Team:UESTC-China/Design
From 2014.igem.org
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<div align="center"><img style="width:60% ;" src="https://static.igem.org/mediawiki/parts/5/5b/Hps1.jpg" naptha_cursor="text"> | <div align="center"><img style="width:60% ;" src="https://static.igem.org/mediawiki/parts/5/5b/Hps1.jpg" naptha_cursor="text"> | ||
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<strong>Fig.1</strong> | <strong>Fig.1</strong> | ||
Schematic Representation of the Bacterial RuMP Pathway and the Plant Calvin-Benson Cycle. HPS and PHI denote 3-hexulose-6-phosphate synthase and 6-phospho-3-hexuloisomerase respectively. The abbreviations for several sugar phosphates are as follows: Ru5P, ribulose 5-phosphate; Hu6P, hexulose 6-phosphate; F6P, fructose 6-phosphate; FBP, fructose 1,6-bisphosphate;RuBP,ribulose1,5-bisphosphate;3-PGA,3-phosphoglyce-rate. The other metabolites in the pathway are symbolized merely by their carbon numbers for simplicity. | Schematic Representation of the Bacterial RuMP Pathway and the Plant Calvin-Benson Cycle. HPS and PHI denote 3-hexulose-6-phosphate synthase and 6-phospho-3-hexuloisomerase respectively. The abbreviations for several sugar phosphates are as follows: Ru5P, ribulose 5-phosphate; Hu6P, hexulose 6-phosphate; F6P, fructose 6-phosphate; FBP, fructose 1,6-bisphosphate;RuBP,ribulose1,5-bisphosphate;3-PGA,3-phosphoglyce-rate. The other metabolites in the pathway are symbolized merely by their carbon numbers for simplicity. | ||
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<div align="center"><img style="width:35% ;" src="https://static.igem.org/mediawiki/parts/a/a7/Faldh.jpg"> | <div align="center"><img style="width:35% ;" src="https://static.igem.org/mediawiki/parts/a/a7/Faldh.jpg"> | ||
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<strong>Fig.2</strong> a. <img align="top" src="https://static.igem.org/mediawiki/2014/0/04/C13-nmr.gif"> spectra from leaf extracts of transgenic tobacco plant treated with gaseous <img align="top" src="https://static.igem.org/mediawiki/2014/e/e7/H13CHO.gif"> for 2 h. b. <img align="top" src="https://static.igem.org/mediawiki/2014/0/04/C13-nmr.gif"> spectra from leaf extracts of WT treated with gaseous <img align="top" src="https://static.igem.org/mediawiki/2014/e/e7/H13CHO.gif"> for 2 h. c. The extract from WT plant leaves without <img align="top" src="https://static.igem.org/mediawiki/2014/e/e7/H13CHO.gif"> treatment was used to monitor the background <img align="top" src="https://static.igem.org/mediawiki/2014/0/04/C13-nmr.gif"> signal levels | <strong>Fig.2</strong> a. <img align="top" src="https://static.igem.org/mediawiki/2014/0/04/C13-nmr.gif"> spectra from leaf extracts of transgenic tobacco plant treated with gaseous <img align="top" src="https://static.igem.org/mediawiki/2014/e/e7/H13CHO.gif"> for 2 h. b. <img align="top" src="https://static.igem.org/mediawiki/2014/0/04/C13-nmr.gif"> spectra from leaf extracts of WT treated with gaseous <img align="top" src="https://static.igem.org/mediawiki/2014/e/e7/H13CHO.gif"> for 2 h. c. The extract from WT plant leaves without <img align="top" src="https://static.igem.org/mediawiki/2014/e/e7/H13CHO.gif"> treatment was used to monitor the background <img align="top" src="https://static.igem.org/mediawiki/2014/0/04/C13-nmr.gif"> signal levels | ||
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<div align="center"><img style="width:50% ;" src="https://static.igem.org/mediawiki/parts/a/a2/FDH.png"> | <div align="center"><img style="width:50% ;" src="https://static.igem.org/mediawiki/parts/a/a2/FDH.png"> | ||
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<strong>Fig.3</strong> The abbreviations are as follows: FALDH:glutathione-dependent formaldehyde dehydrogena-se; FDH: Formate dehydrogenase; HM-GSH: S-Hydroxymethyl glutathione; Forml-GSH: Formyl glutathione; SMM cycle: Methionine cycle. | <strong>Fig.3</strong> The abbreviations are as follows: FALDH:glutathione-dependent formaldehyde dehydrogena-se; FDH: Formate dehydrogenase; HM-GSH: S-Hydroxymethyl glutathione; Forml-GSH: Formyl glutathione; SMM cycle: Methionine cycle. | ||
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<div align="center"><img style="width:40% ;" src="https://static.igem.org/mediawiki/2014/4/47/DdFig._4.png"> | <div align="center"><img style="width:40% ;" src="https://static.igem.org/mediawiki/2014/4/47/DdFig._4.png"> | ||
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<strong>Fig.4</strong> Typical stomata in the epidermis illuminated with light for 30 min (<i>Yin Wang,et al.2014</i>). | <strong>Fig.4</strong> Typical stomata in the epidermis illuminated with light for 30 min (<i>Yin Wang,et al.2014</i>). | ||
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<div align="center"><img style="width:50% ;" src="https://static.igem.org/mediawiki/2014/b/b4/DdFig._5.png"> | <div align="center"><img style="width:50% ;" src="https://static.igem.org/mediawiki/2014/b/b4/DdFig._5.png"> | ||
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<strong>Fig.5</strong> Pollen germination of untransformed control plant and sterile transgenic plantsin vitro. Pollen grains were germinated on sucrose-boric acid medium and over 500 pollen grains were observed. a. Untansformed control plant pollen, b. Sterile pollen.Scale bar 25 μm (<i>Pawan Shukla et al 2014</i>). | <strong>Fig.5</strong> Pollen germination of untransformed control plant and sterile transgenic plantsin vitro. Pollen grains were germinated on sucrose-boric acid medium and over 500 pollen grains were observed. a. Untansformed control plant pollen, b. Sterile pollen.Scale bar 25 μm (<i>Pawan Shukla et al 2014</i>). | ||
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<div align="center"><img style="width:70% ;" src="https://static.igem.org/mediawiki/2014/2/22/Dd.png"><br><br> | <div align="center"><img style="width:70% ;" src="https://static.igem.org/mediawiki/2014/2/22/Dd.png"><br><br> | ||
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<strong>Fig.6</strong> The procedure we constructed our vectors. | <strong>Fig.6</strong> The procedure we constructed our vectors. | ||
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<div align="center"><img width="70%" src="https://static.igem.org/mediawiki/2014/1/11/Vector1.png"> | <div align="center"><img width="70%" src="https://static.igem.org/mediawiki/2014/1/11/Vector1.png"> | ||
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<strong>Fig.7</strong> Schematic of vectors we constructed | <strong>Fig.7</strong> Schematic of vectors we constructed | ||
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Revision as of 12:37, 15 October 2014