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Preliminary proteomic characterisation of primodia and vegetative dikaryotic mycelial cells from tiger’s milk mushroom (Lignosus rhinocerus)

机译:老虎乳菇(Lignosus rhinocerus)的原基和营养性双核菌丝体细胞的初步蛋白质组学表征

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摘要

Tiger’s Milk mushrooms (Lignosus rhinocerus) are polypores with three distinct parts: cap (pileus), stem (stipe) and tuber (sclerotium). The stem of this medicinal mushroom is centrally connected to the brownish woody cap that grows out from the tuber underground rather than from the wood. To date, the biotic and abiotic factors that induce the growth of this mushroom are unclear and information regarding its development is scanty. Hence, the differential protein expressions of vegetative dikaryotic mycelial and primordial cells of this mushroom were investigated. Six two dimensional-sodium dodecyl sulfate-polyacrylamide gel electrophoresis (2D-SDS-PAGE) of 13 cm with pH3-10 containing the intracellular proteins of vegetative mycelial and primordial cells of L. rhinocerus were obtained. Analysis of 2D-SDS-PAGE using Progenesis Samespot version 4.1 yielded approximately 1000 distinct protein spots in the proteome of vegetative mycelial cells, while primordial proteome contained nearly 100 spots. Further comparison between the vegetative mycelial and primordial proteomes yielded significant up-regulation of protein expression of 5 primordial cells proteins that were labeled as P1, P2, P3, P4 and P5. These protein spots were excised, trypsin digested and submitted to mass spectrometry. Protein identification through MASCOT yielded significant identification with P1 and P2 as DnaJ domain protein, P3 and P5 as hypothetical protein while P4 as AP-2rep transcription factor. The present results suggested that P3, P4 and P5 are novel proteins that involved in the initiation of L. rhinocerus primordia. Our findings also suggested that stress response mechanism is present during fruitification of this mushroom.
机译:老虎的牛奶蘑菇(Lignosus rhinocerus)是具有三个不同部分的孢子:帽(菌毛),茎(茎)和块茎(菌核)。这种药用蘑菇的茎中央连接到褐色的木帽上,该木帽是从地下块茎而不是木头长出来的。迄今为止,尚不清楚诱导这种蘑菇生长的生物和非生物因素,有关其发育的信息很少。因此,研究了该蘑菇的营养双核生物菌丝体和原始细胞的差异蛋白表达。获得了六个pH值为13 cm的二维十二烷基硫酸钠聚丙烯酰胺凝胶电泳(2D-SDS-PAGE),pH3-10包含犀牛营养菌丝体和原始细胞的细胞内蛋白。使用Progenesis Samespot 4.1版对2D-SDS-PAGE进行分析,在营养菌丝体细胞的蛋白质组中产生了大约1000个不同的蛋白质斑点,而原始蛋白质组中包含了近100个斑点。营养菌丝体和原始蛋白质组之间的进一步比较显着上调了标记为P1,P2,P3,P4和P5的5种原始细胞蛋白的蛋白表达。切下这些蛋白质斑点,消化胰蛋白酶并进行质谱分析。通过MASCOT进行的蛋白质鉴定可将P1和P2作为DnaJ域蛋白,P3和P5作为假设蛋白,P4作为AP-2rep转录因子进行显着鉴定。目前的结果表明P3,P4和P5是新的蛋白质,参与发起的L. Rhinocerus primordia。我们的发现还表明,该蘑菇的果实化过程中存在应激反应机制。

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