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斑马纹块茎病增强了马铃薯块茎(Solanum tuberosum L.)的呼吸作用和氧化应激。

Zebra chip disease enhances respiration and oxidative stress of potato tubers (Solanum tuberosum L.).

机构信息

Postharvest Physiology and Biochemistry Laboratory, Department of Horticulture, Washington State University, P.O. Box 646414, Pullman, WA, 99164-6414, USA.

出版信息

Planta. 2017 Oct;246(4):625-639. doi: 10.1007/s00425-017-2714-8. Epub 2017 Jun 16.

Abstract

The physiological phenotype of potato tubers afflicted by zebra chip disease is characterized by increased oxidative stress metabolism and upregulation of systems for its mitigation. Starch catabolism and extensive buildup of reducing sugars render potatoes infected with zebra chip (ZC) pathogen (Candidatus Liberibacter solanacearum) unsuitable for fresh market and processing into chips/fries. Here we show that the disease inflicts considerable oxidative stress, which likely constitutes a substantial sink for metabolic energy, resulting in increased respiration rate of afflicted tubers. In contrast to healthy tubers, tissue from diseased tubers had greater ability to reduce 2,3,5-triphenyl-tetrazolium chloride to formazan, indicating enhanced dehydrogenase activity, probable disease-induced changes in cellular redox potential, and increased respiratory activity. The respiration rate of diseased tubers (cv. Atlantic) was 2.4-fold higher than healthy tubers and this correlated with increased activities of glucose-6-phosphate and 6-phosphogluconate dehydrogenases, key enzymes responsible for synthesis of cytosolic reducing equivalents. Wound-induced NADPH oxidase activity was greater for ZC than healthy tubers, but the resulting superoxide was rapidly catabolized by higher superoxide dismutase activity in ZC tubers. Peroxidase, catalase, glutathione reductase and ascorbate free radical reductase activities were also higher in diseased tubers, as was malondialdehyde, a biomarker of peroxidative damage and oxidative stress. Upregulation of the glutathione-ascorbate pathway is a direct response to (and indicator of) oxidative stress, which consumes reducing equivalents (NADPH) to catabolize reactive oxygen species and maintain cellular redox homeostasis. ZC disease substantially altered the oxidative metabolism of tubers, resulting in a physiological phenotype defined by metabolic changes directed toward mitigating oxidative stress. Paradoxically, the increased respiration rate of ZC tubers, which fuels the metabolic pathways responsible for attenuating oxidative stress, likely also contributes to oxidative stress.

摘要

受斑马纹块斑病影响的马铃薯块茎的生理表型特征是氧化应激代谢增加和缓解系统的上调。淀粉分解和大量还原糖的积累使感染斑马纹块斑病(ZC)病原体(Candidatus Liberibacter solanacearum)的马铃薯不适合新鲜市场和加工成薯片/薯条。在这里,我们表明,这种疾病会造成相当大的氧化应激,这可能构成代谢能量的一个重要消耗点,导致受感染块茎的呼吸率增加。与健康块茎相比,来自患病块茎的组织具有更强的将 2,3,5-三苯基氯化四氮唑还原为formazan 的能力,这表明脱氢酶活性增强,可能是疾病引起的细胞氧化还原电位变化,以及呼吸活性增加。患病块茎(大西洋品种)的呼吸率比健康块茎高 2.4 倍,这与葡萄糖-6-磷酸和 6-磷酸葡萄糖酸脱氢酶活性的增加有关,这两种酶是负责合成细胞质还原当量的关键酶。与健康块茎相比,ZC 诱导的 NADPH 氧化酶活性更高,但 ZC 块茎中更高的超氧化物歧化酶活性迅速分解了由此产生的超氧化物。过氧化物酶、过氧化氢酶、谷胱甘肽还原酶和抗坏血酸自由基还原酶的活性在患病块茎中也更高,丙二醛的含量也更高,丙二醛是过氧化损伤和氧化应激的生物标志物。谷胱甘肽-抗坏血酸途径的上调是对氧化应激的直接反应(和指示物),它消耗还原当量(NADPH)来分解活性氧物质并维持细胞氧化还原稳态。ZC 病极大地改变了块茎的氧化代谢,导致一种由代谢变化定义的生理表型,这些变化旨在减轻氧化应激。矛盾的是,ZC 块茎的呼吸率增加,为减轻氧化应激的代谢途径提供燃料,这可能也导致了氧化应激。

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