Difference between revisions of "Part:BBa K1448000"

(GC analysis ofɤ-terpinene in the culture)
 
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<partinfo>BBa_K1448000 short</partinfo>
 
<partinfo>BBa_K1448000 short</partinfo>
  
This part contains ɤ-terpinene synthase region of ''Citrus unshiu'' and was isolated by Mr.Shimada from ''Citrus unshiu''.[[http://www.sciencedirect.com/science/article/pii/S0168945203003777 Shimada et al, 2003]]
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This part contains ɤ-terpinene synthase region of ''Citrus unshiu'' and was isolated by Dr.Shimada from ''Citrus unshiu''.[[http://www.sciencedirect.com/science/article/pii/S0168945203003777 Shimada et al, 2003]]
 
<br><br><br>
 
<br><br><br>
 
<br>
 
<br>
 
'''Further information:'''
 
'''Further information:'''
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* DDBJ entry: [[http://getentry.ddbj.nig.ac.jp/getentry/na/AB110639/?format=flatfile&filetype=html&trace=true&show_suppressed=false&limit=10 AB110639]]
 
* DDBJ entry: [[http://getentry.ddbj.nig.ac.jp/getentry/na/AB110639/?format=flatfile&filetype=html&trace=true&show_suppressed=false&limit=10 AB110639]]
 
* Origin of the enzyme: ''Citrus unshiu''
 
* Origin of the enzyme: ''Citrus unshiu''
  
[[File:Citrus unshiu.png|thumb|250px|right|Image of ''Citrus unshiu'']]
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[[File:Citrus unshiu.png|thumb|250px|right|Image of ''Citrus unshiu'' [http://ja.wikipedia.org/wiki/%E3%82%A6%E3%83%B3%E3%82%B7%E3%83%A5%E3%82%A6%E3%83%9F%E3%82%AB%E3%83%B3 Wikipedia, 2014,10,18]]]
  
  
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== '''Background and principles''' ==
 
== '''Background and principles''' ==
  
[[File:terinene synthesis.png|thumb|600px|left|Fig.2 Reaction catalyzed by ɤ-terpinene synthase.]]
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[[File:terinene synthesis.png|thumb|600px|left|Fig.1 Reaction catalyzed by ɤ-terpinene synthase. [http://iospress.metapress.com/content/ymr9r05l2k6j3ytb/ Suzuki et al, 2004]]]
  
 
<br><br><br>
 
<br><br><br>
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[[File:westernblot of terpinene.png|thumb|500px|right|(Fig.2 Western-bloting analysis of GST and d-limonene synthase (Lane2), ɤ-terpinene synthase (Lane3) and β-pinene synthase(Lane4) fusion proteins expressed in yeast. (A) The gel picture of SDS-PAGE and western-blot; Lanes: 1, p427-TEF; 2, p427-TEF-LS; 3, p427-TEF-ɤTPNS; 4, p427-TEF-βPINS. (B) vector map of plasmids. (C) The names and molecular weights of each mono-terpene synthase.)]]
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[[File:westernblot of terpinene.png|thumb|500px|right|Fig.2 Western-bloting analysis of GST and d-limonene synthase (Lane2), ɤ-terpinene synthase (Lane3) and β-pinene synthase(Lane4) fusion proteins expressed in yeast. (A) The gel picture of SDS-PAGE and western-blot; Lanes: 1, p427-TEF; 2, p427-TEF-LS; 3, p427-TEF-ɤTPNS; 4, p427-TEF-βPINS. (B) Vector map of plasmids. (C) The names and molecular weights of each mono-terpene synthase.]]
 
   
 
   
 
Yeast cells carrying plasmids of p427-TEF-GST-monoterpenoid synthase were cultivated overnight in SD medium (0.67% yeast nitrogen base and 2% glucose with G418) 50mL at 28°C. Cells were collected and kept at -30˚C. Western blot analysis was carried out using anti-GST antibody and 12.5% polyacrylamide gel with SDS.  
 
Yeast cells carrying plasmids of p427-TEF-GST-monoterpenoid synthase were cultivated overnight in SD medium (0.67% yeast nitrogen base and 2% glucose with G418) 50mL at 28°C. Cells were collected and kept at -30˚C. Western blot analysis was carried out using anti-GST antibody and 12.5% polyacrylamide gel with SDS.  
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'''Introduction'''
 
'''Introduction'''
  
Since ɤ-terpinene is a volatile material, we expected that an amount of ɤ-terpinene were detected at the headspace of the culture in which the transformant with ɤ-terpinene generator is cultivated and tried the detection by GC analysis.
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Since ɤ-terpinene is a volatile material, we expected that an amount of ɤ-terpinene were detected at the headspace of the culture in which the transformant with ɤ-terpinene generator was cultivated and tried the detection by GC analysis.
  
  
[[File:detection of ɤ-terpinene using GC-MS.png|thumb|700px|Fig.4 GC-analysis data]]
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[[File:detection of ɤ-terpinene using GC-MS.png|thumb|660px|Fig.3 GC-analysis data]]
  
 
===GC analysis of ɤ-terpinene in the culture===
 
===GC analysis of ɤ-terpinene in the culture===
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We cultivated the transformants containing ɤ-terpinene generator in p427-TEF or only empty p427-TEF in 50 mL SD medium (0.67% yeast nitrogen base and 2% glucose with G418) at 29˚C, 120 rpm for 24 h.  
 
