Difference between revisions of "Part:BBa K2718011"

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===Purification===
 
===Purification===
  
We tried to purify Hmas with Akta pure (GE healthcare) by exchange ion column. We used to eluate 60mL of Tampon B (1M NaCl and Tris 20mM)with gradient of 0 to 100%, figure 3.
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We tried to purify Hmas with Akta pure (GE healthcare) by exchange ion column. We used to eluate 60mL of Tampon B (1M NaCl and Tris 20mM) with gradient of 0 to 100%, figure 3.
  
 
https://static.igem.org/mediawiki/parts/4/44/--Aix-Marseille--HmaS_akta_registry.jpg
 
https://static.igem.org/mediawiki/parts/4/44/--Aix-Marseille--HmaS_akta_registry.jpg
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Figure 3 Elution of HmaS after purification by exchange ion column performed by Akta
 
Figure 3 Elution of HmaS after purification by exchange ion column performed by Akta
  
We can see
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We can see 3 spikes in the elution graph because exchange in chromatography is not a perfect technique to isolate protein. So we decided to do SDS-PAGE (figure 4a and 4b)
  
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https://static.igem.org/mediawiki/parts/3/3f/--Aix-Marseille--HmaS_4a_registry.jpg
  
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Figure 4a SDS-PAGE of eluate after purifiction L. Ladder , 1'X, 2', X ,3' ,4' 5' 3,8,9 and 10 elution samples
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https://static.igem.org/mediawiki/parts/f/f8/--Aix-Marseille--HmaS_4b_registry.jpg
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Figure4 4b SDS-PAGE of eluate after purifiction L. Ladder 11 to 24 elution sample
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We can see a big spot at approxomatively 37kDa, that's may correspond to HmaS. Nevertheless samples are not pure, others proteins are with HmaS. HmaS is on fractions 8 to 17, that's correspon to second spike on figure 3
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===Activity test===
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<span class='h3bb'>Sequence and Features</span>
 
<span class='h3bb'>Sequence and Features</span>

Revision as of 15:36, 16 October 2018


IPTG inductible promotor RBS (strong) HmaS

Usage and Biology

HmaS is used in the metabolic pathway shown in figure 1 to produce benzyl alcohol. HmaS catalyzes the oxidative decarboxylation of phenylpyruvate to produce (S)Mandelate.


T--Aix-Marseille--BenzylAlcohol_pathway.png Figure 1 Metabolic pathway to produce benzyl alcohol


Production

We producted HmaS in E.coli DH5alpha, with 1mm IPTG at OD 0.8, 3 hours

T--Aix-Marseille--HmaS_product_registry.jpg

Figure 2 SDS-PAGE of HmaS production with induction (2, 3 and) 4, without induction ( 1,NI) and with empty plasmid (5)

We see overproduction of HmaS of approximatively 37kDa, that's correspond to molecular wheigt of HmaS. Nonetheless, our inducible promotor is not perfect, and there is basal production of HmaS. Moreover negative control is correct, there is noprodution of HmaS with empty plasmid

Purification

We tried to purify Hmas with Akta pure (GE healthcare) by exchange ion column. We used to eluate 60mL of Tampon B (1M NaCl and Tris 20mM) with gradient of 0 to 100%, figure 3.

--Aix-Marseille--HmaS_akta_registry.jpg

Figure 3 Elution of HmaS after purification by exchange ion column performed by Akta

We can see 3 spikes in the elution graph because exchange in chromatography is not a perfect technique to isolate protein. So we decided to do SDS-PAGE (figure 4a and 4b)

--Aix-Marseille--HmaS_4a_registry.jpg

Figure 4a SDS-PAGE of eluate after purifiction L. Ladder , 1'X, 2', X ,3' ,4' 5' 3,8,9 and 10 elution samples --Aix-Marseille--HmaS_4b_registry.jpg

Figure4 4b SDS-PAGE of eluate after purifiction L. Ladder 11 to 24 elution sample

We can see a big spot at approxomatively 37kDa, that's may correspond to HmaS. Nevertheless samples are not pure, others proteins are with HmaS. HmaS is on fractions 8 to 17, that's correspon to second spike on figure 3

Activity test

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 607
    Illegal BamHI site found at 716
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 556