Botanical Institute, Karlsruhe Institute of Technology, Fritz-Haber-Weg 4, 76131, Karlsruhe, Germany.
Institute of Pharmacy, Martin-Luther-University, Hoher Weg 8, 06120, Halle-WittenbergHalle (Saale), Germany.
Protoplasma. 2023 Mar;260(2):349-369. doi: 10.1007/s00709-022-01781-y. Epub 2022 Jun 13.
Since the discovery of the anticancer drugs vinblastine and vincristine, Catharanthus roseus has been intensively studied for biosynthesis of several terpene indole alkaloids (TIAs). Due to their low abundance in plant tissues at a simultaneously high demand, modes of production alternative to conventional extraction are mandatory. Plant cell fermentation might become one of these alternatives, yet decades of research have shown limited success to certain product classes, leading to the question: how to preserve the intrinsic ability to produce TIAs (metabolic competence) in cell culture? We used the strategy to use the developmental potency of mature embryos to generate such strains. Two cell strains (C1and C4) from seed embryos of Catharanthus roseus were found to differ not only morphologically, but also in their metabolic competence. This differential competence became manifest not only under phytohormone elicitation, but also upon feeding with alkaloid pathway precursors. The more active strain C4 formed larger cell aggregates and was endowed with longer mitochondria. These cellular features were accompanied by higher alkaloid accumulation in response to methyl jasmonate (MeJA) elicitation. The levels of catharanthine could be increased significantly, while the concurrent vindoline branch of the pathway was blocked, such that no bisindole alkaloids were detectable. By feeding vindoline to MeJA-elicited C4 cells, vincristine became detectable; however, only to marginal amounts. In conclusion, these results show that cultured cells are not "de-differentiated", but can differ in metabolic competence. In addition to elicitation and precursor feeding, the cellular properties of the "biomatter" are highly relevant for the success of plant cell fermentation.
自抗癌药物长春碱和长春新碱被发现以来,长春花已被广泛研究以用于合成多种萜类吲哚生物碱(TIAs)。由于 TIAs 在植物组织中的含量较低,而需求量又很高,因此需要替代传统提取方法的生产方式。植物细胞发酵可能成为这些替代方法之一,但数十年的研究表明,对于某些产品类别,这种方法的成功率有限,这就引出了一个问题:如何在细胞培养中保留产生 TIAs 的内在能力(代谢能力)?我们使用利用成熟胚胎的发育潜力来产生这种菌株的策略。从长春花种子胚胎中发现了两个细胞系(C1 和 C4),它们不仅在形态上有所不同,而且在代谢能力上也有所不同。这种差异能力不仅在植物激素诱导下表现出来,而且在添加生物碱途径前体时也表现出来。更活跃的 C4 细胞系形成更大的细胞聚集体,并具有更长的线粒体。这些细胞特征伴随着在茉莉酸甲酯(MeJA)诱导下更高的生物碱积累。长春质碱的水平可以显著提高,而同时通路的长春碱分支被阻断,因此无法检测到双吲哚生物碱。通过向 MeJA 诱导的 C4 细胞中添加长春碱,可以检测到长春新碱;然而,含量非常低。总之,这些结果表明,培养细胞并没有“去分化”,但在代谢能力上可以有所不同。除了诱导和前体喂养外,“生物物质”的细胞特性对于植物细胞发酵的成功也非常重要。