Luna-Palencia Gabriela R, Cerda-García-Rojas Carlos M, Rodríguez-Monroy Mario, Ramos-Valdivia Ana C
Departamento de Biotecnología y Bioingeniería, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, Apartado Postal 14-740, México, DF 07000, Mexico.
Biotechnol Prog. 2005 Jan-Feb;21(1):198-204. doi: 10.1021/bp0497031.
Growth and alkaloid production in Uncaria tomentosa cell suspension cultures were studied in Murashige and Skoog medium supplemented with 10 microM 2,4-dichlorophenoxyacetic acid, 10 microM kinetin, and 58 mM sucrose for maintenance and with 10 microM indole-3-acetic acid, 10 microM kinetin, and 58 mM sucrose for production. A U. tomentosa pale Uth-3 cell line, cultured in the production medium, showed a reduced lag phase and a specific growth rate (mu) of 0.27 day(-1), while cells growing in the maintenance medium showed mu = 0.20 day(-1). U. tomentosa cells growing in the production medium produced monoterpenoid oxindole alkaloids (MOA) in amounts of 10.2 +/- 1.6 microg g(-1) dry weight (DW). The chemical profile of MOA produced by in vitro cell cultures was similar to that found in the plant. After 10 subcultures, maximum MOA production decreased to 2.0 +/- 0.7 microg g(-1) DW, while tryptamine alkaloids (TA) were produced with a maximum of 6.2 +/- 0.4 microg g(-1) DW. The increase of initial sucrose concentration up to 145 mM in the production medium enhanced the cell biomass by 3.2-fold (from 10.2 +/- 0.1 to 32.8 +/- 1.1 g DW L(-1)), reduced mu from 0.27 to 0.23 day(-1), and provoked a substantial accumulation of TA (23.1 +/- 4.7 microg g(-1) DW). A high sucrose concentration stimulated MOA production in the maintenance medium (2.7 +/- 0.5 microg g(-1) DW), even in the presence of 2,4-dichlorophenoxyacetic acid.
在添加了10微摩尔2,4 - 二氯苯氧乙酸、10微摩尔激动素和58毫摩尔蔗糖用于维持培养,以及10微摩尔吲哚 - 3 - 乙酸、10微摩尔激动素和58毫摩尔蔗糖用于生产的Murashige和Skoog培养基中,研究了绒毛钩藤细胞悬浮培养物中的生长和生物碱产生情况。在生产培养基中培养的绒毛钩藤浅色Uth - 3细胞系,其延迟期缩短,比生长速率(μ)为0.27天⁻¹,而在维持培养基中生长的细胞μ = 0.20天⁻¹。在生产培养基中生长的绒毛钩藤细胞产生单萜吲哚生物碱(MOA)的量为10.2±1.6微克/克干重(DW)。体外细胞培养产生的MOA化学谱与植物中发现的相似。经过10次传代培养后,MOA的最大产量降至2.0±0.7微克/克DW,而色胺生物碱(TA)的最大产量为6.2±0.4微克/克DW。生产培养基中初始蔗糖浓度增加至145毫摩尔,使细胞生物量增加了3.2倍(从10.2±0.1克DW/升增加到32.8±1.1克DW/升),μ从0.27降至0.23天⁻¹,并引发了TA的大量积累(23.1±4.7微克/克DW)。高蔗糖浓度刺激了维持培养基中MOA的产生(2.7±0.5微克/克DW),即使存在2,4 - 二氯苯氧乙酸。