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首页> 外文期刊>Chembiochem: A European journal of chemical biology >Biosynthetic and Functional Color–Scent Associations in Flowers of Papaver nudicaulePapaver nudicaule and Their Impact on Pollinators
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Biosynthetic and Functional Color–Scent Associations in Flowers of Papaver nudicaulePapaver nudicaule and Their Impact on Pollinators

机译：罂粟属尿嘧啶的花朵中的生物合成和功能色彩作用关系罂粟属尿布及其对传导素的影响

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Abstract > Despite increasing evidence for biosynthetic connections between flower pigments and volatile compounds, examples of such relationships in polymorphic plant species remains limited. Herein, color–scent associations in flowers from Papaver nudicaule (Papaveraceae) have been investigated. The spectral reflectance and scent composition of flowers of four color cultivars was determined. We found that pigments and volatiles occur in specific combinations in flowers of P.?nudicaule . The presence of indole in the bouquets is strongly associated with the occurrence of yellow pigments called nudicaulins, for which indole is one of the final biosynthetic precursors. Whereas yellow flowers emit an excess of indole, orange flowers consume it during nudicaulin production and lack the substance in their bouquet. By using the honeybee, Apis mellifera , evaluations were made on how color and scent affect the discrimination of these flowers by pollinators. Honeybees were able to discriminate artificial odor mixtures resembling those of the natural flower odors. Bees trained with stimuli combining colors and odors showed an improved discrimination performance. The results indicate that the indole moiety of nudicaulins and emitted indole might be products of the same biochemical pathway. We propose that conserved pathways account for the evolution of color–scent associations in P.?nudicaule and that these associations positively affect flower constancy of pollinators. </abstract> </span> <span class="z_kbtn z_kbtnclass hoverxs" style="display: none;">展开▼</span> </div> <div class="translation abstracttxt"> <span class="zhankaihshouqi fivelineshidden" id="abstract"> <span>机译：</span><Abstract Type =“main”XML：Lang =“en”> <标题类型=“main”>摘要</标题> >尽管花卉颜料和挥发性化合物之间的生物合成连接增加了证据，但多晶型关系的实例植物物种仍然有限。在此，研究了来自罂粟尿嘧啶的鲜花中的颜色 - 气味缔合物（罂粟科e）。测定了四种颜色鲜花的光谱反射率和气味组成。我们发现颜料和挥发物在 P.?内孔的花朵中的特定组合中发生。在束中的吲哚存在吲哚强烈地与称为Nudicaulins的黄色颜料的发生有关，吲哚是最终的生物合成前体之一。虽然黄色花朵发出过量的吲哚，但橙花在尿酸林生成期间消耗它，并且在束缚着束缚物质。通过使用蜜蜂， apis mellifera </ i>，是关于如何通过粉刷者影响这些花的颜色和气味的评估。蜜蜂能够区分类似于天然花气味的人工气味混合物。用刺激训练颜色和气味训练的蜜蜂表现出了改善的辨别性能。结果表明，Nudicaulins的吲哚部分和发射的吲哚可能是相同生物化学途径的产物。我们提出了保守的途径，用于在 p.? nudicaule </ i>中的色彩作业协会的演变，并且这些协会积极影响粉丝器的花常规。 </ p> </ abstract> </span> <span class="z_kbtn z_kbtnclass hoverxs" style="display: none;">展开▼</span> </div> </div> <div class="record"> <h2 class="all_title" id="enpatent33" >著录项</h2> <ul> <li> <span class="lefttit">来源</span> <div style="width: 86%;vertical-align: text-top;display: inline-block;"> <a href='/journal-foreign-16039/'>《Chembiochem: A European journal of chemical biology》</a> <b style="margin: 0 2px;">|</b><span>2018年第14期</span><b style="margin: 0 2px;">|</b><span>共10页</span> </div> </li> <li> <div class="author"> <span class="lefttit">作者</span> <p id="fAuthorthree" class="threelineshidden zhankaihshouqi"> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Martínez‐Harms Jaime&option=202" target="_blank" rel="nofollow">Martínez‐Harms Jaime;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Warskulat Anne‐Christin&option=202" target="_blank" rel="nofollow">Warskulat Anne‐Christin;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Dudek Bettina&option=202" target="_blank" rel="nofollow">Dudek Bettina;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Kunert Grit&option=202" target="_blank" rel="nofollow">Kunert Grit;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Lorenz Sybille&option=202" target="_blank" rel="nofollow">Lorenz Sybille;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Hansson Bill S.