Skip to main content
. 2002 Jun;184(12):3232–3241. doi: 10.1128/JB.184.12.3232-3241.2002

TABLE 2.

β-Galactosidase produced from transcriptional fusionsa

Strain Relevant genotype β-Galactosidase activity (U/mg of protein)
Glutamate plus NH4+ Glutamate Glutamate plus allantoin
HH422 amyE::pucA′-lacZ 1 335 12
CJ13 amyE::pucA′-lacZ pucR::pBOER 1 145 117
LB032 amyE::pucF′-lacZ 1 37 1,818
CJ12 amyE::pucF′-lacZ pucR::pBOER 1 2 19
CO7 amyE::pucH′-lacZ 2 17 354
CJ10 amyE::pucH′-lacZ pucR::pBOER 2 2 3
HØR19 amyE::pucI′-lacZ 1 23 400
HØR29 amyE::pucI′-lacZ pucR::pBOER 1 10 60
LB035 amyE::pucJ′-lacZ 2 1,002 2,336
CJ14 amyE::pucJ′-lacZ pucR::pBOER 1 3 8
CO3 amyE::pucR′-lacZ 1 27 6
LB175 amyE::pucR′-lacZ pucR::pBOER 1 508 420
LB031 amyE::gde′-lacZ 4 12 160
ED441 amyE::gde′-lacZ pucR::pBOER 5 5 3
a

Fusions were between lacZ and the regulatory region upstream of pucA, pucF, pucH, pucI, pucJ, pucR, or gde integrated at the amyE locus of the wild-type B. subtilis strain and a pucR derivative grown under different nitrogen conditions. Cells were grown in glucose minimal medium supplemented with the indicated nitrogen source.