Department of Pharmaceutical Biology and Medicinal Plant Biotechnology, Faculty of Pharmacy with the Laboratory Medicine Division, Medical University of Warsaw, 1 Banacha Str, 02-097, Warsaw, Poland.
Institute of Biochemistry and Biophysics, Laboratory of Plant Pathogenesis, Polish Academy of Sciences, 5A Pawińskiego Str, 02-106, Warsaw, Poland.
Plant Cell Rep. 2019 Jan;38(1):85-99. doi: 10.1007/s00299-018-2351-0. Epub 2018 Nov 7.
Two lines of Taxus × media hairy roots harbouring or not the TXS transgene demonstrated diverse gene expression and taxane yield during cultivation in PFD-supported two liquid-phase culture system. Two lines of Taxus × media hairy roots were subjected to single or twice-repeated supplementation with methyl jasmonate, sodium nitroprusside, L-phenylalanine, and sucrose feeding. One line harboured transgene of taxadiene synthase (ATMA), while the second (KT) did not. Both hairy root lines were cultured in two-phase culture systems containing perfluorodecalin (PFD) in aerated or degassed form. The relationship between TXS (taxadiene synthase), BAPT (baccatin III: 3-amino, 3-phenylpropanoyltransferase), and DBTNBT (3'-N-debenzoyl-2-deoxytaxol-N-benzoyltransferase) genes and taxane production was analysed. The ATMA and KT lines differed in their potential for taxane accumulation, secretion, and taxane profile. In ATMA biomass, both paclitaxel and baccatin III were detected, while in KT roots only paclitaxel. The most suitable conditions for taxane production for ATMA roots were found in single-elicited supported with PFD-degassed cultures (2 473.29 ± 263.85 µg/g DW), whereas in KT roots in single-elicited cultures with PFD-aerated (470.08 ± 25.15 µg/g DW). The extracellular levels of paclitaxel never exceeded 10% for ATMA roots, while for KT increased up to 76%. The gene expression profile was determined in single-elicited cultures supported with PFD-degassed, where in ATMA roots, the highest taxane yield was obtained, while in KT the lowest one. The gene expression pattern in both investigated root lines differed substantially what resulted in taxane yield characterized particular lines. The highest co-expression of TXS, BAPT and DBTNBT genes noted for ATMA roots harvested 48 h after elicitation corresponded with their higher ability for taxane production in comparison with the effects observed for KT roots.
在 PFD 支持的两相液体培养系统中培养时,两条含有或不含有 TXS 转基因的 Taxus × media 发根表现出不同的基因表达和紫杉烷产量。两条 Taxus × media 发根分别进行了一次或两次重复补充茉莉酸甲酯、硝普钠、L-苯丙氨酸和蔗糖喂养。一条根含有紫杉二烯合酶(ATMA)的转基因,而第二条(KT)没有。两条发根均在含有全氟癸烷(PFD)的两相培养系统中进行培养,形式为充气或脱气。分析了 TXS(紫杉二烯合酶)、BAPT(巴卡丁 III:3-氨基、3-苯丙酰基转移酶)和 DBTNBT(3'-N-去苯甲酰基-2-脱氧紫杉醇-N-苯甲酰基转移酶)基因与紫杉烷产量的关系。ATMA 和 KT 系在紫杉烷积累、分泌和紫杉烷谱方面存在差异。在 ATMA 生物量中,同时检测到紫杉醇和巴卡丁 III,而在 KT 根中仅检测到紫杉醇。发现 ATMA 根最适合生产紫杉烷的条件是在 PFD 脱气支持的单一激发培养中(2473.29±263.85μg/g DW),而在 KT 根中在 PFD 充气的单一激发培养中(470.08±25.15μg/g DW)。ATMA 根的细胞外紫杉醇水平从未超过 10%,而 KT 根的紫杉醇水平增加到 76%。在 PFD 脱气支持的单一激发培养中确定了基因表达谱,在 ATMA 根中获得了最高的紫杉烷产量,而在 KT 根中获得了最低的产量。在两条研究发根系中的基因表达模式有很大差异,这导致紫杉烷产量表现出特定系的特点。在 ATMA 根中,在激发后 48 小时收获时观察到 TXS、BAPT 和 DBTNBT 基因的最高共表达,与它们在紫杉烷生产方面的更高能力相对应,而在 KT 根中观察到的效果则相反。