Difference between revisions of "Part:BBa K2271118"
(4 intermediate revisions by 2 users not shown) | |||
Line 1: | Line 1: | ||
− | |||
__NOTOC__ | __NOTOC__ | ||
<partinfo>BBa_K2271118 short</partinfo> | <partinfo>BBa_K2271118 short</partinfo> | ||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here | ||
− | + | ||
<!-- --> | <!-- --> | ||
Line 21: | Line 14: | ||
<partinfo>BBa_K2271118 parameters</partinfo> | <partinfo>BBa_K2271118 parameters</partinfo> | ||
<!-- --> | <!-- --> | ||
+ | |||
+ | <html> | ||
+ | </p> | ||
+ | </html> | ||
+ | __TOC__ | ||
+ | |||
+ | ===Usage and Biology=== | ||
+ | You can use a valencene synthase(ValS) as part of the nootkatone pathway. ValS converts FPP into Valencene. You can chose the ValS from Callitropis nootkatensis, because other valencene synthases perform relatively inefficient in microorganisms[1]. For example, they show a relatively poor product specificity, are less efficient in producing sesquiterpene than other synthases and have a significant amount of side products like germacrene A. In contrast to this, ValS from C. nootkatensis has a good product specificity and is more robust in terms of pH and temperature changes. It has also a better yield than citrus valencene synthases in yeast. | ||
+ | |||
+ | This part is designed for cytosolic expression, for peroxisomal import please choose part: BBa K2271124<br> | ||
+ | |||
+ | |||
+ | ==Characterization== | ||
+ | <div style="text-align:justify;"> | ||
+ | We verified the expression of ValS via western blot. Therefore, we have a 3xFLAG-6xHis-Tag as a part in our plasmids, we can use for the antibodies. The estimated atomic mass of ValS is 69 kDa. | ||
+ | |||
+ | [[File:T--Cologne-Duesseldorf--western-blot-ValS.png|thumb|none| | ||
+ | <strong>Protein abundance in WT and transformed cells from <i>Saccharomyces cerevisiae</i>:</strong> Protein abundance was detected using 6x His Tag Antibody. WT = wild type, ValS = Valencene Synthase, PTS1 = Peroxisom Targeting Signal 1]] | ||
+ | |||
+ | |||
+ | |||
+ | |||
+ | ==References== | ||
+ | <div style="text-align:justify;"> | ||
+ | [1] Jules Beekwilder et al. (2013) Valencene synthase from the heartwood of Nootka cypress (Callitropsis nootkatensis) for biotechnological production of valencene |
Latest revision as of 03:54, 2 November 2017
ValS
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal suffix found in sequence at 2732
Illegal BglII site found at 860 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Usage and Biology
You can use a valencene synthase(ValS) as part of the nootkatone pathway. ValS converts FPP into Valencene. You can chose the ValS from Callitropis nootkatensis, because other valencene synthases perform relatively inefficient in microorganisms[1]. For example, they show a relatively poor product specificity, are less efficient in producing sesquiterpene than other synthases and have a significant amount of side products like germacrene A. In contrast to this, ValS from C. nootkatensis has a good product specificity and is more robust in terms of pH and temperature changes. It has also a better yield than citrus valencene synthases in yeast.
This part is designed for cytosolic expression, for peroxisomal import please choose part: BBa K2271124
Characterization
We verified the expression of ValS via western blot. Therefore, we have a 3xFLAG-6xHis-Tag as a part in our plasmids, we can use for the antibodies. The estimated atomic mass of ValS is 69 kDa.