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Dynamic Analysis of Photosynthate Translocation Into Strawberry Fruits Using Non-invasive 11C-Labeling Supported With Conventional Destructive Measurements Using 13C-Labeling

机译:使用无创11C标签和常规破坏性测量(使用13C标签)支持的光合产物向草莓果实转运的动态分析

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摘要

In protected strawberry (Fragaria × ananassa Duch.) cultivation, environmental control based on the process of photosynthate translocation is essential for optimizing fruit quality and yield, because the process of photosynthate translocation directly affects dry matter partitioning. We visualized photosynthate translocation to strawberry fruits non-invasively with 11CO2 and a positron-emitting tracer imaging system (PETIS). We used PETIS to evaluate real-time dynamics of 11C-labeled photosynthate translocation from a 11CO2-fed leaf, which was immediately below the inflorescence, to individual fruits on an inflorescence in intact plant. Serial photosynthate translocation images and animations obtained by PETIS verified that the 11C-photosynthates from the source leaf reached the sink fruit within 1 h but did not accumulate homogeneously within a fruit. The quantity of photosynthate translocation as represented by 11C radioactivity varied among individual fruits and their positions on the inflorescence. Photosynthate translocation rates to secondary fruit were faster than those to primary or tertiary fruits, even though the translocation pathway from leaf to fruit was the longest for the secondary fruit. Moreover, the secondary fruit was 25% smaller than the primary fruit. Sink activity (11C radioactivity/dry weight [DW]) of the secondary fruit was higher than those of the primary and tertiary fruits. These relative differences in sink activity levels among the three fruit positions were also confirmed by 13C tracer measurement. Photosynthate translocation rates in the pedicels might be dependent on the sink strength of the adjoining fruits. The present study established 11C-photosynthate arrival times to the sink fruits and demonstrated that the translocated material does not uniformly accumulate within a fruit. The actual quantities of translocated photosynthates from a specific leaf differed among individual fruits on the same inflorescence. To the best of our knowledge, this is the first reported observation of real-time translocation to individual fruits in an intact strawberry plant using 11C-radioactive- and 13C-stable-isotope analyses.
机译:在保护草莓(Fragaria×ananassa Duch。)种植中,基于光合产物转运过程的环境控制对于优化果实品质和产量至关重要,因为光合产物转运过程直接影响干物质分配。我们用 11 CO2和正电子发射示踪成像系统(PETIS)非侵入性地观察到光合产物向草莓果实的转运。我们使用PETIS来评估 11 C标记的光合产物从 11 CO2喂养的叶片(紧接在花序下方)到单个果实的实时动态。完整植物的花序。 PETIS获得的系列光合产物易位图像和动画证实,源叶中的 11 C-光合产物在1 h内就到达了宿果,但在果实中并未均匀地积累。以 11 C放射性表示的光合产物易位量在单个果实及其在花序上的位置之间变化。尽管从叶片到果实的转运途径对于次要果实而言最长,但光合产物向次要果实的转运速率比对初生或第三产果实的转运更快。此外,次要水果比主要水果小25%。次生果实的下沉活性( 11 C放射性/干重[DW])高于初生和第三生果实。通过 13 C示踪剂测量也证实了三个水果位置之间的库活动水平的这些相对差异。花梗中光合产物的转运速率可能取决于相邻果实的下沉强度。本研究确定了 11 C-光合产物到达下沉果实的时间,并证明了易位物质在果实中的累积不均匀。同一花序的单个果实之间,来自特定叶片的易位光合产物的实际数量不同。据我们所知,这是首次报道使用 11 C-radioactive-和 13 C-将完整的草莓植株实时转移至单个果实的现象。稳定同位素分析。

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