Difference between revisions of "Part:BBa K2281002"

 
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In our experiments, due to the position of domain, we have to ligate P2A to the downstream of HbOYE by using bridge PCR. Then this integration is ligated to PcGES to form a whole. The product is our part. The diagram below shows the original pathway of citronellol production. However, by using our part, the last two steps will be combined together and the efficiency will be improved.
 
In our experiments, due to the position of domain, we have to ligate P2A to the downstream of HbOYE by using bridge PCR. Then this integration is ligated to PcGES to form a whole. The product is our part. The diagram below shows the original pathway of citronellol production. However, by using our part, the last two steps will be combined together and the efficiency will be improved.
  
[[File:41.jpg|center|940px|img]]
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[[File:Mosquito_parts-figure1.png|center|940px|img]]
  
 
Information about bridge PCR: In MAST (mRNA accessible site tagging), the DNA tags from synthesized library were employed for identifying mRNA accessible sites. A large number of tags were amplified and subcloned for sequencing to verify mRNA binding profiles. A PCR was designed by using one primer which bridges over the tag terminal sequences. In PCR reaction DNA tag fragments were concatemerized by a bridge primer in reaction cycles.
 
Information about bridge PCR: In MAST (mRNA accessible site tagging), the DNA tags from synthesized library were employed for identifying mRNA accessible sites. A large number of tags were amplified and subcloned for sequencing to verify mRNA binding profiles. A PCR was designed by using one primer which bridges over the tag terminal sequences. In PCR reaction DNA tag fragments were concatemerized by a bridge primer in reaction cycles.
  
  
连接成功的胶图
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[[File:Mosquito-bj-jiao3.png|center|380px|img]]
 
The part is successfully ligated into pSB1C3.The left column is the marker, and the two strips on the right are PCR products of the HbOYE+P2A+PcGES.
 
The part is successfully ligated into pSB1C3.The left column is the marker, and the two strips on the right are PCR products of the HbOYE+P2A+PcGES.
  
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NEB-HbOYE+2A+PcGES-R-PstI:ACCTTGCCCTTTTTTGCCGGACTCAAATAGAAGATGGCAA
 
NEB-HbOYE+2A+PcGES-R-PstI:ACCTTGCCCTTTTTTGCCGGACTCAAATAGAAGATGGCAA
  
蛋白胶图
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[[File:Mosquito-bj-jiao2.png|center|380px|img]]
 
Fig 2 Th e SDS-PAGE electrophoresis of recombinant protein
 
Fig 2 Th e SDS-PAGE electrophoresis of recombinant protein
Lane M, protein marker; Lane 1, total protein with IPTG induction of HbOYE+F2A+PcGES-contained pET32a vector ; Lane 2, total protein with IPTG induction of HbOYE+P2A+PcGES-contained pET32a vector; Lane CK, protein produced by empty pET32a vector. Black arrow shows the targeted recombinant proteins.蛋白诱导条件是30℃诱导3 h,IPTG浓度为0.4 mM
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Lane M, protein marker; Lane 1, total protein with IPTG induction of HbOYE+F2A+PcGES-contained pET32a vector ; Lane 2, total protein with IPTG induction of HbOYE+P2A+PcGES-contained pET32a vector; Lane CK, protein produced by empty pET32a vector. Black arrow shows the targeted recombinant proteins. The condition for protein induction is under 30℃ with the IPTG concentration of 0.4 mM for 3 hours.
 
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杂交图
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Fig 3 Western blot result using HIS antibody. Lane M, protein marker; Lane 1, total protein with IPTG induction of HbOYE+F2A+PcGES-contained pET32a vector ; Lane 2, total protein with IPTG induction of HbOYE+P2A+PcGES-contained pET32a vector; Lane CK, protein produced by empty pET32a vector. 蛋白诱导条件是30℃诱导3 h,IPTG浓度为0.4 mM;Western blotting所用第一抗体为康为世纪CW0304S,第二抗体为康为世纪CW0102S。
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[[File:Mosquito-bj-jiao1.png|center|940px|img]]
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Fig 3 Western blot result using HIS antibody. Lane M, protein marker; Lane 1, total protein with IPTG induction of HbOYE+F2A+PcGES-contained pET32a vector ; Lane 2, total protein with IPTG induction of HbOYE+P2A+PcGES-contained pET32a vector; Lane CK, protein produced by empty pET32a vector. The condition for protein induction is under 30℃ with the IPTG concentration of 0.4 mM for 3 hours; The first antibody used in Western blotting is Kangwei biocompany-CW0304S and the second antibody is Kangwei biocompany-CW0102S
  
 
===Purpose for designing this part===
 
===Purpose for designing this part===

Latest revision as of 00:34, 2 November 2017


-HbOYE-P2A-PcGES-

T--CIEI-BJ--part--002.jpg

HbOYE

LOCUS DQ004685

SIZE 1455 bp

DEFINITION Hevea brasiliensis 12-oxophytodienoate reductase (opr).

HbOYE stands for Hevea brasiliensis Old Yellow Enzyme which is the reductase which bolsters the production of cireonellol from geraniol.

(More information about HbOYE is on the page of part BBa_K2281006)

P2A

P2A sequence: GGAAGCGGAGCGACGAATTTTAGTCTACTGAAACAAGCGGGAGACGTGGAGGAAAACCCTGGACCT

2A, known as CHYSEL polypeptides, contains the peptide bond to grow the peptide chain which helps to link two genes. The presence of the conserved CHYSEL residues in the peptides (Donnelly et al., 1997; Ryan et al., 2002) contributes to form a torsion which causes the peptide chain to be released later (Ryan et al., 2002), and then the two genes can express in a cell separately.

