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首页> 外文期刊>Journal of food, agriculture & environment >Dormancy in tulip (Tulipa gesneriana L.) bulbs and freesia (Freesia refracta Klatt.) corms: Changes in soluble proteins and APX activity
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Dormancy in tulip (Tulipa gesneriana L.) bulbs and freesia (Freesia refracta Klatt.) corms: Changes in soluble proteins and APX activity

机译:郁金香(Tulipa gesneriana L.)鳞茎和小苍兰(Freesia refracta Klatt。)球茎的休眠:可溶性蛋白和APX活性的变化

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The bulbs of tulip (Tulipa gesneriana L.) cvs Negrita and Cassini and the corms of freesia (Freesia refracta Klatt.) cvs Polaris and Aladin were used in the study to investigate molecular changes during the storage and sprouting stage besides phenologic observations. One part of the bulbs and corms were directly planted (DP) into greenhouse without any treatment. Another part of the bulbs and corms were either stored in room condition (RC; 18-25°C and 55-65% RH) or in normal atmosphere (NA; 5±1°Cand 70-85% RH)for 120 days before planting. In both storage treatments, the bulbs and corms were transplanted to the greenhouse in three periods with 40 days intervals. In every period, apart of the bulbs and corms were taken for the molecular analyses before planting. In addition, some of DP bulbs and corms were removed from soil at the same periods for molecular analyses. Thestorageof the bulbs and corms reduced the sprouting durations in comparison to the DP treatment. However, NA storage either reduced (in tulip) or inhibit (in freesia) to proportions of plant formation. The highest and the lowest ascorbate peroxidase (APX) activity were found during NA storage and DP treatment, respectively, in both species. In addition APX activity was higher intulip than in freesia. Sharp decrease in total soluble protein (TSP) content particularly after 40 and 60 days of almost all treatments can be an evidence of breakdown of storage proteins. TSP profiles oftulipbulbs showed a major polypeptide, 18 kDa, with different band intensities according to the treatments. In freesia, 66 kDa protein accumulated especially in last two sampling periods of NA storage, whereas 58 kDa protein became invisible in last two sampling periods of NA storage. Since prolonged NAstorage inhibits the sprouting and proportions of plant formation, 66 kDa and 58 kDa bands might be related to dormancy or sprouting in freesia.
机译:除物候观察外,本研究还使用郁金香(Tulipa gesneriana L.)的鳞茎Negrita和Cassini以及小苍兰的球茎(Freesia refracta Klatt。)和北极星和Aladin的鳞茎来研究在贮藏和发芽阶段的分子变化。将一部分鳞茎和球茎未经任何处理直接种植(DP)到温室中。将另一部分球茎和球茎在室温下(RC; 18-25°C和55-65%RH)或在正常气氛下(NA; 5±1°C和70-85%RH)储存120天种植。在两种储存处理中,将鳞茎和球茎以40天为间隔的三个时期移植到温室中。在每个时期,在播种前都要取出鳞茎和球茎进行分子分析。此外,在同一时期从土壤中取出了一些DP球茎和球茎进行分子分析。与DP处理相比,鳞茎和球茎的储存减少了发芽时间。但是,NA的存储量减少了(在郁金香中)或抑制了(在小苍兰中)至植物形成的比例。在两个物种中,分别在NA储存和DP处理期间发现了最高和最低的抗坏血酸过氧化物酶(APX)活性。此外,APX活性高于小苍兰。总可溶性蛋白(TSP)含量的急剧下降,特别是在几乎所有处理中的40天和60天之后,都可以证明存储蛋白的分解。灯泡的TSP谱显示主要多肽18 kDa,根据处理具有不同的条带强度。在小苍兰中,特别是在NA储存的最后两个采样期间积累了66 kDa的蛋白质,而在NA储存的最后两个采样周期中变得看不见58 kDa的蛋白质。由于长时间的NAstorage抑制了发芽和植物形成的比例,因此66 kDa和58 kDa的条带可能与小苍兰的休眠或发芽有关。

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