Instituto de Agroquímica y Tecnología de Alimentos, IATA-CSIC, Calle Agustín Escardino 7, 46980 Paterna, Valencia, Spain.
Food Chem. 2017 Mar 1;218:575-583. doi: 10.1016/j.foodchem.2016.09.089. Epub 2016 Sep 16.
The objective was to investigate whether LED Blue Light (LBL) induces changes in phenolics and ethylene production of sweet oranges, and whether they participate in LBL-elicited resistance against the most important postharvest pathogen (Penicillium digitatum) of citrus fruit. The expression of relevant genes of the phenylpropanoid and ethylene biosynthetic pathways during elicitation of resistance was also determined. Different LBL (wavelength 450nm) quantum fluxes were used within the 60-630μmolms range. The HPLC analysis showed that the most relevant increase in phenylpropanoids occurred in scoparone, which markedly increased 3days after exposing fruits to a very high quantum flux (630μmolms) for 18h. However, phenylpropanoids, including scoparone, were not critical factors in LBL-induced resistance. The genes involved in ethylene biosynthesis were differentially regulated by LBL. Ethylene is not involved in elicited resistance, although high LBL levels increased ethylene production in only 1h.
目的在于研究蓝光 LED(LBL)是否会引起甜橙中酚类物质和乙烯的产生变化,以及它们是否参与了 LBL 诱导的对柑橘果实最重要的采后病原体(指青霉属)的抗性。在诱导抗性过程中,还确定了苯丙烷和乙烯生物合成途径的相关基因的表达。在 60-630μmolms 范围内使用了不同的 LBL(波长 450nm)量子通量。HPLC 分析表明,苯丙烷中最相关的增加发生在罗勒烯,在将果实暴露于非常高的量子通量(630μmolms)18 小时后 3 天,其含量明显增加。然而,苯丙烷,包括罗勒烯,并不是 LBL 诱导抗性的关键因素。参与乙烯生物合成的基因受 LBL 调控。乙烯不参与激发抗性,尽管高水平的 LBL 在仅 1 小时内就增加了乙烯的产生。