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. 2013 Jul 26;3:39. doi: 10.1186/2191-0855-3-39

Table 2.

Sequencing results of vector backbones that were subjected to epMEGAWHOP optimization

pET28a(+)-CelA2 pET22b(+)-BSLA pHY-scarlsberg
bp
Substitution
Region
bp
Substitution
Region
bp
Substitution
Region
 
wt
-
M1
 
 
wt
-
M1
 
 
wt
-
M1
 
488
A
-
T
f1 origin
123
T
-
C
T7 term
209
A
-
G
Tet
850
G
-
C
Kan
2007
A
-
G
na
684
A
-
G
Tet
2233
T
-
C
pBR322 ori
3701
A
-
G
Tet
1584
T
-
C
pTet
2396
T
-
C
na
4563
T
-
C
lacI
3238
T
-
C
pAMP
3170
T
-
C
na
4794
C
-
T
lacI
4221
T
-
C
na
5193 A - T T7 prom           4332 A - - ori-177

The positions of the mutations in the corresponding vector backbones are based on the sequenced vector backbone prior epMEGAWHOP. Alignments of all three vector systems to the corresponding ‘parents’ are included in Additional file 1: Figure S1. Nucleotide position 1 is the base after the stop codon (ATT, TAA) of the inserted genes.

na: no corresponding function of the gene sequence could be assigned.

Kan/Tet: Kanamycin/Tetracyclin resistance gene.

pTET/pAMP: promoter region Tetracyclin/Ampicilin resistance gene (identified with a promoter prediction tool (Reese 2001)).