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. Author manuscript; available in PMC: 2021 Apr 1.
Published in final edited form as: Mol Microbiol. 2020 Feb 5;113(4):841–858. doi: 10.1111/mmi.14449

Table 3.

Expression of lacZ fusions in B. subtilis cells

Strain Fusion type Genotype (codY allele) Additions to the medium β-galactosidase activity (Miller units)
BB2505 bcaPbs codY+bs none 53.9
ILV 7.44
13 aa 13.6
13 aa + ILV 0.14
BB3781 codY+lm none 33.7
ILV 6.90
13 aa 6.03
13 aa + ILV 0.13
BB2548 codY::spc none 119.0
13 aa + ILV 137.0
BB2770 ybgEbs codY+bs none 19.2
ILV 3.49
13 aa 11.7
13 aa + ILV 1.12
BB3782 codY+lm none 14.4
ILV 5.92
13 aa 9.48
13 aa + ILV 1.00
BB2771 codY::spc none 268.0
13 aa + ILV 428.0
BB3776 gdhAlm codY+bs none 676.1
ILV 660.9
13 aa 490.1
13 aa + ILV 236.6
BB3784 codY+lm none 655.2
ILV 635.1
13 aa 516.8
13 aa + ILV 221.8
BB3778 codY::spc none 689.3
13 aa + ILV 636.1

Cells were grown in TSS glucose-ammonium medium with or without mixtures of ILV or 13 aa or both (see Experimental procedures). β-Galactosidase specific activity was assayed and expressed in Miller units. All values are averages of at least two experiments, and the relative standard errors of the mean did not exceed 20%. Some data for the bcaP283-lacZ and ybgE292-lacZ fusions in a wild-type and codY::spc mutant strains were published previously (Belitsky and Sonenshein, 2011).