Difference between revisions of "Part:BBa K517003:Experience"
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===Applications of BBa_K517003=== | ===Applications of BBa_K517003=== | ||
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| + | Beta-pinene synthase expression with pRARE2 in C41 DE3 E.coli that can be used to synthesize alpha- and beta-pinene. | ||
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===User Reviews=== | ===User Reviews=== | ||
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| + | ==Characterization by British Columbia iGEM 2011== | ||
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| + | ===GC-MS analysis of Beta-Pinene Synthase function by British Columbia iGEM 2011=== | ||
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| + | [[Image:Ubcigem2011betapingcms.jpg | frame | center |'''Gas Chromatography Mass Spectrum of Beta-pinene Synthase Products:''' We expressed the beta-pinene synthase (<partinfo>BBa_K517003</partinfo>) in C41 DE3 ''E. coli'' and lysed the cell culture to obtain protein extract which was run through a nickel column to purify the HIS-tagged beta-pinene synthase. The purified synthase was used in an ''in vitro'' enzymatic assay to produce beta-pinene from geranyl diphosphate (GPP) substrate. (A) '''Monoterpene product spectrum of our beta-pinene synthase.''' Through gas chromatography mass spectrometry, we analysed the products of the beta-pinene synthase and found alpha-pinene and beta-pinene. This product spectrum agrees with prior findings (Keeling et al. 2011 BMC Plant Biology). In comparison, the control without GPP indicated by the dark blue link did not produce any monoterpenes. (B) '''Identification of alpha-pinene as a product.''' Cross referencing with standards and a compound library revealed that the beta-pinene product had the characteristic base peaks and retention time of 3.6 minutes. Top panel displays peak spectrum for our sample. Bottom panel displays peak spectrum for library standard. (C) '''Identification of beta-pinene as a product.''' Cross referencing with standards and a compound library revealed that the beta-pinene product had the characteristic base peaks and retention time of 5.6 minutes. Top panel displays peak spectrum for our sample. Bottom panel displays peak spectrum for library standard. ]] | ||
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Latest revision as of 23:42, 28 September 2011
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Applications of BBa_K517003
Beta-pinene synthase expression with pRARE2 in C41 DE3 E.coli that can be used to synthesize alpha- and beta-pinene.
User Reviews
UNIQ4662721e0cebb33e-partinfo-00000000-QINU UNIQ4662721e0cebb33e-partinfo-00000001-QINU
Characterization by British Columbia iGEM 2011
GC-MS analysis of Beta-Pinene Synthase function by British Columbia iGEM 2011
Gas Chromatography Mass Spectrum of Beta-pinene Synthase Products: We expressed the beta-pinene synthase (BBa_K517003) in C41 DE3 E. coli and lysed the cell culture to obtain protein extract which was run through a nickel column to purify the HIS-tagged beta-pinene synthase. The purified synthase was used in an in vitro enzymatic assay to produce beta-pinene from geranyl diphosphate (GPP) substrate. (A) Monoterpene product spectrum of our beta-pinene synthase. Through gas chromatography mass spectrometry, we analysed the products of the beta-pinene synthase and found alpha-pinene and beta-pinene. This product spectrum agrees with prior findings (Keeling et al. 2011 BMC Plant Biology). In comparison, the control without GPP indicated by the dark blue link did not produce any monoterpenes. (B) Identification of alpha-pinene as a product. Cross referencing with standards and a compound library revealed that the beta-pinene product had the characteristic base peaks and retention time of 3.6 minutes. Top panel displays peak spectrum for our sample. Bottom panel displays peak spectrum for library standard. (C) Identification of beta-pinene as a product. Cross referencing with standards and a compound library revealed that the beta-pinene product had the characteristic base peaks and retention time of 5.6 minutes. Top panel displays peak spectrum for our sample. Bottom panel displays peak spectrum for library standard.