Kim Beum Jun, Gibson Donna M, Shuler Michael L
School of Chemical and Biomolecular Engineering, Cornell University, Ithaca, New York 14853, USA.
Biotechnol Prog. 2004 Nov-Dec;20(6):1666-73. doi: 10.1021/bp034274c.
The production of secondary metabolites through plant cell suspension cultures is challenging because the level and pattern of production is often unstable and unpredictable. To investigate the factors affecting instability of secondary metabolite production, high Taxol (paclitaxel)-producing Taxus cultures induced by methyl jasmonate elicitation and their low Taxol-producing counterparts were compared with respect to growth and Taxol production kinetics. With Taxus subcultures we observe alternating states of high and low productivity. Parental cultures and their subcultures from five different cell lines were used to test whether a high-producing culture grows more slowly or dies more rapidly than a low-producing one. These cell lines were of three types: (1) Taxol-producing with and without methyl jasmonate, (2) Taxol-producing only upon elicitation, and (3) nonproducing. High-producing cultures show growth inhibition upon subculture, whereas nonproducing elicited cultures show little growth inhibition. Thus, growth inhibition is primarily due to Taxol or taxane accumulation and not a direct result of methyl jasmonate treatment. Through media exchange between high- and low-producing cultures, it appears that culture components generated by cells alter culture properties. To assess variability as a function of culture lineage, two groups of replicate cultures were generated either with a mixing of the parental flasks or segregation of parental flasks at each subculture. Although parental culture mixing did not reduce flask-to-flask variation, the production level of Taxol in subcultures resulting from mixing inocula was sustained at a higher level relative to segregated subcultures. The results are consistent with the possibility of cell signaling within the population that can induce Taxol production.
通过植物细胞悬浮培养生产次生代谢产物具有挑战性,因为其生产水平和模式往往不稳定且不可预测。为了研究影响次生代谢产物生产不稳定性的因素,比较了茉莉酸甲酯诱导的高产紫杉醇红豆杉培养物及其低产对应物在生长和紫杉醇生产动力学方面的差异。对于红豆杉继代培养物,我们观察到了高产和低产的交替状态。使用来自五个不同细胞系的亲本培养物及其继代培养物来测试高产培养物是否比低产培养物生长更慢或死亡更快。这些细胞系有三种类型:(1) 无论有无茉莉酸甲酯都能产生紫杉醇的,(2) 仅在诱导后产生紫杉醇的,(3) 不产生的。高产培养物在继代培养时表现出生长抑制,而未产生紫杉醇的诱导培养物几乎没有生长抑制。因此,生长抑制主要是由于紫杉醇或紫杉烷的积累,而不是茉莉酸甲酯处理的直接结果。通过高产和低产培养物之间的培养基交换,似乎细胞产生的培养成分会改变培养特性。为了评估作为培养谱系函数的变异性,在每次继代培养时,通过混合亲本烧瓶或分离亲本烧瓶产生了两组重复培养物。虽然亲本培养物混合并没有减少烧瓶间的差异,但相对于分离的继代培养物,混合接种物产生的继代培养物中紫杉醇的生产水平维持在较高水平。结果与群体内细胞信号传导可诱导紫杉醇产生的可能性一致。