Optimization of β-Glucuronidase Activity from Lactobacillus delbrueckii Rh2 and Its Use for Biotransformation of Baicalin and Wogonoside

Scutellariae radix, the root of Scutellaria baicalensis, is a traditional medicinal herb containing baicalin and wogonoside as the main flavonoids. Before absorption, these flavonoids are metabolized into their corresponding aglycones, baicalein and wogonin, by β-glucuronidase produced by the intest...

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Published inApplied biological chemistry Vol. 54; no. 2; pp. 275 - 280
Main Authors Ku, S.M., Seoul National University, Seoul, Republic of Korea, Zheng, Hua, Seoul National University, Seoul, Republic of Korea, Park, M.S., Anyang Science University, Anyang, Republic of Korea, Ji, G.E., Seoul National University, Seoul, Republic of Korea
Format Journal Article
LanguageEnglish
Published New York Springer-Verlag 01.04.2011
Springer Nature B.V
한국응용생명화학회
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Summary:Scutellariae radix, the root of Scutellaria baicalensis, is a traditional medicinal herb containing baicalin and wogonoside as the main flavonoids. Before absorption, these flavonoids are metabolized into their corresponding aglycones, baicalein and wogonin, by β-glucuronidase produced by the intestinal microflora. To develop a method for efficient transformation of these flavonoids, optimal conditions for the production of β-glucuronidase from Lactobacillus delbrueckii Rh2 (Rh2) were determined. Addition of 4% galactose to basal medium increased the enzyme activity of Rh2 by about 8-fold. Optimal pH and temperature for the β-glucuronidase activity of cell extract were 5.0 and 50℃, respectively, and more than 95% of the enzyme activity was maintained at 60℃ for 11 h. Under optimal conditions, more than 90% of the glycones were converted into their corresponding aglycones within 3 h. These results demonstrate that the transformation of baicalin and wogonoside from S. baicalensis by Rh2 would be useful for the efficient production of wogonin and baicalein.
Bibliography:F60
2012000559
G704-000111.2011.54.2.019
ISSN:1738-2203
2468-0834
2234-344X
2468-0842
DOI:10.3839/jksabc.2011.043