Preparative isolation and purification of four prenylflavanones from microbial biotransformation of kurarinone by high-speed counter-current chromatography

Ma, XC; Sun, CK; Huang, SS; Wang, JK; Zhang, BJ; Li, FY; Wang, G; Deng, S; Cui, JA

HERO ID

1116409

Reference Type

Journal Article

Year

2010

Language

English

HERO ID 1116409
In Press No
Year 2010
Title Preparative isolation and purification of four prenylflavanones from microbial biotransformation of kurarinone by high-speed counter-current chromatography
Authors Ma, XC; Sun, CK; Huang, SS; Wang, JK; Zhang, BJ; Li, FY; Wang, G; Deng, S; Cui, JA
Journal Separation and Purification Technology
Volume 76
Issue 2
Page Numbers 140-145
Abstract a- A rapid high-speed counter-current chromatography (HSCCC) method was developed successfully for isolation four transformed products in one-step. a- The novel chemical structures were identified as 4a, 5a-dihydroxy norkurarinone, 7-methoxyl-4a, 5a-dihydroxy norkurarinone and 6a-hydroxykurarinone on the basis of the extensive spectral methods. A preparative high-speed counter-current chromatography (HSCCC) method for isolation and purification of four prenylflavanones from the crud extract after microbial biotransformation of kurarinone was developed successfully using a stepwise elution with two-phase solvent system composed n-hexane-ethyl acetate-methanol-water at the volume ratios of 1:1:0.7:1 (v/v) and 1:1:1.2:1 (v/v). A total of 7mg of 4a,5a-dihydroxy norkurarinone (1), 11mg of 7-methoxyl-4a,5a-dihydroxy norkurarinone (2), 14mg of 6a-hydroxykurarinone (3) and 10mg of norkurarinone (4) were obtained in one-step separation from 520mg of the crude biotransformation sample with purities of 94.0%, 97.8%, 99.5% and 98.7%, respectively. Among them, compounds 1-3 are novel compounds, and their chemical structures were identified on the basis of the extensive spectral methods such as UV, IR, HR-MS and NMR.
Doi 10.1016/j.seppur.2010.09.033
Wosid WOS:000286089800007
Is Certified Translation No
Dupe Override No
Comments Source: Web of Science 000286089800007Scopus URL: https://www.scopus.com/inward/record.uri?eid=2-s2.0-78649448028&doi=10.1016%2fj.seppur.2010.09.033&partnerID=40&md5=23a3651521f24b16e7392764fb5b1b5e
Is Public Yes
Language Text English
Keyword Kurarinone; Biotransformation; Counter-current chromatography; Separation
Is Qa No