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. 2001 Jan 15;29(2):506–514. doi: 10.1093/nar/29.2.506

Table 2. Effect of excess Mlc or NagC on expression of nagE–lacZ fusions.

 
 
Control (pTZ19)
PTZ(Mlc)
 
pTZ(NagC)
 
 
 
Units
Units
Rep
Units
Rep
nagBE–lacZ
looped
1410
25
56
16
88
nagE–lacZ
single site
1120
40
28
420
2.7
nagE–lacZ s.o. single site with super-operator 325 42 8 3.3 98

IBPC529C (nagC, mlc-1) was lysogenised with the three nagE–lacZ fusions and then transformed with plasmids overexpressing Mlc or NagC from the lac promoter in a pTZ vector or the empty vector plasmid (pTZ19, control) as indicated. IBPC529C is Δlac so that expression from the lac promoter of the pTZ plasmids expressing Mlc and NagC is constitutive. Bacteria were grown in MOPS medium with 0.4% glycerol, 0.5% cas amino acids and 0.5 mg/ml ampicillin. β-galactosidase activities were measured throughout the exponential growth phase and the values are the mean of two independent cultures. Rep (repression) is the relative decrease in expression of the fusion caused by the presence of the NagC or Mlc plasmid compared with the empty vector plasmid.