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脆弱愈创木组织培养中罗锅底愈创木薁类生物合成途径基因的生长动力学、代谢产物生成和表达谱分析

Growth Kinetics, Metabolites Production and Expression Profiling of Picrosides Biosynthetic Pathway Genes in Friable Callus Culture of Picrorhiza kurroa Royle ex Benth.

机构信息

Biotechnology Division, CSIR-Institute of Himalayan Bioresource Technology, Palampur, 176061, Himachal Pradesh, India.

Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, 201002, India.

出版信息

Appl Biochem Biotechnol. 2020 Dec;192(4):1298-1317. doi: 10.1007/s12010-020-03391-x. Epub 2020 Jul 28.

Abstract

The rising demand for picrosides commercially and over-exploitation of Picrorhiza kurroa from natural habitat has to initiate alternative strategies for sustainable production of metabolites. In the present research, wild leaf explant of P. kurroa was used to produce friable callus under different culture condition, i.e., dark and light with two temperature variants (15 °C and 25 °C). Afterward, callus cell lines were screened based on growth biomass and metabolites content accumulation. The results revealed, maximum callus growth index along with antioxidant potential (IC-40.88 μg/mL) and total phenol content (41.35 μg/mg) were observed under dark 25 °C. However, under light 15 °C, highest accumulation of picroside II (0.58 μg/mg), cinnamic acid (0.15 μg/mg), p-hydroxy acetophenone (0.30 μg/mg), total flavonoids (77.30 μg/mg), nitrogen (7.06%), carbohydrates (18.03%), and protein (44.12%) were detected. Major reported metabolite in callus was picroside I (1.63 μg/mg) under dark 15 °C. For the first time, picroside III content (range 0.15-0.56 μg/mg) was also detected and quantified in leaf-derived calli. Expression profiling of picroside biosynthetic pathway genes showed a positive correlation with the observed metabolites. Furthermore, an optimized protocol of metabolites enriched callus biomass could be used as potential strategy for sustainable production of picrosides at commercial scale.

摘要

对裂叶獐牙菜中裂环烯醚萜苷类化合物的商业需求不断增加,以及对其在自然栖息地的过度开采,都要求我们必须采取替代策略来实现其代谢产物的可持续生产。本研究以野生裂叶獐牙菜叶片外植体为材料,在不同的培养条件(黑暗和光照,两个温度梯度:15℃和 25℃)下诱导产生疏松愈伤组织,然后基于细胞生长生物量和代谢产物含量的积累对愈伤组织细胞系进行筛选。结果表明,在黑暗、25℃条件下,愈伤组织的生长指数最大,同时具有较高的抗氧化活性(IC₅₀值为 40.88μg/mL)和总酚含量(41.35μg/mg);而在光照、15℃条件下,裂环烯醚萜苷 II(0.58μg/mg)、肉桂酸(0.15μg/mg)、对羟基苯乙酮(0.30μg/mg)、总黄酮(77.30μg/mg)、氮(7.06%)、碳水化合物(18.03%)和蛋白质(44.12%)的含量最高。在黑暗、15℃条件下,愈伤组织中主要代谢产物为裂环烯醚萜苷 I(1.63μg/mg)。本研究首次在叶片来源的愈伤组织中检测到并定量了裂环烯醚萜苷 III(含量范围为 0.15-0.56μg/mg)。裂环烯醚萜苷生物合成途径基因的表达谱与观察到的代谢产物呈正相关。此外,优化后的富含代谢产物的愈伤组织生物量培养方案,可为裂环烯醚萜苷类化合物的商业规模可持续生产提供潜在策略。

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