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首页> 外文期刊>Postharvest Biology and Technology >Pheophytinase activity and gene expression of chlorophyll-degrading enzymes relating to UV-B treatment in postharvest broccoli (Brassica oleracea L. Italica Group) florets.
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Pheophytinase activity and gene expression of chlorophyll-degrading enzymes relating to UV-B treatment in postharvest broccoli (Brassica oleracea L. Italica Group) florets.

机译:与花椰菜(小菜花组)小花中UV-B处理有关的植物植酸酶活性和叶绿素降解酶的基因表达。

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Pheophytinase (PPH) activity and gene expression of chlorophyll (Chl)-degrading enzymes relating to UV-B treatment in postharvest broccoli (Brassica oleracea L. Italica Group) florets were determined. PPH is involved in the dephytylation of Mg-free Chl a, pheophytin (Phy) a. However, in vitro chlorophyllase (Chlase, EC.3.1.1.14) also uses Phy a as a substrate to produce pheophorbide (Pheide) a by dephytylation. For an accurate determination of PPH activity, the PPH protein fraction was separated from Chlase protein by ammonium sulfate precipitation. The protein precipitated by 45-60% saturated ammonium sulfate included a little bit of Chlase activity and was suitable for PPH determination. PPH activity in broccoli florets treated with a UV-B dose of 19 kJ m--2 was repressed for the first 2 d of storage at 15 degrees C, whereas it increased gradually with senescence of control broccoli florets. The expression level of BoCLH1 was reduced in broccoli florets on day 4 of storage, while BoCLH2 and BoCLH3 were up-regulated with UV-B treatment. A high BoPAO expression level was found in senescent broccoli florets, and the up-regulation of this gene was delayed by UV-B treatment. The highest expression level of BoPPH was found in the control, and its expression was clearly repressed by UV-B treatment on day 2 of storage. We suggest that the up-regulation of Chl-degrading enzyme genes could be delayed by UV-B treatment, resulting in the suppression of floret yellowing in stored broccoli. All rights reserved, Elsevier.
机译:测定了花椰菜(小叶芸苔组)小花中的植酸酶(PPH)活性和与UV-B处理有关的叶绿素(Chl)降解酶的基因表达。 PPH参与了不含Mg的Chl a ,脱镁叶绿素(Phy) a 的脱氢。但是,体外叶绿素酶(Chlase,EC.3.1.1.14)也使用Phy a 作为底物,通过以下方法生产脱镁叶绿酸(Pheide) a 脱萘基化。为了准确测定PPH活性,可通过硫酸铵沉淀法从Chlase蛋白中分离PPH蛋白级分。由45-60%饱和硫酸铵沉淀的蛋白质具有一点Chlase活性,适用于PPH测定。在15°C下储存的前2天,用19 kJ m -2 的UV-B剂量处理的西兰花小花中的PPH活性受到抑制,而随着对照西兰花小花的衰老,其PPH活性逐渐升高。 。在存放的第4天,西兰花小花中 BoCLH1 的表达水平降低,而 BoCLH2 和 BoCLH3 的表达被UV-B处理上调。在衰老的西兰花小花中发现高的 BoPAO 表达水平,并且该基因的上调通过UV-B处理而延迟。在对照组中发现 BoPPH 的最高表达水平,并且在储存第2天通过UV-B处理明显抑制了其表达。我们建议通过UV-B处理可以延迟Chl降解酶基因的上调,从而抑制西兰花中所含的小花黄化。保留所有权利,Elsevier。

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