Skip to main content
. Author manuscript; available in PMC: 2017 Jun 1.
Published in final edited form as: Mol Microbiol. 2016 Apr 15;100(6):1039–1065. doi: 10.1111/mmi.13366

TABLE 1.

Mutation in D39 Δcps Δpbp2b suppressor mutants determined by Illumina whole-genome sequencinga

Strainb Gene and mutationc Function nucleotide changed
1. sup2 (IU7477) spd_1346 (mltG) (Δ5 bp at Y403) Hypothetical YceG-like family protein TACTATAG→TAG (Δbp 1212–1216/1656, Y403stop)
2. sup3 (IU7567) spd_1346 (mltG) (Y488D) Hypothetical YceG-like family protein TATGAT (bp 1462/1656)
3. sup4 (IU7570) spd_1346 (mltG)( Δ488 bp at T54) Hypothetical YceG-like family protein Internal out-of-frame Δ488 bp at 165–652/1656
groES (upstream) Co-chaperonin GroES G→T at −48
4. sup5 (IU7765) spd_1346 (mltG) (Ω45 bp)2 Hypothetical YceG-like family protein Out of frame 45 bp (bp 302–346) duplication, TCTTGA (S101stop) at bp 301–303
spd_0115 (G41C) HlyD family secretion protein GGCTGC (bp 121/1253)
a

Illumina whole-genome sequencing was performed as described in Experimental procedures.

b

Strains IU7477, IU7567, IU7570 and IU7765 were isolated from the small number of colonies that arose following independent transformations of unencapsulated D39 Δcps strain IU1945 with a Δpbp2b<>aad9 amplicon (see text and Table S1).

c

Besides the Δpbp2b<>aad9 insertion, the mutational changes shown are compared to the sequence of the IU1945 parent strain.

d

Nucleotide and codon changes are indicated by underlined and bold letters, respectively.