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All mutant strains created in the course of this study are still able to mate with CBS999.97 and also with QF1 despite their deletions.
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Plasmid pJC1 was transformed into the parent strain, creating the att:: hdrABC* strain, as well as into the Δ hdrABC deletion mutant strain, creating the Δ hdrABC att:: hdrABC* mutant strain (see Fig. S1 in the supplemental material).
C65S, C65A, and C65P mutant strains were created.
S. oneidensis mutant strains were created as described previously [28].
The Nse3 mutant strains were created using Cre recombinase-mediated cassette exchange, as detailed in Watson et al. [32].
ΔppsA and ΔpckA mutant strains were created by deletion mutagenesis of wild-type S. Typhimurium using a chloramphenicol cassette as described [76].
The E. coli murA (RM345) and ftsZ (RM349) deletion mutant strains were created using the Lambda Red recombinase system with a derivate of pKD4 as a template (Datsenko and Wanner, 2000).
Alternatively, considering that the chemical mutagens with which most of these mutant strains were created cause specific nucleobase alterations (e.g., G→A by EMS), certain septin proteins could be predisposed to acquire Ts– mutations if the codons representing critical residues are easily mutated to nonconservative amino acid substitutions (e.g., GGA→AGA and Gly→Arg).
An aox1 mutant strain was created using targeted gene disruption, and the mutant strain was reconstituted to wild type using a full-length AOX1.
The ΔlaeAΔrsrA double mutant strain was created by crossing TJW131.1 with RJW135.1 to obtain RJW273 and confirmed by PCR.
Since S. oralis is readily transformable, a ciaR mutant strain was created by integrating a resistance marker into the gene.
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