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首页> 外文期刊>Journal of genetics and genomics >Identification of differentially expressed proteins in poplar leaves induced by Marssonina brunnea f. sp. Multigermtubi
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Identification of differentially expressed proteins in poplar leaves induced by Marssonina brunnea f. sp. Multigermtubi

机译:鉴定Marssonina brunnea f。诱导的杨树叶片中差异表达的蛋白质。 sp。多菌灵

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摘要

Black spot disease in poplar is a disease of the leaf caused by fungus. The major pathogen is Marssonina brunnea f. sp. multigermtubi. To date, little is known about the molecular mechanism of poplar (M. brunnea) interaction. In order to identify the proteins related to disease resistance and understand its molecular basis, the clone "NL895" (P. euramericana CL"NL895"), which is highly resistant to M. brunnea f. sp. multigermtubi, was used in this study. We used two-dimensional gel electrophoresis (2-DE) and mass spectrometry (MS) to identify the proteins in poplar leaves that were differentially expressed in response to black spot disease pathogen, M. brunnea f. sp. multigermtubi. Proteins extracted from poplar leaves at 0, 12, 24, 48, and 72 h after pathogen-inoculation were separated by 2-DE. About 500 reproducible protein spots were detected, of which 40 protein spots displayed differential expression in levels and were subjected to Matrix assisted laser desorption/ionization time of flight mass spectrometry (MALDI-TOF MS) followed by database searching. According to the function, the identified proteins were sorted into five categories, that is, protein synthesis, metabolism, defense response and unclassified proteins.
机译:杨树的黑斑病是由真菌引起的叶病。主要病原体是布鲁氏菌Marssonina brunnea f。 sp。多菌灵迄今为止,关于杨(M. brunnea)相互作用的分子机理了解甚少。为了鉴定与抗病性有关的蛋白质并了解其分子基础,克隆“ NL895”(P。euramericana CL“ NL895”)对布鲁氏菌高度抗性。 sp。在这项研究中使用了multigermtubi。我们使用了二维凝胶电泳(2-DE)和质谱(MS)来鉴定白杨叶片中响应黑斑病病原体M. brunnea f差异表达的蛋白质。 sp。多菌灵接种病原菌后0、12、24、48和72 h从杨树叶片中提取的蛋白质通过2-DE分离。检测到约500个可重现的蛋白质斑点,其中40个蛋白质斑点在水平上表现出差异表达,并经过基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF MS),然后进行数据库搜索。根据功能,将鉴定出的蛋白质分为五类,即蛋白质合成,代谢,防御反应和未分类的蛋白质。

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