Difference between revisions of "Part:BBa K3790005"
TiTong Fudan (Talk | contribs) (→Experimental Results) |
TiTong Fudan (Talk | contribs) (→Experimental Results) |
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===Experimental Results=== | ===Experimental Results=== | ||
− | Since the length of the albA1 fragment is less than 500bp, we chose to synthesize the sequence ourselves by Oligo assembly using Phanta polymerase. We obtained the sequence information from [https://www.ebi.ac.uk/ena/browser/view/AAK42515] and designed synthetic primers for synthesis | + | Since the length of the albA1 fragment is less than 500bp, we chose to synthesize the sequence ourselves by Oligo assembly using Phanta polymerase. We obtained the sequence information from EBI[https://www.ebi.ac.uk/ena/browser/view/AAK42515] and designed synthetic primers for synthesis |
[[File:T--Fudan--Oligo assembly by Taq polymerase.jpg|thumb|none|400px| '''Figure 1. Oligo assembly by PCR.''' It is generally used to construct completely new or special-purpose DNA. This method may have the disadvantage of a high mutation rate when operated. Once, we had to sequence nine clones of the same construct to get a single correct one. The reason for this is most likely due to complex annealing and amplification. We suggest to have 10-15 rounds amplification without F1 or R1 primer, then add those two primers to have another 25 rounds. Must use high-fidelity enzymes for this method. Due to the pricing, we always use 60bp primers, 58 overlapping annealing temperature, to assemble 300-500bp DNA fragment.]] | [[File:T--Fudan--Oligo assembly by Taq polymerase.jpg|thumb|none|400px| '''Figure 1. Oligo assembly by PCR.''' It is generally used to construct completely new or special-purpose DNA. This method may have the disadvantage of a high mutation rate when operated. Once, we had to sequence nine clones of the same construct to get a single correct one. The reason for this is most likely due to complex annealing and amplification. We suggest to have 10-15 rounds amplification without F1 or R1 primer, then add those two primers to have another 25 rounds. Must use high-fidelity enzymes for this method. Due to the pricing, we always use 60bp primers, 58 overlapping annealing temperature, to assemble 300-500bp DNA fragment.]] |
Revision as of 16:35, 21 October 2021
S.ssb
Introduction
S.ssb is a single-stranded binding protein from Sulfolobus solfataricus (the same species as where Sso7d from). We wanted to test whether the single-stranded binding protein could enhance the enzymatic activity of Bst Pol using the change in the activity of the fusion protein composed of it and Bst Pol.
Usage and Biology
In past studies, double-stranded binding proteins, represented by sso7d, were often thought to enhance the activity of DNA polymerase A or DNA polymerase B. However, as a single-stranded binding protein that can also bind DNA, there is no study to prove whether it can increase the activity of DNA polymerase. Therefore, we chose S. ssb, a single-stranded binding protein from the same species as Sso7d, Sulfolobus solfataricus, to verify whether the single-stranded binding protein could enhance the enzymatic activity of Bst Pol.
Experimental Results
Since the length of the albA1 fragment is less than 500bp, we chose to synthesize the sequence ourselves by Oligo assembly using Phanta polymerase. We obtained the sequence information from EBI[1] and designed synthetic primers for synthesis
The length of albA1 DNA was 288 bp, which is approximately 300 bp after adding homology arms to both ends for PCR cloning. We isolated the DNA of interest by gel extraction for subsequent reactions.
Reference
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]