• 제목/요약/키워드: wogonin

검색결과 88건 처리시간 0.022초

Cloning and Expression of $\beta$-Glucuronidase from Lactobacillus brevis in E. coli and Application in Bioconversion of Baicalin and Wogonoside

  • Kim, Hyun-Sung;Kim, Jin-Yong;Park, Myeong-Soo;Zheng, Hua;Ji, Geun-Eog
    • Journal of Microbiology and Biotechnology
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    • 제19권12호
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    • pp.1650-1655
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    • 2009
  • The $\beta$-glucuronidase (GUS) gene from Lactobacillus brevis RO1 was cloned and expressed in Escherichia coli GMS407. The GUS gene was composed of 1,812 bp, encoding a 603-amino-acid protein belonging to glycosyl hydrolase family 2 with three conserved domains. The amino acid similarity was higher than 70% with the $\beta$-glucuronidases of various microorganisms, yet less than 58% with the $\beta$-glucuronidase of L. gasseri ADH. Overexpression and purification of the GUS was performed in $\beta$-glucuronidase-deficient E. coli GMS407. The purified GUS protein was 71 kDa and showed 1,284 U/mg of specific activity at optimum conditions of pH 5.0 and $37^{\circ}C$. At $37^{\circ}C$, the GUS remained stable for 80 min at pH values ranging from 5.0 to 8.0. The purified enzyme exhibited a half-life of 1 h at $60^{\circ}C$ and more than 2 h at $50^{\circ}C$. When the purified GUS was applied to transform baicalin and wogonoside into their corresponding aglycones, $150\;{\mu}M$ of baicalin and $125\;{\mu}M$ of wogonoside were completely transformed into baicalein and wogonin, respectively, within 3 h.

황금(黃芩)과 구성 화합물의 약리작용에 대한 고찰 (Review of Pharmacological Effects of Scutellaria Baicalensis and Its Bioactive Compounds)

  • 이건석;박민희;천목은;홍진우;조수인
    • 대한예방한의학회지
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    • 제15권2호
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    • pp.69-99
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    • 2011
  • Objective : Scutellaria baicalensis is one of the most popular and multi-purpose herb in traditional medicine. It is also useful for its practicability to cultivate in Korea. The purpose of this study is to contribute to researches and applications of scutellaria baicalensis by analyzing and reviewing international researches on the compositions and the effects of scutellaria baicalensis. Methods : This study analyzed 146 articles from PubMed by searching with the keyword "Scutellaria baicalensis", "Huang quin", "Baical Skullcap", "Huang qin", "baical skullcap root", "ogon", "Hwanggeum" and "Hwangkeum", published within the last 10 years(from 2000 to 2009). We reviewed the 146 articles on Scutellaria baicalensis and its active constituents in terms of 'Active constituents', 'Experimental studies', 'Clinical studies', 'Drug interaction', 'Side Effects/Toxicity' and 'Pharmacokinetics'. Results : The active constituents of Scutellaria baicalensis are flavonoids such as baicalein, baicalin, wogonin and oroxylin-A. It is reported that scutellaria baicalensis and its active compounds have antiinflammatory activity, antitumor activity, antioxidant activity, antiviral and antibiotic activity, neuroprotective effects, hepatoprotective effects and cardiovascular effect. Conclusions : This study is aimed to summarize the results obtained within the last 10 years and to contribute to following researches and applications of Scutellaria baicalensis.