&option=202" target="_blank" rel="nofollow">Hansson Bill S.;</a> <a href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=Schneider Bernd&option=202" target="_blank" rel="nofollow">Schneider Bernd;</a> </p> <span class="z_kbtnclass z_kbtnclassall hoverxs" id="zkzz" style="display: none;">展开▼</span> </div> </li> <li> <div style="display: flex;"> <span class="lefttit">作者单位</span> <div style="position: relative;margin-left: 3px;max-width: 639px;"> <div class="threelineshidden zhankaihshouqi" id="fOrgthree"> <p>Max Planck Institute for Chemical EcologyHans-Kn?ll-Strasse 8 07745 Jena Germany;</p> <p>Max Planck Institute for Chemical EcologyHans-Kn?ll-Strasse 8 07745 Jena Germany;</p> <p>Max Planck Institute for Chemical EcologyHans-Kn?ll-Strasse 8 07745 Jena Germany;</p> <p>Max Planck Institute for Chemical EcologyHans-Kn?ll-Strasse 8 07745 Jena Germany;</p> <p>Max Planck Institute for Chemical EcologyHans-Kn?ll-Strasse 8 07745 Jena Germany;</p> <p>Max Planck Institute for Chemical EcologyHans-Kn?ll-Strasse 8 07745 Jena Germany;</p> <p>Max Planck Institute for Chemical EcologyHans-Kn?ll-Strasse 8 07745 Jena Germany;</p> </div> <span class="z_kbtnclass z_kbtnclassall hoverxs" id="zhdw" style="display: none;">展开▼</span> </div> </div> </li> <li > <span class="lefttit">收录信息</span> <span style="width: 86%;vertical-align: text-top;display: inline-block;"></span> </li> <li> <span class="lefttit">原文格式</span> <span>PDF</span> </li> <li> <span class="lefttit">正文语种</span> <span>eng</span> </li> <li> <span class="lefttit">中图分类</span> <span><a href="https://www.zhangqiaokeyan.com/clc/179.html" title="分子生物学">分子生物学;</a></span> </li> <li class="antistop"> <span class="lefttit">关键词</span> <p style="width: 86%;vertical-align: text-top;"> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=alkaloids&option=203" rel="nofollow">alkaloids;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=biosynthesis&option=203" rel="nofollow">biosynthesis;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=color–scent associations&option=203" rel="nofollow">color–scent associations;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=natural products&option=203" rel="nofollow">natural products;</a> <a style="color: #3E7FEB;" href="/search.html?doctypes=4_5_6_1-0_4-0_1_2_3_7_9&sertext=volatile organic compounds&option=203" rel="nofollow">volatile organic compounds;</a> </p> <div class="translation"> 机译：生物碱;生物合成;色彩香味;天然产品;挥发性有机化合物; 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2016-11-16</span> </div> <p class="zwjiyix translation" style="max-width: initial;height: auto;word-break: break-all;white-space: initial;text-overflow: initial;overflow: initial;"> <span>机译：花香色的提取及生产方法 </span> </p> </li> <li> <div> <b>4. </b><a class="enjiyixqcontent" href="/patent-detail/06130449265154.html">SPECIAL MANUFACTURING METHOD FOR KEEPING NATURAL COLOR AND SCENT OF FLOWER</a> <b>[P]</b> . <span> 外国专利： <!-- 日本专利： --> JP2001213702A </span> <span> . 2001-08-07</span> </div> <p class="zwjiyix translation" style="max-width: initial;height: auto;word-break: break-all;white-space: initial;text-overflow: initial;overflow: initial;"> <span>机译：保持花色和花香的特殊制造方法 </span> </p> </li> <li> <div> <b>5. </b><a class="enjiyixqcontent" href="/patent-detail/06130491494217.html">the new rozenvarieteit, hybrid, scented flower, bright blood red color, kleurhoudend, strong branches almost without thorns.</a> <b>[P]</b> . <span> 外国专利： <!-- --> BE584649A </span> <span> . 1960-03-01</span> </div> <p 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