We cultivated the transformants containing ɤ-terpinene generator in p427-TEF or only empty p427-TEF in 50 mL SD medium (0.67% yeast nitrogen base and 2% glucose with G418) at 29˚C, 120 rpm for 24 h.  
  
Analytic instrument: Shimadzu GC14A
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Analytic instrument:
 
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Column: GLScience InertCap1 (15m Length,0.25 mm I.D., 0.25mm film thickness)
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Injection port 200C, Detector port 210 C
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Detector: Flame Ionization Detector
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Column Oven Temperature 40C/5min- 10C/min-200C/5min
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 +
Shimadzu GC14A
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<br>
 +
Column:
 +
GLScience InertCap1 (15m Length,0.25 mm I.D., 0.25mm film thickness)
 +
<br><br>
 +
Injection port 200C
 +
<br><br>
 +
Detector port 210 C
 +
<br><br>
 +
Detector:
 +
Flame Ionization Detector
 +
<br><br>
 +
Column Oven Temperature
 +
40C/5min- 10C/min-200C/5min
 +
<br><br>
 
Carrier Gas: Helium
 
Carrier Gas: Helium
  
  
  
'''Result'''
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'''Results'''
  
  
we uesd  SPME (SOLID PHASE MICROEXTRACTION) to catch ɤ-terpinene at the headspace of the culture. However, any amounts of ɤ-terpinene were not detected at the headspace of the culture (the exposure time is 30min).
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We uesd  SPME (SOLID PHASE MICROEXTRACTION) to catch ɤ-terpinene at the headspace of the culture. However, any amounts of ɤ-terpinene were not detected at the headspace of the culture (the exposure time is 30min).
  
 
Next we tried to catch ɤ-terpinene in the liquid phase of the culture using monotrap (the exposure time is 1h) and an amount of ɤ-terpinene was detected in the liquid phase of the culture.
 
Next we tried to catch ɤ-terpinene in the liquid phase of the culture using monotrap (the exposure time is 1h) and an amount of ɤ-terpinene was detected in the liquid phase of the culture.
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===Growth curve===
 
===Growth curve===
 
<br>
 
<br>
[[File:Growth curve of yeast cells containing ɤ-terpinene generator.png|thumb|500px|right|Fig.4 transformant: BY4742 containing ɤ-terpinene generator inserted in p427-TEF,  control: BY4742 containing empty p427-TEF ]]
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[[File:Growth curve of yeast cells containing ɤ-terpinene generator.png|thumb|500px|right|Fig.4 Transformant: BY4742 containing ɤ-terpinene generator inserted in p427-TEF,  control: BY4742 containing empty p427-TEF ]]
 
'''Introduction''' :
 
'''Introduction''' :
Various mono-terpenoids are known to have an anti-microbial property. In order to evaluate the anti-microbial property of -terpinene, we made the growth curve of yeast cells containing -terpinene generator and compare to that of yeast cells without -terpinene generator.
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Various mono-terpenoids are known to have an anti-microbial property. In order to evaluate the anti-microbial property of ɤ-terpinene, we made the growth curve of yeast cells containing ɤ-terpinene generator and compare to that of yeast cells without ɤ-terpinene generator.
 
<br><br>
 
<br><br>
'''Method''' :
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'''Methods''' :
We cultivated the transformants containing -terpinene generator in p427-TEF or only empty p427-TEF in 50 mL SD medium (0.67% yeast nitrogen base and 2% glucose with G418) at 29˚C, 120 rpm for 24 h. OD600 was measured every 2 h.
+
We cultivated the transformants containing ɤ-terpinene generator in p427-TEF or only empty p427-TEF in 50 mL SD medium (0.67% yeast nitrogen base and 2% glucose with G418) at 29˚C, 120 rpm for 24 h. OD600 was measured every 2 h.
 
<br><br>
 
<br><br>
'''Result''' :
+
'''Results''' :
Yeast cells containing ɤ-terpinene generator showed slower growth than cells containing empty p427-TEF, indicating that γ-terpinene inhibits the growth of yeast cells.
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Yeast cells containing ɤ-terpinene generator showed slower growth than cells containing empty p427-TEF, indicating that ɤ-terpinene inhibits the growth of yeast cells.
 
