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首页> 外文期刊>Postharvest Biology and Technology >Identification of differentially expressed genes from cherry tomato fruit (Lycopersicon esculentum) after application of the biological control yeast Cryptococcus laurentii
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Identification of differentially expressed genes from cherry tomato fruit (Lycopersicon esculentum) after application of the biological control yeast Cryptococcus laurentii

机译:应用生物控制酵母劳氏隐球菌后鉴定樱桃番茄果实(Lycopersicon esculentum)中差异表达的基因

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摘要

Postharvest decay of fruit may be controlled by the use of a variety of diverse microorganisms acting as biocontrol agents, but the mechanisms associated with control are not fully understood. In order to gain insight into the action of antagonistic microorganisms on fruit, a forward subtractive suppression hybridization (SSH) cDNA library was constructed. SSH was performed with cDNA from cherry tomato fruit (Lycopersicon esculentum) inoculated with water as the driver and cDNA from tomato fruit inoculated by Cryptococcus laurentii as the tester. A total of 150 clones in the SSH library were sequenced and found to represent 50 unigenes. BLASTX results reveal that 35 cDNAs had significant sequence homologies with known sequences in the NCBI database. The identified cDNAs encode proteins involved in cellular processes such as primary metabolism, signal transduction, defense and responses to pathogens, stress-related, cell wall assembly, and photosynthesis and transcription related sequences. Six cDNA clones were selected for temporal expression analysis using RT-PCR. The results show that a number of transcripts encoding proteins/enzymes which are known to be up-regulated under some biotic and abiotic stresses are also up-regulated after the application of biological control yeast to cherry tomato fruit. The expression of these proteins may play a role in increasing fruit resistance to postharvest pathogen infection.
机译:可以通过使用多种多样的微生物作为生物防治剂来控制果实的采后腐烂,但与控制有关的机理尚未完全明了。为了深入了解拮抗性微生物对水果的作用,构建了正向消减抑制杂交(SSH)cDNA文库。 SSH是用水驱动的樱桃番茄果实(Lycopersicon esculentum)的cDNA和作为测试者的劳氏隐球菌接种的番茄果实的cDNA进行的。对SSH文库中的150个克隆进行了测序,发现它们代表了50个单基因。 BLASTX结果显示35个cDNA与NCBI数据库中的已知序列具有显着的序列同源性。鉴定出的cDNA编码参与细胞过程的蛋白质,例如初级代谢,信号转导,对病原体的防御和反应,应激相关,细胞壁组装以及光合作用和转录相关序列。选择六个cDNA克隆用于使用RT-PCR的时间表达分析。结果表明,将生物控制酵母应用于樱桃番茄果实后,许多编码蛋白质/酶的转录本(在某些生物和非生物胁迫下也被上调)也被上调。这些蛋白质的表达可能在增加果实对采后病原体感染的抗性中起作用。

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