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. 2014 Jun;80(11):3541–3550. doi: 10.1128/AEM.04160-13

TABLE 3.

Characterization of growth of M. extorquens DM4 and mutants with MMA when provided with plasmid copies of GMAS homologs in trans

Interruptedb CDS(s) and plasmidc Avg generation time (h) ± SD with MMAa provided as:
C + N source C source N source
None
    pCM80 18.9 ± 0.9 18.0 ± 0.4 4.4 ± 0.2
    pME8280 16.2 ± 0.6 15.3 ± 0.3 3.3 ± 0.2
    pME8285 17.5 ± 0.9 18.8 ± 1.6 3.5 ± 0.2
METDI2327
    pCM80 No growth No growth 42.6 ± 1.2
    pME8280 16.9 ± 0.7 15.9 ± 0.3 4.7 ± 0.3
    pME8285 20.2 ± 0.8 16.5 ± 1.3 4.0 ± 0.3
METDI2327, METDI4690
    pCM80 No growth No growth 41.7 ± 1.2
    pME8285 21.5 ± 0.5 19.2 ± 1.5 4.0 ± 0.1
a

MMA was added as the C or N source at 20 or 1.5 mM, respectively. In controls, succinate at 5 mM and (NH4)2SO4 at 1.5 mM were provided as C and N sources, respectively. Similar growth of all strains on succinate (5 mM) and (NH4)2SO4 (1.5 mM) was observed (generation time, 3.4 ± 0.3 h).

b

Interruption of METDI4690 alone conferred no phenotype with MMA as the C or N source (Table 2, mutant DM4Δmetdi4690).

c

pCM80, empty expression vector; pME8280, pCM80 for gmaS expression of METDI2327; pCM8285, pCM80 for expression of METDI4690.