<br>
 
<br>
 
<br><br>
 
<br><br>
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== '''Reference''' ==
 
== '''Reference''' ==
*[[http://www.sciencedirect.com/science/article/pii/S0168945203003777 Shimada et al, 2003]]Takehiko Shimada Tomoko Endoa Hiroshi Fujiia Masakazu Harab Takanori Uedaa Masayuki Kitaa Mitsuo Omura (2003) Molecular cloning and functional characterization of four monoterpene synthase genes from Citrus unshiu Marc.
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*[[http://www.sciencedirect.com/science/article/pii/S0168945203003777 Shimada et al, 2003]]Takehiko Shimada, Tomoko Endo, Hiroshi, Fujii Masakazu Hara, Takanori Ueda, Masayuki Kita, Mitsuo Omura (2003) Molecular cloning and functional characterization of four monoterpene synthase genes from Citrus unshiu.
*[[http://pubs.acs.org/doi/abs/10.1021/jf020993f MARIO C. FOTI et al, 2003]]MARIO C. FOTI*,† AND K. U. INGOLD‡ (2003) Mechanism of Inhibition of Lipid Peroxidation by γ-Terpinene, an Unusual and Potentially Useful Hydrocarbon Antioxidant
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*[[http://pubs.acs.org/doi/abs/10.1021/jf020993f MARIO C. FOTI et al, 2003]]MARIO C. FOTI*,† AND K. U. INGOLD‡ (2003) Mechanism of Inhibition of Lipid Peroxidation by γ-Terpinene, an Unusual and Potentially Useful Hydrocarbon Antioxidant.
  
  

Latest revision as of 03:59, 18 October 2014

gamma-terpinene synthase

This part contains ɤ-terpinene synthase region of Citrus unshiu and was isolated by Dr.Shimada from Citrus unshiu.http://www.sciencedirect.com/science/article/pii/S0168945203003777 Shimada et al, 2003



Further information:

Image of Citrus unshiu [http://ja.wikipedia.org/wiki/%E3%82%A6%E3%83%B3%E3%82%B7%E3%83%A5%E3%82%A6%E3%83%9F%E3%82%AB%E3%83%B3 Wikipedia, 2014,10,18]







Background and principles

Fig.1 Reaction catalyzed by ɤ-terpinene synthase. [http://iospress.metapress.com/content/ymr9r05l2k6j3ytb/ Suzuki et al, 2004]



















Characterization

Western-bloting analysis

Fig.2 Western-bloting analysis of GST and d-limonene synthase (Lane2), ɤ-terpinene synthase (Lane3) and β-pinene synthase(Lane4) fusion proteins expressed in yeast. (A) The gel picture of SDS-PAGE and western-blot; Lanes: 1, p427-TEF; 2, p427-TEF-LS; 3, p427-TEF-ɤTPNS; 4, p427-TEF-βPINS. (B) Vector map of plasmids. (C) The names and molecular weights of each mono-terpene synthase.

Yeast cells carrying plasmids of p427-TEF-GST-monoterpenoid synthase were cultivated overnight in SD medium (0.67% yeast nitrogen base and 2% glucose with G418) 50mL at 28°C. Cells were collected and kept at -30˚C. Western blot analysis was carried out using anti-GST antibody and 12.5% polyacrylamide gel with SDS.

<Results> 

Western blot data (Fig.2) showed clear bands around 90kDa in the lanes of p427-TEF- monoterpenoid synthase but not in the lane of empty vector.






























In vivo detection of ɤ-terpinene using GC

Introduction

Since ɤ-terpinene is a volatile material, we expected that an amount of ɤ-terpinene were detected at the headspace of the culture in which the transformant with ɤ-terpinene generator was cultivated and tried the detection by GC analysis.


Fig.3 GC-analysis data

GC analysis of ɤ-terpinene in the culture

Materials and Methods

We cultivated the transformants containing ɤ-terpinene generator in p427-TEF or only empty p427-TEF in 50 mL SD medium (0.67% yeast nitrogen base and 2% glucose with G418) at 29˚C, 120 rpm for 24 h.

Analytic instrument:

Shimadzu GC14A
Column: GLScience InertCap1 (15m Length,0.25 mm I.D., 0.25mm film thickness)

Injection port 200C

Detector port 210 C

Detector: Flame Ionization Detector

Column Oven Temperature 40C/5min- 10C/min-200C/5min

Carrier Gas: Helium


Results


We uesd SPME (SOLID PHASE MICROEXTRACTION) to catch ɤ-terpinene at the headspace of the culture. However, any amounts of ɤ-terpinene were not detected at the headspace of the culture (the exposure time is 30min).

Next we tried to catch ɤ-terpinene in the liquid phase of the culture using monotrap (the exposure time is 1h) and an amount of ɤ-terpinene was detected in the liquid phase of the culture.


Growth curve


Fig.4 Transformant: BY4742 containing ɤ-terpinene generator inserted in p427-TEF, control: BY4742 containing empty p427-TEF

Introduction : Various mono-terpenoids are known to have an anti-microbial property. In order to evaluate the anti-microbial property of ɤ-terpinene, we made the growth curve of yeast cells containing ɤ-terpinene generator and compare to that of yeast cells without ɤ-terpinene generator.

Methods : We cultivated the transformants containing ɤ-terpinene generator in p427-TEF or only empty p427-TEF in 50 mL SD medium (0.67% yeast nitrogen base and 2% glucose with G418) at 29˚C, 120 rpm for 24 h. OD600 was measured every 2 h.

Results : Yeast cells containing ɤ-terpinene generator showed slower growth than cells containing empty p427-TEF, indicating that ɤ-terpinene inhibits the growth of yeast cells.










Reference



Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 204
    Illegal XhoI site found at 715
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]