Difference between revisions of "Part:BBa K3996012"

 
 
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pXynA
 
pXynA
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== Profile ==
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=== Name: pXynA ===
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=== Base Pairs: 2631bp ===
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=== Origin: synthesis ===
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=== Properties: A Yeast Expression plasmids backbone ===
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==== Usage and Biology ====
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It is formed with pOdd-3 plasmid backbone, FBA1 promoter, AnXlnD orf and CYC1 terminator.
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== Construct design ==
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The plasmid is engineered for further use. (Figure 1).
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[[File:T--Beijing United--BBa K3996012 Figure1.png|500px|thumb|center|Figure 1. DNA map of plasmid pXylan..]]
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== Experimental approach ==
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1. Fragments PCR products Electrophoresis
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To utilize the xylan component contained in the wheat B starch, we cloned the xylanase expression gene from Aspergillus niger.
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[[File:T--Beijing United--BBa K3996007 Figure3.png|500px|thumb|center|Figure 2. Plasmids construction used fragments PCR amplification..]]
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(A) Lane 1: GAP promoter, 695 bp. Lane 2: AnXlnB CDS, 706 bp. Lane 3: CYC1 terminator, 276bp. Lane 4: pXlnB plasmid backbone fragment, 1757 bp. Lane 5: TPI1 promoter, 614 bp. Lane 6: AnXlnD CDS, 2443 bp. Lane 7: pXlnD plasmid backbone fragment, 1804 bp.
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(B) Lane 1: pXlnB plasmid backbone fragment, 1804 bp. Lane 2: pXlnD plasmid backbone fragment, 1804 bp.
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For the pXlnB plasmid construction, the promoter GAP, codon-optimized AnXlnB CDS, and CYC1 terminator PCR bands were shown in the Figure 3A, lane 1, lane2, and lane 3, respectively. The AnXlnB expression cassette was obtained through the overlap PCR. The backbone fragment (kanR with ori) was amplified using two round PCR, the first round and the final fragment band were shown in Figure 3A lane 4 and Figure 3B lane 1, respectively. The backbone was cut with Bsa1 restriction enzyme and ligated with the AnXlnB expression cassette to make the plasmid pXlnB.
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== References ==
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=== 1. 王良东. 小麦B淀粉的组分, 性质和利用的研究[D]. 江南大学, 2004. ===
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=== 2. 赵银峰. 小麦酒精发酵新工艺的研究[D]. 郑州大学, 2005. ===
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=== 3. Claes A, Deparis Q, Foulquié-Moreno M R, et al. Simultaneous secretion of seven lignocellulolytic enzymes by an industrial second-generation yeast strain enables efficient ethanol production from multiple polymeric substrates[J]. Metabolic engineering, 2020, 59: 131-141. ===
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<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Latest revision as of 03:39, 20 October 2021


pXynA

pXynA

Profile

Name: pXynA

Base Pairs: 2631bp

Origin: synthesis

Properties: A Yeast Expression plasmids backbone

Usage and Biology

It is formed with pOdd-3 plasmid backbone, FBA1 promoter, AnXlnD orf and CYC1 terminator.

Construct design

The plasmid is engineered for further use. (Figure 1).

Figure 1. DNA map of plasmid pXylan..

Experimental approach

1. Fragments PCR products Electrophoresis To utilize the xylan component contained in the wheat B starch, we cloned the xylanase expression gene from Aspergillus niger.

Figure 2. Plasmids construction used fragments PCR amplification..

(A) Lane 1: GAP promoter, 695 bp. Lane 2: AnXlnB CDS, 706 bp. Lane 3: CYC1 terminator, 276bp. Lane 4: pXlnB plasmid backbone fragment, 1757 bp. Lane 5: TPI1 promoter, 614 bp. Lane 6: AnXlnD CDS, 2443 bp. Lane 7: pXlnD plasmid backbone fragment, 1804 bp. (B) Lane 1: pXlnB plasmid backbone fragment, 1804 bp. Lane 2: pXlnD plasmid backbone fragment, 1804 bp. For the pXlnB plasmid construction, the promoter GAP, codon-optimized AnXlnB CDS, and CYC1 terminator PCR bands were shown in the Figure 3A, lane 1, lane2, and lane 3, respectively. The AnXlnB expression cassette was obtained through the overlap PCR. The backbone fragment (kanR with ori) was amplified using two round PCR, the first round and the final fragment band were shown in Figure 3A lane 4 and Figure 3B lane 1, respectively. The backbone was cut with Bsa1 restriction enzyme and ligated with the AnXlnB expression cassette to make the plasmid pXlnB.

References

1. 王良东. 小麦B淀粉的组分, 性质和利用的研究[D]. 江南大学, 2004.

2. 赵银峰. 小麦酒精发酵新工艺的研究[D]. 郑州大学, 2005.

3. Claes A, Deparis Q, Foulquié-Moreno M R, et al. Simultaneous secretion of seven lignocellulolytic enzymes by an industrial second-generation yeast strain enables efficient ethanol production from multiple polymeric substrates[J]. Metabolic engineering, 2020, 59: 131-141.

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal PstI site found at 885
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal PstI site found at 885
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 1278
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal PstI site found at 885
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal PstI site found at 885
    Illegal NgoMIV site found at 2062
    Illegal AgeI site found at 1655
  • 1000
    COMPATIBLE WITH RFC[1000]