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了解藏红花球茎发育——组织学和代谢方面的见解

Understanding the Saffron Corm Development-Insights into Histological and Metabolic Aspects.

作者信息

Pallotti Claudia, Renau-Morata Begoña, Cardone Loriana, Nebauer Sergio G, Albiñana Palacios Mireia, Rivas-Sendra Alba, Seguí-Simarro José M, Molina Rosa V

机构信息

Departamento de Producción Vegetal, Universitat Politècnica de València, Camino de Vera s.n., 46022 Valencia, Spain.

Instituto Universitario de Conservación y Mejora de la Agrodiversidad Valenciana (COMAV), Universitat Politècnica de València, Camino de Vera s.n., 46022 Valencia, Spain.

出版信息

Plants (Basel). 2024 Apr 17;13(8):1125. doi: 10.3390/plants13081125.

DOI:10.3390/plants13081125
PMID:38674534
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11055066/
Abstract

The reproduction of L., a sterile triploid plant, is carried out exclusively through corms, whose size determines the saffron yield. The development of daughter corms (DC) is supported by photoassimilates supplied by the leaves as well as by the mother corms (MC). While biomass partitioning during DC development is well studied, growth dynamics in terms of cell number and size, the involved meristems, as well as carbohydrate partition and allocation, are not yet fully understood. We conducted a comprehensive study into saffron corm growth dynamics at the macroscopic and microscopic levels. Variations in carbohydrate content and enzymatic activities related to sucrose metabolism in sources and sinks were measured. Two key meristems were identified. One is involved in vascular connections between DC and MC. The other is a thickening meristem responsible for DC enlargement. This research explains how the previously described phases of corm growth correlate with variations in cell division, enlargement dynamics, and carbohydrate partitioning among organs. Results also elucidated that the end of DC growth relates to a significant drop in MC root biomass, limiting the water supply for the DC growth, and establishing the onset of leaf wilting. The lack of starch accumulation in aged leaf cells is noteworthy, as is the accumulation of lipids. We hypothesize a signaling role of sugars in DC growth initiation, stop, and leaf aging. Finally, we established a predominant role of sucrose synthase as a sucrolytic enzyme in the maintenance of the high flux of carbon for starch synthesis in DC. Together, the obtained results pave the way for the definition of strategies leading to better control of saffron corm development.

摘要

L.是一种不育的三倍体植物,其繁殖完全通过球茎进行,球茎大小决定藏红花产量。子球茎(DC)的发育得到叶片以及母球茎(MC)提供的光合产物的支持。虽然对子球茎发育过程中的生物量分配已有充分研究,但在细胞数量和大小方面的生长动态、所涉及的分生组织以及碳水化合物的分配和分布,仍未完全了解。我们在宏观和微观层面上对藏红花球茎的生长动态进行了全面研究。测量了源库中与蔗糖代谢相关的碳水化合物含量和酶活性的变化。确定了两个关键分生组织。一个参与子球茎与母球茎之间的维管连接。另一个是负责子球茎膨大的增粗分生组织。这项研究解释了先前描述的球茎生长阶段如何与细胞分裂、膨大动态以及器官间碳水化合物分配的变化相关。结果还阐明,子球茎生长的结束与母球茎根生物量的显著下降有关,这限制了子球茎生长的水分供应,并导致叶片枯萎开始。老龄叶细胞中淀粉积累的缺乏以及脂质的积累值得注意。我们推测糖类在子球茎生长启动、停止和叶片衰老中具有信号传导作用。最后,我们确定了蔗糖合酶作为一种蔗糖分解酶在维持子球茎中淀粉合成的高碳通量方面的主要作用。总之,所获得的结果为制定更好地控制藏红花球茎发育的策略铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8618/11055066/bd803b96a13c/plants-13-01125-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8618/11055066/ec91e1c07897/plants-13-01125-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8618/11055066/288f2cd55f6b/plants-13-01125-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8618/11055066/64f2e371b599/plants-13-01125-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8618/11055066/18fab1559022/plants-13-01125-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8618/11055066/0913b4d9c75e/plants-13-01125-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8618/11055066/e867b847c3c0/plants-13-01125-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8618/11055066/eeae671a1c94/plants-13-01125-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8618/11055066/7ebd04de7acd/plants-13-01125-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8618/11055066/bd803b96a13c/plants-13-01125-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8618/11055066/ec91e1c07897/plants-13-01125-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8618/11055066/288f2cd55f6b/plants-13-01125-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8618/11055066/64f2e371b599/plants-13-01125-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8618/11055066/18fab1559022/plants-13-01125-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8618/11055066/0913b4d9c75e/plants-13-01125-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8618/11055066/e867b847c3c0/plants-13-01125-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8618/11055066/eeae671a1c94/plants-13-01125-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8618/11055066/7ebd04de7acd/plants-13-01125-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8618/11055066/bd803b96a13c/plants-13-01125-g009.jpg

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