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. 2009 Jul 31;191(19):6123–6135. doi: 10.1128/JB.00744-09

TABLE 2.

Expression of glnK-lacZ fusion in P. putida and E. coli

Fusion plasmid Structure Strain Other plasmid β-Galactosidase activitya (Miller units ± SD)
Nitrogen excess Nitrogen limitation
P. putida
    pMPO313 glnK-lacZ KT2442 1,167 ± 166 33,204 ± 4,453
    pMPO234 Empty vector KT2442 177 ± 22 153 ± 19
    pMPO313 glnK-lacZ MPO201 (NtrC) 908 ± 126 1,477 ± 90
    pMPO234 Empty vector MPO201 (NtrC) 192 ± 31 152 ± 12
E. coli
    pMPO313 glnK-lacZ ET8000 130 ± 35 13,783 ± 1,774
    pMPO234 Empty vector ET8000 741 ± 178 1,024 ± 260
    pMPO313 glnK-lacZ ET8556 (NtrC) pMPO243 (ntrC) 259 ± 31 8,474 ± 201
    pMPO234 Empty vector ET8556 (NtrC) pMPO243 (ntrC) 535 ± 48 626 ± 70
    pMPO313 glnK-lacZ ET8556 (NtrC) pMPO310 [ntrC(D55E,S161F)] 10,087 ± 1,714 10,212 ± 678
    pMPO234 Empty vector ET8556 (NtrC) pMPO310 [ntrC(D55E,S161F)] 755 ± 101 754 ± 139
    pMPO313 glnK-lacZ ET8556 (NtrC) 189 ± 17 469 ± 68
    pMPO234 Empty vector ET8556 (NtrC) 875 ± 148 1,637 ± 205
a

For P. putida, serine was the nitrogen source, and for E. coli, glutamine was the nitrogen source under nitrogen-limited conditions (see Materials and Methods).