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18 results for “Macleaya”

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zenodo40/100

Macleaya sp. (BR0000012557042)

Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.

opencc-by-sa-4.0May 2019View details →
zenodo40/100

Macleaya cordata (Willd.) R.Br. (BR0000012188871)

Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.

opencc-by-sa-4.0May 2019View details →
zenodo40/100

Macleaya sp. (BR0000021385674)

Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.

opencc-by-sa-4.0May 2019View details →
zenodo40/100

Macleaya cordata (Willd.) R.Br. (BR0000012168576)

Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.

opencc-by-sa-4.0May 2019View details →
zenodo40/100

Macleaya sp. (BR0000012557141)

Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.

opencc-by-sa-4.0May 2019View details →
zenodo40/100

Macleaya kewensis Turrill x (BR0000012451661)

Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.

opencc-by-sa-4.0May 2019View details →
zenodo32/100

Fig. 1 in Establishing the metabolic network of isoquinoline alkaloids from the Macleaya genus

Fig. 1. Diagram of systematic screening of isoquinoline alkaloids by HPLC-Q-TOF-MS combined with a screening method. (a) X, Y, Z, M, and N represent the number of OCH2O, OCH3, OH, glucose, and H groups, respectively. (b) The number of substituent groups connected to the target skeleton is no more than four.

opennotspecifiedMay 2021View details →
zenodo32/100

Fig. 4 in Establishing the metabolic network of isoquinoline alkaloids from the Macleaya genus

Fig. 4. Proposed new biosynthesis pathways for protoberberine (97), sanguinarine (144) and chelerythrine (145).

opennotspecifiedMay 2021View details →
zenodo32/100

Fig. 2 in Establishing the metabolic network of isoquinoline alkaloids from the Macleaya genus

Fig. 2. Proposed metabolic network of isoquinoline alkaloids in the Macleaya genus. a the solid arrow represents verified biosynthesis pathways; b the dotted arrow represents unverified pathways, c the double arrow represents two or more steps needed for biosynthesis; d MT, GOA, and COA are abbreviation for methyl transferase, glycosyltransferase, and cyclooxygenase, respectively; e the red moieties represent the changed substituent groups, and f the blue moieties represent the 13C -labeled benzene ring. (For 6 interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

opennotspecifiedMay 2021View details →
zenodo32/100

Fig. 7 in Preliminary investigations on the pathogenesis-related protein expression profile of the medicinal herb Macleaya cordata and anti-bacterial properties of recombinant proteins

Fig. 7. Antibacterial effects of a series of purified McDef1 concentration against S. aureus (A), E. coli (B), S. pullorum (C) and A. hydrophila (D). 1: 30 μg/ml, 2: 40 μg/ ml, 3: 50 μg/ml, 4: 60 μg/ml, 5: 80 μg/ml, 6: 100 μg/ml, 7: Negative control, empty vector expression supernatant; 8: Positive control, for A̢B̢C: 0.2 mg/mL Ampicillin, for D: 0.5 mg/mL Kanamycin.

opennotspecifiedApr 2021View details →
zenodo32/100

Fig. 6 in Preliminary investigations on the pathogenesis-related protein expression profile of the medicinal herb Macleaya cordata and anti-bacterial properties of recombinant proteins

Fig. 6. Antibacterial effects of recombinant yeasts with McDef1 or McDef2 fermentation supernatant on S. aureus (A), S. pullorum (B), E. coli (C) and A. hydrophila (D). 1: Fermentation supernatant of the recombinant McDef1; 2: Fermentation supernatant of the recombinant McDef2; 3: Negative control, empty vector expression supernatant; 4: Positive control, A̢B̢C: 0.2 mg/mL Ampicillin; D: 0.5 mg/mL Kanamycin.

opennotspecifiedApr 2021View details →
zenodo32/100

Fig. 4 in Preliminary investigations on the pathogenesis-related protein expression profile of the medicinal herb Macleaya cordata and anti-bacterial properties of recombinant proteins

Fig. 4. Multiple sequence alignments of the mature peptides of McLTP1 homologs from different plants with ClustalW2. The target proteins McLTP1 of this study are highlighted with yellow fluorescent background. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

opennotspecifiedApr 2021View details →
zenodo32/100

Fig. 2 in Preliminary investigations on the pathogenesis-related protein expression profile of the medicinal herb Macleaya cordata and anti-bacterial properties of recombinant proteins

Fig. 2. Multiple sequence alignments of the McDef1 (A) and McDef2-5 (B) homologs from different plants with ClustalW2. The conserved domains α-core and γ-core are marked under the homologous sequences respectively. The target proteins McDef1 in (A) and McDef2-5 in (B) of this study are highlighted with yellow fluorescent background. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

opennotspecifiedApr 2021View details →
zenodo32/100

Fig. 1 in Preliminary investigations on the pathogenesis-related protein expression profile of the medicinal herb Macleaya cordata and anti-bacterial properties of recombinant proteins

Fig. 1. The alignment analysis of McDef1-5. The underlined amino acids represent the signal sequence predicted with SignalP. The cysteines are marked in yellow background and the putative disulfide bonds are also shown. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

opennotspecifiedApr 2021View details →
zenodo32/100

Fig. 8 in Preliminary investigations on the pathogenesis-related protein expression profile of the medicinal herb Macleaya cordata and anti-bacterial properties of recombinant proteins

Fig. 8. Antibacterial effects of a series of purified McDef2 concentration against S. aureus (A), E. coli (B), S. pullorum (C) and A. hydrophila (D). 1: 30 μg/ml, 2: 40 μg/ ml, 3: 50 μg/ml, 4: 60 μg/ml, 5: 80 μg/ml, 6: 100 μg/ml, 7: Negative control, empty vector expression supernatant; 8: Positive control, for A̢B̢C: 0.2 mg/mL Ampicillin, for D: 0.5 mg/mL Kanamycin.

opennotspecifiedApr 2021View details →
zenodo28/100

Fig. 3 in Establishing the metabolic network of isoquinoline alkaloids from the Macleaya genus

Fig. 3. TICs of 0-day (A) and 36-day-old (B) tissue culture seedlings.

opennotspecifiedMay 2021View details →
zenodo20/100

Fig. 5 in Preliminary investigations on the pathogenesis-related protein expression profile of the medicinal herb Macleaya cordata and anti-bacterial properties of recombinant proteins

Fig. 5. Tricine-SDS-PAGE analysis of recombinant McDef1 and McDef2 purified from fermentation supernatant. M, Protein standard MW marker; Lane 1, recombinant McDef1; Lane 2, negative control of recombinant McDef1; Lane 3, negative control of recombinant McDef2; Lane 4, recombinant McDef2.

opennotspecifiedApr 2021View details →
zenodo20/100

Fig. 3 in Preliminary investigations on the pathogenesis-related protein expression profile of the medicinal herb Macleaya cordata and anti-bacterial properties of recombinant proteins

Fig. 3. The tertiary structures of McDef1 (A), McDef2-5 (B), McLTP 2 (C) were obtained by SWISS-MODEL.

opennotspecifiedApr 2021View details →

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