LC-ESI-MS/MS를 이용한 용담사간탕의 주요 성분 분석 (Quantitative Analysis of the Marker Constituents in Yongdamsagan-Tang using Liquid Chromatography-Electrospray Ionization-Tandem Mass Spectrometry)

  • 서창섭;하혜경
    • 생약학회지
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    • 제48권4호
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    • pp.320-328
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    • 2017
  • Yongdamsagan-tang has been used to treat the urinary disorders, acute- and chronic-urethritis, and cystitis in Korea. In this study, an ultra-performance liquid chromatography-electrospray ionization-mass spectrometry (UPLC-ESI-MS/MS) method was established for simultaneous analysis of the 20 bioactive marker compounds, geniposidic acid, chlorogenic acid, geniposide, liquiritin apioside, acteoside, calceolarioside B, liquiritin, nodakenin, baicalin, liquiritigenin, wogonoside, baicalein, glycyrrhizin, wogonin, glycyrrhizin, wogonin, saikosaponin A, decursin, decursinol angelate, alisol B, alisol B acetate, and pachymic acid in traditional herbal formula, Yongdamsagan-tang. Chromatographic separations of all marker compounds were conducted using a Waters Acquity UPLC BEH $C_{18}$ analytical column ($2.1{\times}100mm$, $1.7{\mu}m$) at $45^{\circ}C$ using a mobile phase of 0.1% (v/v) formic acid in water and acetonitrile with gradient elution. The MS analysis was performed using a Waters ACQUITY TQD LC-MS/MS coupled with an electrospray ionization source in the positive and negative modes. The flow rate was 0.3 mL/min and injection volume was $2.0{\mu}L$. The correlation coefficient of 20 marker compounds in the test ranges was 0.9943-1.0000. The limits of detection and quantification values of the all marker components were 0.11-6.66 and 0.34-19.99 ng/mL, respectively. As a result of the analysis using the optimized LC-ESI-MS/MS method, three compounds, geniposidic acid (from Plantaginis Semen), alisol B (from Alismatis Rhizoma), and pachymic acid (from Poria Sclerotium), were not detected in this sample. While the amounts of the 17 compounds except for the geniposidic acid, alisol B, and pachymic acid were $0.04-548.13{\mu}g/g$ in Yongdamsagan-tang sample. Among these compounds, baicalin, bioactive marker compound of Scutellariae Radix, was detected at the highest amount as a $548.13{\mu}g/g$.

A Study on the Transformation of Baicalin or Antibacterial, Antitumor Effect of the Active Ingredients in Scutellariae Radix

  • 박성규;안덕균;우은란;박현미
    • 대한한의학회지
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    • 제18권1호
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    • pp.169-186
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    • 1997
  • Scutellariae Radix has been widely used as oriental herbal medicine for the treatment of bacterial infections in the respiratory or the gastrointestinal tract. In partition experiment for better understanding of herbal medicine with various solvents, baicalein or wogonin have more hydrophobic characteristics than baicalin or wogonoside. Unexpectedly, methylene chloride could extract more for baicalin or wogonoside over other active ingredients. New compound from baicalin is discovered casting frointier area on herbal medicine in the future. Application study with new molecule hydrolyzed from baicalin is on the way for better treatment of the patient against specific disease. The baicalin modified with reaction has been shown weak antibacterial activity against Streptococcus pyogenes 308A and Pseudomonas aeruginosa 1771. The minimum inhibitory concentration (MIC) of the baicalin modified compound against those strains were about $600\;{\mu}g/mL$, respectively. In vitro antitumor experiment, $EC_{50}$ of baicalin modified with reaction was more than $300\;{\mu}g/mL$ and $EC_{50}$ of baicalein was $100\;{\mu}g/mL$. Among these compounds, baicalin exhibited high level of antitumor activity. $EC_{50}$ of baicalin was less than $33.3\;{\mu}g/mL$.

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수치에 의한 황금의 성분변화 (Change of Flavonoid Composition in Scutellaria baicalensis by Processing)

  • 김장희;양기숙;김태희
    • 약학회지
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    • 제43권1호
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    • pp.16-22
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    • 1999
  • Scutellaria baicalensis Georgi (Labiatae) has been extensively used in treatment of diarrhea, conjunctivitis, gastritis, enteritis and skin disease. As instructed in old description, the Scutellariae Radix should sometimes be processed before use. To 노디 light on the changes of chemical compositions by processing as well as processing method-activity relationships, Scutellariae Radix was heated at 16$0^{\circ}C$-20$0^{\circ}C$ for 30 min. in furnace or soaked with 20% EtOH (SPE) and boy's urine(SPU), respectively, which are one of processing methods and then heated at 17$0^{\circ}C$ for 30 min. To isolate the chemical components, Scutellariae Radix with/without processing were extracted with EtOH and EtOH extract was fractionated with ether, ethyl acetate and butanol to give respective fractions. Ether and EtOAc fractions obtained from the processed drug with urine (SPU) were subjected to chromatography to obtainsix components, oroxylin A, Wogonin, chrysin, baicalein, baicalein 7-O-$\beta$-D-glucopyranoside and $\beta$-sitosterol 3-O-$\beta$-D-glucopyranoside. All the isolated compounds were identified by means of physicochemical and spectroscopic methods (IR, $^1H-NMR,{\;}^13C-NMR$, Mass). By HPLC determination, the changes of the contents for each isolated components from SPE and SPU samples were observed. It was found that the content of nonglycosidic flavones such as oroxylin A, wogonin, chrysin and baicalein was increased markedly, whereas the content of baicalin and baicalein 7-O-$\beta$-D-glucopyranoside was significantly decreased in both samples as compared with those of Scutellariae Radix. When the sample was soaked with boy's urine, the total amount of nonglycosidic flavones was higher than that of processing with 20% EtOH.

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Analysis of Scutellaria baicaleinsis Georgi (Scutellariae Radix) by LC-DAD and LC-ESI/MS

  • Yu, Youngbob;Choi, Pil-Son;Koo, Sungtae;Chang, Suhwan
    • 한국자원식물학회지
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    • 제31권6호
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    • pp.652-659
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    • 2018
  • In this study, baicalin, as a marker substance of Scutellariae Radix, was quantitatively analyzed by a high performance liquid chromatography-photodiode array detector (HPLC-DAD). We identified wogonoside, baicalein, and wogonin in the Scutellariae Radix by a high performance liquid chromatography-electrospray ionization-mass spectrometer (HPLC-ESI-MS). The baicalin was separated on a Xterra C18 column ($5{\mu}m$, $4.6{\times}250mm$) using mobile phase consisting of 38% acetonitrile in 0.68% phosphoric acid. The baicalin spectrum in the Scutellariae Radix extracts was coincided by comparing with UV-visible spectrum (200-550 nm) of baicalin standard in the library. The amount of baicalin in Scutellariae Radix was 10.46%, which is higher than KFDA's guideline. The marker substances of Scutellariae Radix showed a strong base peak $[M]^+$ in the positive detection mode following as; baicalin (m/z; $271[MH^+-sugar]^+$, $447[M+H]^+$), wogonoside (m/z; $285[MH^+-sugar]^+$, $461[M+H]^+$), baicalein (m/z; $271\;[M+H]^+$), wogonin (m/z; $285[M+H]^+$). These results are consistent with the fragment pattern and molecular weight of standard components from literature.

토성(土性) 및 시비조건(施肥條件)이 황금(黃芩)의 생육(生育), 수량(收量) 및 품질(品質)에 미치는 영향(影響) (Effect of Soil Textures and Fertilizer Application Conditions on the Growth, Yield and Quality of Scutellaria baicalensis G.)

  • 김명석;박장현;정병준;박규철;박태동;김상철;심재한
    • 한국약용작물학회지
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    • 제9권2호
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    • pp.91-98
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    • 2001
  • 남부지방의 황금재배시 토성 및 시비조건에 따른 증수효과(增收效果)를 구명하고자 여천(麗川) 재래종(在來種)을 공시(供試)하여 재식거리를 $40{\times}10cm$로 콘크리트 pot에 토성별 시비조건을 달리하여 4월(月) 1일(日)에 점파하였고 시험을 수행한 결과를 요약하면 다음과 같다. 1. 공시토양의 화학성을 보면 유기물, 유효인산(有效燐酸), 칼리함량은 식양토, 양토, 사양토 순으로 증가되는 경향을 보였고 토양의 물리성은 사양토에서 고상(固相)비율, 식양토에서 공극율이 가장 높았으며 퇴비의 전질소(全窒素) 및 칼리함량이 각각 2.25, 1.59%였고 C/N율은 21.4로 분해가 용역(容易)하였다. 2. 입모률(立毛率)은 퇴비시용구가 $86{\sim}88%$로 높았고 토성 및 시비조건의 생육(生育)은 양토 및 퇴비시용이 경장 및 경태가 각각 $44{\sim}47\;cm$, $7.50{\sim}8.17\;mm$로 가장 길고 굵어져 주당 분지수 및 건경엽중이 각각 $16.6{\sim}18.5$개, $22.1{\sim}26.0\;g$정도로 증가되었다. 3. 지하부 생육을 보면 식양토와 무비구에 비해 양토 및 퇴비 시용구가 주근장 및 주근경은 각각 $2.2{\sim}3.0\;cm$, $1.09{\sim}1.81\;mm$ 정도로 길고 굵어져 상근중 비율도 $2{\sim}6%$ 높아졌으며 주당 건근중이 $2.3{\sim}3.2\;g$으로 무거워 생장량이 증대되었다. 4, 근(根)의 baicalin, baicalein, wogonin 함량은 토성 간에는 식양토가 각각(各各) 9.03%, 2.72%, 1.62% 높은 함량으로 나타났고 시비조건은 무비구(無肥區)(7.13%, 1.35%, 0.49%)에 비해 퇴비 시용구에서 각각 2.80%, 2.45%, 1.91% 높은 함량을 보였다. 5. 토성 및 시비조건에 따른 상관관계는 경장, 주당 분지수, 주근장, 건근중 등의 지참, 지하부생육과 근의 전질소, 가리간에는 정(正)의 상관을 보였고 근의 baicalin, baicalein, wogonin 등의 총 유효성분함량과는 유의적(有意的)인 부(負)의 상관이 인정되었다.

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천연방부제 개발을 위한 자원식물을 활용한 발효 전·후 물질 변화와 항균활성 비교 (Comparison of Substance Change and Antibacterial Activity Before and After Fermentation Using Resource Plants for The Development of Natural Preservatives)

