Callus growth kinetics and accumulation of secondary metabolites of Bletilla striata Rchb.f. using a callus suspension culture

• Published in: PloS one 2020-02, Vol.15 (2), p.e0220084-e0220084
• Main Authors: Pan, Yinchi, Li, Lin, Xiao, Shiji, Chen, Zhongjie, Sarsaiya, Surendra, Zhang, Shebo, ShangGuan, Yanni, Liu, Houbo, Xu, Delin
• Format: Article
• Language: English
• Subjects: Acceleration; Accumulation; Biology; Biology and Life Sciences; Biosynthesis; Bletilla striata; Bony Callus - growth & development; Callus; Cell Culture Techniques - methods; Cultivation; Endangered plants; Germplasm; Glucosides - analysis; Growth; Growth curves; Growth kinetics; Growth stage; Herbal medicine; Kinetics; Mathematical models; Medical research; Medicinal plants; Metabolites; Models, Theoretical; Pharmacy; Physical Sciences; Plant metabolites; Plants, Medicinal - metabolism; Reaction kinetics; Regeneration; Research and Analysis Methods; Secondary Metabolism; Secondary metabolites; Seeds; Seeds - chemistry; Stationary phase; Succinates - analysis; Suspension culture; Weight
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0220084

Bletilla striata is an endangered traditional Chinese medicinal plant with multiple uses and a slow regeneration rate of its germplasm resources. To evaluate the callus growth kinetics and accumulation of secondary metabolites (SMs), a callus suspension culture was proven to be a valuable approach for acquiring high yields of medicinal compounds. An effective callus suspension culture for obtaining B. striata callus growth and its SMs was achieved with the in vitro induction of calluses from B. striata seeds. The callus growth kinetics and accumulation of SMs were analyzed using a mathematical model. The resulting callus growth kinetic model revealed that the growth curves of B. striata suspension-cultured calluses were sigmoidal, indicating changes in the growth of the suspension-cultured calluses. Improved Murashige and Skoog callus growth medium was the most favorable medium for B. striata callus formation, with the highest callus growth occurring during the stationary phase of the cultivation period. Callus growth acceleration started after 7 days and thereafter gradually decreased until day 24 of the cultivation period and reached its highest at day 36 period in both the dry weight and fresh weight analyses. The coelonin concentration peaked during the exponential growth stage and decreased afterward during the stationary stage of the callus suspension culture. The maximum content of coelonin (approximately 0.3323 mg/g callus dry weight) was observed on the 18th day of the cultivation cycle, while dactylorhin A and militarine reached the highest concentrations at day 24, and p-hydroxybenzyl alcohol at day 39. This investigation also laid a foundation for a multimathematical model to better describe the accumulation variation of SMs. The production of SMs showed great specificity during callus growth and development. This research provided a well-organized way to increase the accumulation and production of SMs during the scaled-up biosynthesis of calluses in B. striata callus suspension cultures.