Skip to main content
. 2014 Jun 4;9(6):e98791. doi: 10.1371/journal.pone.0098791

Table 1. E. coli strains, plasmid DNAs and oligonucleotides used in this study.

E. coli strains
Strain Relevant genotype Source
RW118 a lamB+ dnaN+ lexA+ sulA211 [65]
RW120 RW118: ΔumuDC595::cat [65]
MS139 lamB::(His6 -dnaN+–cam) [6]
MS198 RW118: lamB::(His6 -dnaN+–cam) dnaN+ This work
MS199 RW118: lamB::(His6 -dnaN+–cam) dnaN–1FS–tet–recF+ This work
MS200 RW118: lamB::(His6 -dnaN+–cam) dnaN–1FS–tet–recF+ (pAMPdnaN+) This work
GS20 lamB20::Tn5 CGSC b
MS201 RW118: lamB20::Tn5 dnaN–1FS–tet–recF+ (pAMPdnaN+) This work
MS202 c RW118: lamB20::Tn5 dnaN–1FS–tet–recF+ (pACMdnaN+) This work
MS203 c RW118: lamB20::Tn5 dnaN–1FS–tet–recF+ (pACMQ61K) This work
MS204 c RW118: lamB20::Tn5 dnaN–1FS–tet–recF+ (pACMS107L) This work
MS205 c RW118: lamB20::Tn5 dnaN–1FS–tet–recF+ (pACMG157S) This work
MS206 c RW118: lamB20::Tn5 dnaN–1FS–tet–recF+ (pACMV170M) This work
MS207 c RW118: lamB20::Tn5 dnaN–1FS–tet–recF+ (pACME202K) This work
MS208 c RW118: lamB20::Tn5 dnaN–1FS–tet–recF+ (pACMM204K) This work
AB1157 d dnaN+ umuD+C+ lexA+ Lab stock
MG1655 e dnaN+ umuD+C+ lexA+ Lab stock
a

The complete annotated genotype for strain RW118 is: rpsL31 xyl-5 mtl-1 galK2 lacY1 tsx-33 supE44 thi-1 hisG4(Oc) argE3(Oc) araD139 thr-1 Δ(gpt-proA)62 sulA211.

b

CGSC: E. coli Genetic Stock Center, Yale University, New Haven, CT 06520, USA.

c

These strains were generated by plasmid shuffle; see Material and Methods for a detailed description of the dnaN plasmid shuffle assay. For strains MS202-MS208, the sequence of each plasmid encoded dnaN allele was verified by automated nucleotide sequence analysis, and the –1 frameshift mutation in the dnaN–1FS allele was confirmed by diagnostic PCR and XhoI restriction analysis.

d

The complete annotated genotype for strain AB1157 is: xyl-5 mtl-1 galK2 rpsL31 kdgK51 lacY1 tsx-33 supE44 thi-1 leuB6 hisG4(Oc) mgl-51 argE3(Oc) rfbD1 proA2 ara-14 thr-1 qsr-9 qin-111.

e

The complete annotated genotype for strain MG1655 is: ilvG rfb-50 rph-1.

f

The sequence corresponding to the XhoI restriction endonuclease site (CTCGAG) within the dnaN 1FS allele, which contains a C→T substitution and −1 dG frameshift (CTTAG), is shown in lower case italics.