SOURCE

 Teschovirus is a genus of viruses in the order Picornavirales, in the family Picornaviridae. 
 Pigs serve as natural hosts. There is currently only one species in this genus: the type species Porcine teschovirus, 
 which is responsible for the porcine enteroviral encephalomyelitis disease caused in pigs.
 The genus name comes from its type species and the disease it causes: 
 Teschen disease (a severe and fatal form of pig encephalomyelitis), 
 which itself was named for the town in the Czech Republic where the disease was first recognised in 1929.

PcGES

LOCUS KF926075

SIZE 1734 bp

DEFINITION Pogostemon cablin geraniol synthase (GS1) mRNA, partial cds.

PcGES stands for Pogostemon cablin geraniol synthase (GS1) mRNA which is an enzyme which bolsters the production of geraniol. Through the MVA or DXP pathway, Geranyl Diphosphate (GPP) can be produced. Then PcGES helps convert GPP to geraniol.

SOURCE Pogostemon cablin (patchouli)

 ORGANISM  Pogostemon cablin
           Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;
           Spermatophyta; Magnoliophyta; eudicotyledons; Gunneridae;
           Pentapetalae; asterids; lamiids; Lamiales; Lamiaceae; Lamioideae;
           Pogostemoneae; Pogostemon.
                                 T--CIEI-BJ--part002--source.jpg

Patchouli (Pogostemon cablin) is a species of plant from the genus Pogostemon. It is a bushy herb of the mint family, with erect stems, reaching around 75 centimetres (2.5 ft) in height and bearing small, pale pink-white flowers. The plant is native to tropical regions of Asia, and is now extensively cultivated in China, Indonesia, Cambodia, Myanmar, India, Maldives, Malaysia, Mauritius, Seychelles, Madagascar, Taiwan, Philippines, Thailand, Vietnam, South America and the Caribbean.

Experiments

In our experiments, due to the position of domain, we have to ligate P2A to the downstream of HbOYE by using bridge PCR. Then this integration is ligated to PcGES to form a whole. The product is our part. The diagram below shows the original pathway of citronellol production. However, by using our part, the last two steps will be combined together and the efficiency will be improved.

img

Information about bridge PCR: In MAST (mRNA accessible site tagging), the DNA tags from synthesized library were employed for identifying mRNA accessible sites. A large number of tags were amplified and subcloned for sequencing to verify mRNA binding profiles. A PCR was designed by using one primer which bridges over the tag terminal sequences. In PCR reaction DNA tag fragments were concatemerized by a bridge primer in reaction cycles.


img

The part is successfully ligated into pSB1C3.The left column is the marker, and the two strips on the right are PCR products of the HbOYE+P2A+PcGES.

Primer sequence NEB-HbOYE-F-EcoRI:TTTCGCTAAGGATGATTTCTGGATGGCTGAAACTGGAAC

NEB-HbOYE+2A+PcGES-R-PstI:ACCTTGCCCTTTTTTGCCGGACTCAAATAGAAGATGGCAA

img

Fig 2 Th e SDS-PAGE electrophoresis of recombinant protein Lane M, protein marker; Lane 1, total protein with IPTG induction of HbOYE+F2A+PcGES-contained pET32a vector ; Lane 2, total protein with IPTG induction of HbOYE+P2A+PcGES-contained pET32a vector; Lane CK, protein produced by empty pET32a vector. Black arrow shows the targeted recombinant proteins. The condition for protein induction is under 30℃ with the IPTG concentration of 0.4 mM for 3 hours.

img

Fig 3 Western blot result using HIS antibody. Lane M, protein marker; Lane 1, total protein with IPTG induction of HbOYE+F2A+PcGES-contained pET32a vector ; Lane 2, total protein with IPTG induction of HbOYE+P2A+PcGES-contained pET32a vector; Lane CK, protein produced by empty pET32a vector. The condition for protein induction is under 30℃ with the IPTG concentration of 0.4 mM for 3 hours; The first antibody used in Western blotting is Kangwei biocompany-CW0304S and the second antibody is Kangwei biocompany-CW0102S

Purpose for designing this part

The whole purpose of our project is to optimize the efficiency of producing citronellol, so as we combine GES and OYE with 2A, the productive efficiency will be achieved. As for this goal, this part is essential for our project. When functioning, since 2A functions as separating GES gene and OYE gene, which can be automatic removed by cell itself, two independent proteins can be synthesized properly throughout the process. Therefore, but only the final product will be same as before, but also the efficiency is improved.

References

REFERENCE 1 (bases 1 to 1734)

 AUTHORS   Ouyang,P., Zeng,S. and Mo,X.
 TITLE     Cloning and Expression Analysis patchouli geraniol synthase Clone
           and Expression Analysis of Geraniol Synthase Gene in Pogostemon
           cablin
 JOURNAL   Xibei Zhiwu Xuebao 36, 5 (2016)

REFERENCE 2 (bases 1 to 1734)

 AUTHORS   Ouyang,P. and Mo,X.
 TITLE     Direct Submission
 JOURNAL   Submitted (26-NOV-2013) Traditional Chinese Medicine, Guangdong
           Food and Grug Vocational College, Longdong North Road No. 321,
           Tianhe District, Guangzhou, Guangdong 510520, China


REFERENCE 3

 AUTHORS   Mao, Jian Ping
 TITLE   Bridge PCR,An Easy Way for Concatemerizing DNA Tags
 JOURNAL   China Biotechnology (2009).


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]