞有45种上调蛋白和73种下调蛋白。通过基因本体富集、KEGG通路和STRING分析对差异表达蛋白进行功能分类。细胞膜合成相关蛋白、抗氧化应激相关蛋白、代谢相关蛋白和毒力因子在复苏过程中表现出不同的表达模式。这些发现有助于理解冷冻存活的[某种微生物]的复苏机制,可能有助于开发新技术以改进冷冻食品中食源性病原体的检测和控制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c583/5943506/d27e2e0d9c27/fmicb-09-00866-g002.jpg

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