BBa_K1621009 1 BBa_K1621009 pOP - protein expression vector compatible with RFC[25] 2015-08-29T11:00:00Z 2015-09-01T01:44:49Z The sequence is a modified version of the common expression vector pET22b+. Five fragments that were needed for the assembly of the whole part were synthesized by Integrated DNA Technologies. This part contains the sequence for a plasmid backbone that is designed for efficient overexpression of proteins in ''Escherichia coli''. Usually, vectors that are optimized for protein overexpression are low- to medium-copy plasmids. In contrast to cloning purposes, this is sufficient for protein expression. When a certain copy number is reached, the expression machinery of the cell is saturated and a further increase will not result in higher expression yields. High copy plasmids rather result in lower expression rates because more metabolic capacity is shared for replication. <br> <br> Many ''E. coli'' strains optimized for overexpression carry a chloramphenicol resistance gene as a selective marker. Plasmids carrying the same marker are not suitable for protein expression for two reasons. First, double selection for successfully transformed colonies on a medium with two antibiotics is not possible. Second, there is no selective pressure which makes it an advantage for the cell to even keep the plasmid. <br> The iGEM standard vector pSB1C3 was designed for cloning purposes and thus is provided with an origin of replication yielding high plasmid copy numbers. Moreover, it carries a chloramphenicol resistance gene as selection marker which makes it a tough task to use this vector for expression purposes. <br> <br> Using a modified version of pSB1C3 (plasmid map pIG15_001) for overexpression resulted in an unsatisfying protein amount. Working with a common expression vector increased the overexpression efficiency significantly. <br> <br> Obviously, it is a lot of work to clone every part you want to send to the registry into an expression vector and additionally into pSB1C3 which exhibits a completely different cloning site. For those reasons, this new vector backbone was added to the iGEM registry which is suitable for efficient protein overexpression and compatible for cloning parts derived from the registry in a standardized procedure. <br> <br> The new vector, called pOP ??? plasmid for Overexpression of Proteins - combines features needed for efficient overexpression of proteins with standardized elements derived from pSB1C3. Based on the commonly used expression vector pET22b+, some changes had to be applied to fit all the iGEM standards. <br> First, one of the standard cloning sites had to be inserted instead of the original multiple cloning site. RFC[25] seemed to be the most suitable for protein expression purposes, because it allows the assembly of several coding sequences because the scar which is left between the sequences does not result in a frameshift or a stop codon. This is advantageous for expression of fusion proteins on the one hand and enables to genetically fuse the protein of interest to a specific tag for affinity purification on the other hand. Additionally, signal sequences can be added to cause secretion of the protein which is a commonly used tool for simplification of protein purification. <br> Next, recognition sites for restriction enzymes which are used for the insertion of coding sequences had to be eliminated in the backbone, so those enzymes (namely AgeI, EcoRI, NgoMIV, NotI, SpeI, PstI and XbaI) remain single cutters. <br> To allow sequence analysis in a standardized way, the binding sites of the primers VF2 and VR as they are used by the iGEM registry have been inserted in an appropriate distance to the insertion site. <br> <br> The final vector was designed theoretically based on pET22b+. Because the sites where adaptations had to be applied were distributed all over the vector, a multi-step mutagenesis approach was difficult. Instead, the vector was divided into five fragments. In the first step, two or three of the fragments were assembled by fusion PCR. The two resulting fragments were pieced together by Gibson Assembly. The resulting plasmid is shown in figure 1. <br> <br> Taken together, we designed a new plasmid for the overexpression of proteins that is compatible with iGEM cloning standards. We are happy to provide this new backbone to the iGEM registry and help future iGEM teams to reach high expression yields in an easy way. <br> false false _2038_ 25598 25598 9 false The original sequence of pET22b+ was modified to make it compatible to iGEM standard cloning procedures. This includes the removal of recognition sites of several restriction enzymes as well as the insertion of RFC[25] as a multiple cloning site. Further details can be found on the main page. false Ramona Emig, Julika Neumann, Lara Stuehn annotation2441409 1 RBS range2441409 1 4876 4900 annotation2441410 1 VF2 range2441410 1 4906 4924 annotation2441401 1 BioBrick suffix RFC[25] range2441401 1 1 30 annotation2441407 1 lacI range2441407 1 3391 4470 annotation2441403 1 T7 terminator range2441403 1 105 151 annotation2441405 1 beta-lactamase range2441405 1 339 1196 annotation2441402 1 BioBrick prefix RFC[25] range2441402 1 4984 5012 annotation2441408 1 T7 promoter range2441408 1 4857 4873 annotation2441404 1 VR range2441404 1 159 178 annotation2441406 1 ColE1 ori range2441406 1 1354 1973 BBa_K1621009_sequence 1 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tagatggccggc igem2sbol 1 iGEM to SBOL conversion Conversion of the iGEM parts registry to SBOL2.1 James Alastair McLaughlin Chris J. Myers 2017-03-06T15:00:00.000Z