Response Surface Methodology to Optimize Enzymatic Preparation of Deapio-Platycodin D and Platycodin D from Radix Platycodi

doi:10.3390/ijms13044089

Open AccessThis article is

freely available
re-usable

Int. J. Mol. Sci. 2012, 13(4), 4089-4100; doi:10.3390/ijms13044089

Article

Response Surface Methodology to Optimize Enzymatic Preparation of Deapio-Platycodin D and Platycodin D from Radix Platycodi

Wei Li^1,†, Li-Chun Zhao^2,†, Zi Wang¹, Yi-Nan Zheng¹, Jian Liang^2,* and Hui Wang^3,*

¹ College of Chinese Medicinal Materials, Jilin Agricultural University, Changchun 130118, China ² The Affiliated Ruikang Hospital of Guangxi Traditional Chinese Medical College, Nanning 530011, China ³ China-Japan Union Hospital, Jilin University, Changchun 130033, China ^† These authors contributed equally to this work.

* Authors to whom correspondence should be addressed.

Received: 3 February 2012; in revised form: 8 March 2012 / Accepted: 19 March 2012 / Published: 28 March 2012

(This article belongs to the Section Bioactives and Nutraceuticals)

Download PDF Full-Text [554 KB, uploaded 28 March 2012 10:42 CEST]

Abstract: In the present work, we reported the enzymatic preparation of deapio-platycodin D (dPD) and platycodin D (PD) optimized by response surface methodology (RSM) from Radix Platycodi. During investigation of the hydrolysis of crude platycosides by various glycoside hydrolases, snailase showed a strong ability to transform deapio-platycoside E (dPE) and platycoside E (PE) into dPD and PD with 100% conversion. RSM was used to optimize the effects of the reaction temperature (35–45 °C), enzyme load (5–20%), and reaction time (4–24 h) on the conversion process. Validation of the RSM model was verified by the good agreement between the experimental and the predicted values of dPD and PD conversion yield. The optimum preparation conditions were as follows: temperature, 43 °C; enzyme load, 15%; reaction time, 22 h. The biotransformation pathways were dPE→dPD3→dPD and PE→PD3→PD, respectively. The determined method may be highly applicable for the enzymatic preparation of dPD and PD for medicinal purposes and also for commercial use.

Keywords: snailase; deapio-platycodin D; platycodin D; radix platycodi; response surface methodology

Article Statistics

Load and display the download statistics.

Citations to this Article

Load and display citations from CrossRef.

Cite This Article

MDPI and ACS Style

Li, W.; Zhao, L.-C.; Wang, Z.; Zheng, Y.-N.; Liang, J.; Wang, H. Response Surface Methodology to Optimize Enzymatic Preparation of Deapio-Platycodin D and Platycodin D from Radix Platycodi. Int. J. Mol. Sci. 2012, 13, 4089-4100.

AMA Style

Li W, Zhao L-C, Wang Z, Zheng Y-N, Liang J, Wang H. Response Surface Methodology to Optimize Enzymatic Preparation of Deapio-Platycodin D and Platycodin D from Radix Platycodi. International Journal of Molecular Sciences. 2012; 13(4):4089-4100.

Chicago/Turabian Style

Li, Wei; Zhao, Li-Chun; Wang, Zi; Zheng, Yi-Nan; Liang, Jian; Wang, Hui. 2012. "Response Surface Methodology to Optimize Enzymatic Preparation of Deapio-Platycodin D and Platycodin D from Radix Platycodi." Int. J. Mol. Sci. 13, no. 4: 4089-4100.

Int. J. Mol. Sci. EISSN 1422-0067 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert