<p>The reaction time was 30: CHCl<sub>3</sub>-CH<sub>3</sub>OH-H<sub>2</sub>O (65∶35∶10, lower phase). (S, S1, S2, S3), ginsenoside standards (PPD type ginsenoside mixtures); Standards: 1, 3, 5, 7, 9, 11, 13; Reaction mixture: 2, 4, 6, 8, 10, 12, 14; 1, Rb<sub>1</sub>; 2, reaction mixture of Rb<sub>1</sub>; 3, Rd; 4, reaction mixture of Rd; 5, Gyp XVII; 6, reaction mixture of Gyp XVII; 7, Rg<sub>3</sub>(<i>S</i>); 8, reaction mixture of Rg<sub>3</sub>(<i>S</i>); 9, Rb<sub>2</sub>; 10, reaction mixture of Rb<sub>2</sub>; 11, Rb<sub>3</sub>; 12, reaction mixture of Rb<sub>3</sub>; 13, Rc; 14, reaction mixture of Rc. Abbreviations: C-K, compound K.</p
<p>(<b>A</b>) Four mixtures of <sup>32</sup>P-cdiGMP were heated, cooled, spotted on PEI-cellulose T...
<p>Lane: 1, uninduced crude extract; 2, soluble fraction of the crude extract of the induced recombi...
Fig. 4. UPLC-MS analysis of isoquercitrin converted from quercetin by ArUGTs using heterologous expr...
<p>The sampling times were 10: CHCl<sub>3</sub>-CH<sub>3</sub>OH-H<sub>2</sub>O (65∶35∶10, v/v, lowe...
<p>(a), transformation of ginsenoside Re; (b), transformation of ginsenoside Rg<sub>1</sub>. Develop...
400-406Bacterium Lysinibacillus massiliensis No. 24 was tested for its ability to transform the majo...
<p>Example single ion monitoring chromatograms (SIM, m/z = 503.22) obtained for samples taken immedi...
<p>(A) Reaction products from monosaccharides and Glc1<i>P</i>. Reactions were performed with 2 mg/m...
<p>GCMS analysis (extracted ion chromatograms) of products formed <i>in vitro</i> with (<b>A</b>) <i...
<p>GCMS analysis (extracted ion chromatograms) of products formed <i>in vitro</i> with (<b>A</b>) <i...
AbstractBackgroundSome differences have been reported in the biotransformation of ginsenosides, prob...
Fig. 3. UPLC-MS analysis of isoquercitrin converted from quercetin by ArUGTs expressed in TX-TL. (A)...
<p>Lanes: M, molecular weight standard; 1, insoluble fraction of the crude extract of the induced re...
<p>TLC analysis of products are shown. The standards are marked as M: marker, including <i>p</i>NPGl...
Fig. 2. UPLC-MS analysis of isoquercitrin converted from quercetin by AtUGTs expressed in TX-TL. (A)...
<p>(<b>A</b>) Four mixtures of <sup>32</sup>P-cdiGMP were heated, cooled, spotted on PEI-cellulose T...
<p>Lane: 1, uninduced crude extract; 2, soluble fraction of the crude extract of the induced recombi...
Fig. 4. UPLC-MS analysis of isoquercitrin converted from quercetin by ArUGTs using heterologous expr...
<p>The sampling times were 10: CHCl<sub>3</sub>-CH<sub>3</sub>OH-H<sub>2</sub>O (65∶35∶10, v/v, lowe...
<p>(a), transformation of ginsenoside Re; (b), transformation of ginsenoside Rg<sub>1</sub>. Develop...
400-406Bacterium Lysinibacillus massiliensis No. 24 was tested for its ability to transform the majo...
<p>Example single ion monitoring chromatograms (SIM, m/z = 503.22) obtained for samples taken immedi...
<p>(A) Reaction products from monosaccharides and Glc1<i>P</i>. Reactions were performed with 2 mg/m...
<p>GCMS analysis (extracted ion chromatograms) of products formed <i>in vitro</i> with (<b>A</b>) <i...
<p>GCMS analysis (extracted ion chromatograms) of products formed <i>in vitro</i> with (<b>A</b>) <i...
AbstractBackgroundSome differences have been reported in the biotransformation of ginsenosides, prob...
Fig. 3. UPLC-MS analysis of isoquercitrin converted from quercetin by ArUGTs expressed in TX-TL. (A)...
<p>Lanes: M, molecular weight standard; 1, insoluble fraction of the crude extract of the induced re...
<p>TLC analysis of products are shown. The standards are marked as M: marker, including <i>p</i>NPGl...
Fig. 2. UPLC-MS analysis of isoquercitrin converted from quercetin by AtUGTs expressed in TX-TL. (A)...
<p>(<b>A</b>) Four mixtures of <sup>32</sup>P-cdiGMP were heated, cooled, spotted on PEI-cellulose T...
<p>Lane: 1, uninduced crude extract; 2, soluble fraction of the crude extract of the induced recombi...
Fig. 4. UPLC-MS analysis of isoquercitrin converted from quercetin by ArUGTs using heterologous expr...