  • 정서아;정연옥;송가현;박노복
    • 현장농수산연구지
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    • 제25권1호
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    • pp.20-35
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    • 2023
  • 화학방부제는 항균활성은 좋지만 많은 부작용이 보고되고 있어 최근에는 인체에 해가 없으며 방부 기능과 자체 효능이 있는 천연방부제의 개발이 활발하다. 또한 천연물의 흡수율을 높이기 위한 방법으로 분자량이 커서 인체에 잘 흡수되지 않아 저분자화를 시키기 위한 방법으로 균주를 이용하여 발효하는 것도 늘어나고 있는 추세이다. 이에 천연방부제가 방부 효과는 지속되어야 하고 첨가했을 때 품질에 손상을 주지 않아야 하며, 향, 색과 성분에 영향을 끼치지 않아야 한다는 요건들을 충족시켜야 한다. 따라서 본 연구는 인체에 해가 없으며 항균활성이 좋은 황금, 단삼, 관중을 선정하였다. 식물은 모두 에탄올로 추출하였고, 발효균주로는 B. subtilis, L. casei, S. cerevisiae와 누룩에서 분리한 Asp. oryzae로 액체와 고체발효를 하여 발효 전과 발효 후의 유효성분의 함량을 비교하였다. 항균활성을 알아보기 위해 C. albicans, S. aureus, P. aeruginosa 세균 3종과 진균은 E. coli로 억제력을 탐색하였다. 천연방부제 개발로 사용하기 위해서는 항균활성이 있고 이러한 실험을 수행하여 다음과 같은 결과를 얻었다. 1. 원산지, 굵기와 용매에 따른 수율은 황금은 중국산이며 굵기는 2,800㎛로 50% ethyl alcohol 추출물에서 21.88%, 단삼은 국내산으로 굵기는 2,800㎛이며 50% ethyl alcohol 추출물에서 25.62%, 관중은 중국산으로 굵기는 2,800㎛, 70% ethyl alcohol 추출물에서 6.50%의 수율을 얻었다. 2. L. casei로 1일 액체 발효했을 때 수율은 황금 66.8%, 단삼 84.8%, 관중 73.0%였다. B. subtilis로 고체발효한 황금과 단삼은 24.40%, 39.30%, 관중은 L. casei로 발효 했을 때 11.10%의 수율을 얻었다. 3. 액체발효 후 황금에서 S. aureus 균주에 대하여 9mm 정도의 clear zone이 확인되었고, 단삼과 관중 발효에서는 항균력이 확인되지 않았다. 4. 황금을 L. casei로 고체발효 했을 때 C. albicans와 S. aureus에서 높은 항균활성을 보였다. 단삼은 S. cerevisiae로 고체발효 했을 때 S. aureus에서 항균활성을 보였다. 관중은 L. casei, S. cerevisiae로 고체발효 했을 때 E. coli와 S. aureus에서 항균활성이 높게 나타났다. 발효하지 않았을 때보다 발효 후의 항균활성이 매우 높았다. 5. 유효성분의 변화는 고체발효하지 않은 황금에서는 baicalin 101.57, baicalein 28.26, wogonin 5.33mg/g이었고, S. cerevisiae로 고체발효 했을 때는 baicalin 94.31, baicalein 30.41, wogonin 3.57mg/g로 baicalein의 함량은 증가된 것으로 확인되었다. 발효하지 않은 단삼에서는 salvianolic acid A가 1.82mg/g 이었으며, S. cerevisiae로 고체발효했을 때는 5.70mg/g으로 증가하였다. 관중의 유효성분은 flavaspidic acid AP, flavaspidic acid PB, flavaspidic acid AB, flavaspidic acid BB로 나타났다.

Flavonoids with Bradykinin Antagonistic Effects from Scutellariae Radix

  • YunChoi, Hye-Sook;Yoo, Kyung-Sook;Chung, Sung-Hyun;Yang, Hyun-Sook;Choi, Jin-Jae;Kim, Young-Joo
    • 생약학회지
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    • 제23권4호
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    • pp.234-239
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    • 1992
  • Seven flavonoid components were isolated from fr. C of Scutellariae radix which showed antagonistic effects against bradykinin(BK). The results indicated that two oxygen functions (either -OH or $-OCH_3$) at 2'- and 6'-positions and/or an oxygen function at 6-position of flavone seemed to be favored for the BK inhibitory activities. Skullcapflavone-II(IV) which contains $6-OCH_3$, 2'-OH and $6-OCH_3$ in the structure was the most active among the flavones tested.

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시호(柴胡)함유 한방제(漢方劑)중 황금(黃芩) 지표성분(指標成分)의 확인(確認) 및 Baicalin 정량(定量) (Identification of Index Components of Scutellariae Radix and Quantitative Determination of Baicalin from Curde Drug Preparation Containing Bupleuri Radix)

  • 최강주;고성룡;양재원
    • 생약학회지
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    • 제21권2호
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    • pp.158-162
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    • 1990
  • As a part of studies on the quality control of crude drug preparation, So-Shi-Ho-Tang, index components of Scutellariae Radix were identified by TLC and quantified by HPLC. Wogonin and baicalein were identified in ethyl ether fraction on silica gel plate with benzene/ethyl acetate (1 : 1, v/v). The content of baicalin was determined by HPLC on ${\mu}-Bondapak\;C_18$ column with 0.5%-phosphoric acid/acetonitrile (73 : 27, v/v). Its recovery rate in the extract granules, compared to the content in the Scutellariae Radix, was $52.1\;{\pm}\;0.7%$.

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