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首页> 外文期刊>Postharvest Biology and Technology >Identification of bitter pit protein markers in Malus domestica using differential in-gel electrophoresis (DIGE) and LC-MS/MS
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Identification of bitter pit protein markers in Malus domestica using differential in-gel electrophoresis (DIGE) and LC-MS/MS

机译:使用差动凝胶电泳(DIGE)和LC-MS / MS鉴定Malus Domestica中苦坑蛋白标记物的鉴定

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摘要

Bitter pit is a physiological disorder that occurs in apple, pear and quince and has long been associated with calcium uptake or lack thereof. In the present study, pooled biological Malus domestica proteins were collected from healthy and naturally occurring bitter pit fruit. Protein samples (bitter pit and healthy) were analyzed with differential in-gel electrophoresis (DIGE) and SameSpots software was used to compare gel spots by intensity. Identified spots (p 0.05) were spot picked and trypsin digested. Peptides were separated by liquid chromatography (LC) and submitted to LTQ-Orbitrap mass spectrometer to infer protein identification. A total of 200 +/- 5 protein spots were detected, 41 spots classified as having p 0.05 and were successfully identified by their peptide sequence listed in an online M. domestica database. Thirteen spots were identified as having p 0.05 and a minimum 2-fold change. Several pathogenesis-related (PR) proteins belonging to three PR families, PR-5 (10.3-fold), PR8/chitinase (35.5-fold) and PR-10 (6.8-fold) were upregulated in bitter pit sampled tissues. Three proteins involved in several metabolic processes including ethylene biosynthesis (3.3-fold), glycosyltransferase reactions in metabolism (2.3-fold) and metal biding (11.1-fold) were found to be overly expressed in healthy sampled tissues. This research provides a significant advance in the knowledge of protein expression alterations occurring in bitter pit in comparison with sound tissues. (C) 2015 Elsevier B.V. All rights reserved.
机译:苦坑是一种在苹果,梨和柑橘中发生的生理疾病,长期与钙吸收或缺乏有关。在本研究中,从健康和天然存在的苦坑果实中收集了汇集的生物明星蛋白。用差动凝胶电泳(DIGE)分析蛋白质样品(苦坑和健康),并且SAMESPOS软件用于通过强度比较凝胶斑点。鉴定的斑点(p <0.05)是挑选的,胰蛋白酶消化。用液相色谱(LC)分离肽,并提交至LTQ-甲叠质谱仪,以推断蛋白质鉴定。检测到总共200 +/- 5蛋白斑点,归类为具有P&的41个斑点。 0.05并通过其在线M. Domestica数据库中列出的肽序列成功鉴定。将十三个斑点鉴定为具有p& 0.05和至少2倍的变化。属于三个PR家族的几种致病性相关(PR)蛋白,PR-5(10.3倍),PR8 / Chitinase(35.5倍)和Pr-10(6.8倍)在苦坑采样组织中上调。参与包括乙烯生物合成(3.3倍)的几种代谢过程的三种蛋白质,发现代谢中的糖基转移酶反应(2.3倍)和金属凸糊(11.1倍)在健康的采样组织中过度表达。该研究在与声音组织相比,在苦坑中发生的蛋白质表达改变的知识提供了显着提前。 (c)2015 Elsevier B.v.保留所有权利。

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