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在暴露于营养性磷酸盐缺乏的细胞培养物中,马铃薯的碳通量保持稳定。

Carbon Fluxes in Potato () Remain Stable in Cell Cultures Exposed to Nutritional Phosphate Deficiency.

作者信息

He Jiang Zhou, Dorion Sonia, Carmona-Rojas Laura Michell, Rivoal Jean

机构信息

Institut de Recherche en Biologie Végétale, Université de Montréal, 4101 Rue Sherbrooke Est, Montréal, QC H1X 2B2, Canada.

Grupo de Biotecnologiía, Facultad de Ciencias Exactas y Naturales, Universidad de Antioquia, Medelliín 050010, Colombia.

出版信息

Biology (Basel). 2023 Sep 1;12(9):1190. doi: 10.3390/biology12091190.

DOI:10.3390/biology12091190
PMID:37759596
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10525292/
Abstract

Nutritional phosphate deficiency is a major limitation to plant growth. Here, we monitored fluxes in pathways supporting respiratory metabolism in potato () cell cultures growing in control or limiting phosphate conditions. Sugar uptake was quantified using [U-C]sucrose as precursor. Carbohydrate degradation through glycolysis and respiratory pathways was estimated using the catabolism of [U-C]sucrose to CO. Anaplerotic carbon flux was assessed by labeling with NaHCO. The data showed that these metabolic fluxes displayed distinct patterns over culture time. However, phosphate depletion had relatively little impact on the various fluxes. Sucrose uptake was higher during the first six days of culture, followed by a decline, which was steeper in Pi-sufficient cells. Anaplerotic pathway flux was more important at day three and decreased thereafter. In contrast, the flux between sucrose and CO was at a maximum in the mid-log phase of the culture, with a peak at Day 6. Metabolization of [U-C]sucrose into neutral, basic and acidic fractions was also unaffected by phosphate nutrition. Hence, the well-documented changes in central metabolism enzymes activities in response to Pi deficiency do not drastically modify metabolic fluxes, but rather result in the maintenance of the carbon fluxes that support respiration.

摘要

营养性磷缺乏是植物生长的主要限制因素。在此,我们监测了在对照或磷限制条件下生长的马铃薯()细胞培养物中支持呼吸代谢的途径中的通量。使用[U-C]蔗糖作为前体对糖摄取进行定量。通过[U-C]蔗糖分解为CO来估计通过糖酵解和呼吸途径的碳水化合物降解。通过用NaHCO标记来评估回补碳通量。数据表明,这些代谢通量在培养时间内呈现出不同的模式。然而,磷耗竭对各种通量的影响相对较小。培养的前六天蔗糖摄取较高,随后下降,在磷充足的细胞中下降更陡。回补途径通量在第三天更重要,此后下降。相反,蔗糖与CO之间的通量在培养的对数中期达到最大值,在第6天出现峰值。[U-C]蔗糖代谢为中性、碱性和酸性部分也不受磷营养的影响。因此,充分记录的响应磷缺乏时中心代谢酶活性的变化不会大幅改变代谢通量,而是导致维持支持呼吸的碳通量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e100/10525292/a741fb32222d/biology-12-01190-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e100/10525292/cf38d723e678/biology-12-01190-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e100/10525292/9a9255aee622/biology-12-01190-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e100/10525292/82a619b0c7f1/biology-12-01190-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e100/10525292/a741fb32222d/biology-12-01190-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e100/10525292/cf38d723e678/biology-12-01190-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e100/10525292/9a9255aee622/biology-12-01190-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e100/10525292/82a619b0c7f1/biology-12-01190-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e100/10525292/a741fb32222d/biology-12-01190-g004.jpg

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