Abstract

Atractylodes chinensis is a medicinal plant widely used for the treatment of gastric disorders, and its main bioactive compounds are atractylon and β-eudesmol. This study was purposed to establish the adventitious root culture system of A. chinensis for in vitro production of atractylon and β-eudesmol. The main parameters in the adventitious root induction and suspension cultures were optimized to maximize the culture efficiency. Adventitious roots were induced most efficiently from leaf explants on Murashige and Skoog (MS) solid medium containing 1.5mg/L naphthaleneacetic acid (NAA) and 30g/L sucrose with the highest root induction rate of approximately 92% and 12.9 roots per explant. During the adventitious root suspension culture, the root biomass and the accumulated content of the target compounds simultaneously increased to reach the maximum values after 8weeks of culture. The maximum yield of the target compounds (total concentration 3.38mg/g DW, total yield 2.66mg) was achieved in the roots cultured in ½ MS liquid medium supplemented with 2.0mg/L IBA, 3.2mg/L NAA, and 40g/L sucrose with the inoculum density of 8g/L. Through the central composite design experiment, it was found that the combined use of different types of auxins in the suspension culture could further improve root growth and metabolite accumulation than the application of only one type of auxin. This work provides a new possibility to have a promising candidate for the industrial production of A. chinensis pharmaceuticals without relying on wild resources or field cultivation. KEY POINTS: • The induction culture was optimized for efficient root induction. • Suspension culture was optimized for the atractylon and β-eudesmol production. • Combined use of different auxins improves root growth and metabolite accumulation.

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